| ID: 132088771 | Neanderthal introgressed variant-containing enhancer experimental_53950 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159784803..159784972) | | |
| ID: 132088770 | Neanderthal introgressed variant-containing enhancer experimental_53909 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159761790..159761959) | | |
| ID: 129934998 | ATAC-STARR-seq lymphoblastoid active region 16696 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159940217..159940266) | | |
| ID: 129934997 | ATAC-STARR-seq lymphoblastoid silent region 12047 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159922001..159922110) | | |
| ID: 129934996 | ATAC-STARR-seq lymphoblastoid active region 16695 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159904228..159904307) | | |
| ID: 129934995 | ATAC-STARR-seq lymphoblastoid active region 16694 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159904038..159904087) | | |
| ID: 129934994 | ATAC-STARR-seq lymphoblastoid active region 16693 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159903768..159903817) | | |
| ID: 129934993 | ATAC-STARR-seq lymphoblastoid active region 16692 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159903668..159903717) | | |
| ID: 129934992 | ATAC-STARR-seq lymphoblastoid active region 16691 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159896559..159896798) | | |
| ID: 129934991 | ATAC-STARR-seq lymphoblastoid active region 16690 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159895739..159895918) | | |
| ID: 129934990 | ATAC-STARR-seq lymphoblastoid silent region 12045 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159894253..159894332) | | |
| ID: 129934989 | ATAC-STARR-seq lymphoblastoid active region 16689 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159891128..159891397) | | |
| ID: 129934988 | ATAC-STARR-seq lymphoblastoid active region 16688 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159891048..159891097) | | |
| ID: 129934987 | ATAC-STARR-seq lymphoblastoid silent region 12044 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159712985..159713104) | | |
| ID: 129660833 | ReSE screen-validated silencer GRCh37_chr2:160761228-160761469 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159904488..159904958) | | |
| ID: 127275108 | OCT4-NANOG hESC enhancer GRCh37_chr2:160911725-160912406 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (160055214..160055895) | | |
| ID: 127275107 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:160594100-160595092 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159737589..159738581) | | |
| ID: 127275106 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:160568592-160569258 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159711955..159712794) | | |
| ID: 127275105 | H3K4me1 hESC enhancer GRCh37_chr2:160480245-160480746 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159623734..159624235) | | |
| ID: 127275104 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:160472595-160473121 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159616084..159616637) | | |