ID: 132089896 | Neanderthal introgressed variant-containing enhancer experimental_18813 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (112705135..112705304) | | |
ID: 130006770 | ATAC-STARR-seq lymphoblastoid silent region 3908 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (113314394..113314643) | | |
ID: 130006769 | ATAC-STARR-seq lymphoblastoid active region 5536 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (112761920..112762029) | | |
ID: 129390361 | MPRA-validated peak1472 silencer [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (112734313..112734513) | | |
ID: 127822517 | OCT4-NANOG hESC enhancer GRCh37_chr11:113017979-113018497 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (113147257..113147775) | | |
ID: 127822516 | H3K4me1 hESC enhancer GRCh37_chr11:112832085-112832862 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (112961363..112962140) | | |
ID: 127822515 | H3K4me1 hESC enhancer GRCh37_chr11:112752465-112752965 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (112881742..112882242) | | |
ID: 127822514 | H3K4me1 hESC enhancer GRCh37_chr11:112748461-112748976 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (112877738..112878253) | | |
ID: 127822513 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:112693347-112694212 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (112822624..112823489) | | |
ID: 127822512 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:112692479-112693346 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (112821756..112822623) | | |
ID: 127822511 | H3K4me1 hESC enhancer GRCh37_chr11:112669341-112670018 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (112798618..112799295) | | |
ID: 127822510 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:112668663-112669340 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (112797940..112798617) | | |
ID: 126861342 | MED14-independent group 3 enhancer GRCh37_chr11:113214693-113215892 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (113343971..113345170) | | |
ID: 126861341 | BRD4-independent group 4 enhancer GRCh37_chr11:113202304-113203503 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (113331582..113332781) | | |
ID: 124902814 | TTC12 divergent transcript [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (113278437..113314456, complement) | | |
ID: 124902801 | uncharacterized LOC124902801 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (112774542..112775575, complement) | | |
ID: 124625839 | Sharpr-MPRA regulatory region 9915 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (113314667..113314961) | | |
ID: 106479095 | RNA, U7 small nuclear 187 pseudogene [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (112977353..112977420) | | |
ID: 105369498 | uncharacterized LOC105369498 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (112821285..112835437, complement) | | |
ID: 105369496 | uncharacterized LOC105369496 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (112698772..112737541, complement) | | |