| ID: 132088844 | Neanderthal introgressed variant-containing enhancer experimental_58486 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4136182..4136351) | | |
| ID: 129933010 | ATAC-STARR-seq lymphoblastoid silent region 11117 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4533969..4534038) | | |
| ID: 129660576 | ReSE screen-validated silencer GRCh37_chr2:4972372-4972579 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4924782..4924989) | | |
| ID: 129660575 | ReSE screen-validated silencer GRCh37_chr2:4241556-4242093 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4193966..4194503) | | |
| ID: 127272420 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:4932007-4932507 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4884417..4884917) | | |
| ID: 127272419 | H3K27ac hESC enhancer GRCh37_chr2:4570459-4570958 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4522869..4523368) | | |
| ID: 127272418 | NANOG hESC enhancer GRCh37_chr2:4437428-4437943 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4389838..4390353) | | |
| ID: 127272417 | OCT4-NANOG hESC enhancer GRCh37_chr2:4429087-4429804 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4381497..4382214) | | |
| ID: 127272416 | OCT4-NANOG hESC enhancer GRCh37_chr2:4428368-4429086 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4380778..4381496) | | |
| ID: 127272415 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr2:4293747-4294616 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4246157..4247026) | | |
| ID: 126806112 | MED14-independent group 3 enhancer GRCh37_chr2:4827862-4829061 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4780272..4781471) | | |
| ID: 126806111 | MED14-independent group 3 enhancer GRCh37_chr2:4635935-4637134 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4588345..4589544) | | |
| ID: 126806110 | MED14-independent group 3 enhancer GRCh37_chr2:4268419-4269618 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4220829..4222028) | | |
| ID: 124900523 | uncharacterized LOC124900523 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4827001..4827155, complement) | | |
| ID: 107985841 | uncharacterized LOC107985841 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4135997..4140725, complement) | | |
| ID: 106479854 | RNA, U6 small nuclear 649, pseudogene [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4945277..4945383) | | |
| ID: 727982 | long intergenic non-protein coding RNA 1249 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4628218..4656222, complement) | | |
| ID: 442006 | nucleophosmin 1 pseudogene 48 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (4514119..4515152, complement) | | |