| ID: 132088820 | Neanderthal introgressed variant-containing enhancer experimental_56992 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217425973..217426142) | | |
| ID: 132088819 | Neanderthal introgressed variant-containing enhancer experimental_56991 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217412014..217412183) | | |
| ID: 132088818 | Neanderthal introgressed variant-containing enhancer experimental_56990 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217405981..217406150) | | |
| ID: 132088817 | Neanderthal introgressed variant-containing enhancer experimental_56989 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217404099..217404268) | | |
| ID: 132088816 | Neanderthal introgressed variant-containing enhancer experimental_56988 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217388241..217388410) | | |
| ID: 127275725 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:218199087-218199799 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217334364..217335076) | | |
| ID: 127275724 | H3K27ac hESC enhancer GRCh37_chr2:218156639-218157139 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217291916..217292416) | | |
| ID: 127275723 | H3K27ac hESC enhancer GRCh37_chr2:218156138-218156638 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217291415..217291915) | | |
| ID: 127275722 | OCT4-NANOG hESC enhancer GRCh37_chr2:218134772-218135400 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217270049..217270677) | | |
| ID: 126806510 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr2:218291011-218292210 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217426288..217427487) | | |
| ID: 126806509 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr2:218234719-218235918 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217369996..217371195) | | |
| ID: 126806508 | BRD4-independent group 4 enhancer GRCh37_chr2:218125637-218126836 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217260914..217262113) | | |
| ID: 124907981 | uncharacterized LOC124907981 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217412521..217413097) | | |
| ID: 112806078 | Sharpr-MPRA regulatory region 8768 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217331686..217331980) | | |
| ID: 106481806 | RN7SK pseudogene 43 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217251556..217251875) | | |
| ID: 105373877 | DIRC3 antisense RNA 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217282733..217344204) | | |
| ID: 101928278 | IGFBP5 antisense RNA 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (216694446..216811073) | | |
| ID: 729582 | disrupted in renal carcinoma 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (217284019..217790443, complement) | | 608262 |