| ID: 129388911 | MPRA-validated peak3852 silencer [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127255199..127255399) | | |
| ID: 127274690 | NANOG-H3K4me1 hESC enhancer GRCh37_chr2:127966173-127966722 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127208597..127209146) | | |
| ID: 127274689 | H3K4me1 hESC enhancer GRCh37_chr2:127940541-127941097 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127182965..127183521) | | |
| ID: 127274688 | H3K4me1 hESC enhancer GRCh37_chr2:127928522-127929073 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127170946..127171497) | | |
| ID: 127274687 | H3K4me1 hESC enhancer GRCh37_chr2:127923313-127923906 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127165737..127166330) | | |
| ID: 127274686 | H3K4me1 hESC enhancer GRCh37_chr2:127922719-127923312 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127165143..127165736) | | |
| ID: 127274685 | H3K4me1 hESC enhancer GRCh37_chr2:127915365-127915865 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127157789..127158289) | | |
| ID: 127274684 | H3K4me1 hESC enhancer GRCh37_chr2:127914864-127915364 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127157288..127157788) | | |
| ID: 127274683 | H3K4me1 hESC enhancer GRCh37_chr2:127894055-127894554 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127136479..127136978) | | |
| ID: 127274682 | H3K4me1 hESC enhancer GRCh37_chr2:127893553-127894054 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127135977..127136478) | | |
| ID: 124907883 | uncharacterized LOC124907883 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127226819..127229300) | | |
| ID: 122819151 | Sharpr-MPRA regulatory region 1591 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127196953..127197247) | | |
| ID: 122819150 | Sharpr-MPRA regulatory region 2128 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127107002..127107387) | | |
| ID: 106480805 | NIFK pseudogene 9 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127170011..127170231) | MKI67IPP9 | |
| ID: 105373605 | uncharacterized LOC105373605 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127107145..127135826) | | |
| ID: 100130102 | WBP11 pseudogene 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127247703..127250284) | | |
| ID: 339761 | cytochrome P450 family 27 subfamily C member 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127183832..127220299, complement) | | 620605 |
| ID: 2071 | ERCC excision repair 3, TFIIH core complex helicase subunit [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127257290..127294144, complement) | BTF2, GTF2H, RAD25, Ssl2, TFIIH, TTD2, XPB | 133510 |
| ID: 274 | bridging integrator 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127048023..127107154, complement) | AMPH2, AMPHL, CNM2, SH3P9 | 601248 |