ID: 127275229 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:172291003-172291562 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171433984..171435052) | | |
ID: 127275228 | OCT4-H3K27ac hESC enhancer GRCh37_chr2:172289881-172290441 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171433371..171433931) | | |
ID: 127275227 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:172243459-172244043 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171386949..171387533) | | |
ID: 127275226 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:172242874-172243458 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171386364..171386948) | | |
ID: 127275225 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr2:172183340-172183864 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171326830..171327354) | | |
ID: 127275224 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:172175660-172176482 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171319150..171319972) | | |
ID: 127275223 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr2:172172370-172173192 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171315860..171316682) | | |
ID: 126806403 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr2:172100813-172102012 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171244303..171245502) | | |
ID: 124906093 | small integral membrane protein 26-like [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171277493..171277809) | | |
ID: 122847316 | Sharpr-MPRA regulatory region 8774 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171323979..171324273) | | |
ID: 122847315 | Sharpr-MPRA regulatory region 707 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171316759..171317053) | | |
ID: 115945201 | CRISPRi-validated cis-regulatory element chr2.5458 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171513679..171514152) | | |
ID: 107983995 | uncharacterized LOC107983995 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171244633..171264920, complement) | | |
ID: 105373737 | uncharacterized LOC105373737 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171265626..171301140, complement) | | |
ID: 644166 | ribosomal protein S26 pseudogene 20 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171374862..171375299, complement) | RPS26_7_290 | |
ID: 359774 | death associated protein 3 pseudogene 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171491417..171492129) | MRPS29P2 | |
ID: 80067 | DDB1 and CUL4 associated factor 17 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171434226..171485052) | C20orf37, C2orf37 | 612515 |
ID: 79828 | methyltransferase 8, tRNA N3-cytidine [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171315746..171434772, complement) | TIP | 609525 |