ID: 127275646 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:209010074-209010697 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (208145350..208145973) | | |
ID: 127275645 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr2:209007684-209008466 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (208142960..208143742) | | |
ID: 127275644 | H3K4me1 hESC enhancer GRCh37_chr2:208996508-208997008 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (208131784..208132284) | | |
ID: 127275643 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:208976214-208976954 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (208111490..208112230) | | |
ID: 100533727 | replication factor C subunit 2 pseudogene [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (208135246..208137547, complement) | | |
ID: 100507443 | uncharacterized LOC100507443 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (208119129..208156762) | | |
ID: 200575 | crystallin gamma E, pseudogene [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (208108164..208112668, complement) | CCL, CRYG51, D2S1472, G2, CRYGEP | |
ID: 1421 | crystallin gamma D [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (208121607..208124524, complement) | CACA, CCA3, CCP, CRYG4, CTRCT4, PCC, cry-g-D | 123690 |
ID: 1420 | crystallin gamma C [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (208128137..208129828, complement) | CCL, CRYG3, CTRCT2 | 123680 |
ID: 1419 | crystallin gamma B [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (208142573..208146158, complement) | CRYG2, CTRCT39 | 123670 |
ID: 1418 | crystallin gamma A [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (208160740..208163589, complement) | CRY-g-A, CRYG1, CRYG5 | 123660 |