ID: 127276074 | NANOG hESC enhancer GRCh37_chr2:234125377-234125936 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233216731..233217290) | | |
ID: 127276073 | H3K4me1 hESC enhancer GRCh37_chr2:234072305-234072918 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233163659..233164272) | | |
ID: 127276072 | H3K4me1 hESC enhancer GRCh37_chr2:233993677-233994176 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233128967..233129466) | | |
ID: 127276071 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:233989436-233989982 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233124726..233125272) | | |
ID: 127276070 | H3K4me1 hESC enhancer GRCh37_chr2:233988888-233989435 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233124178..233124725) | | |
ID: 127276069 | H3K27ac hESC enhancer GRCh37_chr2:233987251-233987751 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233122541..233123041) | | |
ID: 127276068 | H3K4me1 hESC enhancer GRCh37_chr2:233982267-233982860 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233117557..233118150) | | |
ID: 127276067 | H3K4me1 hESC enhancer GRCh37_chr2:233972623-233973122 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233107913..233108412) | | |
ID: 127276066 | H3K4me1 hESC enhancer GRCh37_chr2:233972121-233972622 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233107411..233107912) | | |
ID: 127276065 | H3K4me1 hESC enhancer GRCh37_chr2:233953501-233954000 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233088791..233089290) | | |
ID: 127276064 | H3K4me1 hESC enhancer GRCh37_chr2:233937995-233938700 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233073285..233073990) | | |
ID: 127276063 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:233927377-233927970 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233062647..233063260) | | |
ID: 127276062 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:233926783-233927376 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233062073..233062666) | | |
ID: 126806555 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr2:234155927-234157126 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233247281..233248480) | | |
ID: 122861316 | Sharpr-MPRA regulatory region 10619 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233084539..233084833) | | |
ID: 106480930 | RNA, 7SL, cytoplasmic 32, pseudogene [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233205199..233205479) | | |
ID: 101928881 | uncharacterized LOC101928881 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233012614..233015885) | | |
ID: 25791 | neuronal guanine nucleotide exchange factor [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (232878701..233013256, complement) | ARHGEF27, EPHEXIN | 605991 |
ID: 4759 | neuraminidase 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233032672..233035057) | SIAL2 | 605528 |
ID: 3635 | inositol polyphosphate-5-phosphatase D [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (233060342..233207903) | SHIP, SHIP-1, SHIP1, SIP-145, hp51CN, p150Ship | 601582 |