ID: 127892709 | H3K27ac hESC enhancer GRCh37_chr20:19998307-19998807 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (20017663..20018163) | | |
ID: 127892708 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:19973649-19974520 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (19993005..19993876) | | |
ID: 127892707 | H3K27ac hESC enhancer GRCh37_chr20:19961489-19961988 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (19980845..19981344) | | |
ID: 127892706 | H3K27ac hESC enhancer GRCh37_chr20:19960987-19961488 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (19980343..19980844) | | |
ID: 127892705 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr20:19939385-19940116 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (19958741..19959472) | | |
ID: 127892704 | H3K4me1 hESC enhancer GRCh37_chr20:19938653-19939384 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (19958009..19958740) | | |
ID: 127892703 | H3K4me1 hESC enhancer GRCh37_chr20:19866384-19866884 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (19885740..19886240) | | |
ID: 127892702 | H3K4me1 hESC enhancer GRCh37_chr20:19819023-19819524 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (19838379..19838880) | | |
ID: 127892701 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr20:19739291-19739865 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (19758647..19759221) | | |
ID: 127892700 | H3K4me1 hESC enhancer GRCh37_chr20:19691947-19692447 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (19711303..19711803) | | |
ID: 127892699 | H3K27ac hESC enhancer GRCh37_chr20:19659231-19660207 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (19678587..19679563) | | |
ID: 127892698 | NANOG-H3K27ac hESC enhancer GRCh37_chr20:19658252-19659230 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (19677608..19678586) | | |
ID: 126862992 | MED14-independent group 3 enhancer GRCh37_chr20:19999269-20000468 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (20018625..20019824) | | |
ID: 124908104 | translation initiation factor IF-2-like [Homo sapiens (human)] | | | |
ID: 121627896 | Sharpr-MPRA regulatory region 11499 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (19802445..19802739) | | |
ID: 100421663 | cutaneous T cell lymphoma-associated antigen 1 pseudogene [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (19809088..19810021) | | |
ID: 85824 | ribosomal protein L12 pseudogene 12 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (19823407..19824031, complement) | RPL12L3, RPL12_16_1689, dJ999L4.1 | |
ID: 57419 | solute carrier family 24 member 3 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (19212642..19722926) | NCKX3 | 609839 |
ID: 54453 | Ras and Rab interactor 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (19757599..20002456) | MACS, RASSF4 | 610222 |
ID: 51126 | N-alpha-acetyltransferase 20, NatB catalytic subunit [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (20017290..20033655) | MRT73, NAT3, NAT3P, NAT5, NAT5P, dJ1002M8.1 | 610833 |