ID: 130007904 | ATAC-STARR-seq lymphoblastoid active region 6367 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (51047772..51047851) | | |
ID: 130007903 | ATAC-STARR-seq lymphoblastoid active region 6366 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (51047602..51047721) | | |
ID: 130007902 | ATAC-STARR-seq lymphoblastoid active region 6365 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50924129..50924338) | | |
ID: 129390458 | MPRA-validated peak1733 silencer [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50981693..50981893) | | |
ID: 129390457 | MPRA-validated peak1732 silencer [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50912453..50912653) | | |
ID: 127824162 | H3K27ac hESC enhancer GRCh37_chr12:51442355-51442893 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (51048572..51049110) | | |
ID: 127824161 | H3K27ac hESC enhancer GRCh37_chr12:51441816-51442354 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (51047942..51048571) | | |
ID: 127824160 | H3K27ac hESC enhancer GRCh37_chr12:51419741-51420352 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (51025958..51026764) | | |
ID: 127824159 | H3K27ac hESC enhancer GRCh37_chr12:51419127-51419740 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (51025344..51025957) | | |
ID: 127824158 | H3K4me1 hESC enhancer GRCh37_chr12:51346409-51346909 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50952626..50953126) | | |
ID: 127824157 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:51319135-51319678 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50925352..50925895) | | |
ID: 127824156 | H3K4me1 hESC enhancer GRCh37_chr12:51251733-51252232 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50857950..50858449) | | |
ID: 127824155 | H3K4me1 hESC enhancer GRCh37_chr12:51251231-51251732 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50857448..50857949) | | |
ID: 124906973 | uncharacterized LOC124906973 [Homo sapiens (human)] | | | |
ID: 116268439 | CRISPRi-validated cis-regulatory element chr12.1615 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50901497..50902266) | | |
ID: 112163601 | Sharpr-MPRA regulatory region 4642 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50933826..50934120) | | |
ID: 106481947 | RNA, U6 small nuclear 1273, pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (51037499..51037602) | | |
ID: 106481204 | RNA, U6 small nuclear 87, pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (51014134..51014241, complement) | | |
ID: 100147826 | RNA, U7 small nuclear 39 pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (51010999..51011057) | U7.39 | |
ID: 613227 | HIG1 hypoxia inducible domain family member 1C [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50931110..50972592) | GM921 | 620803 |