ID: 130056106 | ATAC-STARR-seq lymphoblastoid active region 8735 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (75064195..75064364) | | |
ID: 130056105 | ATAC-STARR-seq lymphoblastoid silent region 5939 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (75051080..75051269) | | |
ID: 130056104 | ATAC-STARR-seq lymphoblastoid active region 8734 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (75002468..75002557) | | |
ID: 130056103 | ATAC-STARR-seq lymphoblastoid active region 8733 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74963326..74963475) | | |
ID: 130056102 | ATAC-STARR-seq lymphoblastoid silent region 5938 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74955644..74955743) | | |
ID: 130056101 | ATAC-STARR-seq lymphoblastoid silent region 5937 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74955394..74955463) | | |
ID: 130056100 | ATAC-STARR-seq lymphoblastoid silent region 5936 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74946459..74946508) | | |
ID: 127828001 | H3K27ac hESC enhancer GRCh37_chr14:75536539-75537090 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (75069836..75070387) | | |
ID: 127828000 | H3K27ac hESC enhancer GRCh37_chr14:75535987-75536538 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (75069284..75069835) | | |
ID: 127827999 | H3K27ac hESC enhancer GRCh37_chr14:75469302-75469982 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (75002599..75003279) | | |
ID: 127827998 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:75447877-75448500 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74981174..74981797) | | |
ID: 127827997 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:75447251-75447876 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74980548..74981173) | | |
ID: 127827996 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:75446625-75447250 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74979922..74980547) | | |
ID: 126862002 | BRD4-independent group 4 enhancer GRCh37_chr14:75431938-75433137 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74965235..74966434) | | |
ID: 107984690 | uncharacterized LOC107984690 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74942729..74950227) | | |
ID: 106479870 | RNA, U6 small nuclear 689, pseudogene [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (75020761..75020867) | | |
ID: 91754 | NIMA related kinase 9 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (75079353..75127202, complement) | APUG, LCCS10, NC, NERCC, NERCC1 | 609798 |
ID: 79696 | zinc finger C2HC-type containing 1C [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (75069641..75079988) | C14orf140, FAM164C | |
ID: 27030 | mutL homolog 3 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (75013775..75051467, complement) | HNPCC7 | 604395 |
ID: 8892 | eukaryotic translation initiation factor 2B subunit beta [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (75002921..75012366) | EIF-2Bbeta, EIF2B, EIF2Bbeta, VWM2 | 606454 |