| ID: 130056092 | ATAC-STARR-seq lymphoblastoid active region 8726 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74303023..74303382) | | |
| ID: 130056091 | ATAC-STARR-seq lymphoblastoid silent region 5929 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74302683..74302762) | | |
| ID: 130056090 | ATAC-STARR-seq lymphoblastoid silent region 5928 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74257531..74257710) | | |
| ID: 130056089 | ATAC-STARR-seq lymphoblastoid silent region 5927 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74251628..74251787) | | |
| ID: 129390646 | MPRA-validated peak2199 silencer [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74202173..74202373) | | |
| ID: 127827966 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:74758461-74759313 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74291758..74292610) | | |
| ID: 127827965 | H3K27ac hESC enhancer GRCh37_chr14:74732232-74732732 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74265529..74266029) | | |
| ID: 127827964 | H3K4me1 hESC enhancer GRCh37_chr14:74712311-74712812 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74245608..74246109) | | |
| ID: 127827963 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:74707503-74708468 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74240800..74241765) | | |
| ID: 112268141 | small ubiquitin-related modifier 2-like [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74191896..74193277) | | |
| ID: 105370564 | uncharacterized LOC105370564 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74208861..74217764, complement) | | |
| ID: 100287680 | SUB1 pseudogene 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74305423..74306063) | | |
| ID: 338917 | visual system homeobox 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74239449..74262738) | CHX10, HOX10, MCOP2, MCOPCB3, RET1 | 142993 |
| ID: 91750 | lin-52 DREAM MuvB core complex component [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74084956..74201493) | C14orf46, c14_5549 | |
| ID: 55237 | vertebrae development associated [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74302993..74360008) | C14orf115, vertnin | 620468 |
| ID: 5826 | ATP binding cassette subfamily D member 4 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74285269..74302934, complement) | ABC41, EST352188, MAHCJ, P70R, P79R, PMP69, PXMP1L | 603214 |