ID: 130055909 | ATAC-STARR-seq lymphoblastoid active region 8585 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67696032..67696081) | | |
ID: 130055908 | ATAC-STARR-seq lymphoblastoid active region 8584 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67695962..67696011) | | |
ID: 130055907 | ATAC-STARR-seq lymphoblastoid silent region 5866 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67694872..67694931) | | |
ID: 130055906 | ATAC-STARR-seq lymphoblastoid silent region 5865 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67680311..67680410) | | |
ID: 130055905 | ATAC-STARR-seq lymphoblastoid silent region 5864 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67674517..67674956) | | |
ID: 130055904 | ATAC-STARR-seq lymphoblastoid silent region 5863 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67674307..67674416) | | |
ID: 130055903 | ATAC-STARR-seq lymphoblastoid silent region 5862 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67668795..67668844) | | |
ID: 130055902 | ATAC-STARR-seq lymphoblastoid silent region 5861 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67668655..67668784) | | |
ID: 127827812 | H3K4me1 hESC enhancer GRCh37_chr14:68195910-68196540 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67729193..67729823) | | |
ID: 127827811 | H3K27ac hESC enhancer GRCh37_chr14:68161998-68162634 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67695281..67695917) | | |
ID: 112272549 | Sharpr-MPRA regulatory region 4541 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67680992..67681286) | | |
ID: 106480979 | RNA, 7SL, cytoplasmic 213, pseudogene [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67751228..67751544, complement) | | |
ID: 106480694 | RNA, 7SL, cytoplasmic 369, pseudogene [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67705954..67706252) | | |
ID: 100873641 | RNA, 5S ribosomal pseudogene 386 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67657105..67657211, complement) | RN5S386 | |
ID: 100421541 | DnaJ heat shock protein family (Hsp40) member C9 pseudogene [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67799004..67799806) | | |
ID: 283562 | ribosomal protein L21 pseudogene 9 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67714505..67715225) | | |
ID: 145226 | retinol dehydrogenase 12 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67701886..67734451) | LCA13, RP53, SDR7C2 | 608830 |
ID: 51109 | retinol dehydrogenase 11 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67676800..67695764, complement) | ARSDR1, CGI82, HCBP12, MDT1, PSDR1, RALR1, RDJCSS, SCALD, SDR7C1 | 607849 |
ID: 23503 | zinc finger FYVE-type containing 26 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67728892..67816590, complement) | FYVE-CENT, SPG15 | 612012 |
ID: 10490 | vesicle transport through interaction with t-SNAREs 1B [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67647085..67674632, complement) | VTI1, VTI1-LIKE, VTI1L, VTI2, v-SNARE, vti1-rp1 | 603207 |