ID: 132090255 | Neanderthal introgressed variant-containing enhancer experimental_36264 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67367077..67367246) | | |
ID: 130055892 | ATAC-STARR-seq lymphoblastoid active region 8578 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67359784..67360583) | | |
ID: 130055891 | ATAC-STARR-seq lymphoblastoid silent region 5855 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67241047..67242016) | | |
ID: 130055890 | ATAC-STARR-seq lymphoblastoid active region 8576 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67240787..67241066) | | |
ID: 129663445 | ReSE screen-validated silencer GRCh37_chr14:67723162-67723330 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67256445..67256613) | | |
ID: 129390638 | MPRA-validated peak2181 silencer [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67277859..67278059) | | |
ID: 127827803 | H3K27ac hESC enhancer GRCh37_chr14:67825632-67826418 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67358915..67359763) | | |
ID: 125024506 | Sharpr-MPRA regulatory region 12737 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67389292..67389586) | | |
ID: 124903330 | uncharacterized LOC124903330 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67228238..67241409, complement) | | |
ID: 326276 | splicing factor 3b, subunit 4 pseudogene 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67199041..67200552) | SF3B4P | |
ID: 161142 | golgi associated RAB2 interactor family member 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67189440..67228558) | C14orf54, FAM71D, GARI-L1, GARI-L2 | 619898 |
ID: 64398 | protein associated with LIN7 1, MAGUK p55 family member [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67241435..67336061) | MPP5 | 606958 |
ID: 51382 | ATPase H+ transporting V1 subunit D [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67337872..67359804, complement) | ATP6M, VATD, VMA8 | 609398 |
ID: 26499 | pleckstrin 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67386984..67412165, complement) | | 608007 |
ID: 10243 | gephyrin [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (66508147..67735355) | GEPH, GPH, GPHRYN, HKPX1, MOCODC | 603930 |
ID: 1965 | eukaryotic translation initiation factor 2 subunit alpha [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67360328..67386516) | EIF-2, EIF-2A, EIF-2alpha, EIF2, EIF2A | 603907 |