ID: 127827811 | H3K27ac hESC enhancer GRCh37_chr14:68161998-68162634 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67695281..67695917) | | |
ID: 124907417 | uncharacterized LOC124907417 [Homo sapiens (human)] | | | |
ID: 124903331 | uncharacterized LOC124903331 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67625867..67639713, complement) | | |
ID: 112272549 | Sharpr-MPRA regulatory region 4541 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67680992..67681286) | | |
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: 100420100 | high mobility group box 1 pseudogene 34 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67615484..67616094) | | |
ID: 100419668 | protein kinase C eta pseudogene [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67610986..67613873) | | |
ID: 319098 | cytochrome c oxidase subunit 7A2 pseudogene 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67652229..67652629, complement) | COX7A3P, COX7AP1 | |
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: 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 |
ID: 10243 | gephyrin [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (66508147..67735355) | GEPH, GPH, GPHRYN, HKPX1, MOCODC | 603930 |
ID: 384 | arginase 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67619920..67651708) | | 107830 |