ID: 132090403 | Neanderthal introgressed variant-containing enhancer experimental_44716 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (76695354..76695523) | | |
ID: 132090402 | Neanderthal introgressed variant-containing enhancer experimental_44671 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (76671949..76672118) | | |
ID: 127884581 | NANOG hESC enhancer GRCh37_chr16:76716883-76717434 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (76682986..76683537) | | |
ID: 126862405 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr16:76838358-76839557 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (76804461..76805660) | | |
ID: 126862404 | MED14-independent group 3 enhancer GRCh37_chr16:76749983-76751182 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (76716086..76717285) | | |
ID: 106480475 | RN7SK pseudogene 233 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (76287630..76287739) | | |
ID: 105376774 | uncharacterized LOC105376774 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (76770539..76772931) | | |
ID: 101928203 | long intergenic non-protein coding RNA 2125 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (76634998..76658478) | | |
ID: 100616172 | microRNA 4719 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (76868936..76869019) | | |
ID: 441775 | ribosomal protein L18 pseudogene 13 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (76235017..76235658, complement) | RPL18_5_1500 | |
ID: 85445 | contactin associated protein family member 4 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (76277401..76560757) | CASPR4 | 610518 |