ID: 129663771 | ReSE screen-validated silencer GRCh37_chr16:15607777-15607948 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15513920..15514091) | | |
ID: 129663770 | ReSE screen-validated silencer GRCh37_chr16:15506027-15506244 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15412170..15412387) | | |
ID: 127898555 | MPV17L-BMERB1 readthrough [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15395754..15588259) | | |
ID: 127883270 | H3K27ac hESC enhancer GRCh37_chr16:15603978-15604478 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15510121..15510621) | | |
ID: 127883269 | H3K4me1 hESC enhancer GRCh37_chr16:15528749-15529371 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15434892..15435514) | | |
ID: 127525787 | phospholipase A2 group XG, pseudogene [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15358978..15362674) | | |
ID: 126862298 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr16:15587399-15588598 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15493542..15494741) | | |
ID: 112340379 | Sharpr-MPRA regulatory region 1380 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15502292..15502586) | | |
ID: 105371102 | uncharacterized LOC105371102 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15504720..15521011, complement) | | |
ID: 100288332 | nuclear pore complex interacting protein family member A5 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15363624..15381646, complement) | NPIP | |
ID: 653190 | ATP binding cassette subfamily C member 6 pseudogene 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (18571248..18598289) | | |
ID: 255027 | MPV17 mitochondrial inner membrane protein like [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15395754..15413271) | M-LPH, M-LPH1, M-LPH2, MLPH1, MLPH21, MPV17L | 618100 |
ID: 89927 | bMERB domain containing 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15434588..15588259) | C16orf45, MINP | |