ID: 128966723 | nuclear pore complex-interacting protein family member A5-like [Homo sapiens (human)] | | | |
ID: 127883600 | H3K4me1 hESC enhancer GRCh37_chr16:29393875-29394494 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29382554..29383173) | | |
ID: 127883599 | H3K4me1 hESC enhancer GRCh37_chr16:29393253-29393874 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29381932..29382553) | | |
ID: 127883598 | H3K4me1 hESC enhancer GRCh37_chr16:29340729-29341590 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29329408..29330269) | | |
ID: 127883597 | H3K4me1 hESC enhancer GRCh37_chr16:29339867-29340728 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29328546..29329407) | | |
ID: 127883435 | H3K27ac hESC enhancer GRCh37_chr16:22593503-22594003 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (22582182..22582682) | | |
ID: 124905419 | small nucleolar RNA U13 [Homo sapiens (human)] | | | |
ID: 124903796 | small nucleolar RNA U13 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29437497..29437600, complement) | | |
ID: 112268378 | zinc finger protein ENSP00000375192-like [Homo sapiens (human)] | | | |
ID: 112268175 | uncharacterized LOC112268175 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (22577464..22608063, complement) | | |
ID: 107282092 | BOLA2-SMG1P6 readthrough [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29442905..29454964, complement) | | |
ID: 100505915 | uncharacterized LOC100505915 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15094411..15109197) | | |
ID: 100422558 | SMG1 pseudogene 6 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29425411..29447026, complement) | | |
ID: 728888 | nuclear pore complex interacting protein family member B11 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29381167..29406711, complement) | NPIP | |
ID: 653786 | OTOA pseudogene 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (22545698..22576865) | | |
ID: 606724 | coronin 1A pseudogene [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29449345..29449915) | | |
ID: 440352 | sorting nexin 29 pseudogene 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29302287..29365059) | RUNDC2C | |