ID: 130059328 | ATAC-STARR-seq lymphoblastoid silent region 7671 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70288722..70288851) | | |
ID: 130059327 | ATAC-STARR-seq lymphoblastoid active region 11051 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70252157..70252346) | | |
ID: 130059326 | ATAC-STARR-seq lymphoblastoid active region 11050 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70252067..70252116) | | |
ID: 130059325 | ATAC-STARR-seq lymphoblastoid silent region 7670 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70251597..70251686) | | |
ID: 130059324 | ATAC-STARR-seq lymphoblastoid silent region 7669 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70251147..70251466) | | |
ID: 129663870 | ReSE screen-validated silencer GRCh37_chr16:70317824-70318022 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70283921..70284119) | | |
ID: 129663869 | ReSE screen-validated silencer GRCh37_chr16:70294233-70294475 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70260330..70260572) | | |
ID: 127884416 | H3K27ac hESC enhancer GRCh37_chr16:70380425-70381042 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70346522..70347147) | | |
ID: 127884415 | H3K27ac hESC enhancer GRCh37_chr16:70379806-70380424 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70345903..70346521) | | |
ID: 127884414 | H3K4me1 hESC enhancer GRCh37_chr16:70286884-70287384 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70252981..70253481) | | |
ID: 126862386 | MED14-independent group 3 enhancer GRCh37_chr16:70366483-70367682 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70332580..70333779) | | |
ID: 124903795 | small nucleolar RNA U13 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70232979..70233082, complement) | | |
ID: 112486204 | Sharpr-MPRA regulatory region 7868 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70299006..70299300) | | |
ID: 106480998 | RNA, 7SL, cytoplasmic 279, pseudogene [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70276069..70276352) | | |
ID: 100506083 | DDX19A divergent transcript [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70315640..70346747, complement) | | |
ID: 100506060 | SMG1 pseudogene 7 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70219581..70246617, complement) | | |
ID: 118460 | exosome component 6 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70246778..70251940, complement) | EAP4, MTR3, Mtr3p, hMtr3p, p11 | 606490 |
ID: 55308 | DEAD-box helicase 19A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70346903..70373383) | DDX19-DDX19L, DDX19L | |
ID: 11269 | DEAD-box helicase 19B [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70289767..70335305) | DBP5, DDX19, RNAh | 605812 |
ID: 16 | alanyl-tRNA synthetase 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70252298..70289506, complement) | AARS, CMT2N, DEE29, EIEE29, HDLS2, TTD8 | 601065 |