ID: 130060934 | ATAC-STARR-seq lymphoblastoid silent region 8550 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43025055..43025194) | | |
ID: 129664047 | ReSE screen-validated silencer GRCh37_chr17:41224055-41224260 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43072038..43072243) | | |
ID: 127886932 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:41311429-41311959 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43159412..43159942) | | |
ID: 127886931 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr17:41298599-41299208 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43146582..43147191) | | |
ID: 127886930 | OCT4-NANOG hESC enhancer GRCh37_chr17:41214996-41215531 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43062979..43063514) | | |
ID: 127886929 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:41195058-41195600 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43043041..43043583) | | |
ID: 126862571 | BRD4-independent group 4 enhancer GRCh37_chr17:41243136-41244335 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43091119..43092318) | | |
ID: 125177482 | Sharpr-MPRA regulatory region 8675 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43036292..43036586) | | |
ID: 111589216 | BRCA1 intron 2 regulatory region [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43119737..43120061) | | |
ID: 111589215 | BRCA1 promoter region [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43124495..43127556) | | |
ID: 110485085 | BRCA1P1 intergenic recombination region [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43156563..43157234) | | |
ID: 110485084 | BRCA1 intronic recombination region [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43119629..43120300) | | |
ID: 101929767 | uncharacterized LOC101929767 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43148366..43170403, complement) | | |
ID: 100885865 | high mobility group nucleosome binding domain 1 pseudogene 29 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43144845..43145323) | | |
ID: 140660 | ribosomal protein L21 pseudogene 4 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43079261..43079816) | RPL21_58_1548 | |
ID: 10493 | vesicle amine transport 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43014607..43022385, complement) | VATI | 604631 |
ID: 10230 | neighbor of BRCA1 lncRNA 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43125557..43153671) | NCRNA00192 | 618708 |
ID: 8153 | Rho family GTPase 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43025231..43032041) | ARHN, RHO7, RhoN | 601555 |
ID: 672 | BRCA1 DNA repair associated [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43044295..43170327, complement) | BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4, PPP1R53, PSCP, RNF53 | 113705 |