ID: 130060550 | ATAC-STARR-seq lymphoblastoid silent region 8340 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28406054..28406393) | | |
ID: 130060549 | ATAC-STARR-seq lymphoblastoid silent region 8339 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28405694..28405853) | | |
ID: 130060548 | ATAC-STARR-seq lymphoblastoid active region 11926 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28398496..28398585) | | |
ID: 130060547 | ATAC-STARR-seq lymphoblastoid active region 11925 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28384947..28385016) | | |
ID: 130060546 | ATAC-STARR-seq lymphoblastoid silent region 8338 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28372077..28372246) | | |
ID: 130060545 | ATAC-STARR-seq lymphoblastoid silent region 8337 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28371427..28371756) | | |
ID: 129390846 | MPRA-validated peak2778 silencer [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28380056..28380256) | | |
ID: 127886334 | H3K27ac hESC enhancer GRCh37_chr17:26735385-26736225 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28408367..28409207) | | |
ID: 127886333 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:26731519-26732244 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28404501..28405226) | | |
ID: 127886332 | OCT4-NANOG hESC enhancer GRCh37_chr17:26729147-26729889 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28402129..28402871) | | |
ID: 127886331 | H3K4me1 hESC enhancer GRCh37_chr17:26724067-26724750 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28397048..28397731) | | |
ID: 127886330 | H3K4me1 hESC enhancer GRCh37_chr17:26722700-26723383 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28395681..28396364) | | |
ID: 124903964 | uncharacterized LOC124903964 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28410702..28413581) | | |
ID: 100616388 | microRNA 4723 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28360654..28360734) | mir-4723 | |
ID: 100420410 | H3 histone pseudogene 41 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28416911..28417489) | H3F3BP2, p51 | |
ID: 645832 | SEBOX homeobox [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28363506..28365199, complement) | OG-9, OG9, OG9X | 610975 |
ID: 147007 | transmembrane protein 199 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28357647..28363683) | C17orf32, CDG2P, VMA12, VPH2 | 616815 |
ID: 113235 | solute carrier family 46 member 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28394642..28406592, complement) | G21, HCP1, HsPCFT, PCFT, hPCFT | 611672 |
ID: 23098 | sterile alpha and TIR motif containing 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28371694..28404049) | HsTIR, MyD88-5, SAMD2, SARM, hSARM1 | 607732 |
ID: 7448 | vitronectin [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28367284..28370307, complement) | V75, VN, VNT | 193190 |