ID: 130060998 | ATAC-STARR-seq lymphoblastoid silent region 8605 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44970430..44970499) | | |
ID: 130060997 | ATAC-STARR-seq lymphoblastoid silent region 8604 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44968234..44968593) | | |
ID: 130060996 | ATAC-STARR-seq lymphoblastoid active region 12267 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44947491..44947550) | | |
ID: 130060995 | ATAC-STARR-seq lymphoblastoid silent region 8603 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44911506..44911575) | | |
ID: 130060994 | ATAC-STARR-seq lymphoblastoid active region 12266 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44911186..44911295) | | |
ID: 129664056 | ReSE screen-validated silencer GRCh37_chr17:43031038-43031303 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44953670..44953935) | | |
ID: 127887033 | H3K4me1 hESC enhancer GRCh37_chr17:43039086-43039586 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44961718..44962218) | | |
ID: 127887032 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:43025111-43025630 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44947743..44948262) | | |
ID: 127887031 | H3K4me1 hESC enhancer GRCh37_chr17:42997401-42997900 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44920033..44920532) | | |
ID: 127887030 | OCT4-NANOG hESC enhancer GRCh37_chr17:42969539-42970081 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44892171..44892713) | | |
ID: 112268183 | basic proline-rich protein-like [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44970176..44988626, complement) | | |
ID: 106479373 | RNA, 7SL, cytoplasmic 405, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44883986..44884274) | | |
ID: 105371793 | uncharacterized LOC105371793 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44918719..44924797) | | |
ID: 102466734 | microRNA 6783 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44934618..44934681, complement) | hsa-mir-6783 | |
ID: 100528020 | family with sequence similarity 187 member A [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44903433..44905390) | | |
ID: 388389 | dynein axonemal assembly factor 19 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44899729..44905390) | CCDC103, CILD17, PR46b, SMH | 614677 |
ID: 146909 | kinesin family member 18B [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44924711..44947773, complement) | | 614570 |
ID: 10882 | complement C1q like 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44959693..44968303, complement) | C1QRF, C1QTNF14, CRF, CTRP14 | 611586 |
ID: 9343 | elongation factor Tu GTP binding domain containing 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44849948..44899445, complement) | MFDGA, MFDM, SNRNP116, Snrp116, Snu114, U5-116KD | 603892 |
ID: 2670 | glial fibrillary acidic protein [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44903159..44915500, complement) | ALXDRD | 137780 |