| 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: 129664055 | ReSE screen-validated silencer GRCh37_chr17:42943931-42944112 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44866563..44866744) | | |
| 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: 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: 51751 | HIG1 hypoxia inducible domain family member 1B [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44844860..44850476) | CLST11240, CLST11240-15 | 620420 |
| 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 |