| ID: 130061171 | ATAC-STARR-seq lymphoblastoid silent region 8702 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50520666..50520725) | | |
| ID: 130061170 | ATAC-STARR-seq lymphoblastoid silent region 8701 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50511406..50511495) | | |
| ID: 130061169 | ATAC-STARR-seq lymphoblastoid active region 12386 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50511106..50511305) | | |
| ID: 130061168 | ATAC-STARR-seq lymphoblastoid active region 12385 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50508535..50508664) | | |
| ID: 130061167 | ATAC-STARR-seq lymphoblastoid active region 12384 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50508455..50508514) | | |
| ID: 130061166 | ATAC-STARR-seq lymphoblastoid silent region 8700 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50508145..50508434) | | |
| ID: 130061165 | ATAC-STARR-seq lymphoblastoid silent region 8699 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50478626..50479115) | | |
| ID: 130061164 | ATAC-STARR-seq lymphoblastoid silent region 8697 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50397500..50397569) | | |
| ID: 129664079 | ReSE screen-validated silencer GRCh37_chr17:48557048-48557434 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50479687..50480073) | | |
| ID: 127887321 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:48546157-48547114 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50468796..50469753) | | |
| ID: 127887320 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:48545198-48546156 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50467837..50468795) | | |
| ID: 127887319 | NANOG-H3K4me1 hESC enhancer GRCh37_chr17:48508611-48509306 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50431250..50431945) | | |
| ID: 127887318 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:48503111-48503655 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50425750..50426350) | | |
| ID: 125177502 | Sharpr-MPRA regulatory region 13074 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50412268..50412562) | | |
| ID: 112533651 | Sharpr-MPRA regulatory region 9450 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50482508..50482802) | | |
| ID: 359772 | mitochondrial ribosomal protein S21 pseudogene 9 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50450469..50450735, complement) | | |
| ID: 146956 | essential meiotic structure-specific endonuclease 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50373229..50381483) | MMS4L, SLX2A | 610885 |
| ID: 84073 | MYCBP associated protein [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50507778..50531501) | AMAP-1, AMAP1 | 609835 |
| ID: 80221 | acyl-CoA synthetase family member 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50426218..50474845) | ACSMW, AVYV493 | 610465 |
| ID: 55379 | leucine rich repeat containing 59 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50381238..50397523, complement) | PRO1855, p34 | 614854 |