Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:57256968-57257045 | Rare:33 | ||||
chr17:57850008-57850282 | Common:1; Rare:86 | ||||
chr17:58006336-58006720 | Common:2; Rare:105 | ||||
chr17:58006934-58007006 | Rare:9 | ||||
chr17:58007146-58007421 | Common:1; Rare:130 | ||||
chr17:58007540-58007751 | Common:1; Rare:42 | ||||
chr17:58083116-58083487 | Common:6; Rare:143 | ||||
chr17:58219185-58219375 | Common:1; Rare:76; Clinvar:5; Clinvar (benign):5 | ||||
chr17:58328763-58328941 | Common:1; Rare:50 | ||||
chr17:58352125-58352451 | Common:5; Rare:131 | ||||
chr17:58514537-58514755 | Rare:51 | ||||
chr17:58692365-58692749 | Common:3; Rare:168; Clinvar:27; Clinvar (benign):27; Clinvar (pathogenic):2 | ||||
chr17:59106695-59107141 | Common:2; Rare:148; Clinvar:4; Clinvar (benign):3 | ||||
chr17:59155101-59155357 | Common:1; Rare:72 | ||||
chr17:59155398-59155784 | Rare:97 |