Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42017531-42017580 | Rare:12 | ||||
chr17:42154948-42155223 | Common:3; Rare:67 | ||||
chr17:42422997-42423290 | Common:1; Rare:95; Clinvar:3 | ||||
chr17:42458820-42458920 | Rare:31 | ||||
chr17:42577651-42577838 | Rare:89 | ||||
chr17:42609320-42609732 | Common:8; Rare:173; Clinvar (benign):2 | ||||
chr17:43125324-43125642 | Rare:82; Clinvar:3; Clinvar (benign):3 | ||||
chr17:43171003-43171274 | Common:1; Rare:92 | ||||
chr17:43398878-43398995 | Common:1; Rare:34 | ||||
chr17:43778925-43779076 | Rare:31 | ||||
chr17:44186687-44186998 | Common:1; Rare:106 | ||||
chr17:44187142-44187274 | Rare:36 | ||||
chr17:44324780-44324982 | Common:2; Rare:71 | ||||
chr17:44345072-44345321 | Rare:52; Clinvar:5; Clinvar (benign):3 | ||||
chr17:44503377-44503657 | Rare:120 |