Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42017388-42017482 | Rare:41 | ||||
chr17:42115946-42116147 | Rare:37 | ||||
chr17:42458738-42458906 | Common:1; Rare:67 | ||||
chr17:42535960-42536266 | Common:3; Rare:87; Clinvar:8; Clinvar (benign):2 | ||||
chr17:42577685-42577844 | Rare:76 | ||||
chr17:42609253-42609715 | Common:9; Rare:194; Clinvar (benign):1 | ||||
chr17:42681841-42681942 | Rare:22 | ||||
chr17:42773392-42773499 | Rare:35 | ||||
chr17:42834331-42834544 | Common:2; Rare:56 | ||||
chr17:42964425-42964518 | Rare:47 | ||||
chr17:42998126-42998461 | Common:3; Rare:87 | ||||
chr17:43125362-43125664 | Rare:64; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43170205-43170502 | Common:2; Rare:67 | ||||
chr17:43171024-43171258 | Rare:75 | ||||
chr17:43211750-43211906 | Common:1; Rare:35 |