Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:8162911-8163093 | Rare:62 | ||||
chr17:8176313-8176487 | Rare:55 | ||||
chr17:8248042-8248182 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
chr17:8435687-8435927 | Common:2; Rare:97 | ||||
chr17:10059777-10059939 | Common:1; Rare:29 | ||||
chr17:10697481-10697654 | Common:3; Rare:78; Clinvar:5; Clinvar (benign):2 | ||||
chr17:14069354-14069549 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
chr17:15699500-15699773 | Common:3; Rare:71 | ||||
chr17:15999593-15999761 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):3 | ||||
chr17:16217048-16217227 | Rare:37 | ||||
chr17:17281194-17281395 | Rare:81 | ||||
chr17:17591589-17591926 | Common:2; Rare:96 | ||||
chr17:17782022-17782080 | Rare:18 | ||||
chr17:18087778-18087999 | Rare:63 | ||||
chr17:18183649-18183925 | Rare:119 |