Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:6640646-6641070 | Common:7; Rare:126 | ||||
chr17:6651574-6651689 | Common:1; Rare:38 | ||||
chr17:7012300-7012737 | Rare:140 | ||||
chr17:7221425-7221549 | Common:7; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
chr17:7251967-7252308 | Common:1; Rare:132 | ||||
chr17:7308679-7308971 | Rare:63 | ||||
chr17:7484229-7484371 | Common:1; Rare:58 | ||||
chr17:7484504-7484834 | Common:2; Rare:130 | ||||
chr17:7583542-7583865 | Common:1; Rare:132; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:7687468-7687558 | Rare:21 | ||||
chr17:7857467-7857735 | Common:2; Rare:84 | ||||
chr17:7885519-7885653 | Rare:27 | ||||
chr17:7931906-7932248 | Common:5; Rare:94 | ||||
chr17:8162884-8163081 | Rare:63 | ||||
chr17:8176354-8176455 | Rare:32 |