| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7219817-7220074 | Common:7; Rare:188; Clinvar:12; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr17:7234164-7234727 | Common:6; Rare:539 | ||||
| chr17:7237577-7238010 | Common:5; Rare:337 | ||||
| chr17:7238234-7240146 | Common:24; Rare:1019 | ||||
| chr17:7240633-7241623 | Common:5; Rare:470 | ||||
| chr17:7241766-7241965 | Common:6; Rare:103 | ||||
| chr17:7242265-7242606 | Common:3; Rare:277 | ||||
| chr17:7242737-7243167 | Common:4; Rare:238 | ||||
| chr17:7251540-7252441 | Common:12; Rare:632 | ||||
| chr17:7260994-7261347 | Common:6; Rare:231 | ||||
| chr17:7261448-7261858 | Common:4; Rare:138 | ||||
| chr17:7262271-7262856 | Common:9; Rare:268 | ||||
| chr17:7263175-7263395 | Common:3; Rare:136 | ||||
| chr17:7263523-7263923 | Common:2; Rare:131 | ||||
| chr17:7281255-7281821 | Common:9; Rare:420 |