| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7223618-7224069 | Rare:144; Clinvar:16; Clinvar (benign):6; Clinvar (pathogenic):16 | ||||
| chr17:7224481-7224903 | Common:2; Rare:146; Clinvar:12; Clinvar (benign):16; Clinvar (pathogenic):4 | ||||
| chr17:7234463-7234637 | Common:2; Rare:94 | ||||
| chr17:7241777-7241885 | Common:1; Rare:25 | ||||
| chr17:7242240-7242639 | Common:1; Rare:118 | ||||
| chr17:7243005-7243121 | Common:1; Rare:63 | ||||
| chr17:7251935-7252314 | Common:2; Rare:150 | ||||
| chr17:7252485-7252720 | Common:2; Rare:88 | ||||
| chr17:7260937-7261234 | Common:1; Rare:87 | ||||
| chr17:7261379-7261529 | Rare:36 | ||||
| chr17:7262405-7262705 | Common:2; Rare:68 | ||||
| chr17:7262810-7262954 | Common:2; Rare:30 | ||||
| chr17:7262960-7263312 | Common:1; Rare:68 | ||||
| chr17:7263561-7263699 | Common:2; Rare:19 | ||||
| chr17:7263950-7264112 | Rare:30 |