| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7219817-7219944 | Common:3; Rare:61; Clinvar:5; Clinvar (benign):1 | ||||
| chr17:7234362-7234648 | Common:2; Rare:133 | ||||
| chr17:7239405-7239819 | Common:4; Rare:125 | ||||
| chr17:7242246-7242536 | Common:1; Rare:94 | ||||
| chr17:7251963-7252322 | Common:1; Rare:141 | ||||
| chr17:7307245-7307746 | Common:6; Rare:140 | ||||
| chr17:7315036-7315451 | Common:4; Rare:149 | ||||
| chr17:7479551-7479730 | Rare:31 | ||||
| chr17:7484214-7484396 | Common:2; Rare:82 | ||||
| chr17:7561784-7561996 | Common:2; Rare:58 | ||||
| chr17:7573758-7573971 | Common:1; Rare:70 | ||||
| chr17:7580209-7580486 | Common:1; Rare:86 | ||||
| chr17:7583542-7583865 | Common:1; Rare:132; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584054-7584112 | Rare:16 | ||||
| chr17:7614542-7614674 | Rare:34 |