| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:18857828-18858228 | Common:16; Rare:212 | ||||
| chr17:18858601-18858781 | Rare:29 | ||||
| chr17:19004038-19004450 | Common:3; Rare:178 | ||||
| chr17:19004477-19005049 | Common:8; Rare:305 | ||||
| chr17:19237060-19237600 | Common:3; Rare:174 | ||||
| chr17:19362280-19362402 | Common:1; Rare:14 | ||||
| chr17:19362563-19363245 | Common:7; Rare:325; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:19377380-19378168 | Common:22; Rare:582 | ||||
| chr17:19378098-19378589 | Common:10; Rare:548 | ||||
| chr17:19495088-19495488 | Common:8; Rare:156 | ||||
| chr17:19977582-19978078 | Common:6; Rare:482 | ||||
| chr17:19978119-19978519 | Common:1; Rare:80 | ||||
| chr17:20009117-20009517 | Common:23; Rare:389 | ||||
| chr17:20009678-20010171 | Common:2; Rare:167 | ||||
| chr17:20010110-20010600 | Common:3; Rare:217 |