| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41785922-41786201 | Common:1; Rare:88 | ||||
| chr17:41786370-41786746 | Common:3; Rare:81; Clinvar:3; Clinvar (benign):4 | ||||
| chr17:41810992-41811222 | Common:1; Rare:159 | ||||
| chr17:41812584-41813263 | Common:6; Rare:309; Clinvar:16 | ||||
| chr17:41836174-41836322 | Rare:81 | ||||
| chr17:41865351-41865559 | Rare:156 | ||||
| chr17:41918887-41919331 | Common:4; Rare:295; Clinvar:2 | ||||
| chr17:41930320-41930800 | Common:1; Rare:187 | ||||
| chr17:41966579-41966870 | Common:3; Rare:189 | ||||
| chr17:42017040-42017310 | Rare:102 | ||||
| chr17:42017379-42017596 | Common:2; Rare:136 | ||||
| chr17:42017720-42018090 | Common:2; Rare:175 | ||||
| chr17:42019970-42020186 | Common:2; Rare:118 | ||||
| chr17:42121250-42121413 | Common:1; Rare:58 | ||||
| chr17:42154893-42155273 | Common:7; Rare:186 |