| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:139291944-139291964 | Rare:1 | ||||
| chr6:139374522-139374781 | Common:1; Rare:109 | ||||
| chr6:142147079-142147290 | Common:3; Rare:77 | ||||
| chr6:143450597-143450936 | Common:1; Rare:126; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143843161-143843391 | Common:2; Rare:72 | ||||
| chr6:144095524-144095831 | Common:6; Rare:90 | ||||
| chr6:145735254-145735546 | Common:7; Rare:85; Clinvar:16; Clinvar (benign):12 | ||||
| chr6:145814753-145814950 | Common:1; Rare:98 | ||||
| chr6:145964220-145964616 | Common:1; Rare:127 | ||||
| chr6:149483148-149483217 | Rare:13 | ||||
| chr6:149484908-149485220 | Common:4; Rare:55 | ||||
| chr6:149545998-149546141 | Rare:60 | ||||
| chr6:149648584-149648833 | Common:1; Rare:75 | ||||
| chr6:149718055-149718193 | Common:3; Rare:49 | ||||
| chr6:149746488-149746617 | Common:2; Rare:63 |