| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34665373-34665665 | Rare:94 | ||||
| chr9:35072336-35072675 | Rare:90; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35162286-35162298 | Rare:3 | ||||
| chr9:35489922-35490139 | Common:2; Rare:61 | ||||
| chr9:35563863-35563969 | Rare:35 | ||||
| chr9:35619533-35619704 | Rare:38 | ||||
| chr9:35646835-35646961 | Rare:25 | ||||
| chr9:35657841-35658440 | Common:11; Rare:472; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 | ||||
| chr9:35689702-35690120 | Common:4; Rare:129; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35691110-35691225 | Common:1; Rare:27 | ||||
| chr9:35703791-35704054 | Common:1; Rare:74 | ||||
| chr9:35731983-35732326 | Common:2; Rare:86 | ||||
| chr9:35732365-35732676 | Common:2; Rare:79 | ||||
| chr9:35748982-35749369 | Common:2; Rare:143 | ||||
| chr9:35814983-35815275 | Rare:74 |