| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111599643-111599869 | Common:1; Rare:65 | ||||
| chr9:111661486-111661703 | Common:3; Rare:61 | ||||
| chr9:112333573-112333949 | Rare:120 | ||||
| chr9:112379834-112380146 | Common:3; Rare:129 | ||||
| chr9:112718011-112718351 | Common:2; Rare:80 | ||||
| chr9:113056649-113056879 | Common:1; Rare:75; Clinvar:1 | ||||
| chr9:113150862-113151041 | Common:1; Rare:60 | ||||
| chr9:113221230-113221628 | Common:1; Rare:126 | ||||
| chr9:113275359-113275746 | Common:5; Rare:125; Clinvar (pathogenic):1 | ||||
| chr9:113340237-113340431 | Common:3; Rare:49 | ||||
| chr9:113401242-113401523 | Common:6; Rare:105; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410289-113410729 | Common:3; Rare:133 | ||||
| chr9:114387983-114388111 | Common:1; Rare:43 | ||||
| chr9:115118007-115118274 | Common:3; Rare:61 | ||||
| chr9:116687221-116687364 | Common:3; Rare:50; Clinvar:2; Clinvar (benign):1 |