| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113056657-113056833 | Common:1; Rare:63; Clinvar:1 | ||||
| chr9:113150714-113151052 | Common:4; Rare:89 | ||||
| chr9:113188015-113188173 | Common:2; Rare:19 | ||||
| chr9:113221230-113221649 | Common:1; Rare:130 | ||||
| chr9:113275204-113275351 | Rare:41 | ||||
| chr9:113275359-113275734 | Common:5; Rare:119; Clinvar (pathogenic):1 | ||||
| chr9:113340237-113340431 | Common:3; Rare:49 | ||||
| chr9:113376858-113377087 | Common:8; Rare:71 | ||||
| chr9:113401236-113401537 | Common:6; Rare:111; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410214-113410737 | Common:3; Rare:161 | ||||
| chr9:113463581-113463781 | Common:1; Rare:70 | ||||
| chr9:113565353-113565668 | Common:1; Rare:75 | ||||
| chr9:113580672-113580957 | Common:3; Rare:52 | ||||
| chr9:114387970-114388111 | Common:1; Rare:48 | ||||
| chr9:114505484-114505662 | Common:1; Rare:49 |