| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113056446-113056933 | Common:1; Rare:166; Clinvar:1 | ||||
| chr9:113150835-113151041 | Common:2; Rare:63 | ||||
| chr9:113221186-113221607 | Common:1; Rare:138 | ||||
| chr9:113275359-113275723 | Common:5; Rare:115; Clinvar (pathogenic):1 | ||||
| chr9:113340168-113340487 | Common:6; Rare:81 | ||||
| chr9:113376921-113377151 | Common:8; Rare:73 | ||||
| chr9:113401245-113401601 | Common:6; Rare:123; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410331-113410873 | Common:4; Rare:163 | ||||
| chr9:113463442-113463842 | Common:7; Rare:268 | ||||
| chr9:113593790-113594156 | Common:4; Rare:130 | ||||
| chr9:113875889-113876381 | Common:1; Rare:194 | ||||
| chr9:113876380-113876811 | Common:6; Rare:195 | ||||
| chr9:114387979-114388205 | Common:1; Rare:61 | ||||
| chr9:114505436-114505729 | Common:2; Rare:84 | ||||
| chr9:114587516-114587830 | Common:3; Rare:127 |