| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113221212-113221603 | Common:1; Rare:130 | ||||
| chr9:113275376-113275745 | Common:5; Rare:120; Clinvar (pathogenic):1 | ||||
| chr9:113340243-113340375 | Common:2; Rare:31 | ||||
| chr9:113375476-113375912 | Common:5; Rare:69 | ||||
| chr9:113376728-113377118 | Common:10; Rare:110 | ||||
| chr9:113401235-113401357 | Common:4; Rare:64; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410289-113410790 | Common:4; Rare:162 | ||||
| chr9:114387949-114388119 | Common:1; Rare:53 | ||||
| chr9:114587400-114587901 | Common:4; Rare:171 | ||||
| chr9:115117986-115118237 | Common:3; Rare:58 | ||||
| chr9:116687221-116687373 | Common:3; Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:120532494-120532709 | Rare:45 | ||||
| chr9:120714458-120714704 | Common:2; Rare:74 | ||||
| chr9:120793242-120793499 | Common:1; Rare:89 | ||||
| chr9:120842890-120843281 | Common:1; Rare:130 |