| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111599389-111599726 | Common:1; Rare:77 | ||||
| chr9:111661484-111661703 | Common:3; Rare:61 | ||||
| chr9:112333576-112333945 | Rare:119 | ||||
| chr9:112379770-112380150 | Common:4; Rare:147 | ||||
| chr9:113150641-113151024 | Common:5; Rare:86 | ||||
| chr9:113221230-113221612 | Common:1; Rare:121 | ||||
| chr9:113275359-113275745 | Common:5; Rare:125; Clinvar (pathogenic):1 | ||||
| chr9:113410281-113410705 | Common:3; Rare:125 | ||||
| chr9:114587565-114587910 | Common:3; Rare:136 | ||||
| chr9:115118140-115118435 | Rare:69 | ||||
| chr9:116687228-116687361 | Common:1; Rare:43; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120793242-120793538 | Common:2; Rare:108 | ||||
| chr9:120842905-120843095 | Common:1; Rare:66 | ||||
| chr9:120877148-120877518 | Common:3; Rare:127 | ||||
| chr9:121074858-121074969 | Rare:54 |