| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:100429423-100429614 | Rare:31 | ||||
| chr9:101398580-101398855 | Rare:96 | ||||
| chr9:101533680-101533943 | Common:1; Rare:81 | ||||
| chr9:104093988-104094369 | Common:5; Rare:93 | ||||
| chr9:104747570-104747757 | Rare:48 | ||||
| chr9:105447966-105448144 | Common:2; Rare:64 | ||||
| chr9:105558079-105558159 | Rare:22; Clinvar (benign):1 | ||||
| chr9:108934063-108934484 | Common:7; Rare:166; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:110256418-110256611 | Common:1; Rare:73 | ||||
| chr9:112333530-112333910 | Rare:115 | ||||
| chr9:112379834-112380146 | Common:3; Rare:129 | ||||
| chr9:113221262-113221620 | Rare:111 | ||||
| chr9:113275376-113275734 | Common:5; Rare:114; Clinvar (pathogenic):1 | ||||
| chr9:113410428-113410772 | Common:3; Rare:97 | ||||
| chr9:113517124-113517304 | Common:1; Rare:39 |