| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97803330-97803720 | Common:3; Rare:202 | ||||
| chr9:97853910-97854270 | Rare:197; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr9:98010951-98011540 | Rare:212 | ||||
| chr9:98867740-98868050 | Common:3; Rare:45 | ||||
| chr9:98929650-98930220 | Common:2; Rare:134 | ||||
| chr9:99819860-99820280 | Common:3; Rare:195 | ||||
| chr9:100411624-100412024 | Common:9; Rare:182 | ||||
| chr9:104968250-104968610 | Common:6; Rare:182 | ||||
| chr9:104991470-104991980 | Common:9; Rare:218 | ||||
| chr9:107504600-107505116 | Common:7; Rare:184 | ||||
| chr9:107548330-107548700 | Common:8; Rare:116 | ||||
| chr9:107734405-107734971 | Common:8; Rare:141 | ||||
| chr9:107749730-107750060 | Rare:112 | ||||
| chr9:111482630-111483050 | Common:6; Rare:151 | ||||
| chr9:111728560-111728960 | Rare:93 |