| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35657681-35657817 | Common:2; Rare:84; Clinvar:11; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
| chr9:35657846-35658409 | Common:10; Rare:459; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35665165-35665313 | Common:1; Rare:55 | ||||
| chr9:35691059-35691183 | Rare:24 | ||||
| chr9:35732076-35732334 | Common:2; Rare:70 | ||||
| chr9:35732365-35732677 | Common:3; Rare:79 | ||||
| chr9:35748954-35749361 | Common:2; Rare:148 | ||||
| chr9:35814983-35815293 | Rare:79 | ||||
| chr9:36190687-36190973 | Common:1; Rare:97 | ||||
| chr9:36258386-36258629 | Common:2; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36572770-36572957 | Rare:53 | ||||
| chr9:37120110-37120615 | Common:2; Rare:160 | ||||
| chr9:37422587-37422735 | Common:2; Rare:76 | ||||
| chr9:37465239-37465576 | Common:3; Rare:108 | ||||
| chr9:37485772-37486017 | Common:2; Rare:91 |