| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129568236-129569295 | Common:3; Rare:283 | ||||
| chr9:129596719-129596888 | Common:1; Rare:31 | ||||
| chr9:129597337-129597737 | Common:2; Rare:122 | ||||
| chr9:129607556-129607956 | Common:2; Rare:123 | ||||
| chr9:129712353-129713053 | Common:10; Rare:325 | ||||
| chr9:129737812-129738247 | Common:2; Rare:129 | ||||
| chr9:129777130-129777390 | Common:1; Rare:58 | ||||
| chr9:129884490-129884683 | Rare:50 | ||||
| chr9:129962753-129963153 | Common:3; Rare:93 | ||||
| chr9:129963177-129964508 | Common:16; Rare:336 | ||||
| chr9:130101956-130102208 | Common:3; Rare:45 | ||||
| chr9:130109942-130110342 | Common:2; Rare:130 | ||||
| chr9:130138297-130138537 | Common:3; Rare:52 | ||||
| chr9:130214420-130214690 | Common:3; Rare:46 | ||||
| chr9:130681129-130681566 | Common:4; Rare:142; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 |