| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:131676833-131676982 | Common:2; Rare:40 | ||||
| chr9:132897541-132897815 | Common:7; Rare:62; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr9:132901659-132901949 | Common:3; Rare:55; Clinvar:3; Clinvar (benign):6 | ||||
| chr9:133126326-133126508 | Common:1; Rare:25 | ||||
| chr9:133127528-133127762 | Common:1; Rare:51 | ||||
| chr9:134025172-134025522 | Common:17; Rare:109 | ||||
| chr9:134372896-134373148 | Rare:52 | ||||
| chr9:134753781-134753894 | Common:3; Rare:33; Clinvar:2; Clinvar (benign):5 | ||||
| chr9:136094161-136094275 | Rare:31 | ||||
| chr9:136311615-136311741 | Rare:16 | ||||
| chr9:136418331-136418590 | Common:3; Rare:64 | ||||
| chr9:136441798-136441893 | Common:2; Rare:34 | ||||
| chr9:136644469-136644576 | Common:1; Rare:24 | ||||
| chr9:136664731-136665017 | Common:1; Rare:69 | ||||
| chr9:136670744-136671008 | Common:1; Rare:70 |