| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:214723-214879 | Common:2; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:215076-215205 | Common:3; Rare:73; Clinvar (benign):1 | ||||
| chr9:470136-470369 | Common:16; Rare:101 | ||||
| chr9:2015060-2015387 | Common:3; Rare:96 | ||||
| chr9:2017483-2017694 | Rare:61 | ||||
| chr9:2844049-2844314 | Common:5; Rare:100 | ||||
| chr9:3525990-3526115 | Common:1; Rare:64 | ||||
| chr9:3526420-3526527 | Common:2; Rare:57 | ||||
| chr9:4299962-4300257 | Common:5; Rare:109; Clinvar (benign):1 | ||||
| chr9:4662268-4662323 | Common:1; Rare:18 | ||||
| chr9:4679423-4679891 | Common:1; Rare:209 | ||||
| chr9:4741083-4741373 | Common:4; Rare:136 | ||||
| chr9:4792674-4793079 | Common:2; Rare:154 | ||||
| chr9:4793331-4793546 | Common:1; Rare:63 | ||||
| chr9:4984673-4985124 | Common:2; Rare:163 |