| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136866238-136866515 | Common:3; Rare:108 | ||||
| chr9:136886237-136886534 | Common:2; Rare:90 | ||||
| chr9:136886940-136887240 | Common:1; Rare:85 | ||||
| chr9:136992120-136992430 | Rare:92 | ||||
| chr9:137027753-137027853 | Rare:28 | ||||
| chr9:137028130-137028570 | Common:1; Rare:122 | ||||
| chr9:137046020-137046440 | Common:2; Rare:103 | ||||
| chr9:137070513-137070830 | Common:2; Rare:67 | ||||
| chr9:137070913-137071313 | Common:1; Rare:105 | ||||
| chr9:137086660-137087136 | Common:2; Rare:199; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:137169398-137169557 | Common:1; Rare:64 | ||||
| chr9:137188519-137188752 | Common:2; Rare:113 | ||||
| chr9:137188821-137189494 | Common:4; Rare:265 | ||||
| chr9:137200730-137201062 | Common:3; Rare:96 | ||||
| chr9:137240786-137241024 | Common:1; Rare:98 |