| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136944519-136944950 | Common:4; Rare:315 | ||||
| chr9:136949200-136949650 | Common:2; Rare:189 | ||||
| chr9:136949860-136950260 | Common:2; Rare:141 | ||||
| chr9:136981890-136982340 | Common:6; Rare:70 | ||||
| chr9:136982570-136982900 | Common:6; Rare:128 | ||||
| chr9:136992150-136992483 | Rare:182 | ||||
| chr9:136996551-136996690 | Common:2; Rare:89 | ||||
| chr9:137028138-137028413 | Common:2; Rare:140 | ||||
| chr9:137028800-137029160 | Common:6; Rare:103 | ||||
| chr9:137044496-137044807 | Common:1; Rare:65 | ||||
| chr9:137045347-137045570 | Common:2; Rare:57 | ||||
| chr9:137046014-137046299 | Common:4; Rare:128 | ||||
| chr9:137070474-137070781 | Common:4; Rare:103 | ||||
| chr9:137077287-137077535 | Common:2; Rare:71 | ||||
| chr9:137086541-137087176 | Common:5; Rare:496; Clinvar:11; Clinvar (benign):3 |