| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113275359-113275728 | Common:5; Rare:118; Clinvar (pathogenic):1 | ||||
| chr9:113376921-113377124 | Common:8; Rare:68 | ||||
| chr9:113410301-113410715 | Common:3; Rare:121 | ||||
| chr9:114587447-114587893 | Common:4; Rare:158 | ||||
| chr9:116687203-116687330 | Common:2; Rare:44 | ||||
| chr9:120793257-120793507 | Common:1; Rare:87 | ||||
| chr9:120842917-120843107 | Common:1; Rare:63 | ||||
| chr9:120877186-120877466 | Common:1; Rare:90 | ||||
| chr9:121074851-121074959 | Rare:54 | ||||
| chr9:121201840-121202156 | Common:2; Rare:89 | ||||
| chr9:122159725-122159898 | Rare:59 | ||||
| chr9:122264810-122264925 | Common:1; Rare:32 | ||||
| chr9:122905276-122905503 | Common:1; Rare:100 | ||||
| chr9:122931490-122931667 | Common:3; Rare:33 | ||||
| chr9:124415412-124415539 | Common:1; Rare:57 |