| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:93187632-93187752 | Not yet | Rare:22 | 88 | ||
| chr9:96484248-96484468 | Not yet | Common:1; Rare:28 | 139 | ||
| chr9:97687241-97687397 | Not yet | Common:1; Rare:36; Clinvar:1; Clinvar (pathogenic):1 | 109 | ||
| chr9:113256003-113256271 | Not yet | Common:1; Rare:56 | 154 | ||
| chr9:123339985-123340146 | Not yet | Rare:38 | 108 | ||
| chr9:125537994-125538283 | Not yet | Rare:47 | 130 | ||
| chr9:127818349-127818547 | Not yet | Common:1; Rare:46; Clinvar:1; Clinvar (benign):4 | 149 | ||
| chr9:127819621-127819708 | Not yet | Rare:29; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | 59 | ||
| chr9:128630168-128630342 | Not yet | Common:3; Rare:43; Clinvar (benign):3 | 99 | ||
| chr9:130712960-130713053 | Not yet | Common:1; Rare:29 | 71 | ||
| chr9:131373437-131373671 | Not yet | Common:1; Rare:55 | 151 | ||
| chr9:131483488-131483714 | Not yet | Common:1; Rare:42 | 173 | ||
| chr9:136669675-136669932 | Not yet | Common:1; Rare:71 | 134 | ||
| chr9:136839444-136839764 | Not yet | Common:1; Rare:118 | 158 | ||
| chr9:136847916-136848069 | Not yet | Rare:29 | 88 |