| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128726275-128726356 | Common:1; Rare:17; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:128879417-128879669 | Common:4; Rare:122; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129160994-129161466 | Common:2; Rare:150 | ||||
| chr3:129183831-129184058 | Common:2; Rare:73 | ||||
| chr3:129249552-129249657 | Common:1; Rare:31 | ||||
| chr3:129278578-129279078 | Common:5; Rare:125 | ||||
| chr3:129315765-129316098 | Common:2; Rare:101 | ||||
| chr3:129316282-129316338 | Rare:21 | ||||
| chr3:129439739-129440158 | Common:1; Rare:129; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:130746779-130746976 | Common:3; Rare:57 | ||||
| chr3:130893956-130894202 | Common:2; Rare:76 | ||||
| chr3:131026734-131026940 | Common:2; Rare:54 | ||||
| chr3:131381467-131381811 | Common:2; Rare:88 | ||||
| chr3:132417423-132417528 | Common:1; Rare:31 | ||||
| chr3:132659855-132659981 | Common:2; Rare:29 |