| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127628949-127629263 | Common:1; Rare:102 | ||||
| chr3:127822478-127822539 | Rare:13 | ||||
| chr3:127823180-127823340 | Common:3; Rare:31 | ||||
| chr3:128052139-128052495 | Common:4; Rare:119 | ||||
| chr3:128123760-128123928 | Rare:46 | ||||
| chr3:128879385-128879675 | Common:5; Rare:138; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129161013-129161152 | Common:1; Rare:54 | ||||
| chr3:129183814-129184084 | Common:2; Rare:93 | ||||
| chr3:129249492-129249682 | Common:3; Rare:57 | ||||
| chr3:129278777-129278882 | Common:3; Rare:30 | ||||
| chr3:129316230-129316344 | Rare:57 | ||||
| chr3:129439847-129440371 | Common:1; Rare:160; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893535-129893891 | Rare:139 | ||||
| chr3:129974551-129974757 | Common:1; Rare:47 | ||||
| chr3:130746766-130746947 | Common:3; Rare:56 |