| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:101561770-101561915 | Common:1; Rare:47 | ||||
| chr3:101686672-101686870 | Common:2; Rare:83 | ||||
| chr3:107522810-107522995 | Rare:42 | ||||
| chr3:112561623-112561702 | Rare:26 | ||||
| chr3:112561920-112562072 | Rare:46 | ||||
| chr3:113746773-113747067 | Common:4; Rare:64 | ||||
| chr3:114056500-114056778 | Common:2; Rare:111 | ||||
| chr3:120742503-120742782 | Common:2; Rare:78 | ||||
| chr3:121835051-121835231 | Common:2; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:122383199-122383345 | Common:2; Rare:42 | ||||
| chr3:122384077-122384247 | Rare:65 | ||||
| chr3:128052139-128052468 | Common:4; Rare:110 | ||||
| chr3:129183843-129184113 | Common:1; Rare:101 | ||||
| chr3:129439916-129440151 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:134485461-134485741 | Rare:65 |