| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:113746989-113747093 | Common:3; Rare:14 | ||||
| chr3:114056481-114056816 | Common:2; Rare:129 | ||||
| chr3:114624915-114625024 | Common:1; Rare:17 | ||||
| chr3:115100256-115100400 | Rare:22 | ||||
| chr3:119436929-119437033 | Rare:27 | ||||
| chr3:119463591-119463780 | Common:4; Rare:55 | ||||
| chr3:119468826-119469018 | Rare:73 | ||||
| chr3:119498406-119498638 | Common:3; Rare:80 | ||||
| chr3:120094436-120094567 | Common:1; Rare:54 | ||||
| chr3:120596158-120596457 | Common:1; Rare:116 | ||||
| chr3:120742500-120742777 | Common:2; Rare:78 | ||||
| chr3:121749631-121750021 | Common:1; Rare:89 | ||||
| chr3:121834977-121835231 | Common:3; Rare:82; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383192-122383323 | Common:1; Rare:41 | ||||
| chr3:122384030-122384268 | Rare:84 |