| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:108589436-108589722 | Common:3; Rare:71 | ||||
| chr3:112561635-112561709 | Rare:25 | ||||
| chr3:112561960-112562072 | Rare:34 | ||||
| chr3:113515166-113515261 | Rare:23 | ||||
| chr3:113745962-113746381 | Common:2; Rare:151 | ||||
| chr3:114624939-114624992 | Rare:5 | ||||
| chr3:119463606-119463813 | Common:3; Rare:61 | ||||
| chr3:119468848-119468984 | Rare:46 | ||||
| chr3:119498403-119498620 | Common:3; Rare:75 | ||||
| chr3:120742508-120742782 | Common:2; Rare:76 | ||||
| chr3:121749647-121749767 | Rare:30 | ||||
| chr3:121834990-121835209 | Common:3; Rare:72; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122564239-122564421 | Common:3; Rare:53 | ||||
| chr3:122794967-122795069 | Rare:34 | ||||
| chr3:123692357-123692439 | Rare:17 |