| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119498710-119499060 | Rare:190 | ||||
| chr3:119677374-119677523 | Rare:49 | ||||
| chr3:119781933-119782172 | Common:2; Rare:39 | ||||
| chr3:119782454-119782854 | Common:6; Rare:113 | ||||
| chr3:120093691-120094091 | Common:6; Rare:224 | ||||
| chr3:120094287-120094742 | Common:8; Rare:266 | ||||
| chr3:120348720-120349463 | Common:8; Rare:360 | ||||
| chr3:120596067-120596371 | Common:3; Rare:99 | ||||
| chr3:120682114-120682368 | Rare:100; Clinvar:8 | ||||
| chr3:120742479-120742789 | Common:4; Rare:172 | ||||
| chr3:121749010-121749340 | Rare:78 | ||||
| chr3:121749600-121750041 | Common:3; Rare:194 | ||||
| chr3:121834956-121835241 | Common:3; Rare:93; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383164-122383345 | Common:4; Rare:107 | ||||
| chr3:122384041-122384292 | Common:6; Rare:155 |