| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:114624904-114625024 | Common:1; Rare:18 | ||||
| chr3:115100267-115100412 | Rare:26 | ||||
| chr3:119468834-119469004 | Rare:63 | ||||
| chr3:119498700-119498886 | Rare:67 | ||||
| chr3:119660872-119661129 | Rare:42 | ||||
| chr3:119677297-119677519 | Common:1; Rare:83 | ||||
| chr3:120093582-120093942 | Rare:108 | ||||
| chr3:120094429-120094539 | Common:2; Rare:47 | ||||
| chr3:120742511-120742788 | Common:2; Rare:77 | ||||
| chr3:121592993-121593093 | Rare:16 | ||||
| chr3:121593230-121593465 | Common:1; Rare:39 | ||||
| chr3:121749220-121749304 | Rare:21 | ||||
| chr3:121749473-121749528 | Rare:11 | ||||
| chr3:121749646-121749785 | Rare:33 | ||||
| chr3:121834956-121835231 | Common:3; Rare:89; Clinvar:6; Clinvar (benign):2 |