| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:114625032-114625146 | Rare:20 | ||||
| chr3:115100181-115100404 | Rare:39 | ||||
| chr3:115100518-115100529 | Rare:1 | ||||
| chr3:115147226-115147667 | Common:5; Rare:116 | ||||
| chr3:119240850-119241060 | Common:1; Rare:59 | ||||
| chr3:119294144-119294464 | Rare:62; Clinvar:1 | ||||
| chr3:119294523-119294699 | Rare:35; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:119436855-119437071 | Rare:51 | ||||
| chr3:119462117-119462268 | Common:1; Rare:17 | ||||
| chr3:119468826-119469024 | Common:1; Rare:75 | ||||
| chr3:119498412-119498723 | Common:4; Rare:99 | ||||
| chr3:119498792-119498846 | Rare:16 | ||||
| chr3:119498853-119498891 | Rare:17 | ||||
| chr3:119676909-119677061 | Common:8; Rare:44 | ||||
| chr3:119677249-119677523 | Common:1; Rare:106 |