| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:101677091-101677285 | Rare:70 | ||||
| chr3:101686519-101686901 | Common:2; Rare:151 | ||||
| chr3:105868976-105869184 | Common:4; Rare:89 | ||||
| chr3:108589383-108589722 | Common:3; Rare:104 | ||||
| chr3:112561593-112561697 | Rare:36 | ||||
| chr3:112561936-112562065 | Rare:35 | ||||
| chr3:113515122-113515261 | Rare:44 | ||||
| chr3:114056503-114056845 | Common:2; Rare:127 | ||||
| chr3:119463606-119463798 | Common:3; Rare:52 | ||||
| chr3:119468837-119469010 | Rare:63 | ||||
| chr3:119498371-119498659 | Common:5; Rare:97 | ||||
| chr3:119677340-119677577 | Common:1; Rare:80 | ||||
| chr3:120596160-120596354 | Common:1; Rare:63 | ||||
| chr3:120742503-120742777 | Common:2; Rare:77 | ||||
| chr3:121834987-121835231 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 |