| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:113515122-113515257 | Rare:41 | ||||
| chr3:113746129-113746348 | Common:1; Rare:88 | ||||
| chr3:113746993-113747072 | Common:3; Rare:10 | ||||
| chr3:114056530-114056850 | Common:2; Rare:108 | ||||
| chr3:119240865-119241048 | Common:1; Rare:54 | ||||
| chr3:119463598-119463817 | Common:3; Rare:66 | ||||
| chr3:119468834-119469010 | Rare:65 | ||||
| chr3:119498416-119498613 | Common:3; Rare:66 | ||||
| chr3:119677340-119677517 | Common:1; Rare:62 | ||||
| chr3:120094338-120094569 | Common:2; Rare:93 | ||||
| chr3:120596182-120596462 | Common:1; Rare:108 | ||||
| chr3:120742503-120742783 | Common:2; Rare:78 | ||||
| chr3:121545922-121546080 | Common:1; Rare:45 | ||||
| chr3:121749646-121750074 | Common:2; Rare:107 | ||||
| chr3:121834956-121835248 | Common:3; Rare:99; Clinvar:6; Clinvar (benign):2 |