| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119437551-119437628 | Common:1; Rare:17 | ||||
| chr3:119463589-119463813 | Common:4; Rare:69 | ||||
| chr3:119468824-119469014 | Rare:68 | ||||
| chr3:119498396-119498930 | Common:4; Rare:179 | ||||
| chr3:120450892-120451319 | Rare:130 | ||||
| chr3:120742473-120742797 | Common:2; Rare:98 | ||||
| chr3:121749639-121750045 | Common:2; Rare:95 | ||||
| chr3:121834970-121835243 | Common:3; Rare:89; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122384103-122384295 | Common:4; Rare:71 | ||||
| chr3:122416002-122416230 | Common:1; Rare:75 | ||||
| chr3:122514760-122515029 | Common:3; Rare:74 | ||||
| chr3:122564231-122564429 | Common:3; Rare:58 | ||||
| chr3:122795027-122795168 | Common:3; Rare:68 | ||||
| chr3:123201730-123201985 | Common:1; Rare:81 | ||||
| chr3:123585014-123585284 | Common:1; Rare:86 |