| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:114056486-114056788 | Common:2; Rare:118 | ||||
| chr3:119498310-119498625 | Common:4; Rare:100 | ||||
| chr3:120742508-120742783 | Common:2; Rare:76 | ||||
| chr3:121834990-121835238 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122416169-122416225 | Rare:19 | ||||
| chr3:122564240-122564419 | Common:3; Rare:52 | ||||
| chr3:126084097-126084219 | Common:1; Rare:51 | ||||
| chr3:127590711-127590902 | Common:2; Rare:38 | ||||
| chr3:128052149-128052526 | Common:3; Rare:127 | ||||
| chr3:129439845-129440264 | Common:1; Rare:124; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:131026792-131026949 | Common:2; Rare:38 | ||||
| chr3:131381472-131381801 | Common:2; Rare:83 | ||||
| chr3:132659783-132659981 | Common:3; Rare:46 | ||||
| chr3:134485966-134486060 | Common:2; Rare:36 | ||||
| chr3:136862039-136862289 | Common:1; Rare:72 |