| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129249545-129249711 | Common:1; Rare:52 | ||||
| chr3:129316274-129316415 | Common:1; Rare:40 | ||||
| chr3:129439869-129440345 | Common:1; Rare:146; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893539-129893891 | Rare:138 | ||||
| chr3:130746771-130746946 | Common:3; Rare:56 | ||||
| chr3:130893905-130894263 | Common:3; Rare:105 | ||||
| chr3:131026749-131026942 | Common:2; Rare:50 | ||||
| chr3:131381496-131381801 | Common:2; Rare:76 | ||||
| chr3:131502793-131502995 | Common:1; Rare:91 | ||||
| chr3:132417200-132417534 | Common:2; Rare:102 | ||||
| chr3:132659792-132659950 | Common:3; Rare:38 | ||||
| chr3:133661837-133662021 | Rare:42 | ||||
| chr3:134374369-134374678 | Common:2; Rare:89 | ||||
| chr3:134485414-134485766 | Rare:85 | ||||
| chr3:134485957-134486092 | Common:2; Rare:49 |