| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129249492-129249659 | Common:3; Rare:48 | ||||
| chr3:129278742-129278898 | Common:4; Rare:45 | ||||
| chr3:129316284-129316340 | Rare:21 | ||||
| chr3:129439823-129440412 | Common:1; Rare:181; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:129578026-129578255 | Common:1; Rare:33 | ||||
| chr3:129893592-129893887 | Rare:129 | ||||
| chr3:130094241-130094317 | Rare:18 | ||||
| chr3:130746796-130746913 | Common:3; Rare:37 | ||||
| chr3:130893914-130894224 | Common:3; Rare:91 | ||||
| chr3:131026734-131026942 | Common:2; Rare:54 | ||||
| chr3:131381518-131381801 | Common:2; Rare:67 | ||||
| chr3:131502799-131502851 | Rare:22 | ||||
| chr3:131502860-131503004 | Common:1; Rare:62 | ||||
| chr3:132317241-132317448 | Rare:41 | ||||
| chr3:132417400-132417706 | Common:3; Rare:103 |