| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129249503-129249690 | Common:3; Rare:53 | ||||
| chr3:129278761-129278882 | Common:4; Rare:40 | ||||
| chr3:129439861-129440335 | Common:1; Rare:145; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893580-129893871 | Rare:126 | ||||
| chr3:130746753-130746934 | Common:3; Rare:55 | ||||
| chr3:130893919-130894237 | Common:3; Rare:91 | ||||
| chr3:131026735-131026962 | Common:2; Rare:58 | ||||
| chr3:131381478-131381825 | Common:2; Rare:93 | ||||
| chr3:131502869-131503004 | Common:1; Rare:58 | ||||
| chr3:134485687-134485772 | Rare:35 | ||||
| chr3:134485950-134486060 | Common:3; Rare:46 | ||||
| chr3:136862032-136862277 | Common:1; Rare:68 | ||||
| chr3:138834874-138835013 | Rare:42 | ||||
| chr3:139389608-139389876 | Common:2; Rare:82 | ||||
| chr3:140941514-140941878 | Common:3; Rare:119 |