| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:131026720-131026968 | Common:2; Rare:64 | ||||
| chr3:131381479-131381832 | Common:2; Rare:96 | ||||
| chr3:132417177-132417534 | Common:5; Rare:117 | ||||
| chr3:132659799-132659918 | Common:3; Rare:26 | ||||
| chr3:132660057-132660340 | Common:2; Rare:59 | ||||
| chr3:132722137-132722210 | Common:1; Rare:34; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:133661796-133662033 | Rare:57 | ||||
| chr3:134485381-134485773 | Rare:92 | ||||
| chr3:134485964-134486200 | Common:2; Rare:78 | ||||
| chr3:136022528-136022779 | Common:2; Rare:44 | ||||
| chr3:136862014-136862269 | Common:1; Rare:75 | ||||
| chr3:138115570-138115772 | Common:4; Rare:49 | ||||
| chr3:138594209-138594431 | Rare:61 | ||||
| chr3:138608957-138609133 | Common:1; Rare:50 | ||||
| chr3:139389568-139389878 | Common:2; Rare:98 |