| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184182113-184182162 | Rare:11 | ||||
| chr3:184185874-184186240 | Common:4; Rare:141 | ||||
| chr3:184248869-184249021 | Rare:81; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249510-184249741 | Common:1; Rare:67 | ||||
| chr3:184298947-184299327 | Common:5; Rare:118 | ||||
| chr3:184314440-184314663 | Common:3; Rare:65 | ||||
| chr3:184320118-184320490 | Rare:73 | ||||
| chr3:184325275-184325639 | Common:1; Rare:92 | ||||
| chr3:184335855-184336035 | Rare:61 | ||||
| chr3:184361575-184361770 | Rare:52 | ||||
| chr3:184362140-184362257 | Common:1; Rare:17 | ||||
| chr3:184711915-184712243 | Common:2; Rare:108 | ||||
| chr3:184812030-184812207 | Common:2; Rare:54 | ||||
| chr3:184812319-184812441 | Common:2; Rare:26 | ||||
| chr3:185152711-185153087 | Common:5; Rare:140 |