| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184155777-184157393 | Common:8; Rare:752 | ||||
| chr3:184174433-184174949 | Common:9; Rare:259 | ||||
| chr3:184176487-184176910 | Common:14; Rare:223 | ||||
| chr3:184185775-184186270 | Common:29; Rare:853 | ||||
| chr3:184248785-184249258 | Common:8; Rare:640; Clinvar:30; Clinvar (benign):13 | ||||
| chr3:184249414-184249814 | Common:7; Rare:671 | ||||
| chr3:184261500-184261840 | Rare:70 | ||||
| chr3:184298849-184299318 | Common:30; Rare:799 | ||||
| chr3:184314276-184314734 | Common:20; Rare:513 | ||||
| chr3:184314780-184314880 | Rare:24 | ||||
| chr3:184314923-184315323 | Common:1; Rare:233 | ||||
| chr3:184319465-184319806 | Common:3; Rare:153 | ||||
| chr3:184335490-184336091 | Common:7; Rare:344 | ||||
| chr3:184336189-184337075 | Common:15; Rare:359 | ||||
| chr3:184361481-184362370 | Common:3; Rare:566 |