| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:80677895-80678107 | Common:1; Rare:47 | ||||
| chr3:105798682-105798878 | Rare:51 | ||||
| chr3:105802273-105802382 | Rare:26 | ||||
| chr3:106255932-106256314 | Common:4; Rare:71 | ||||
| chr3:107240566-107240724 | Rare:66 | ||||
| chr3:107325641-107325671 | Rare:8 | ||||
| chr3:111739380-111739444 | Rare:13 | ||||
| chr3:125055000-125055176 | Common:2; Rare:23 | ||||
| chr3:133466616-133466800 | Common:2; Rare:26 | ||||
| chr3:134912186-134912525 | Common:1; Rare:61 | ||||
| chr3:150091104-150091279 | Rare:32 | ||||
| chr3:157174870-157175223 | Common:3; Rare:154 | ||||
| chr3:169764989-169765300 | Common:1; Rare:111; Clinvar:7; Clinvar (pathogenic):3 | ||||
| chr3:169932052-169932343 | Common:2; Rare:55 | ||||
| chr3:184756301-184756547 | Common:3; Rare:42 |