| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39153834-39154817 | Common:10; Rare:344 | ||||
| chr3:39383030-39384004 | Common:16; Rare:633; Clinvar:26; Clinvar (benign):10 | ||||
| chr3:39406369-39407320 | Common:58; Rare:1292 | ||||
| chr3:39408250-39408922 | Common:7; Rare:269; Clinvar (pathogenic):1 | ||||
| chr3:39809320-39809780 | Common:3; Rare:139 | ||||
| chr3:40309431-40309883 | Common:63; Rare:946 | ||||
| chr3:40309960-40310120 | Common:3; Rare:75 | ||||
| chr3:40310278-40311145 | Common:5; Rare:252 | ||||
| chr3:40386690-40387290 | Common:5; Rare:247 | ||||
| chr3:40457059-40457459 | Common:27; Rare:749 | ||||
| chr3:40457576-40457854 | Common:4; Rare:93 | ||||
| chr3:40476630-40476890 | Rare:47 | ||||
| chr3:40477012-40477600 | Common:13; Rare:371 | ||||
| chr3:40477580-40477980 | Common:5; Rare:121 | ||||
| chr3:40505660-40506170 | Rare:374 |