| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:133475260-133475396 | Rare:25 | ||||
| chr3:133475714-133475932 | Common:3; Rare:23 | ||||
| chr3:133477551-133477784 | Common:1; Rare:42 | ||||
| chr3:133491058-133491323 | Rare:56 | ||||
| chr3:133492238-133492419 | Common:2; Rare:26 | ||||
| chr3:141311772-141311977 | Common:3; Rare:58 | ||||
| chr3:153163451-153163591 | Rare:34 | ||||
| chr3:153762503-153762708 | Common:3; Rare:50 | ||||
| chr3:155111454-155111581 | Common:1; Rare:16 | ||||
| chr3:155113147-155113300 | Common:1; Rare:33 | ||||
| chr3:157174851-157175253 | Common:3; Rare:174 | ||||
| chr3:168165774-168166099 | Common:1; Rare:52 | ||||
| chr3:169765051-169765192 | Rare:64; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr3:169932205-169932410 | Common:2; Rare:45 | ||||
| chr3:169940460-169940713 | Common:3; Rare:39 |