| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:19946974-19947468 | Common:7; Rare:182 | ||||
| chr3:20186161-20186415 | Common:2; Rare:81 | ||||
| chr3:21751097-21751370 | Common:2; Rare:87 | ||||
| chr3:23202926-23203201 | Common:1; Rare:99 | ||||
| chr3:23916880-23917236 | Rare:133 | ||||
| chr3:23917624-23917862 | Common:2; Rare:64 | ||||
| chr3:24495191-24495384 | Common:4; Rare:47 | ||||
| chr3:25428107-25428412 | Rare:69 | ||||
| chr3:25783371-25783621 | Common:2; Rare:88; Clinvar (benign):3 | ||||
| chr3:25789997-25790119 | Common:3; Rare:46 | ||||
| chr3:27369360-27369568 | Rare:44 | ||||
| chr3:28348644-28348735 | Rare:20 | ||||
| chr3:28348765-28349186 | Common:4; Rare:135 | ||||
| chr3:29280864-29281417 | Common:15; Rare:106 | ||||
| chr3:30606701-30606819 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):1 |