| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:19946974-19947412 | Common:5; Rare:164 | ||||
| chr3:21751086-21751261 | Common:1; Rare:56 | ||||
| chr3:23202938-23203207 | Common:1; Rare:91 | ||||
| chr3:23916878-23917181 | Rare:116 | ||||
| chr3:23917666-23917960 | Common:2; Rare:79; Clinvar (benign):1 | ||||
| chr3:24494738-24494906 | Rare:45 | ||||
| chr3:25428107-25428398 | Rare:66 | ||||
| chr3:25783392-25783640 | Common:2; Rare:77; Clinvar (benign):3 | ||||
| chr3:25790007-25790106 | Common:2; Rare:38 | ||||
| chr3:28348622-28348744 | Rare:28 | ||||
| chr3:28348784-28348908 | Common:1; Rare:29 | ||||
| chr3:28348994-28349185 | Common:2; Rare:54 | ||||
| chr3:29280864-29281363 | Common:14; Rare:96 | ||||
| chr3:30606754-30606958 | Common:1; Rare:63; Clinvar:5; Clinvar (benign):4 | ||||
| chr3:31532362-31532668 | Common:4; Rare:94 |