| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:41200071-41200122 | Rare:20 | ||||
| chr3:41224273-41224595 | Rare:76; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:41224667-41224990 | Common:1; Rare:67; Clinvar (pathogenic):1 | ||||
| chr3:41962053-41962377 | Common:4; Rare:74 | ||||
| chr3:42013536-42013762 | Common:5; Rare:70 | ||||
| chr3:42160077-42160263 | Common:2; Rare:36 | ||||
| chr3:42581889-42582137 | Common:3; Rare:78 | ||||
| chr3:42582256-42582323 | Rare:17 | ||||
| chr3:42590683-42590958 | Common:3; Rare:85 | ||||
| chr3:42600331-42600777 | Common:3; Rare:172 | ||||
| chr3:42635105-42635365 | Rare:74 | ||||
| chr3:42773215-42773334 | Common:1; Rare:34 | ||||
| chr3:42804242-42804705 | Common:2; Rare:134 | ||||
| chr3:42843695-42844030 | Common:2; Rare:43 | ||||
| chr3:43286431-43286654 | Common:2; Rare:97 |