| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:148996388-148996624 | Rare:77; Clinvar (pathogenic):1 | ||||
| chr3:149009013-149009285 | Common:4; Rare:49; Clinvar (pathogenic):1 | ||||
| chr3:149129447-149129718 | Common:3; Rare:116; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149375122-149375370 | Common:1; Rare:47 | ||||
| chr3:149377447-149377946 | Common:1; Rare:124 | ||||
| chr3:149657504-149657537 | Rare:7 | ||||
| chr3:149657682-149658048 | Common:3; Rare:79 | ||||
| chr3:149970740-149970830 | Rare:15 | ||||
| chr3:149970855-149971014 | Rare:86 | ||||
| chr3:150408024-150408380 | Common:2; Rare:119 | ||||
| chr3:150408539-150408667 | Rare:41 | ||||
| chr3:150408828-150409024 | Rare:58 | ||||
| chr3:150411080-150411134 | Rare:17 | ||||
| chr3:150411147-150411249 | Common:1; Rare:29 | ||||
| chr3:150456868-150457127 | Common:1; Rare:38 |