| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:146160987-146161105 | Rare:50; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:146161139-146161255 | Common:1; Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:146161302-146161415 | Common:2; Rare:21; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:146469366-146469485 | Common:2; Rare:24 | ||||
| chr3:146544506-146544796 | Common:4; Rare:68 | ||||
| chr3:149060645-149060793 | Rare:46 | ||||
| chr3:149129539-149129735 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149198563-149198802 | Rare:48 | ||||
| chr3:149333362-149333651 | Common:4; Rare:56 | ||||
| chr3:149658023-149658209 | Rare:46 | ||||
| chr3:149813721-149813859 | Common:1; Rare:22 | ||||
| chr3:149969361-149969457 | Common:1; Rare:28 | ||||
| chr3:149970831-149971055 | Common:1; Rare:100 | ||||
| chr3:149971093-149971336 | Common:4; Rare:104 | ||||
| chr3:149971456-149971534 | Rare:32 |