| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:88149856-88150007 | Rare:46 | ||||
| chr3:94062930-94063040 | Rare:32 | ||||
| chr3:97764476-97764805 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:99638510-99638648 | Rare:31 | ||||
| chr3:99817566-99817904 | Rare:97 | ||||
| chr3:99876126-99876312 | Common:1; Rare:51 | ||||
| chr3:100260701-100261024 | Rare:86 | ||||
| chr3:100492404-100492619 | Common:2; Rare:76 | ||||
| chr3:101561796-101561904 | Common:1; Rare:34 | ||||
| chr3:101573995-101574218 | Rare:76 | ||||
| chr3:101677098-101677164 | Rare:30 | ||||
| chr3:101686672-101686949 | Common:2; Rare:104 | ||||
| chr3:105868828-105869186 | Common:6; Rare:125 | ||||
| chr3:108090936-108091110 | Rare:64 | ||||
| chr3:108589390-108589518 | Common:1; Rare:40 |