| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:195271510-195271810 | Common:1; Rare:71 | ||||
| chr3:195442940-195443473 | Common:5; Rare:152 | ||||
| chr3:195543221-195543481 | Common:3; Rare:102 | ||||
| chr3:195583797-195584197 | Common:11; Rare:109 | ||||
| chr3:195892712-195893011 | Common:2; Rare:51 | ||||
| chr3:196081191-196081802 | Common:5; Rare:241 | ||||
| chr3:196082029-196082298 | Common:5; Rare:105 | ||||
| chr3:196287652-196288022 | Common:2; Rare:114 | ||||
| chr3:196288076-196288476 | Common:4; Rare:108 | ||||
| chr3:196317650-196318070 | Common:4; Rare:114; Clinvar (pathogenic):1 | ||||
| chr3:196318127-196318435 | Common:1; Rare:128 | ||||
| chr3:196432304-196432686 | Common:1; Rare:139 | ||||
| chr3:196503686-196503975 | Common:6; Rare:98 | ||||
| chr3:196568400-196568870 | Common:5; Rare:140 | ||||
| chr3:196712197-196712431 | Common:4; Rare:83 |