| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184314438-184314612 | Common:3; Rare:54 | ||||
| chr3:196568546-196568643 | Rare:24 | ||||
| chr3:196942375-196942677 | Common:1; Rare:127 | ||||
| chr3:197949894-197950240 | Common:4; Rare:106; Clinvar (benign):2 | ||||
| chr4:499121-499275 | Common:3; Rare:58 | ||||
| chr4:673872-673965 | Rare:43 | ||||
| chr4:674219-674507 | Rare:133 | ||||
| chr4:705578-705955 | Common:1; Rare:128 | ||||
| chr4:932264-932487 | Common:2; Rare:87 | ||||
| chr4:986909-987024 | Common:1; Rare:29; Clinvar:1 | ||||
| chr4:2468942-2469154 | Common:1; Rare:64 | ||||
| chr4:2934664-2934954 | Common:5; Rare:97 | ||||
| chr4:4290113-4290244 | Common:1; Rare:51 | ||||
| chr4:6640590-6640716 | Common:2; Rare:50 | ||||
| chr4:15681567-15681773 | Common:3; Rare:68 |