| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:113746540-113747161 | Common:14; Rare:256 | ||||
| chr3:113838780-113839212 | Common:13; Rare:229 | ||||
| chr3:113947532-113948043 | Common:6; Rare:324 | ||||
| chr3:113948094-113948370 | Common:3; Rare:204 | ||||
| chr3:114055708-114056345 | Common:9; Rare:182 | ||||
| chr3:114056454-114056898 | Common:6; Rare:437 | ||||
| chr3:115147241-115147448 | Common:1; Rare:50 | ||||
| chr3:115147686-115148093 | Rare:129 | ||||
| chr3:119034610-119035220 | Common:9; Rare:324 | ||||
| chr3:119240460-119240816 | Common:2; Rare:121 | ||||
| chr3:119240802-119241112 | Common:3; Rare:197 | ||||
| chr3:119293660-119293960 | Common:1; Rare:50 | ||||
| chr3:119293950-119294389 | Common:1; Rare:188 | ||||
| chr3:119463528-119463897 | Common:12; Rare:220 | ||||
| chr3:119468832-119469054 | Common:2; Rare:152; Clinvar (pathogenic):1 |