| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:114899631-114899849 | Rare:30 | ||||
| chr3:115100110-115100750 | Common:3; Rare:114 | ||||
| chr3:115146628-115146835 | Rare:64 | ||||
| chr3:115147686-115147918 | Rare:72 | ||||
| chr3:115623135-115623336 | Rare:32 | ||||
| chr3:115623519-115623681 | Rare:60 | ||||
| chr3:116445460-116445782 | Common:1; Rare:60 | ||||
| chr3:119240870-119241036 | Common:1; Rare:51 | ||||
| chr3:119462913-119463313 | Common:1; Rare:98 | ||||
| chr3:119463606-119463865 | Common:3; Rare:78 | ||||
| chr3:119468817-119469047 | Common:1; Rare:89; Clinvar (pathogenic):1 | ||||
| chr3:119498340-119498605 | Common:4; Rare:91 | ||||
| chr3:119579660-119580320 | Common:4; Rare:150 | ||||
| chr3:119676853-119677253 | Common:30; Rare:176 | ||||
| chr3:119677375-119677559 | Rare:60 |