| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:130980328-130980593 | Rare:57; Clinvar (pathogenic):1 | ||||
| chr3:131026725-131026955 | Common:2; Rare:58 | ||||
| chr3:131381467-131381809 | Common:2; Rare:87 | ||||
| chr3:131502733-131503022 | Common:1; Rare:116 | ||||
| chr3:132659618-132660054 | Common:3; Rare:106; Clinvar:1 | ||||
| chr3:132675311-132675611 | Rare:50; Clinvar (pathogenic):1 | ||||
| chr3:133574080-133574281 | Common:1; Rare:53 | ||||
| chr3:133608685-133608967 | Rare:70 | ||||
| chr3:133661772-133662015 | Rare:56 | ||||
| chr3:134250849-134251080 | Rare:74 | ||||
| chr3:134374373-134374657 | Common:1; Rare:79 | ||||
| chr3:134485393-134485773 | Rare:92 | ||||
| chr3:134485931-134486273 | Common:4; Rare:121 | ||||
| chr3:136195806-136195998 | Common:1; Rare:80 | ||||
| chr3:136196220-136196492 | Common:1; Rare:99 |