| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:16264907-16265225 | Common:2; Rare:96 | ||||
| chr3:16605403-16605503 | Rare:41 | ||||
| chr3:16884972-16885223 | Common:7; Rare:76 | ||||
| chr3:17742514-17742961 | Common:4; Rare:161 | ||||
| chr3:19946966-19947412 | Common:5; Rare:167 | ||||
| chr3:20186204-20186390 | Common:2; Rare:53 | ||||
| chr3:23202913-23203207 | Common:1; Rare:102 | ||||
| chr3:23916911-23917177 | Rare:99 | ||||
| chr3:23917611-23917955 | Common:2; Rare:92; Clinvar (benign):1 | ||||
| chr3:24494977-24495265 | Common:2; Rare:89 | ||||
| chr3:25428107-25428289 | Rare:34 | ||||
| chr3:25783390-25783634 | Common:2; Rare:78; Clinvar (benign):3 | ||||
| chr3:25789987-25790120 | Common:3; Rare:50 | ||||
| chr3:27369340-27369537 | Rare:41 | ||||
| chr3:28241558-28241672 | Common:1; Rare:42 |