| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15601512-15601815 | Common:4; Rare:129; Clinvar:2 | ||||
| chr3:15601853-15602046 | Common:1; Rare:99; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:15756513-15756652 | Common:2; Rare:30 | ||||
| chr3:15859777-15860099 | Common:4; Rare:97 | ||||
| chr3:16264866-16265243 | Common:2; Rare:128 | ||||
| chr3:16472571-16472712 | Rare:34 | ||||
| chr3:16604459-16604566 | Common:2; Rare:32 | ||||
| chr3:16605226-16605560 | Common:5; Rare:134 | ||||
| chr3:16884795-16885228 | Common:8; Rare:109 | ||||
| chr3:17699995-17700097 | Rare:21 | ||||
| chr3:17742500-17743015 | Common:5; Rare:183 | ||||
| chr3:19946881-19946949 | Common:3; Rare:21 | ||||
| chr3:19946951-19947450 | Common:7; Rare:186 | ||||
| chr3:20012199-20012348 | Common:2; Rare:18 | ||||
| chr3:20185885-20185983 | Rare:27 |