| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:16264868-16265243 | Common:2; Rare:127 | ||||
| chr3:16513505-16513558 | Rare:9 | ||||
| chr3:16513563-16513851 | Common:4; Rare:72 | ||||
| chr3:16884962-16885208 | Common:7; Rare:74 | ||||
| chr3:17742529-17742956 | Common:4; Rare:155 | ||||
| chr3:19946951-19947442 | Common:7; Rare:182 | ||||
| chr3:20186161-20186415 | Common:2; Rare:81 | ||||
| chr3:23805830-23806056 | Common:1; Rare:47 | ||||
| chr3:23916848-23917354 | Rare:173 | ||||
| chr3:23917666-23918031 | Common:2; Rare:97; Clinvar (benign):1 | ||||
| chr3:25428107-25428346 | Rare:52 | ||||
| chr3:25783392-25783627 | Common:2; Rare:76; Clinvar (benign):3 | ||||
| chr3:25790008-25790126 | Common:4; Rare:45 | ||||
| chr3:28241441-28241796 | Common:2; Rare:121 | ||||
| chr3:28348644-28348724 | Rare:18 |