| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:185937958-185938175 | Common:2; Rare:93 | ||||
| chr3:186567274-186567491 | Common:3; Rare:61 | ||||
| chr3:186783215-186783639 | Common:2; Rare:188 | ||||
| chr3:186806416-186806588 | Rare:60 | ||||
| chr3:186930227-186930771 | Common:5; Rare:130 | ||||
| chr3:186931281-186931360 | Common:1; Rare:21 | ||||
| chr3:187139397-187139548 | Common:1; Rare:57 | ||||
| chr3:187291626-187291924 | Common:1; Rare:102 | ||||
| chr3:187291932-187292065 | Common:14; Rare:46 | ||||
| chr3:187292247-187292274 | Rare:3 | ||||
| chr3:188153649-188153986 | Common:1; Rare:64 | ||||
| chr3:188154041-188154227 | Rare:60 | ||||
| chr3:190120319-190120509 | Common:1; Rare:77; Clinvar (pathogenic):1 | ||||
| chr3:190120881-190121018 | Rare:45 | ||||
| chr3:192917838-192918033 | Common:2; Rare:85 |