| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:185937798-185938088 | Common:2; Rare:130 | ||||
| chr3:185938091-185938282 | Rare:61 | ||||
| chr3:186567293-186567470 | Common:3; Rare:40 | ||||
| chr3:186570926-186571039 | Common:2; Rare:39 | ||||
| chr3:186783257-186783709 | Common:1; Rare:214 | ||||
| chr3:186784085-186784261 | Common:2; Rare:80 | ||||
| chr3:186791759-186792005 | Common:1; Rare:51 | ||||
| chr3:186806405-186806587 | Rare:63 | ||||
| chr3:186930411-186930819 | Common:2; Rare:97 | ||||
| chr3:187180704-187181239 | Common:7; Rare:129 | ||||
| chr3:187291735-187291863 | Rare:45 | ||||
| chr3:188153686-188153938 | Common:1; Rare:49 | ||||
| chr3:188154082-188154224 | Rare:47 | ||||
| chr3:190120251-190120592 | Common:1; Rare:146; Clinvar (pathogenic):1 | ||||
| chr3:190120775-190121065 | Rare:82 |