| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184319246-184319764 | Common:54; Rare:441 | ||||
| chr3:184335776-184336029 | Common:1; Rare:83 | ||||
| chr3:184361525-184361958 | Rare:224 | ||||
| chr3:184362128-184362972 | Common:1; Rare:360 | ||||
| chr3:184380170-184380361 | Rare:52 | ||||
| chr3:184561616-184561800 | Common:1; Rare:46 | ||||
| chr3:184711246-184711564 | Common:2; Rare:104; Clinvar (benign):1 | ||||
| chr3:184711580-184712293 | Common:8; Rare:480 | ||||
| chr3:184812024-184812231 | Common:2; Rare:64 | ||||
| chr3:184812135-184812267 | Common:2; Rare:41 | ||||
| chr3:185152680-185153250 | Common:14; Rare:424 | ||||
| chr3:185253987-185254256 | Common:2; Rare:128; Clinvar:3 | ||||
| chr3:185282784-185283097 | Common:3; Rare:213 | ||||
| chr3:185498220-185498610 | Rare:82 | ||||
| chr3:185498822-185499216 | Rare:329 |