| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:100492410-100492831 | Common:11; Rare:118 | ||||
| chr3:100709194-100709748 | Common:9; Rare:164; Clinvar (benign):1 | ||||
| chr3:101513126-101513245 | Common:7; Rare:27 | ||||
| chr3:101561785-101561971 | Common:2; Rare:66 | ||||
| chr3:101677096-101677385 | Rare:96 | ||||
| chr3:101685546-101685913 | Common:2; Rare:91 | ||||
| chr3:101686446-101686884 | Common:2; Rare:179 | ||||
| chr3:101779175-101779328 | Common:4; Rare:47 | ||||
| chr3:101850500-101850653 | Rare:36 | ||||
| chr3:101855186-101855500 | Common:2; Rare:86 | ||||
| chr3:101856316-101856358 | Rare:13 | ||||
| chr3:101856713-101857043 | Common:4; Rare:54 | ||||
| chr3:105366417-105366777 | Common:3; Rare:97 | ||||
| chr3:105367234-105367463 | Common:2; Rare:65 | ||||
| chr3:105868875-105869191 | Common:6; Rare:113 |