| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:100260932-100261061 | Rare:47 | ||||
| chr3:100334652-100334780 | Common:1; Rare:56 | ||||
| chr3:100401068-100401246 | Rare:54 | ||||
| chr3:100401378-100401688 | Common:2; Rare:68 | ||||
| chr3:100492460-100492653 | Common:1; Rare:61 | ||||
| chr3:100709207-100709994 | Common:11; Rare:206; Clinvar (benign):1 | ||||
| chr3:101513122-101513343 | Common:8; Rare:48 | ||||
| chr3:101561662-101561955 | Common:2; Rare:95 | ||||
| chr3:101574049-101574262 | Common:1; Rare:74 | ||||
| chr3:101677025-101677196 | Rare:66 | ||||
| chr3:101686489-101686875 | Common:2; Rare:155 | ||||
| chr3:101687032-101687343 | Common:1; Rare:73 | ||||
| chr3:101724583-101724670 | Rare:36 | ||||
| chr3:101724886-101725008 | Rare:27 | ||||
| chr3:101779112-101779267 | Common:3; Rare:50 |