| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:99817560-99817924 | Rare:108 | ||||
| chr3:99876079-99876287 | Common:2; Rare:59 | ||||
| chr3:100260713-100261059 | Rare:103 | ||||
| chr3:100334565-100334780 | Common:2; Rare:74 | ||||
| chr3:100401057-100401192 | Rare:41 | ||||
| chr3:100401398-100401586 | Common:1; Rare:35 | ||||
| chr3:100492420-100492658 | Common:2; Rare:78 | ||||
| chr3:100709157-100709716 | Common:9; Rare:164; Clinvar (benign):1 | ||||
| chr3:101513109-101513343 | Common:8; Rare:52 | ||||
| chr3:101561759-101561915 | Common:1; Rare:56 | ||||
| chr3:101574064-101574242 | Rare:63 | ||||
| chr3:101677026-101677072 | Rare:15 | ||||
| chr3:101677074-101677185 | Rare:47 | ||||
| chr3:101685816-101686036 | Common:3; Rare:58 | ||||
| chr3:101686480-101686887 | Common:2; Rare:162 |