| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:88149828-88150036 | Common:4; Rare:69 | ||||
| chr3:93979849-93980165 | Common:3; Rare:97; Clinvar:1 | ||||
| chr3:94062894-94063033 | Rare:41 | ||||
| chr3:97764439-97764552 | Rare:25 | ||||
| chr3:97764707-97764795 | Common:1; Rare:17; Clinvar (benign):1 | ||||
| chr3:97821924-97822074 | Rare:55 | ||||
| chr3:97972385-97972534 | Common:3; Rare:56 | ||||
| chr3:99638559-99638672 | Rare:24 | ||||
| chr3:99876113-99876320 | Common:1; Rare:56 | ||||
| chr3:100260731-100261024 | Rare:76 | ||||
| chr3:100401398-100401580 | Common:1; Rare:34 | ||||
| chr3:100492413-100492785 | Common:11; Rare:112 | ||||
| chr3:100709187-100709362 | Common:4; Rare:60 | ||||
| chr3:100993382-100993729 | Common:3; Rare:61 | ||||
| chr3:101513156-101513343 | Common:8; Rare:39 |