| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49104699-49104910 | Common:1; Rare:92; Clinvar:1; Clinvar (benign):5 | ||||
| chr3:49132939-49133161 | Rare:41; Clinvar:2 | ||||
| chr3:49166289-49166367 | Rare:19 | ||||
| chr3:49199248-49199552 | Common:1; Rare:68 | ||||
| chr3:49340029-49340267 | Common:3; Rare:76 | ||||
| chr3:49411876-49412213 | Common:1; Rare:115 | ||||
| chr3:49429262-49429451 | Common:1; Rare:40 | ||||
| chr3:49674225-49674395 | Common:1; Rare:64 | ||||
| chr3:49689460-49689597 | Rare:42 | ||||
| chr3:49723937-49724211 | Common:8; Rare:94 | ||||
| chr3:49786491-49786769 | Rare:89 | ||||
| chr3:49856544-49856645 | Common:1; Rare:26 | ||||
| chr3:50267404-50267674 | Common:2; Rare:84 | ||||
| chr3:50299334-50299683 | Common:1; Rare:87 | ||||
| chr3:50328177-50328362 | Rare:54 |