| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:107957165-107957419 | Rare:50 | ||||
| chr6:107957974-107958450 | Common:2; Rare:158; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:108074250-108074291 | Rare:13 | ||||
| chr6:108074621-108074866 | Common:1; Rare:84; Clinvar:1 | ||||
| chr6:108294765-108295097 | Common:1; Rare:90 | ||||
| chr6:108559689-108559829 | Common:1; Rare:56 | ||||
| chr6:108560729-108560987 | Rare:105 | ||||
| chr6:109009432-109009690 | Common:2; Rare:80 | ||||
| chr6:109095053-109095188 | Common:2; Rare:44 | ||||
| chr6:109095412-109095563 | Rare:30 | ||||
| chr6:109382374-109382548 | Common:4; Rare:79; Clinvar (benign):1 | ||||
| chr6:109382784-109382886 | Common:2; Rare:31 | ||||
| chr6:109440575-109441035 | Common:3; Rare:137 | ||||
| chr6:109455630-109455803 | Common:3; Rare:50 | ||||
| chr6:109455872-109456074 | Rare:43 |