| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:34424734-34425225 | Common:3; Rare:123; Clinvar (benign):8 | ||||
| chr6:34696764-34696975 | Common:1; Rare:50 | ||||
| chr6:34757285-34757586 | Common:2; Rare:84 | ||||
| chr6:34887953-34888146 | Common:1; Rare:43 | ||||
| chr6:35058094-35058293 | Rare:38 | ||||
| chr6:35214212-35214385 | Common:1; Rare:46 | ||||
| chr6:35259399-35259542 | Rare:44 | ||||
| chr6:36197224-36197396 | Rare:60 | ||||
| chr6:36442744-36443083 | Common:2; Rare:112 | ||||
| chr6:36547417-36547585 | Rare:79 | ||||
| chr6:36594170-36594378 | Common:3; Rare:78 | ||||
| chr6:36676368-36676524 | Common:2; Rare:22 | ||||
| chr6:36678408-36678805 | Common:1; Rare:94 | ||||
| chr6:36874768-36874898 | Rare:48 | ||||
| chr6:36875008-36875153 | Common:1; Rare:18 |