| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32894573-32894790 | Common:9; Rare:60 | ||||
| chr6:33425650-33425846 | Common:1; Rare:49; Clinvar (benign):1 | ||||
| chr6:34299042-34299174 | Rare:19 | ||||
| chr6:35016891-35017136 | Common:3; Rare:27 | ||||
| chr6:35017336-35017638 | Common:2; Rare:84 | ||||
| chr6:35490099-35490408 | Common:1; Rare:89 | ||||
| chr6:35601276-35601490 | Common:1; Rare:38 | ||||
| chr6:36680154-36680467 | Common:6; Rare:61 | ||||
| chr6:36834763-36834931 | Common:1; Rare:32 | ||||
| chr6:36844243-36844629 | Common:1; Rare:62 | ||||
| chr6:36849145-36849449 | Common:3; Rare:56 | ||||
| chr6:37131226-37131532 | Common:2; Rare:56 | ||||
| chr6:39819806-39819975 | Common:3; Rare:39 | ||||
| chr6:40998604-40998854 | Common:1; Rare:47 | ||||
| chr6:41451700-41451818 | Rare:21 |