| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:2764520-2764817 | Common:4; Rare:95 | ||||
| chr6:2989671-2989973 | Common:7; Rare:81 | ||||
| chr6:3068951-3069065 | Common:1; Rare:48 | ||||
| chr6:3155696-3155995 | Common:3; Rare:60; Clinvar (benign):2 | ||||
| chr6:3194660-3194831 | Rare:34 | ||||
| chr6:3226593-3226925 | Common:5; Rare:65; Clinvar:1 | ||||
| chr6:3228482-3228845 | Common:2; Rare:82 | ||||
| chr6:3228903-3229061 | Common:9; Rare:39 | ||||
| chr6:3229070-3229161 | Common:1; Rare:10 | ||||
| chr6:3229203-3229382 | Common:4; Rare:38 | ||||
| chr6:3229676-3229812 | Common:1; Rare:19 | ||||
| chr6:3233514-3233601 | Common:1; Rare:13 | ||||
| chr6:3247885-3248045 | Common:1; Rare:34 | ||||
| chr6:3254095-3254407 | Common:4; Rare:110 | ||||
| chr6:4018548-4018789 | Common:3; Rare:78 |