| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:181207553-181207751 | Common:4; Rare:59 | ||||
| chr6:1607812-1607882 | Common:1; Rare:19 | ||||
| chr6:1608915-1609257 | Rare:94 | ||||
| chr6:1612548-1613075 | Common:4; Rare:102; Clinvar (pathogenic):1 | ||||
| chr6:1613291-1613443 | Common:2; Rare:28 | ||||
| chr6:7885959-7886235 | Common:1; Rare:80 | ||||
| chr6:11227544-11227686 | Common:1; Rare:23 | ||||
| chr6:11230858-11231015 | Common:1; Rare:25 | ||||
| chr6:13056827-13056894 | Rare:11 | ||||
| chr6:13058296-13058504 | Common:2; Rare:31 | ||||
| chr6:13184774-13184814 | Rare:11 | ||||
| chr6:13229866-13230143 | Common:1; Rare:59 | ||||
| chr6:13616345-13616520 | Common:1; Rare:41 | ||||
| chr6:15524648-15524744 | Rare:35; Clinvar:2 | ||||
| chr6:21595872-21596017 | Common:1; Rare:55 |