| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42929963-42930362 | Common:4; Rare:73 | ||||
| chr6:42978318-42978487 | Rare:57; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr6:43096766-43096856 | Rare:15 | ||||
| chr6:43172144-43172427 | Common:1; Rare:66 | ||||
| chr6:43174552-43174932 | Common:2; Rare:82 | ||||
| chr6:43224374-43224622 | Common:2; Rare:54 | ||||
| chr6:43247195-43247384 | Rare:46 | ||||
| chr6:43338240-43338609 | Common:1; Rare:125 | ||||
| chr6:43339111-43339461 | Common:2; Rare:104 | ||||
| chr6:43368118-43368388 | Rare:47 | ||||
| chr6:43376891-43376958 | Common:1; Rare:9 | ||||
| chr6:43380991-43381115 | Rare:17 | ||||
| chr6:43383685-43383987 | Common:2; Rare:51 | ||||
| chr6:43393281-43393491 | Rare:43 | ||||
| chr6:43725166-43725270 | Common:1; Rare:20 |