| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:125749401-125749682 | Common:5; Rare:116 | ||||
| chr6:125781059-125781156 | Rare:18 | ||||
| chr6:125791047-125791115 | Rare:17 | ||||
| chr6:125986421-125986548 | Rare:48 | ||||
| chr6:127118966-127119249 | Rare:74 | ||||
| chr6:127119806-127119862 | Rare:17 | ||||
| chr6:127266811-127266916 | Common:1; Rare:40 | ||||
| chr6:127343337-127343420 | Rare:16 | ||||
| chr6:127343547-127343564 | Rare:4 | ||||
| chr6:128520559-128520763 | Rare:77 | ||||
| chr6:130365613-130365742 | Rare:23 | ||||
| chr6:130366042-130366483 | Common:3; Rare:96 | ||||
| chr6:131572991-131573234 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:131628116-131628433 | Common:3; Rare:86 | ||||
| chr6:131951370-131951402 | Rare:11 |