| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:118895098-118895270 | Rare:49 | ||||
| chr6:119269423-119269508 | Common:1; Rare:15 | ||||
| chr6:119350586-119350737 | Common:2; Rare:33 | ||||
| chr6:129392750-129393124 | Common:1; Rare:93; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr6:129395396-129395515 | Rare:24 | ||||
| chr6:129427575-129427851 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:129476536-129476783 | Common:1; Rare:39 | ||||
| chr6:129486376-129486632 | Common:3; Rare:74; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr6:132817023-132817187 | Common:1; Rare:53 | ||||
| chr6:135880819-135880859 | Rare:6 | ||||
| chr6:136783966-136784144 | Common:1; Rare:31 | ||||
| chr6:137218046-137218099 | Rare:10 | ||||
| chr6:137218690-137218760 | Common:1; Rare:13 | ||||
| chr6:137868211-137868236 | Rare:3 | ||||
| chr6:139978192-139978388 | Common:2; Rare:33 |