| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:132814262-132814621 | Common:4; Rare:132 | ||||
| chr6:133953031-133953313 | Common:2; Rare:87 | ||||
| chr6:134174840-134175036 | Common:1; Rare:96 | ||||
| chr6:134317611-134317755 | Common:1; Rare:24 | ||||
| chr6:135054745-135055017 | Common:6; Rare:83 | ||||
| chr6:135497604-135497936 | Common:4; Rare:126; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:135851463-135851717 | Rare:40 | ||||
| chr6:136289744-136290024 | Common:1; Rare:124 | ||||
| chr6:136526163-136526328 | Common:4; Rare:30 | ||||
| chr6:136526405-136526665 | Common:3; Rare:60 | ||||
| chr6:136550404-136550669 | Common:2; Rare:75 | ||||
| chr6:137219310-137219463 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:138773324-138773547 | Common:3; Rare:98 | ||||
| chr6:138773646-138773836 | Common:3; Rare:88 | ||||
| chr6:139028464-139028858 | Common:1; Rare:79 |