| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:132734495-132734950 | Common:2; Rare:119 | ||||
| chr6:133888998-133889114 | Common:1; Rare:18 | ||||
| chr6:133953038-133953252 | Common:2; Rare:64 | ||||
| chr6:134174833-134175105 | Common:1; Rare:131 | ||||
| chr6:134177843-134178091 | Common:1; Rare:37 | ||||
| chr6:135054676-135054990 | Common:6; Rare:106 | ||||
| chr6:135497588-135497928 | Common:4; Rare:127; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:136289767-136290041 | Common:2; Rare:119 | ||||
| chr6:136550388-136550687 | Common:2; Rare:88 | ||||
| chr6:137219113-137219193 | Rare:20 | ||||
| chr6:137219284-137219503 | Common:3; Rare:76; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:138773657-138773839 | Common:3; Rare:85 | ||||
| chr6:139028616-139028853 | Common:1; Rare:52 | ||||
| chr6:139028869-139029160 | Common:8; Rare:87 | ||||
| chr6:142147140-142147290 | Rare:56 |