| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:134175787-134176118 | Common:2; Rare:55 | ||||
| chr6:134317780-134317969 | Common:1; Rare:40 | ||||
| chr6:135054785-135054990 | Common:6; Rare:62 | ||||
| chr6:135497586-135497954 | Common:4; Rare:136; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:136037717-136038080 | Common:2; Rare:75 | ||||
| chr6:136289767-136290057 | Common:2; Rare:126 | ||||
| chr6:136550372-136550709 | Common:2; Rare:101 | ||||
| chr6:136792970-136793311 | Common:1; Rare:85 | ||||
| chr6:137219111-137219180 | Rare:17 | ||||
| chr6:137219264-137219518 | Common:4; Rare:87; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:137866935-137867275 | Rare:78 | ||||
| chr6:138107196-138107233 | Rare:14 | ||||
| chr6:138773343-138773586 | Common:2; Rare:109 | ||||
| chr6:138773646-138773865 | Common:3; Rare:97 | ||||
| chr6:138988208-138988411 | Common:3; Rare:58 |