| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:133953031-133953241 | Common:2; Rare:63 | ||||
| chr6:134174509-134174665 | Rare:68 | ||||
| chr6:134174710-134175032 | Common:1; Rare:160 | ||||
| chr6:134175648-134175741 | Rare:34 | ||||
| chr6:134177843-134178008 | Rare:26 | ||||
| chr6:135497604-135497877 | Common:4; Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289767-136290032 | Common:1; Rare:115 | ||||
| chr6:136550394-136550669 | Common:2; Rare:81 | ||||
| chr6:137219111-137219199 | Common:1; Rare:23 | ||||
| chr6:137219254-137219493 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:138107079-138107572 | Common:4; Rare:160 | ||||
| chr6:138404057-138404233 | Common:1; Rare:50 | ||||
| chr6:138773613-138773836 | Common:3; Rare:101 | ||||
| chr6:139028553-139028813 | Common:1; Rare:51 | ||||
| chr6:142147140-142147290 | Rare:56 |