| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:133953047-133953306 | Common:2; Rare:84 | ||||
| chr6:134174833-134174989 | Common:1; Rare:75 | ||||
| chr6:135054784-135054990 | Common:6; Rare:62 | ||||
| chr6:135497596-135497944 | Common:4; Rare:130; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289756-136290014 | Common:1; Rare:111 | ||||
| chr6:136550372-136550687 | Common:2; Rare:94 | ||||
| chr6:137219316-137219511 | Common:4; Rare:67; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:138499418-138499654 | Common:2; Rare:47 | ||||
| chr6:138773646-138773836 | Common:3; Rare:88 | ||||
| chr6:139028628-139028842 | Common:1; Rare:44 | ||||
| chr6:142147140-142147304 | Rare:67 | ||||
| chr6:142301832-142302131 | Common:6; Rare:87 | ||||
| chr6:143060724-143060983 | Common:8; Rare:93 | ||||
| chr6:143450651-143450961 | Common:1; Rare:115; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511670-143511733 | Common:3; Rare:18 |