| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:132401435-132401596 | Common:1; Rare:47 | ||||
| chr6:132513042-132513264 | Common:1; Rare:56 | ||||
| chr6:133888998-133889130 | Common:1; Rare:21 | ||||
| chr6:133952948-133953264 | Common:2; Rare:90 | ||||
| chr6:134174855-134175105 | Common:1; Rare:113 | ||||
| chr6:135054784-135054980 | Common:6; Rare:57 | ||||
| chr6:135497604-135497890 | Common:4; Rare:105; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289758-136290014 | Common:1; Rare:111 | ||||
| chr6:136550379-136550701 | Common:2; Rare:96 | ||||
| chr6:137219109-137219479 | Common:4; Rare:133; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:138773646-138773814 | Common:3; Rare:78 | ||||
| chr6:139028592-139028850 | Common:1; Rare:54 | ||||
| chr6:142147140-142147290 | Rare:56 | ||||
| chr6:142301832-142302146 | Common:6; Rare:91 | ||||
| chr6:142302408-142302677 | Common:1; Rare:54 |