| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:124968337-124968391 | Rare:16 | ||||
| chr6:125297589-125297730 | Common:2; Rare:22 | ||||
| chr6:127281777-127281835 | Rare:9 | ||||
| chr6:129315530-129315778 | Common:1; Rare:75; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr6:130874659-130874717 | Common:1; Rare:7 | ||||
| chr6:130875079-130875281 | Common:3; Rare:31 | ||||
| chr6:130920957-130921011 | Rare:8 | ||||
| chr6:130921026-130921054 | Common:1; Rare:4 | ||||
| chr6:130980482-130980564 | Rare:11 | ||||
| chr6:131598375-131598610 | Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:131949585-131950176 | Common:2; Rare:142 | ||||
| chr6:131950177-131950738 | Common:4; Rare:174 | ||||
| chr6:132816794-132817000 | Common:3; Rare:87 | ||||
| chr6:132817472-132817709 | Common:2; Rare:61 | ||||
| chr6:134908932-134909104 | Rare:31 |