| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:128882905-128883059 | Rare:33 | ||||
| chr6:128883068-128883428 | Common:2; Rare:98; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr6:128883470-128883593 | Common:2; Rare:28 | ||||
| chr6:129710138-129710322 | Rare:49 | ||||
| chr6:129710337-129710356 | Common:1; Rare:3 | ||||
| chr6:130365403-130365569 | Common:1; Rare:38 | ||||
| chr6:130366113-130366489 | Common:3; Rare:82 | ||||
| chr6:131015835-131016052 | Rare:32 | ||||
| chr6:131063148-131063468 | Rare:94 | ||||
| chr6:131628107-131628461 | Common:3; Rare:93 | ||||
| chr6:132401452-132401593 | Common:1; Rare:41 | ||||
| chr6:132814274-132814611 | Common:3; Rare:122 | ||||
| chr6:133241033-133241387 | Common:5; Rare:108 | ||||
| chr6:133888982-133889227 | Common:1; Rare:42 | ||||
| chr6:133889305-133889604 | Common:4; Rare:100; Clinvar:1 |