| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32668274-32668695 | Common:39; Rare:31 | ||||
| chr6:32741406-32741443 | Common:3; Rare:8 | ||||
| chr6:32816850-32817207 | Common:4; Rare:73 | ||||
| chr6:32843848-32844135 | Common:3; Rare:81; Clinvar:1; Clinvar (benign):3 | ||||
| chr6:32844303-32844858 | Common:1; Rare:122 | ||||
| chr6:32853640-32854287 | Common:5; Rare:194; Clinvar:2; Clinvar (benign):4 | ||||
| chr6:32940847-32941078 | Common:1; Rare:40 | ||||
| chr6:32948867-32949378 | Common:4; Rare:98 | ||||
| chr6:32952812-32953275 | Rare:93 | ||||
| chr6:32968510-32968665 | Common:3; Rare:49 | ||||
| chr6:32970610-32970716 | Common:1; Rare:25 | ||||
| chr6:33009514-33009826 | Common:5; Rare:69 | ||||
| chr6:33075903-33076134 | Common:3; Rare:44 | ||||
| chr6:33080138-33080491 | Common:11; Rare:54 | ||||
| chr6:33200654-33200923 | Common:2; Rare:82 |