| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:133308829-133309094 | Common:2; Rare:107 | ||||
| chr10:133309151-133309463 | Common:2; Rare:124 | ||||
| chr10:133347211-133347422 | Rare:44 | ||||
| chr10:133356941-133357234 | Common:1; Rare:92 | ||||
| chr10:133357933-133358221 | Common:5; Rare:80 | ||||
| chr10:133373245-133373397 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr10:133525034-133525224 | Common:2; Rare:31 | ||||
| chr10:133526879-133527577 | Common:7; Rare:147 | ||||
| chr10:133531466-133531747 | Common:1; Rare:78 | ||||
| chr11:207363-207719 | Common:7; Rare:109 | ||||
| chr11:208615-208884 | Rare:97 | ||||
| chr11:212471-212692 | Common:1; Rare:74 | ||||
| chr11:236300-236491 | Common:7; Rare:65 | ||||
| chr11:236871-237059 | Common:1; Rare:71 | ||||
| chr11:288811-289169 | Common:3; Rare:97 |