| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:129279489-129279741 | Common:3; Rare:109 | ||||
| chr11:129895516-129895687 | Common:2; Rare:68 | ||||
| chr11:130069567-130070067 | Common:2; Rare:188 | ||||
| chr11:130314395-130314520 | Common:1; Rare:42 | ||||
| chr11:130448430-130448652 | Rare:53 | ||||
| chr11:130916389-130916658 | Common:7; Rare:80 | ||||
| chr11:131911364-131911471 | Common:1; Rare:47 | ||||
| chr11:133957024-133957105 | Rare:25 | ||||
| chr11:134224533-134224695 | Rare:61 | ||||
| chr11:134253286-134253608 | Common:2; Rare:118; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:134331673-134332127 | Common:10; Rare:114 | ||||
| chr12:389230-389383 | Rare:60 | ||||
| chr12:389483-389703 | Common:6; Rare:99 | ||||
| chr12:401436-401644 | Rare:58 | ||||
| chr12:643616-643642 | Rare:7 |