| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130916376-130916686 | Common:7; Rare:95 | ||||
| chr11:133956956-133957201 | Common:1; Rare:73 | ||||
| chr11:134223882-134224229 | Common:2; Rare:133 | ||||
| chr11:134224475-134224789 | Common:2; Rare:128 | ||||
| chr11:134253277-134253640 | Common:3; Rare:138; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:388424-388731 | Common:1; Rare:74 | ||||
| chr12:389003-389131 | Common:5; Rare:67 | ||||
| chr12:389205-389422 | Common:1; Rare:87 | ||||
| chr12:389449-389739 | Common:7; Rare:113 | ||||
| chr12:401390-401781 | Common:2; Rare:102 | ||||
| chr12:642636-643288 | Common:9; Rare:179 | ||||
| chr12:643370-643496 | Rare:27 | ||||
| chr12:643609-644059 | Common:2; Rare:98 | ||||
| chr12:752294-752770 | Common:1; Rare:141 | ||||
| chr12:752925-753080 | Common:1; Rare:38; Clinvar (benign):1 |