| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:133309076-133309426 | Common:2; Rare:135 | ||||
| chr10:133357300-133357418 | Common:2; Rare:22 | ||||
| chr10:133357424-133357517 | Rare:16 | ||||
| chr10:133357656-133357809 | Common:1; Rare:26 | ||||
| chr10:133357914-133358047 | Common:2; Rare:41 | ||||
| chr10:133373264-133373657 | Common:3; Rare:163; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr10:133373673-133373804 | Common:1; Rare:47 | ||||
| chr10:133378839-133379345 | Common:21; Rare:106 | ||||
| chr10:133393976-133394553 | Common:3; Rare:222 | ||||
| chr11:207106-207840 | Common:12; Rare:213 | ||||
| chr11:207915-208146 | Common:1; Rare:44 | ||||
| chr11:208160-208258 | Common:3; Rare:18 | ||||
| chr11:208588-208933 | Common:1; Rare:123 | ||||
| chr11:209406-209726 | Rare:108 | ||||
| chr11:210217-210377 | Rare:30 |