| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:5689617-5689902 | Common:3; Rare:58 | ||||
| chr11:5690238-5690425 | Rare:28 | ||||
| chr11:5690491-5691212 | Common:6; Rare:139 | ||||
| chr11:5691219-5691357 | Common:2; Rare:42 | ||||
| chr11:6234566-6234878 | Common:3; Rare:98 | ||||
| chr11:6235045-6235365 | Rare:75 | ||||
| chr11:6320237-6320278 | Rare:16 | ||||
| chr11:6320484-6320681 | Common:2; Rare:64 | ||||
| chr11:6320925-6321208 | Common:2; Rare:50 | ||||
| chr11:6390160-6390598 | Common:3; Rare:128; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:6473831-6474156 | Common:1; Rare:98 | ||||
| chr11:6481201-6481663 | Common:5; Rare:168 | ||||
| chr11:6603156-6603414 | Common:2; Rare:71 | ||||
| chr11:6603522-6603916 | Common:4; Rare:116; Clinvar (benign):3 | ||||
| chr11:6604417-6604615 | Rare:42 |