| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66059517-66060008 | Common:1; Rare:102 | ||||
| chr11:66061681-66061999 | Rare:76 | ||||
| chr11:66199313-66199371 | Rare:10 | ||||
| chr11:66247505-66247624 | Rare:19 | ||||
| chr11:66682590-66682748 | Rare:25 | ||||
| chr11:66683603-66683892 | Common:2; Rare:53 | ||||
| chr11:66684664-66684943 | Common:2; Rare:51 | ||||
| chr11:66714096-66714345 | Common:1; Rare:64; Clinvar (benign):2 | ||||
| chr11:66771751-66771791 | Rare:6 | ||||
| chr11:66790584-66790803 | Rare:25 | ||||
| chr11:66844955-66845262 | Common:2; Rare:96 | ||||
| chr11:66905947-66906226 | Common:2; Rare:47 | ||||
| chr11:66967677-66967862 | Common:1; Rare:27 | ||||
| chr11:67317218-67317295 | Common:1; Rare:14 | ||||
| chr11:67369038-67369053 | Rare:5 |