| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65919111-65919499 | Rare:136 | ||||
| chr11:65919616-65919730 | Rare:35 | ||||
| chr11:65961412-65961793 | Common:1; Rare:123 | ||||
| chr11:65961991-65962262 | Common:5; Rare:92 | ||||
| chr11:66001717-66001837 | Common:1; Rare:25 | ||||
| chr11:66002060-66002402 | Common:3; Rare:96; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:66002417-66002852 | Common:2; Rare:124; Clinvar:1 | ||||
| chr11:66002911-66002949 | Common:2; Rare:11 | ||||
| chr11:66051928-66052463 | Common:9; Rare:166 | ||||
| chr11:66069952-66070449 | Common:2; Rare:143 | ||||
| chr11:66100770-66100992 | Common:2; Rare:55 | ||||
| chr11:66257061-66257403 | Common:2; Rare:55 | ||||
| chr11:66257465-66257677 | Rare:53 | ||||
| chr11:66258345-66258477 | Rare:26 | ||||
| chr11:66267951-66268113 | Common:1; Rare:26 |