| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:72008674-72009007 | Common:2; Rare:102 | ||||
| chr11:72080351-72080854 | Common:2; Rare:121; Clinvar:9 | ||||
| chr11:72112201-72112530 | Rare:87 | ||||
| chr11:72112644-72112898 | Common:3; Rare:114 | ||||
| chr11:72114658-72115104 | Rare:67 | ||||
| chr11:72224317-72224407 | Common:1; Rare:16 | ||||
| chr11:72225459-72225495 | Rare:5 | ||||
| chr11:72228887-72229179 | Rare:62; Clinvar (pathogenic):1 | ||||
| chr11:72721851-72722038 | Common:1; Rare:42 | ||||
| chr11:72722187-72722405 | Rare:50 | ||||
| chr11:72752345-72752707 | Common:3; Rare:103 | ||||
| chr11:72814064-72814446 | Common:4; Rare:112 | ||||
| chr11:73218230-73218381 | Rare:32 | ||||
| chr11:73308157-73308294 | Common:1; Rare:54 | ||||
| chr11:73760196-73760313 | Rare:23 |