| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:94543784-94543957 | Common:3; Rare:39 | ||||
| chr11:94768255-94768427 | Rare:50 | ||||
| chr11:94973537-94973705 | Rare:50 | ||||
| chr11:95066844-95066939 | Rare:20 | ||||
| chr11:95067446-95067573 | Rare:46 | ||||
| chr11:95089731-95089944 | Common:3; Rare:90 | ||||
| chr11:95789478-95789893 | Common:4; Rare:191 | ||||
| chr11:95790338-95790598 | Common:1; Rare:102 | ||||
| chr11:95923835-95924161 | Common:2; Rare:142; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96342753-96342881 | Rare:23 | ||||
| chr11:96389831-96390043 | Common:1; Rare:88 | ||||
| chr11:100687097-100687258 | Common:4; Rare:39 | ||||
| chr11:101583469-101583636 | Common:1; Rare:59; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:101914767-101915094 | Common:4; Rare:79 | ||||
| chr11:101915108-101915330 | Common:3; Rare:65 |