| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:746895-746919 | Rare:7 | ||||
| chr11:747227-747540 | Rare:123; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:777071-777127 | Common:1; Rare:16 | ||||
| chr11:777388-777794 | Common:3; Rare:156 | ||||
| chr11:796163-796378 | Rare:62; Clinvar:1 | ||||
| chr11:797236-797543 | Common:2; Rare:87 | ||||
| chr11:797545-797803 | Rare:76 | ||||
| chr11:797872-798072 | Common:1; Rare:55 | ||||
| chr11:798163-798492 | Common:2; Rare:114 | ||||
| chr11:805178-805466 | Common:8; Rare:102 | ||||
| chr11:809269-809676 | Common:5; Rare:101 | ||||
| chr11:809740-810131 | Common:3; Rare:153 | ||||
| chr11:819366-819645 | Common:2; Rare:107; Clinvar:3 | ||||
| chr11:830285-830403 | Common:1; Rare:40 | ||||
| chr11:832829-833033 | Common:7; Rare:66 |