| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130314071-130314090 | Rare:2 | ||||
| chr11:130314299-130314555 | Common:1; Rare:87 | ||||
| chr11:130314602-130314697 | Rare:28 | ||||
| chr11:130314845-130315171 | Common:3; Rare:101 | ||||
| chr11:130916373-130916709 | Common:9; Rare:106 | ||||
| chr11:134223886-134224184 | Common:2; Rare:114 | ||||
| chr11:134224445-134224769 | Common:2; Rare:138 | ||||
| chr11:134225445-134225549 | Rare:28 | ||||
| chr11:134252850-134252866 | Rare:4 | ||||
| chr11:134253304-134253628 | Common:3; Rare:117; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:389209-389408 | Common:1; Rare:79 | ||||
| chr12:389442-389744 | Common:7; Rare:120 | ||||
| chr12:401385-401715 | Common:2; Rare:95 | ||||
| chr12:643579-644053 | Common:2; Rare:105 | ||||
| chr12:752057-752130 | Rare:5 |