| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111977137-111977395 | Common:3; Rare:57 | ||||
| chr11:111988853-111988996 | Rare:29 | ||||
| chr11:112025298-112025495 | Common:2; Rare:47; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:112073995-112074424 | Common:1; Rare:87 | ||||
| chr11:112086662-112086932 | Rare:125; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr11:112164079-112164136 | Rare:10 | ||||
| chr11:112226250-112226650 | Common:1; Rare:156; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112961276-112961654 | Common:4; Rare:174 | ||||
| chr11:113314454-113314602 | Rare:51 | ||||
| chr11:113875475-113875771 | Common:4; Rare:106 | ||||
| chr11:114059410-114059793 | Rare:80 | ||||
| chr11:114059836-114059897 | Rare:9 | ||||
| chr11:114059952-114060251 | Common:3; Rare:75 | ||||
| chr11:114257514-114257825 | Rare:60 | ||||
| chr11:114296237-114296572 | Rare:63 |