| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111937300-111937429 | Common:1; Rare:29 | ||||
| chr11:111937483-111937567 | Rare:27 | ||||
| chr11:111976681-111977024 | Rare:62 | ||||
| chr11:111977028-111977664 | Common:10; Rare:151 | ||||
| chr11:112024784-112024933 | Common:3; Rare:28; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:112024981-112025232 | Rare:60; Clinvar:2 | ||||
| chr11:112025252-112025535 | Common:3; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
| chr11:112073937-112074097 | Common:1; Rare:32 | ||||
| chr11:112074172-112074425 | Common:1; Rare:56 | ||||
| chr11:112074573-112074763 | Common:1; Rare:41 | ||||
| chr11:112074856-112074924 | Common:1; Rare:7 | ||||
| chr11:112085972-112086244 | Common:2; Rare:46 | ||||
| chr11:112086283-112086552 | Common:1; Rare:63 | ||||
| chr11:112086650-112086978 | Common:1; Rare:144; Clinvar:10; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr11:112163730-112163923 | Common:1; Rare:29 |