| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:103109280-103109521 | Common:1; Rare:65; Clinvar (benign):1 | ||||
| chr11:103109524-103109823 | Common:2; Rare:87; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:104164283-104164316 | Common:1; Rare:14 | ||||
| chr11:104967579-104968116 | Common:4; Rare:90 | ||||
| chr11:104968327-104968410 | Rare:20 | ||||
| chr11:104968492-104968694 | Common:3; Rare:61 | ||||
| chr11:104969021-104969082 | Rare:13 | ||||
| chr11:105035126-105035255 | Rare:38 | ||||
| chr11:105045294-105045463 | Rare:46 | ||||
| chr11:106021749-106021818 | Common:2; Rare:21 | ||||
| chr11:106021979-106022636 | Common:5; Rare:181 | ||||
| chr11:106076655-106077099 | Rare:76 | ||||
| chr11:106077288-106077748 | Common:2; Rare:151 | ||||
| chr11:106077792-106077898 | Common:1; Rare:43 | ||||
| chr11:106077992-106078093 | Common:2; Rare:22 |