| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61361835-61361957 | Common:1; Rare:28 | ||||
| chr11:61362267-61362417 | Common:1; Rare:41; Clinvar:6 | ||||
| chr11:61392527-61392652 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:61429892-61430152 | Common:1; Rare:111; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:61792573-61792955 | Common:5; Rare:102 | ||||
| chr11:61816244-61816296 | Rare:22 | ||||
| chr11:61816786-61816981 | Rare:57 | ||||
| chr11:61967313-61967806 | Common:3; Rare:184; Clinvar:4 | ||||
| chr11:62545589-62545987 | Common:1; Rare:90 | ||||
| chr11:62546708-62546924 | Common:1; Rare:69 | ||||
| chr11:62591500-62591804 | Rare:98 | ||||
| chr11:62621949-62622212 | Common:2; Rare:82 | ||||
| chr11:62653257-62653436 | Common:1; Rare:63 | ||||
| chr11:62665061-62665418 | Common:5; Rare:163 | ||||
| chr11:62671754-62672002 | Common:1; Rare:93; Clinvar (benign):1 |