| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68903763-68903932 | Common:4; Rare:77; Clinvar (benign):6 | ||||
| chr11:69640984-69641238 | Common:1; Rare:53 | ||||
| chr11:70398431-70398614 | Common:2; Rare:68 | ||||
| chr11:71448295-71448671 | Common:4; Rare:102; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71452954-71453247 | Common:4; Rare:78 | ||||
| chr11:72041062-72041275 | Common:1; Rare:36 | ||||
| chr11:72224110-72224218 | Common:3; Rare:26 | ||||
| chr11:72793536-72793781 | Rare:50 | ||||
| chr11:73760267-73760332 | Rare:13 | ||||
| chr11:73876784-73877032 | Common:5; Rare:69 | ||||
| chr11:74170865-74171343 | Common:2; Rare:152 | ||||
| chr11:74949074-74949310 | Common:6; Rare:67 | ||||
| chr11:76783051-76783353 | Common:9; Rare:100 | ||||
| chr11:78139587-78139756 | Rare:62; Clinvar:2 | ||||
| chr11:78188593-78188992 | Common:3; Rare:125 |