| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1032805-1032903 | Common:2; Rare:33 | ||||
| chr11:1033187-1033460 | Common:3; Rare:74 | ||||
| chr11:1036608-1036884 | Rare:84 | ||||
| chr11:1157601-1158218 | Common:5; Rare:149 | ||||
| chr11:1222905-1223153 | Common:2; Rare:66 | ||||
| chr11:1257881-1258144 | Common:3; Rare:79; Clinvar (benign):1 | ||||
| chr11:1309554-1309785 | Common:2; Rare:102 | ||||
| chr11:1486758-1487048 | Common:1; Rare:50 | ||||
| chr11:1834222-1834434 | Rare:50 | ||||
| chr11:1868400-1868875 | Common:2; Rare:101 | ||||
| chr11:1871086-1871432 | Common:4; Rare:95 | ||||
| chr11:1919435-1919730 | Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:2137274-2137473 | Rare:46 | ||||
| chr11:2138230-2138585 | Common:2; Rare:70 | ||||
| chr11:2138626-2138736 | Rare:24 |