| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62592162-62592730 | Common:2; Rare:184 | ||||
| chr11:62599168-62599580 | Common:3; Rare:230 | ||||
| chr11:62599751-62600512 | Common:1; Rare:195 | ||||
| chr11:62600511-62600825 | Common:1; Rare:130 | ||||
| chr11:62600781-62601352 | Common:3; Rare:384 | ||||
| chr11:62601306-62601645 | Common:5; Rare:221 | ||||
| chr11:62601588-62602240 | Common:8; Rare:726 | ||||
| chr11:62602273-62602673 | Common:12; Rare:348 | ||||
| chr11:62611208-62612861 | Common:25; Rare:1484; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:62612870-62613300 | Common:4; Rare:198; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:62621854-62622255 | Common:12; Rare:614 | ||||
| chr11:62646041-62646441 | Common:4; Rare:155 | ||||
| chr11:62646553-62646953 | Common:8; Rare:601; Clinvar (pathogenic):4 | ||||
| chr11:62652313-62652928 | Common:2; Rare:251 | ||||
| chr11:62653180-62653720 | Common:7; Rare:529 |