| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118111176-118111589 | Common:11; Rare:192 | ||||
| chr11:118251890-118252570 | Common:4; Rare:362 | ||||
| chr11:118342586-118342733 | Rare:79; Clinvar:4 | ||||
| chr11:118342713-118343113 | Common:4; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:118344112-118344512 | Common:4; Rare:150; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr11:118359410-118359880 | Common:22; Rare:663 | ||||
| chr11:118401066-118402231 | Common:5; Rare:1064 | ||||
| chr11:118435586-118437515 | Common:29; Rare:1675; Clinvar (benign):6 | ||||
| chr11:118530380-118530793 | Common:2; Rare:278 | ||||
| chr11:118530840-118531420 | Common:3; Rare:488 | ||||
| chr11:118565872-118566324 | Common:2; Rare:182 | ||||
| chr11:118572168-118572568 | Common:13; Rare:296 | ||||
| chr11:118572710-118573150 | Common:2; Rare:87 | ||||
| chr11:118573252-118573652 | Common:3; Rare:121 | ||||
| chr11:118607189-118608507 | Common:28; Rare:729 |