| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68751380-68751780 | Common:4; Rare:266 | ||||
| chr11:68839057-68839651 | Common:9; Rare:406 | ||||
| chr11:68839907-68840516 | Common:3; Rare:180 | ||||
| chr11:68841760-68842160 | Common:1; Rare:157; Clinvar (benign):3 | ||||
| chr11:68903642-68904042 | Common:35; Rare:713; Clinvar:21; Clinvar (benign):49 | ||||
| chr11:68904195-68904725 | Common:7; Rare:156 | ||||
| chr11:69048586-69049127 | Common:45; Rare:874 | ||||
| chr11:69049514-69049914 | Common:3; Rare:96 | ||||
| chr11:69293839-69294239 | Common:12; Rare:153 | ||||
| chr11:69295180-69295652 | Common:5; Rare:483 | ||||
| chr11:69298238-69298895 | Common:12; Rare:267 | ||||
| chr11:69640801-69641389 | Common:2; Rare:271 | ||||
| chr11:69643110-69643760 | Common:2; Rare:312 | ||||
| chr11:69674377-69674907 | Common:16; Rare:208 | ||||
| chr11:69675135-69675632 | Common:11; Rare:550 |