| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62546673-62546905 | Common:1; Rare:73 | ||||
| chr11:62591494-62591857 | Rare:122 | ||||
| chr11:62601209-62601502 | Common:1; Rare:88 | ||||
| chr11:62601615-62601976 | Common:1; Rare:115 | ||||
| chr11:62611546-62611860 | Rare:77 | ||||
| chr11:62621903-62622234 | Common:2; Rare:103 | ||||
| chr11:62646560-62646810 | Common:1; Rare:101; Clinvar (pathogenic):1 | ||||
| chr11:62653262-62653505 | Common:1; Rare:72 | ||||
| chr11:62664850-62665474 | Common:6; Rare:262 | ||||
| chr11:62671622-62672059 | Common:2; Rare:161; Clinvar (benign):3 | ||||
| chr11:62678866-62679219 | Rare:116 | ||||
| chr11:62706214-62706439 | Common:3; Rare:95; Clinvar (benign):5 | ||||
| chr11:62709508-62709659 | Rare:69 | ||||
| chr11:62727913-62728197 | Common:6; Rare:74 | ||||
| chr11:62728404-62728597 | Common:3; Rare:109 |