| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66288917-66289490 | Common:6; Rare:391 | ||||
| chr11:66344983-66345290 | Common:3; Rare:189 | ||||
| chr11:66347480-66347890 | Common:13; Rare:227; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:66347990-66348270 | Common:1; Rare:184 | ||||
| chr11:66371250-66371530 | Rare:200 | ||||
| chr11:66371537-66372041 | Common:8; Rare:415 | ||||
| chr11:66371942-66372360 | Common:6; Rare:162 | ||||
| chr11:66372387-66372568 | Rare:78 | ||||
| chr11:66437439-66438587 | Common:1; Rare:372 | ||||
| chr11:66438704-66439400 | Common:5; Rare:243 | ||||
| chr11:66466652-66466972 | Rare:236 | ||||
| chr11:66479840-66480140 | Common:2; Rare:92 | ||||
| chr11:66480121-66480695 | Common:11; Rare:297 | ||||
| chr11:66510551-66510706 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr11:66545962-66546351 | Common:15; Rare:267 |