| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69640979-69641508 | Common:1; Rare:131 | ||||
| chr11:69675251-69675531 | Rare:84 | ||||
| chr11:70203133-70203366 | Common:3; Rare:87 | ||||
| chr11:70203472-70203742 | Rare:95; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:70270477-70270743 | Common:2; Rare:107 | ||||
| chr11:70371390-70371481 | Common:4; Rare:9 | ||||
| chr11:70397907-70397958 | Rare:10 | ||||
| chr11:70398004-70398017 | Rare:1 | ||||
| chr11:70398231-70398408 | Common:2; Rare:55 | ||||
| chr11:70398421-70398640 | Common:2; Rare:81 | ||||
| chr11:70422742-70422990 | Common:1; Rare:74 | ||||
| chr11:71448295-71448681 | Common:4; Rare:106; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71928398-71928722 | Rare:89 | ||||
| chr11:71928884-71929123 | Common:1; Rare:83 | ||||
| chr11:72080420-72080858 | Common:2; Rare:106; Clinvar:8 |