| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64359270-64359510 | Common:2; Rare:119 | ||||
| chr11:64723060-64723380 | Common:2; Rare:71 | ||||
| chr11:64742801-64743374 | Common:1; Rare:353; Clinvar:1 | ||||
| chr11:64769070-64769480 | Common:1; Rare:118 | ||||
| chr11:64777347-64777991 | Common:3; Rare:501 | ||||
| chr11:64778342-64778823 | Common:10; Rare:562 | ||||
| chr11:64803101-64803439 | Rare:309 | ||||
| chr11:64809812-64810026 | Rare:46; Clinvar:11; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr11:64810461-64810843 | Common:6; Rare:167; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:64844543-64844942 | Common:11; Rare:245 | ||||
| chr11:64878447-64879039 | Common:8; Rare:360 | ||||
| chr11:64879294-64879603 | Common:2; Rare:61 | ||||
| chr11:64917084-64917615 | Common:9; Rare:291 | ||||
| chr11:64923980-64924800 | Common:6; Rare:261 | ||||
| chr11:64935871-64936013 | Rare:32 |