| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64304708-64304838 | Common:1; Rare:29 | ||||
| chr11:64335167-64335380 | Rare:38 | ||||
| chr11:64358123-64358379 | Common:1; Rare:47 | ||||
| chr11:64372934-64373301 | Common:5; Rare:75 | ||||
| chr11:64405347-64405490 | Common:1; Rare:23 | ||||
| chr11:64406300-64406410 | Rare:13 | ||||
| chr11:64406634-64406944 | Common:1; Rare:55 | ||||
| chr11:64407307-64407531 | Common:1; Rare:52 | ||||
| chr11:64439358-64439531 | Rare:25 | ||||
| chr11:64448781-64449137 | Common:5; Rare:69 | ||||
| chr11:64449619-64449829 | Rare:50 | ||||
| chr11:64566285-64566619 | Common:4; Rare:66 | ||||
| chr11:64566624-64566943 | Common:1; Rare:64 | ||||
| chr11:64804003-64804101 | Common:3; Rare:14; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:64842313-64842416 | Common:1; Rare:17 |