| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95789478-95789598 | Common:1; Rare:62 | ||||
| chr11:95790359-95790591 | Common:1; Rare:89 | ||||
| chr11:96389860-96390061 | Common:1; Rare:84 | ||||
| chr11:101914752-101915025 | Common:1; Rare:59 | ||||
| chr11:101915106-101915329 | Common:3; Rare:65 | ||||
| chr11:102110233-102110454 | Rare:88 | ||||
| chr11:102347111-102347298 | Common:2; Rare:62 | ||||
| chr11:102452551-102452864 | Common:1; Rare:104 | ||||
| chr11:103092017-103092211 | Common:1; Rare:57 | ||||
| chr11:105045308-105045448 | Rare:39 | ||||
| chr11:106077319-106077740 | Common:2; Rare:136 | ||||
| chr11:108008873-108009369 | Common:1; Rare:154 | ||||
| chr11:108121378-108121678 | Common:5; Rare:101; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr11:108222603-108223115 | Common:1; Rare:162; Clinvar:7; Clinvar (benign):1 | ||||
| chr11:111766359-111766433 | Common:1; Rare:43 |