| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:103091887-103092229 | Common:1; Rare:100 | ||||
| chr11:104163998-104164162 | Common:1; Rare:39 | ||||
| chr11:105034826-105035016 | Common:1; Rare:41 | ||||
| chr11:105610065-105610116 | Rare:9 | ||||
| chr11:106022175-106022559 | Common:3; Rare:112 | ||||
| chr11:106077306-106077730 | Common:2; Rare:131 | ||||
| chr11:108008875-108009250 | Common:1; Rare:98 | ||||
| chr11:108009273-108009415 | Rare:62 | ||||
| chr11:108121424-108121672 | Common:4; Rare:94; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr11:108222544-108223158 | Common:1; Rare:198; Clinvar:9; Clinvar (benign):1 | ||||
| chr11:108223186-108223447 | Rare:67; Clinvar (benign):2 | ||||
| chr11:108223973-108224105 | Rare:28 | ||||
| chr11:108286941-108287073 | Rare:26 | ||||
| chr11:108498296-108498462 | Common:2; Rare:50 | ||||
| chr11:108593532-108593945 | Common:5; Rare:111 |