| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102347100-102347445 | Common:3; Rare:99 | ||||
| chr11:102451845-102451912 | Rare:21 | ||||
| chr11:102451913-102451995 | Rare:18 | ||||
| chr11:102452509-102452951 | Common:2; Rare:143 | ||||
| chr11:103092012-103092236 | Common:1; Rare:63 | ||||
| chr11:103109311-103109576 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:104163803-104164408 | Common:5; Rare:184 | ||||
| chr11:105610584-105610760 | Rare:39 | ||||
| chr11:106077307-106077730 | Common:2; Rare:131 | ||||
| chr11:107457793-107458115 | Common:6; Rare:90 | ||||
| chr11:108008804-108008977 | Rare:50 | ||||
| chr11:108009070-108009192 | Rare:24 | ||||
| chr11:108009254-108009369 | Rare:53 | ||||
| chr11:108121356-108121677 | Common:5; Rare:110; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr11:108134094-108134316 | Common:1; Rare:55; Clinvar:1; Clinvar (pathogenic):1 |