| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61362097-61362235 | Rare:42 | ||||
| chr11:61362239-61362339 | Common:2; Rare:36; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:61362341-61362458 | Rare:25; Clinvar:3 | ||||
| chr11:61391996-61392021 | Rare:5 | ||||
| chr11:61392264-61392445 | Common:1; Rare:30; Clinvar:1 | ||||
| chr11:61392493-61392692 | Common:2; Rare:64; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:61392744-61392884 | Rare:30 | ||||
| chr11:61429421-61429597 | Common:2; Rare:54 | ||||
| chr11:61429838-61430205 | Common:2; Rare:154; Clinvar:3; Clinvar (benign):9 | ||||
| chr11:61430346-61430393 | Rare:9 | ||||
| chr11:61508301-61508351 | Rare:11 | ||||
| chr11:61508501-61508799 | Common:1; Rare:79 | ||||
| chr11:61509221-61509572 | Common:1; Rare:77 | ||||
| chr11:61580454-61580698 | Rare:55 | ||||
| chr11:61580979-61581316 | Common:2; Rare:108 |