| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36346301-36346510 | Common:3; Rare:59; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:36346632-36346787 | Common:4; Rare:44 | ||||
| chr13:36999265-36999470 | Rare:83 | ||||
| chr13:37000235-37000407 | Common:2; Rare:31 | ||||
| chr13:37000704-37000839 | Rare:57; Clinvar (pathogenic):1 | ||||
| chr13:37059453-37059729 | Common:1; Rare:81 | ||||
| chr13:38349542-38349919 | Common:4; Rare:128; Clinvar (pathogenic):1 | ||||
| chr13:39037709-39038056 | Common:1; Rare:108 | ||||
| chr13:39038107-39038433 | Common:1; Rare:81 | ||||
| chr13:39655627-39655802 | Common:2; Rare:88; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:40771032-40771355 | Common:3; Rare:113 | ||||
| chr13:40789359-40789617 | Common:2; Rare:87; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:41061395-41061665 | Common:2; Rare:81 | ||||
| chr13:41132692-41133021 | Common:1; Rare:78 | ||||
| chr13:41194466-41194692 | Common:2; Rare:48 |