| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:32586227-32586597 | Common:2; Rare:114 | ||||
| chr13:36346301-36346505 | Common:3; Rare:58; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:36999265-36999451 | Rare:75 | ||||
| chr13:37000736-37000815 | Rare:33; Clinvar (pathogenic):1 | ||||
| chr13:37059584-37059751 | Common:1; Rare:55 | ||||
| chr13:38349796-38350056 | Common:3; Rare:119 | ||||
| chr13:38350214-38350349 | Rare:45 | ||||
| chr13:39038059-39038499 | Common:1; Rare:106 | ||||
| chr13:40771131-40771444 | Common:3; Rare:93 | ||||
| chr13:40789359-40789644 | Common:2; Rare:99; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:41060356-41060528 | Rare:67 | ||||
| chr13:41060838-41061068 | Common:16; Rare:135 | ||||
| chr13:41061131-41061609 | Common:4; Rare:158 | ||||
| chr13:41132732-41132996 | Rare:72 | ||||
| chr13:41194454-41194781 | Common:2; Rare:75 |