| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36999260-36999451 | Rare:78 | ||||
| chr13:37000755-37000805 | Rare:24 | ||||
| chr13:37059578-37059754 | Common:1; Rare:58 | ||||
| chr13:37869751-37869926 | Common:1; Rare:41 | ||||
| chr13:38350215-38350474 | Common:1; Rare:79 | ||||
| chr13:39038094-39038482 | Common:1; Rare:95 | ||||
| chr13:39655625-39655755 | Common:2; Rare:74; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:40982858-40983032 | Common:3; Rare:27 | ||||
| chr13:41060121-41060527 | Common:3; Rare:143 | ||||
| chr13:41060838-41061068 | Common:16; Rare:135 | ||||
| chr13:41061126-41061654 | Common:4; Rare:179 | ||||
| chr13:41132701-41132986 | Rare:74 | ||||
| chr13:41457289-41457547 | Common:2; Rare:76 | ||||
| chr13:43786713-43787012 | Common:1; Rare:81 | ||||
| chr13:43879467-43879609 | Rare:39 |