| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36297804-36297923 | Rare:46 | ||||
| chr13:36345543-36345671 | Common:1; Rare:25 | ||||
| chr13:36346282-36346454 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36346632-36346781 | Common:3; Rare:44 | ||||
| chr13:37000736-37000808 | Rare:29 | ||||
| chr13:37059585-37059726 | Common:1; Rare:49 | ||||
| chr13:38349786-38349932 | Common:1; Rare:70 | ||||
| chr13:38350215-38350291 | Rare:37 | ||||
| chr13:39038079-39038460 | Common:1; Rare:91 | ||||
| chr13:39603122-39603284 | Common:1; Rare:55 | ||||
| chr13:41019279-41019398 | Rare:18 | ||||
| chr13:41060868-41061038 | Common:16; Rare:105 | ||||
| chr13:41061352-41061579 | Common:2; Rare:67 | ||||
| chr13:41132759-41133029 | Common:1; Rare:68 | ||||
| chr13:42992168-42992393 | Common:3; Rare:47 |