| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:39655608-39655802 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:40789368-40789628 | Common:2; Rare:87; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:41019233-41019415 | Rare:28 | ||||
| chr13:41060815-41061081 | Common:17; Rare:153 | ||||
| chr13:41061131-41061285 | Common:1; Rare:54 | ||||
| chr13:41061352-41061586 | Common:2; Rare:69 | ||||
| chr13:41132759-41132980 | Rare:57 | ||||
| chr13:41194392-41194575 | Common:2; Rare:42 | ||||
| chr13:41263551-41263601 | Rare:12 | ||||
| chr13:41457222-41457565 | Common:2; Rare:88 | ||||
| chr13:41457649-41457756 | Rare:27 | ||||
| chr13:41463437-41463698 | Common:1; Rare:45 | ||||
| chr13:42271776-42272041 | Common:2; Rare:76 | ||||
| chr13:42992143-42992346 | Common:2; Rare:47 | ||||
| chr13:43879460-43879913 | Common:19; Rare:120 |