| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:38349529-38349910 | Common:4; Rare:126; Clinvar (pathogenic):1 | ||||
| chr13:38350215-38350287 | Rare:37 | ||||
| chr13:39038087-39038426 | Common:1; Rare:87 | ||||
| chr13:40771141-40771319 | Common:3; Rare:52 | ||||
| chr13:40789377-40789611 | Common:2; Rare:76; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:41060875-41061598 | Common:20; Rare:290 | ||||
| chr13:41132732-41132980 | Rare:68 | ||||
| chr13:41194467-41194771 | Common:2; Rare:71 | ||||
| chr13:41263552-41263612 | Rare:13 | ||||
| chr13:41311189-41311340 | Common:1; Rare:65 | ||||
| chr13:41457331-41457547 | Common:2; Rare:63 | ||||
| chr13:42992184-42992279 | Common:1; Rare:23 | ||||
| chr13:43023550-43023678 | Common:1; Rare:60 | ||||
| chr13:43879449-43879600 | Rare:40 | ||||
| chr13:43879686-43879928 | Common:18; Rare:67 |