| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36345543-36345657 | Common:1; Rare:23 | ||||
| chr13:36346301-36346459 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36999275-36999457 | Rare:74 | ||||
| chr13:37000227-37000397 | Common:2; Rare:30 | ||||
| chr13:37000748-37000805 | Rare:25 | ||||
| chr13:37059610-37059775 | Common:1; Rare:56 | ||||
| chr13:39038081-39038426 | Common:1; Rare:87 | ||||
| chr13:40771130-40771299 | Common:2; Rare:53 | ||||
| chr13:40789377-40789615 | Common:2; Rare:78; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:41060938-41061598 | Common:11; Rare:239 | ||||
| chr13:41132732-41133002 | Rare:72 | ||||
| chr13:42271760-42272033 | Common:2; Rare:78 | ||||
| chr13:43879464-43879920 | Common:19; Rare:120 | ||||
| chr13:44435170-44435441 | Common:3; Rare:77 | ||||
| chr13:44436783-44436997 | Common:2; Rare:65 |