| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36346307-36346453 | Common:2; Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:37000233-37000452 | Common:2; Rare:46 | ||||
| chr13:37059621-37059745 | Common:1; Rare:38 | ||||
| chr13:39038079-39038439 | Common:1; Rare:88 | ||||
| chr13:39655627-39655742 | Common:1; Rare:67; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr13:41060883-41060949 | Common:11; Rare:47 | ||||
| chr13:41061352-41061633 | Common:2; Rare:88 | ||||
| chr13:41132782-41132984 | Rare:54 | ||||
| chr13:43023477-43023717 | Common:1; Rare:94 | ||||
| chr13:43879476-43879910 | Common:19; Rare:117 | ||||
| chr13:44989432-44989607 | Rare:67 | ||||
| chr13:45120348-45120560 | Common:2; Rare:65 | ||||
| chr13:45341036-45341609 | Common:4; Rare:259 | ||||
| chr13:45464713-45464996 | Common:1; Rare:67 | ||||
| chr13:46052704-46052852 | Common:2; Rare:40 |