| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:32538703-32538966 | Common:1; Rare:71 | ||||
| chr13:33285686-33285954 | Common:1; Rare:60 | ||||
| chr13:33817979-33818247 | Common:2; Rare:125 | ||||
| chr13:34942160-34942351 | Common:3; Rare:62 | ||||
| chr13:35476312-35476857 | Common:1; Rare:99 | ||||
| chr13:36297768-36297914 | Common:1; Rare:54 | ||||
| chr13:36346294-36346469 | Common:2; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36346591-36346796 | Common:4; Rare:56 | ||||
| chr13:36920124-36920437 | Common:8; Rare:135; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:37000355-37000412 | Rare:9 | ||||
| chr13:37000686-37000811 | Rare:51; Clinvar (pathogenic):1 | ||||
| chr13:37059550-37059741 | Common:1; Rare:65 | ||||
| chr13:37598545-37598893 | Common:2; Rare:102 | ||||
| chr13:39037872-39038482 | Common:2; Rare:164 | ||||
| chr13:39655583-39655732 | Common:3; Rare:84; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 |