| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49936219-49936598 | Common:2; Rare:221 | ||||
| chr13:49996759-49997088 | Common:2; Rare:117 | ||||
| chr13:50081935-50082312 | Common:2; Rare:189 | ||||
| chr13:50909575-50909822 | Rare:55; Clinvar:2 | ||||
| chr13:51451980-51452297 | Common:6; Rare:162 | ||||
| chr13:51452647-51452817 | Rare:47 | ||||
| chr13:51452915-51453418 | Common:2; Rare:333 | ||||
| chr13:51584276-51584760 | Common:5; Rare:220 | ||||
| chr13:51803713-51803863 | Rare:81 | ||||
| chr13:51804086-51804301 | Common:4; Rare:109 | ||||
| chr13:52011302-52011702 | Common:4; Rare:200; Clinvar:15; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:52011856-52012460 | Common:2; Rare:213; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr13:52159405-52159917 | Common:8; Rare:229 | ||||
| chr13:52449880-52450280 | Common:1; Rare:105 | ||||
| chr13:52455318-52455551 | Common:6; Rare:144 |