| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:38349548-38349936 | Common:3; Rare:135; Clinvar (pathogenic):1 | ||||
| chr13:38350215-38350299 | Rare:39 | ||||
| chr13:39038086-39038495 | Common:1; Rare:99 | ||||
| chr13:39603116-39603444 | Common:2; Rare:117 | ||||
| chr13:40771139-40771333 | Common:3; Rare:57 | ||||
| chr13:41060868-41061598 | Common:20; Rare:293 | ||||
| chr13:41132731-41132959 | Rare:62 | ||||
| chr13:41457274-41457552 | Common:2; Rare:77 | ||||
| chr13:42271794-42272190 | Common:4; Rare:105 | ||||
| chr13:43879464-43879659 | Common:1; Rare:51 | ||||
| chr13:43879691-43879910 | Common:18; Rare:62 | ||||
| chr13:44435164-44435463 | Common:3; Rare:86 | ||||
| chr13:44436712-44437033 | Common:3; Rare:91 | ||||
| chr13:44989432-44989614 | Rare:68 | ||||
| chr13:45120392-45120597 | Common:1; Rare:65 |