| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:79405595-79405766 | Rare:41 | ||||
| chr13:79405786-79405941 | Rare:51 | ||||
| chr13:79405948-79406357 | Common:4; Rare:118 | ||||
| chr13:79406411-79406606 | Common:2; Rare:35 | ||||
| chr13:79406714-79406796 | Rare:13 | ||||
| chr13:79480975-79481517 | Common:3; Rare:208 | ||||
| chr13:80339300-80339461 | Common:2; Rare:44 | ||||
| chr13:80340552-80340586 | Common:1; Rare:6 | ||||
| chr13:80340652-80340975 | Rare:61 | ||||
| chr13:80341065-80341160 | Rare:34 | ||||
| chr13:80341243-80341532 | Rare:85 | ||||
| chr13:91398501-91398645 | Rare:42 | ||||
| chr13:93226471-93226871 | Common:3; Rare:79; Clinvar (benign):1 | ||||
| chr13:93226907-93226992 | Rare:15 | ||||
| chr13:93227245-93227353 | Rare:19; Clinvar:2 |