| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:76886837-76886932 | Rare:21 | ||||
| chr13:76991863-76992287 | Common:5; Rare:178; Clinvar:25; Clinvar (benign):24; Clinvar (pathogenic):5 | ||||
| chr13:76992299-76992458 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chr13:76992471-76992850 | Common:4; Rare:65 | ||||
| chr13:77026504-77026887 | Common:3; Rare:114 | ||||
| chr13:77027087-77027382 | Common:6; Rare:106 | ||||
| chr13:77325769-77326196 | Common:2; Rare:78 | ||||
| chr13:77326591-77326890 | Common:1; Rare:86 | ||||
| chr13:77326970-77327351 | Common:1; Rare:149 | ||||
| chr13:77535578-77535767 | Rare:36 | ||||
| chr13:78658409-78658781 | Rare:99 | ||||
| chr13:78659087-78659450 | Common:15; Rare:206 | ||||
| chr13:79405595-79405970 | Common:1; Rare:109 | ||||
| chr13:79405977-79406352 | Common:4; Rare:104 | ||||
| chr13:79406416-79406614 | Common:2; Rare:36 |