| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:76886342-76886693 | Common:2; Rare:109 | ||||
| chr13:76991522-76991620 | Rare:16 | ||||
| chr13:76991895-76992256 | Common:4; Rare:157; Clinvar:25; Clinvar (benign):20; Clinvar (pathogenic):4 | ||||
| chr13:76992364-76992449 | Common:1; Rare:14 | ||||
| chr13:76992465-76992854 | Common:5; Rare:66 | ||||
| chr13:77026536-77026864 | Common:3; Rare:96 | ||||
| chr13:77027063-77027333 | Common:6; Rare:97 | ||||
| chr13:77326931-77327381 | Common:1; Rare:162 | ||||
| chr13:77697340-77697809 | Common:2; Rare:136 | ||||
| chr13:78659082-78659249 | Common:2; Rare:113 | ||||
| chr13:79405769-79405967 | Rare:65 | ||||
| chr13:79406109-79406616 | Common:6; Rare:120 | ||||
| chr13:79406738-79406784 | Rare:9 | ||||
| chr13:79480983-79481527 | Common:3; Rare:208 | ||||
| chr13:80339777-80340072 | Common:2; Rare:71 |