| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:163437260-163437668 | Common:1; Rare:116 | ||||
| chr5:163460011-163460677 | Common:7; Rare:184 | ||||
| chr5:163505433-163505752 | Common:1; Rare:109 | ||||
| chr5:168844810-168844903 | Common:1; Rare:24 | ||||
| chr5:169300972-169301309 | Common:3; Rare:99 | ||||
| chr5:169583592-169583895 | Common:7; Rare:89 | ||||
| chr5:171387520-171387898 | Rare:174 | ||||
| chr5:172006604-172007047 | Common:2; Rare:115 | ||||
| chr5:172188175-172188533 | Common:1; Rare:94 | ||||
| chr5:172958776-172958938 | Common:3; Rare:48 | ||||
| chr5:172959365-172959496 | Common:1; Rare:47 | ||||
| chr5:173144509-173144627 | Rare:45 | ||||
| chr5:173888637-173889068 | Common:1; Rare:69 | ||||
| chr5:174724521-174724713 | Common:1; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:176361603-176361898 | Common:1; Rare:79 |