| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43637117-43637334 | Common:2; Rare:71 | ||||
| chr2:44361483-44362010 | Common:4; Rare:166 | ||||
| chr2:46297012-46297370 | Common:6; Rare:143 | ||||
| chr2:46297675-46297796 | Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46375372-46375730 | Common:2; Rare:85 | ||||
| chr2:46617019-46617262 | Common:7; Rare:106 | ||||
| chr2:46915722-46915910 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46941566-46941637 | Common:1; Rare:30; Clinvar:1 | ||||
| chr2:46941662-46941779 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:47176427-47176660 | Common:1; Rare:139; Clinvar (benign):5 | ||||
| chr2:47782979-47783189 | Common:2; Rare:91; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:48314629-48314769 | Rare:51 | ||||
| chr2:48440631-48440962 | Common:7; Rare:148 | ||||
| chr2:53767549-53767867 | Common:5; Rare:108 | ||||
| chr2:53786842-53787191 | Common:1; Rare:135 |