| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38875886-38876049 | Common:1; Rare:59 | ||||
| chr2:39437078-39437453 | Common:4; Rare:134 | ||||
| chr2:43595978-43596158 | Common:1; Rare:57 | ||||
| chr2:44361483-44361986 | Common:3; Rare:160 | ||||
| chr2:46073691-46073943 | Common:1; Rare:52 | ||||
| chr2:46297545-46297792 | Common:1; Rare:69; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:46617012-46617257 | Common:6; Rare:105 | ||||
| chr2:46915722-46916135 | Common:4; Rare:133; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47176440-47176820 | Common:4; Rare:180; Clinvar (benign):5 | ||||
| chr2:47345075-47345148 | Rare:20 | ||||
| chr2:47782939-47783198 | Common:2; Rare:112; Clinvar:4; Clinvar (benign):7 | ||||
| chr2:48440631-48440851 | Common:7; Rare:108 | ||||
| chr2:53767650-53767866 | Common:3; Rare:72 | ||||
| chr2:53786846-53787191 | Common:1; Rare:132 | ||||
| chr2:53970750-53971126 | Common:10; Rare:130 |