| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46297675-46297820 | Rare:59; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:46542538-46542657 | Rare:40 | ||||
| chr2:46616982-46617262 | Common:7; Rare:122 | ||||
| chr2:46699080-46699340 | Common:1; Rare:79 | ||||
| chr2:46914146-46914262 | Rare:21 | ||||
| chr2:46915704-46915939 | Common:2; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:46916007-46916189 | Common:2; Rare:56 | ||||
| chr2:46941694-46941807 | Common:3; Rare:41; Clinvar (benign):1 | ||||
| chr2:47176439-47176565 | Rare:91; Clinvar (benign):5 | ||||
| chr2:47345052-47345148 | Rare:26 | ||||
| chr2:47369229-47369539 | Common:3; Rare:133; Clinvar:10; Clinvar (benign):4 | ||||
| chr2:47782946-47783198 | Common:2; Rare:108; Clinvar:4; Clinvar (benign):7 | ||||
| chr2:47905497-47905847 | Common:3; Rare:172 | ||||
| chr2:48440614-48440907 | Common:8; Rare:127 | ||||
| chr2:48568493-48568816 | Common:5; Rare:71 |