| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:42792563-42792846 | Common:3; Rare:78 | ||||
| chr2:43595917-43596205 | Common:1; Rare:101 | ||||
| chr2:44361433-44362032 | Common:4; Rare:198 | ||||
| chr2:44941804-44942036 | Common:1; Rare:48 | ||||
| chr2:46297173-46297409 | Common:3; Rare:94 | ||||
| chr2:46616978-46617289 | Common:7; Rare:131 | ||||
| chr2:46915733-46915950 | Common:2; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916016-46916187 | Common:2; Rare:54 | ||||
| chr2:47176164-47176948 | Common:9; Rare:352; Clinvar (benign):5 | ||||
| chr2:47345045-47345174 | Rare:34 | ||||
| chr2:47369239-47369576 | Common:4; Rare:145; Clinvar:14; Clinvar (benign):5 | ||||
| chr2:47402824-47403194 | Common:1; Rare:167; Clinvar:50; Clinvar (benign):27 | ||||
| chr2:47905497-47905848 | Common:3; Rare:173 | ||||
| chr2:48314306-48314626 | Rare:104 | ||||
| chr2:48440614-48440865 | Common:8; Rare:117 |