| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:39437071-39437453 | Common:4; Rare:136 | ||||
| chr2:42169164-42169431 | Common:1; Rare:133 | ||||
| chr2:43595978-43596207 | Common:1; Rare:79 | ||||
| chr2:44361479-44361982 | Common:3; Rare:159 | ||||
| chr2:46617019-46617262 | Common:7; Rare:106 | ||||
| chr2:46915722-46915910 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916012-46916137 | Common:2; Rare:39 | ||||
| chr2:47176439-47176759 | Common:4; Rare:157; Clinvar (benign):5 | ||||
| chr2:47345053-47345148 | Rare:26 | ||||
| chr2:47782947-47783202 | Common:2; Rare:112; Clinvar:4; Clinvar (benign):8 | ||||
| chr2:48314871-48315066 | Common:1; Rare:85 | ||||
| chr2:48440615-48440815 | Common:6; Rare:83 | ||||
| chr2:53767559-53767829 | Common:4; Rare:91 | ||||
| chr2:53786842-53787213 | Common:1; Rare:143 | ||||
| chr2:53970788-53971152 | Common:11; Rare:131 |