| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46941122-46941290 | Common:1; Rare:73 | ||||
| chr2:46941707-46941873 | Common:3; Rare:55; Clinvar (benign):1 | ||||
| chr2:47173969-47174247 | Common:1; Rare:65 | ||||
| chr2:47176398-47176598 | Rare:136; Clinvar (benign):5 | ||||
| chr2:47782881-47783214 | Common:3; Rare:147; Clinvar:6; Clinvar (benign):10 | ||||
| chr2:47905491-47905700 | Common:3; Rare:105 | ||||
| chr2:48314777-48315072 | Common:1; Rare:121 | ||||
| chr2:48440614-48440956 | Common:8; Rare:150 | ||||
| chr2:53767518-53767879 | Common:5; Rare:121 | ||||
| chr2:53786819-53787375 | Common:1; Rare:211 | ||||
| chr2:53870876-53870921 | Common:1; Rare:13 | ||||
| chr2:53970755-53971122 | Common:10; Rare:125 | ||||
| chr2:54456078-54456514 | Common:1; Rare:161 | ||||
| chr2:54457084-54457295 | Common:2; Rare:85 | ||||
| chr2:54662250-54662633 | Common:2; Rare:72 |