| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47783679-47783955 | Common:7; Rare:58; Clinvar (benign):2 | ||||
| chr2:47905490-47905911 | Common:3; Rare:197 | ||||
| chr2:48314183-48314802 | Common:1; Rare:217 | ||||
| chr2:48440621-48440861 | Common:8; Rare:114 | ||||
| chr2:53767525-53768019 | Common:5; Rare:185 | ||||
| chr2:53786826-53787372 | Common:1; Rare:209 | ||||
| chr2:53870460-53870638 | Rare:49 | ||||
| chr2:53970569-53971129 | Common:11; Rare:210 | ||||
| chr2:54457035-54457268 | Common:1; Rare:99 | ||||
| chr2:54557661-54558110 | Common:3; Rare:102 | ||||
| chr2:54558257-54558570 | Common:4; Rare:103 | ||||
| chr2:54558613-54558882 | Common:1; Rare:78 | ||||
| chr2:54723367-54723685 | Common:1; Rare:101 | ||||
| chr2:54973558-54973867 | Common:3; Rare:96 | ||||
| chr2:55050093-55050871 | Common:8; Rare:261 |