| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:23927065-23927329 | Common:3; Rare:93 | ||||
| chr2:23940363-23940514 | Common:3; Rare:53 | ||||
| chr2:24076204-24076597 | Rare:107 | ||||
| chr2:24123282-24123510 | Common:1; Rare:61 | ||||
| chr2:24793133-24793161 | Rare:12 | ||||
| chr2:24971907-24972138 | Common:1; Rare:75 | ||||
| chr2:25673513-25673740 | Common:1; Rare:85 | ||||
| chr2:25878445-25878699 | Common:2; Rare:76 | ||||
| chr2:25982448-25982636 | Common:1; Rare:45 | ||||
| chr2:26244564-26244977 | Common:2; Rare:154; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345785-26346165 | Common:1; Rare:115 | ||||
| chr2:26764210-26764347 | Common:1; Rare:53 | ||||
| chr2:27032862-27033016 | Rare:59 | ||||
| chr2:27071324-27071878 | Common:2; Rare:174 | ||||
| chr2:27078228-27078838 | Common:3; Rare:138 |