| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:232776535-232776566 | Rare:5; Clinvar:1 | ||||
| chr2:233854471-233854782 | Common:5; Rare:89 | ||||
| chr2:234951790-234952109 | Common:2; Rare:84 | ||||
| chr2:236507426-236507651 | Common:6; Rare:78 | ||||
| chr2:236569622-236569898 | Common:8; Rare:52 | ||||
| chr2:237085790-237085973 | Common:1; Rare:73 | ||||
| chr2:237487157-237487287 | Common:2; Rare:36 | ||||
| chr2:237966728-237967078 | Common:4; Rare:108 | ||||
| chr2:238060701-238061057 | Common:4; Rare:113 | ||||
| chr2:238203583-238203821 | Common:3; Rare:101 | ||||
| chr2:238426880-238427067 | Common:1; Rare:69 | ||||
| chr2:239309178-239309296 | Rare:24 | ||||
| chr2:239401641-239401732 | Rare:40 | ||||
| chr2:240025291-240025429 | Common:1; Rare:56; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240136264-240136403 | Common:1; Rare:62 |