| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:232550545-232550736 | Rare:79 | ||||
| chr2:232550748-232551125 | Common:3; Rare:95 | ||||
| chr2:232697095-232697377 | Common:2; Rare:93 | ||||
| chr2:233251520-233251729 | Common:3; Rare:74 | ||||
| chr2:233419052-233419247 | Common:2; Rare:39 | ||||
| chr2:233854472-233854779 | Common:5; Rare:88 | ||||
| chr2:236167313-236167503 | Common:3; Rare:74 | ||||
| chr2:237085761-237085973 | Common:2; Rare:79 | ||||
| chr2:238060723-238061143 | Common:6; Rare:134 | ||||
| chr2:238203616-238203821 | Common:3; Rare:89 | ||||
| chr2:238426641-238426986 | Common:6; Rare:90 | ||||
| chr2:238434496-238434747 | Common:1; Rare:33 | ||||
| chr2:239401641-239401739 | Rare:45 | ||||
| chr2:240025292-240025452 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240136264-240136404 | Common:1; Rare:63 |