| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:232550545-232550723 | Rare:70 | ||||
| chr2:232697130-232697379 | Common:2; Rare:81 | ||||
| chr2:232776515-232776573 | Rare:10; Clinvar:1 | ||||
| chr2:233854493-233854741 | Common:4; Rare:71 | ||||
| chr2:236167285-236167645 | Common:4; Rare:127 | ||||
| chr2:236507410-236507672 | Common:7; Rare:87 | ||||
| chr2:237085803-237085951 | Common:1; Rare:60 | ||||
| chr2:237966728-237967089 | Common:4; Rare:112 | ||||
| chr2:238203554-238203810 | Common:5; Rare:101 | ||||
| chr2:238426890-238427073 | Common:1; Rare:69 | ||||
| chr2:240025225-240025496 | Common:3; Rare:103; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:240560760-240560926 | Common:2; Rare:82 | ||||
| chr2:241102259-241102395 | Common:2; Rare:50 | ||||
| chr2:241149434-241149649 | Common:3; Rare:68 | ||||
| chr2:241240031-241240311 | Common:1; Rare:71 |