| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:231961652-231961748 | Rare:28; Clinvar:1 | ||||
| chr2:232550531-232550716 | Rare:73 | ||||
| chr2:232550850-232551125 | Common:1; Rare:59 | ||||
| chr2:233418929-233419364 | Common:3; Rare:85 | ||||
| chr2:233854480-233854741 | Common:5; Rare:76 | ||||
| chr2:234951811-234952148 | Common:1; Rare:86 | ||||
| chr2:236167272-236167504 | Common:3; Rare:84 | ||||
| chr2:237085807-237085963 | Common:1; Rare:66 | ||||
| chr2:238060702-238061121 | Common:6; Rare:135 | ||||
| chr2:238203616-238203797 | Common:3; Rare:76 | ||||
| chr2:240025282-240025407 | Common:1; Rare:51; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240560764-240560910 | Common:2; Rare:69 | ||||
| chr2:241102276-241102357 | Common:2; Rare:31 | ||||
| chr2:241149439-241149583 | Common:1; Rare:47 | ||||
| chr2:241272770-241272947 | Rare:68 |