| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:233854505-233854757 | Common:4; Rare:68 | ||||
| chr2:236507446-236507639 | Common:6; Rare:69 | ||||
| chr2:236569619-236569871 | Common:8; Rare:47 | ||||
| chr2:237085761-237085955 | Common:2; Rare:72 | ||||
| chr2:237627385-237627644 | Common:2; Rare:94 | ||||
| chr2:237966756-237967078 | Common:4; Rare:98 | ||||
| chr2:238060738-238061067 | Common:4; Rare:101 | ||||
| chr2:238203555-238203808 | Common:5; Rare:100 | ||||
| chr2:238426896-238427067 | Common:1; Rare:63 | ||||
| chr2:240025240-240025455 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:240136252-240136374 | Rare:48 | ||||
| chr2:240457176-240457443 | Common:3; Rare:88 | ||||
| chr2:240560766-240560873 | Common:1; Rare:46 | ||||
| chr2:240820150-240820445 | Rare:69 | ||||
| chr2:241102276-241102412 | Common:2; Rare:43 |