| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:222861500-222861736 | Common:2; Rare:85 | ||||
| chr2:223836793-223837460 | Common:3; Rare:182 | ||||
| chr2:223837448-223837969 | Common:5; Rare:232 | ||||
| chr2:223945219-223945398 | Rare:87 | ||||
| chr2:223957173-223957518 | Common:8; Rare:208; Clinvar (benign):2 | ||||
| chr2:223957655-223957872 | Rare:48; Clinvar (benign):1 | ||||
| chr2:224039220-224039473 | Rare:95 | ||||
| chr2:224485190-224485650 | Rare:200 | ||||
| chr2:224585204-224585975 | Common:20; Rare:633 | ||||
| chr2:225042190-225042580 | Common:2; Rare:167 | ||||
| chr2:225042600-225042910 | Common:2; Rare:95 | ||||
| chr2:226794943-226795301 | Rare:200 | ||||
| chr2:226795463-226796376 | Common:6; Rare:358; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:226798857-226800155 | Common:14; Rare:713 | ||||
| chr2:226835820-226836200 | Common:3; Rare:363 |