| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3575107-3575385 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:8682295-8682913 | Common:8; Rare:237 | ||||
| chr2:9420400-9420590 | Common:1; Rare:32 | ||||
| chr2:9422811-9422852 | Rare:6 | ||||
| chr2:9423108-9423715 | Common:2; Rare:164 | ||||
| chr2:9474425-9474633 | Common:7; Rare:78 | ||||
| chr2:9555412-9555460 | Rare:9 | ||||
| chr2:9555530-9555966 | Common:2; Rare:150; Clinvar:2 | ||||
| chr2:9843255-9843519 | Common:6; Rare:76 | ||||
| chr2:10302715-10302991 | Common:5; Rare:85 | ||||
| chr2:10448312-10448731 | Common:1; Rare:132 | ||||
| chr2:10689797-10690024 | Common:2; Rare:95 | ||||
| chr2:10812680-10812823 | Rare:68 | ||||
| chr2:11344967-11345121 | Common:3; Rare:52 | ||||
| chr2:11466004-11466286 | Common:6; Rare:82 |