| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:230416094-230416306 | Rare:63 | ||||
| chr2:231198505-231198684 | Common:1; Rare:63 | ||||
| chr2:231464343-231464727 | Common:3; Rare:132 | ||||
| chr2:231707804-231707835 | Rare:11 | ||||
| chr2:231708483-231708746 | Common:3; Rare:131 | ||||
| chr2:231710296-231710518 | Common:2; Rare:109 | ||||
| chr2:231961638-231961748 | Rare:33; Clinvar:1 | ||||
| chr2:232550540-232550747 | Rare:86 | ||||
| chr2:233854493-233854716 | Common:4; Rare:62 | ||||
| chr2:237085761-237085955 | Common:2; Rare:72 | ||||
| chr2:238060761-238061115 | Common:6; Rare:114 | ||||
| chr2:240025299-240025508 | Common:1; Rare:90; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:240560764-240560873 | Common:1; Rare:47 | ||||
| chr2:241102276-241102406 | Common:2; Rare:42 | ||||
| chr2:241272770-241273016 | Rare:83 |