| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190880548-190880868 | Common:4; Rare:108 | ||||
| chr2:191014145-191014441 | Common:3; Rare:98; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191020259-191020587 | Common:1; Rare:116 | ||||
| chr2:191246070-191246470 | Common:2; Rare:109 | ||||
| chr2:191677822-191678161 | Common:4; Rare:96 | ||||
| chr2:192194811-192195211 | Common:2; Rare:122 | ||||
| chr2:195656802-195656948 | Rare:48 | ||||
| chr2:195657901-195658150 | Common:2; Rare:54 | ||||
| chr2:196068280-196068640 | Common:6; Rare:91 | ||||
| chr2:196068818-196068980 | Common:1; Rare:47 | ||||
| chr2:196170640-196171430 | Common:7; Rare:229 | ||||
| chr2:196171527-196171787 | Common:1; Rare:79 | ||||
| chr2:196592430-196592980 | Common:2; Rare:126 | ||||
| chr2:196639439-196639776 | Rare:115 | ||||
| chr2:196799450-196799930 | Common:2; Rare:153 |