| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201260396-201260609 | Common:1; Rare:46 | ||||
| chr2:201451467-201451813 | Common:2; Rare:88 | ||||
| chr2:201642668-201642740 | Rare:36 | ||||
| chr2:201780887-201781001 | Common:2; Rare:33; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:202238540-202238701 | Common:1; Rare:50 | ||||
| chr2:202265669-202265873 | Rare:75 | ||||
| chr2:202634695-202635039 | Common:6; Rare:114 | ||||
| chr2:202912137-202912286 | Common:2; Rare:51 | ||||
| chr2:203238874-203239030 | Rare:60 | ||||
| chr2:206085941-206085986 | Rare:9 | ||||
| chr2:206086073-206086144 | Rare:13 | ||||
| chr2:206159380-206159913 | Common:4; Rare:146; Clinvar (benign):1 | ||||
| chr2:206274911-206275028 | Rare:44 | ||||
| chr2:207165928-207166383 | Common:3; Rare:142 | ||||
| chr2:207166826-207166937 | Rare:49 |