| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219229577-219229891 | Common:2; Rare:95 | ||||
| chr2:219245383-219245537 | Common:1; Rare:45 | ||||
| chr2:219253914-219254093 | Common:2; Rare:59 | ||||
| chr2:219279190-219279545 | Common:3; Rare:108; Clinvar (benign):1 | ||||
| chr2:219498670-219498944 | Common:2; Rare:61 | ||||
| chr2:219597708-219597909 | Common:1; Rare:84 | ||||
| chr2:221572266-221572464 | Common:2; Rare:71 | ||||
| chr2:221573963-221573996 | Rare:5 | ||||
| chr2:222656047-222656433 | Common:3; Rare:121 | ||||
| chr2:223837508-223837879 | Common:1; Rare:86 | ||||
| chr2:223957256-223957475 | Common:4; Rare:81 | ||||
| chr2:226835918-226836088 | Rare:67 | ||||
| chr2:227164099-227164362 | Rare:78; Clinvar:2 | ||||
| chr2:227164435-227164621 | Rare:37; Clinvar:3 | ||||
| chr2:227325182-227325425 | Common:5; Rare:87 |