| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218322982-218323355 | Common:6; Rare:124 | ||||
| chr2:218381874-218382374 | Common:3; Rare:100 | ||||
| chr2:218398567-218398751 | Common:2; Rare:68 | ||||
| chr2:218399531-218399756 | Common:1; Rare:101 | ||||
| chr2:218568232-218568632 | Common:3; Rare:106 | ||||
| chr2:218568756-218568961 | Common:1; Rare:62 | ||||
| chr2:218659339-218659743 | Common:4; Rare:95 | ||||
| chr2:218671966-218672334 | Common:2; Rare:93 | ||||
| chr2:218782014-218782183 | Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:219176818-219177119 | Common:4; Rare:88 | ||||
| chr2:219178128-219178496 | Common:6; Rare:144 | ||||
| chr2:219206683-219206946 | Rare:92 | ||||
| chr2:219229549-219229896 | Common:2; Rare:110 | ||||
| chr2:219245383-219245531 | Rare:43 | ||||
| chr2:219253872-219254056 | Common:1; Rare:57 |