| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219177690-219178040 | Common:16; Rare:130 | ||||
| chr2:219178113-219178313 | Common:12; Rare:205 | ||||
| chr2:219206681-219206923 | Rare:87 | ||||
| chr2:219217780-219218290 | Common:2; Rare:162; Clinvar:2 | ||||
| chr2:219229541-219229912 | Common:4; Rare:227 | ||||
| chr2:219245389-219245536 | Common:2; Rare:77 | ||||
| chr2:219253879-219254056 | Common:1; Rare:60 | ||||
| chr2:219278960-219279535 | Common:4; Rare:284 | ||||
| chr2:219441786-219442186 | Rare:124 | ||||
| chr2:219498495-219498954 | Common:5; Rare:153 | ||||
| chr2:219543044-219543163 | Common:1; Rare:29 | ||||
| chr2:219543081-219543210 | Common:1; Rare:33 | ||||
| chr2:219543519-219544076 | Common:6; Rare:329 | ||||
| chr2:219571399-219571611 | Common:2; Rare:99; Clinvar:6 | ||||
| chr2:219571830-219572330 | Common:24; Rare:187 |