| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218568747-218568966 | Common:1; Rare:63 | ||||
| chr2:218659310-218659854 | Common:4; Rare:135 | ||||
| chr2:218662120-218662261 | Rare:39; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:218671966-218672385 | Common:2; Rare:109 | ||||
| chr2:218710771-218711021 | Common:2; Rare:61 | ||||
| chr2:219160767-219160931 | Common:1; Rare:50 | ||||
| chr2:219176648-219176793 | Common:3; Rare:56 | ||||
| chr2:219176827-219177074 | Common:4; Rare:73 | ||||
| chr2:219178146-219178315 | Common:6; Rare:97 | ||||
| chr2:219206660-219206923 | Rare:94 | ||||
| chr2:219229320-219229422 | Rare:33 | ||||
| chr2:219229553-219229924 | Common:2; Rare:114 | ||||
| chr2:219245383-219245534 | Common:1; Rare:44 | ||||
| chr2:219252977-219253243 | Common:1; Rare:75 | ||||
| chr2:219253254-219253382 | Common:3; Rare:46 |