| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218381936-218382251 | Common:1; Rare:58 | ||||
| chr2:218418971-218419162 | Rare:38 | ||||
| chr2:218424004-218424295 | Common:1; Rare:53 | ||||
| chr2:218568276-218568622 | Common:2; Rare:93 | ||||
| chr2:218568733-218568966 | Common:1; Rare:65 | ||||
| chr2:218659334-218659785 | Common:4; Rare:113 | ||||
| chr2:218671973-218672357 | Common:2; Rare:96 | ||||
| chr2:218782011-218782189 | Rare:39; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218984459-218984591 | Rare:25 | ||||
| chr2:219124685-219124917 | Rare:32 | ||||
| chr2:219176814-219177119 | Common:4; Rare:90 | ||||
| chr2:219177147-219177238 | Common:1; Rare:16 | ||||
| chr2:219178142-219178436 | Common:6; Rare:127 | ||||
| chr2:219206658-219206923 | Rare:95 | ||||
| chr2:219229544-219229920 | Common:2; Rare:117 |