| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:42568340-42568810 | Common:12; Rare:221 | ||||
| chr2:42569053-42569453 | Common:2; Rare:106 | ||||
| chr2:42569610-42569860 | Rare:44 | ||||
| chr2:43225683-43226170 | Common:12; Rare:622 | ||||
| chr2:43226262-43226371 | Rare:53 | ||||
| chr2:43226310-43226946 | Common:25; Rare:1245 | ||||
| chr2:43226978-43227461 | Common:4; Rare:260 | ||||
| chr2:43595788-43596290 | Common:7; Rare:792 | ||||
| chr2:43636998-43637398 | Common:7; Rare:263 | ||||
| chr2:43637746-43638146 | Common:2; Rare:89 | ||||
| chr2:43676220-43676751 | Common:10; Rare:360 | ||||
| chr2:43773781-43774181 | Common:16; Rare:306; Clinvar (pathogenic):2 | ||||
| chr2:43995910-43996527 | Common:30; Rare:1269; Clinvar:12; Clinvar (benign):12; Clinvar (pathogenic):5 | ||||
| chr2:44167740-44168475 | Common:26; Rare:1211 | ||||
| chr2:44168382-44169702 | Common:13; Rare:1431 |