| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130342686-130342939 | Common:3; Rare:84 | ||||
| chr2:131093349-131093530 | Common:1; Rare:79 | ||||
| chr2:131493050-131493118 | Common:1; Rare:20 | ||||
| chr2:134918585-134918862 | Common:1; Rare:109 | ||||
| chr2:135531158-135531526 | Common:1; Rare:79 | ||||
| chr2:135741665-135741971 | Common:1; Rare:114 | ||||
| chr2:138501647-138502011 | Common:4; Rare:134 | ||||
| chr2:144517324-144517579 | Rare:75; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:148020686-148021125 | Common:2; Rare:103; Clinvar (benign):2 | ||||
| chr2:148021486-148021652 | Rare:42 | ||||
| chr2:148875580-148875629 | Rare:19; Clinvar (benign):1 | ||||
| chr2:149330354-149330624 | Common:1; Rare:116 | ||||
| chr2:149587326-149587390 | Rare:14 | ||||
| chr2:149587685-149587862 | Common:1; Rare:50; Clinvar:1 | ||||
| chr2:152098693-152098714 | Rare:6 |