Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:30146585-30147049 | Common:5; Rare:152 | ||||
chr2:30147882-30147964 | Common:1; Rare:23 | ||||
chr2:30234285-30234477 | Rare:74 | ||||
chr2:31234004-31234158 | Rare:40 | ||||
chr2:31414691-31414963 | Common:2; Rare:56; Clinvar (benign):1 | ||||
chr2:32009849-32010160 | Common:2; Rare:97 | ||||
chr2:32010570-32010758 | Rare:44 | ||||
chr2:32010999-32011125 | Rare:39 | ||||
chr2:32039419-32039612 | Rare:55 | ||||
chr2:32039747-32039906 | Rare:56 | ||||
chr2:32063345-32063685 | Common:1; Rare:121; Clinvar:1 | ||||
chr2:32165720-32165918 | Common:1; Rare:79 | ||||
chr2:32277777-32277986 | Common:1; Rare:52 | ||||
chr2:32627987-32628128 | Rare:45 | ||||
chr2:33476306-33476612 | Common:5; Rare:64 |