Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:1421152-1421348 | Common:3; Rare:48 | ||||
chr2:1421898-1422205 | Common:1; Rare:61 | ||||
chr2:1422942-1423141 | Common:3; Rare:61; Clinvar:1 | ||||
chr2:1443525-1443692 | Common:6; Rare:24 | ||||
chr2:1444060-1444303 | Common:4; Rare:25 | ||||
chr2:1453649-1454142 | Rare:142; Clinvar:4 | ||||
chr2:1461534-1461871 | Common:5; Rare:73 | ||||
chr2:1462049-1462273 | Common:3; Rare:44 | ||||
chr2:1472583-1472610 | Rare:7 | ||||
chr2:1473283-1473459 | Rare:33 | ||||
chr2:1480750-1481045 | Common:11; Rare:68 | ||||
chr2:1482586-1482897 | Common:3; Rare:55 | ||||
chr2:1483897-1483976 | Common:1; Rare:13 | ||||
chr2:1493345-1493582 | Common:11; Rare:55 | ||||
chr2:1517600-1517835 | Common:1; Rare:17 |