Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:18560640-18560800 | Rare:46 | ||||
chr2:19901945-19902049 | Common:1; Rare:35 | ||||
chr2:20051496-20051903 | Common:1; Rare:116 | ||||
chr2:20823059-20823159 | Rare:40 | ||||
chr2:23927056-23927325 | Common:3; Rare:92 | ||||
chr2:24076241-24076594 | Rare:95 | ||||
chr2:24123272-24123510 | Common:1; Rare:63 | ||||
chr2:24793113-24793160 | Rare:24 | ||||
chr2:24971908-24972126 | Common:1; Rare:74 | ||||
chr2:26244536-26244966 | Common:2; Rare:155; Clinvar:6; Clinvar (benign):9 | ||||
chr2:26345841-26346156 | Common:1; Rare:93 | ||||
chr2:26764194-26764344 | Common:1; Rare:60 | ||||
chr2:27032765-27033017 | Rare:85 | ||||
chr2:27051535-27051706 | Rare:51 | ||||
chr2:27078540-27078892 | Common:2; Rare:84 |