Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:40399971-40400033 | Rare:12 | ||||
chr22:40400444-40400811 | Rare:65 | ||||
chr22:40777056-40777312 | Common:1; Rare:75 | ||||
chr22:40951960-40951988 | Rare:5 | ||||
chr22:41092544-41092624 | Rare:46 | ||||
chr22:41256005-41256293 | Common:1; Rare:92 | ||||
chr22:41302507-41302854 | Common:2; Rare:80 | ||||
chr22:41356006-41356316 | Rare:75 | ||||
chr22:41413940-41414053 | Rare:37 | ||||
chr22:41518527-41518669 | Common:1; Rare:38; Clinvar (benign):1 | ||||
chr22:41522944-41523274 | Rare:100; Clinvar:2 | ||||
chr22:41576627-41576943 | Rare:45 | ||||
chr22:41619765-41620029 | Rare:48 | ||||
chr22:41677258-41677568 | Common:1; Rare:56 | ||||
chr22:41694171-41694193 | Rare:4 |