Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:121755406-121755844 | Common:5; Rare:142 | ||||
chr2:127106863-127106942 | Rare:16; Clinvar:2 | ||||
chr2:127106944-127107392 | Common:5; Rare:132; Clinvar:8; Clinvar (benign):3 | ||||
chr2:127220078-127220358 | Common:3; Rare:67 | ||||
chr2:127294062-127294258 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):2 | ||||
chr2:127387946-127388257 | Common:8; Rare:133 | ||||
chr2:127526382-127526619 | Common:2; Rare:91 | ||||
chr2:127526792-127526837 | Rare:14 | ||||
chr2:127811149-127811333 | Common:1; Rare:65 | ||||
chr2:127858050-127858368 | Common:4; Rare:125 | ||||
chr2:127885951-127885965 | Rare:3 | ||||
chr2:128027248-128027577 | Common:1; Rare:126 | ||||
chr2:128091052-128091354 | Common:8; Rare:98 | ||||
chr2:128318823-128318994 | Common:2; Rare:69 | ||||
chr2:130129313-130129590 | Common:4; Rare:75 |