Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:113627041-113627272 | Common:1; Rare:68 | ||||
chr2:113889761-113890174 | Common:8; Rare:130 | ||||
chr2:118014041-118014221 | Common:2; Rare:100 | ||||
chr2:118088322-118088570 | Common:1; Rare:67 | ||||
chr2:119366811-119367045 | Common:1; Rare:67 | ||||
chr2:119679072-119679219 | Common:3; Rare:46 | ||||
chr2:120252656-120252955 | Common:2; Rare:92 | ||||
chr2:121530568-121530880 | Common:7; Rare:125 | ||||
chr2:121649418-121649715 | Common:2; Rare:85 | ||||
chr2:121755402-121755737 | Common:3; Rare:107 | ||||
chr2:127294100-127294219 | Common:2; Rare:48; Clinvar (benign):2 | ||||
chr2:127387970-127388267 | Common:7; Rare:131 | ||||
chr2:127811143-127811264 | Rare:36 | ||||
chr2:127858112-127858356 | Common:3; Rare:86 | ||||
chr2:127885891-127885972 | Rare:18 |