Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:38199093-38199223 | Common:1; Rare:29 | ||||
chr2:47803161-47803450 | Common:2; Rare:99; Clinvar:7; Clinvar (benign):12 | ||||
chr2:47906476-47906910 | Common:2; Rare:151 | ||||
chr2:55282204-55282368 | Common:5; Rare:57 | ||||
chr2:55523475-55523797 | Common:2; Rare:67 | ||||
chr2:61764226-61764486 | Common:3; Rare:86 | ||||
chr2:62475825-62476149 | Common:3; Rare:63 | ||||
chr2:65089043-65089314 | Rare:57 | ||||
chr2:69794131-69794182 | Rare:7 | ||||
chr2:70086246-70086485 | Common:4; Rare:93 | ||||
chr2:70087954-70088196 | Rare:58 | ||||
chr2:70088209-70088477 | Common:1; Rare:79 | ||||
chr2:74120284-74120383 | Rare:41 | ||||
chr2:74120562-74120669 | Common:2; Rare:27 | ||||
chr2:74370464-74370820 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):3 |