Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:47795724-47795934 | Common:3; Rare:57; Clinvar:6; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr2:47803162-47803461 | Common:2; Rare:106; Clinvar:12; Clinvar (benign):13 | ||||
chr2:47906490-47906818 | Common:2; Rare:115 | ||||
chr2:60468814-60468949 | Rare:20; Clinvar:1 | ||||
chr2:65436540-65436691 | Rare:40 | ||||
chr2:66431982-66432091 | Common:1; Rare:18 | ||||
chr2:70088052-70088359 | Common:1; Rare:79 | ||||
chr2:70088436-70088816 | Rare:75 | ||||
chr2:70089013-70089087 | Rare:21 | ||||
chr2:70281127-70281436 | Common:1; Rare:73 | ||||
chr2:73902262-73902428 | Common:1; Rare:31; Clinvar:1 | ||||
chr2:73984960-73985060 | Rare:30 | ||||
chr2:74120210-74120381 | Rare:63 | ||||
chr2:74370776-74371067 | Common:2; Rare:80; Clinvar:4; Clinvar (benign):3 | ||||
chr2:87521295-87521349 | Rare:10 |