Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:70049645-70049719 | Rare:16 | ||||
chr2:70088233-70088358 | Common:1; Rare:34 | ||||
chr2:70088583-70088804 | Rare:35 | ||||
chr2:70089015-70089088 | Rare:20 | ||||
chr2:70281142-70281436 | Common:1; Rare:65 | ||||
chr2:73984960-73985131 | Rare:53 | ||||
chr2:74370801-74371179 | Common:2; Rare:103; Clinvar:5; Clinvar (benign):4 | ||||
chr2:86136810-86137019 | Common:1; Rare:40 | ||||
chr2:95526728-95526834 | Common:1; Rare:37 | ||||
chr2:109128016-109128263 | Common:2; Rare:69 | ||||
chr2:111207565-111207843 | Common:2; Rare:49 | ||||
chr2:131682377-131682561 | Common:3; Rare:55 | ||||
chr2:150571981-150572182 | Common:3; Rare:42 | ||||
chr2:164947215-164947321 | Common:1; Rare:18 | ||||
chr2:176105215-176105476 | Common:1; Rare:47 |