Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:202238515-202238615 | Rare:34 | ||||
chr2:202912147-202912298 | Common:1; Rare:53 | ||||
chr2:202912528-202912582 | Rare:19 | ||||
chr2:203014672-203014933 | Common:1; Rare:78 | ||||
chr2:203238925-203239051 | Common:1; Rare:51 | ||||
chr2:203239226-203239329 | Rare:34 | ||||
chr2:203535246-203535546 | Common:3; Rare:131 | ||||
chr2:205682353-205682498 | Rare:25 | ||||
chr2:206085772-206085981 | Common:1; Rare:60 | ||||
chr2:206086281-206086303 | Rare:3 | ||||
chr2:206159389-206159672 | Common:2; Rare:95 | ||||
chr2:206274921-206275041 | Rare:44 | ||||
chr2:206765284-206765645 | Common:3; Rare:96; Clinvar:4; Clinvar (benign):4 | ||||
chr2:207529796-207530104 | Common:2; Rare:87 | ||||
chr2:208255014-208255217 | Common:2; Rare:53 |