Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:201642637-201642789 | Rare:73 | ||||
chr2:201643403-201643553 | Common:1; Rare:48; Clinvar:4; Clinvar (benign):2 | ||||
chr2:202911898-202912024 | Rare:26 | ||||
chr2:202912128-202912293 | Common:2; Rare:56 | ||||
chr2:203238846-203239040 | Rare:76 | ||||
chr2:203239226-203239298 | Rare:24 | ||||
chr2:203328150-203328437 | Common:2; Rare:108 | ||||
chr2:203535173-203535546 | Common:3; Rare:147 | ||||
chr2:206159380-206159989 | Common:4; Rare:182; Clinvar (benign):1 | ||||
chr2:206213358-206213533 | Rare:26 | ||||
chr2:206765330-206765643 | Common:3; Rare:79; Clinvar:4; Clinvar (benign):4 | ||||
chr2:207165928-207166128 | Rare:36 | ||||
chr2:207529701-207530113 | Common:3; Rare:119 | ||||
chr2:207625226-207625364 | Common:1; Rare:35 | ||||
chr2:208255032-208255238 | Common:2; Rare:54 |