Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:26674951-26675347 | Rare:68 | ||||
chr22:27674847-27675041 | Rare:31 | ||||
chr22:27742078-27742304 | Rare:39 | ||||
chr22:27742920-27742968 | Rare:9 | ||||
chr22:27743730-27743796 | Common:1; Rare:24 | ||||
chr22:27744260-27744527 | Common:3; Rare:57 | ||||
chr22:28699845-28700202 | Rare:82; Clinvar:19; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
chr22:29031388-29031448 | Rare:9 | ||||
chr22:29287097-29287207 | Rare:27 | ||||
chr22:29299595-29300469 | Common:7; Rare:257 | ||||
chr22:29481019-29481125 | Common:1; Rare:45 | ||||
chr22:30245973-30246196 | Common:1; Rare:43 | ||||
chr22:30937684-30937885 | Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
chr22:30968984-30969329 | Common:3; Rare:102 | ||||
chr22:30970091-30970320 | Common:2; Rare:46 |