Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:23751129-23751180 | Rare:13 | ||||
chr22:24554981-24555485 | Common:4; Rare:186 | ||||
chr22:24555617-24556025 | Rare:125 | ||||
chr22:26512444-26512555 | Common:1; Rare:50 | ||||
chr22:26590069-26590220 | Common:3; Rare:64 | ||||
chr22:27919195-27919437 | Common:4; Rare:110 | ||||
chr22:28741794-28742078 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
chr22:28800463-28800688 | Common:5; Rare:91 | ||||
chr22:29268012-29268337 | Common:2; Rare:105 | ||||
chr22:29766971-29767393 | Common:4; Rare:113 | ||||
chr22:29767531-29767599 | Common:1; Rare:30 | ||||
chr22:30356864-30356989 | Common:1; Rare:40 | ||||
chr22:30607047-30607258 | Common:3; Rare:65; Clinvar:3; Clinvar (benign):3 | ||||
chr22:37019423-37019848 | Common:5; Rare:122 | ||||
chr22:37560340-37560517 | Common:1; Rare:65 |