Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52926994-52927363 | Common:8; Rare:146 | ||||
chr1:53090903-53091129 | Common:3; Rare:57 | ||||
chr1:53196689-53196897 | Rare:126; Clinvar:6; Clinvar (benign):1 | ||||
chr1:53220121-53220548 | Common:1; Rare:328 | ||||
chr1:53220558-53220760 | Common:4; Rare:184 | ||||
chr1:53238448-53238614 | Common:3; Rare:136 | ||||
chr1:53327958-53328248 | Common:3; Rare:130 | ||||
chr1:53838135-53838950 | Common:3; Rare:282 | ||||
chr1:53945566-53946106 | Common:16; Rare:278 | ||||
chr1:53946255-53946544 | Common:2; Rare:173 | ||||
chr1:54053178-54053668 | Common:12; Rare:322 | ||||
chr1:54199975-54200309 | Rare:179 | ||||
chr1:54356190-54356410 | Common:1; Rare:124 | ||||
chr1:54406356-54406544 | Common:6; Rare:152 | ||||
chr1:54715756-54715898 | Common:2; Rare:49 |