Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:212791684-212792076 | Common:10; Rare:257 | ||||
chr1:212858056-212858394 | Common:11; Rare:166; Clinvar:6; Clinvar (benign):2 | ||||
chr1:212950320-212950604 | Common:2; Rare:100 | ||||
chr1:213015417-213015633 | Rare:118 | ||||
chr1:213015742-213015933 | Rare:88 | ||||
chr1:213051176-213051370 | Rare:115 | ||||
chr1:214280689-214281346 | Common:7; Rare:338 | ||||
chr1:214281414-214281565 | Common:2; Rare:77 | ||||
chr1:214551180-214551460 | Common:4; Rare:128 | ||||
chr1:214551536-214552054 | Common:4; Rare:276 | ||||
chr1:214552437-214552596 | Common:2; Rare:30 | ||||
chr1:214602919-214603322 | Common:8; Rare:217 | ||||
chr1:215567134-215567454 | Common:1; Rare:152 | ||||
chr1:215567479-215567779 | Common:2; Rare:183 | ||||
chr1:217631001-217631379 | Common:4; Rare:205 |