Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:5593318-5593573 | Rare:76 | ||||
chr7:5603293-5603550 | Common:2; Rare:93 | ||||
chr7:6009015-6009320 | Common:3; Rare:131; Clinvar:9; Clinvar (benign):14; Clinvar (pathogenic):2 | ||||
chr7:6059033-6059331 | Common:5; Rare:113 | ||||
chr7:6104617-6105009 | Common:5; Rare:138 | ||||
chr7:6272514-6272786 | Common:1; Rare:126 | ||||
chr7:6447852-6448094 | Common:2; Rare:101 | ||||
chr7:6484043-6484289 | Common:2; Rare:121 | ||||
chr7:6577370-6577495 | Common:1; Rare:41 | ||||
chr7:6706685-6707124 | Common:3; Rare:157 | ||||
chr7:6826171-6826350 | Common:4; Rare:43 | ||||
chr7:7182308-7182685 | Common:6; Rare:139 | ||||
chr7:7566979-7567047 | Rare:21 | ||||
chr7:7970309-7970472 | Common:1; Rare:47 | ||||
chr7:8262234-8262625 | Common:3; Rare:123 |