Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:123748976-123749218 | Common:2; Rare:85 | ||||
chr7:131327715-131327894 | Rare:63 | ||||
chr7:139359692-139359968 | Common:2; Rare:113 | ||||
chr7:152676103-152676288 | Common:2; Rare:71; Clinvar (benign):6 | ||||
chr7:155644389-155644667 | Common:2; Rare:85 | ||||
chr8:232223-232425 | Common:2; Rare:81 | ||||
chr8:6406543-6406661 | Common:3; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
chr8:11802450-11802767 | Common:6; Rare:166 | ||||
chr8:17246814-17247027 | Common:2; Rare:90 | ||||
chr8:22245022-22245150 | Rare:66 | ||||
chr8:23164022-23164118 | Rare:18 | ||||
chr8:26382779-26383108 | Rare:109 | ||||
chr8:29263071-29263288 | Rare:66 | ||||
chr8:30156268-30156379 | Rare:27 | ||||
chr8:38176426-38176863 | Common:5; Rare:123 |