Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:94409318-94409608 | Rare:83; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr7:94420172-94420315 | Rare:39; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr7:94420387-94420645 | Rare:69; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr7:100335858-100336146 | Common:1; Rare:96 | ||||
chr7:101804739-101805002 | Common:1; Rare:48 | ||||
chr7:102822453-102822588 | Common:1; Rare:17 | ||||
chr7:105013031-105013202 | Rare:60 | ||||
chr7:113118548-113118671 | Common:1; Rare:41 | ||||
chr7:116211460-116211539 | Rare:18 | ||||
chr7:121330220-121330307 | Rare:17 | ||||
chr7:130500335-130500526 | Common:2; Rare:45 | ||||
chr7:130541196-130541218 | |||||
chr7:131108089-131108119 | Rare:4 | ||||
chr7:148987246-148987529 | Common:8; Rare:92 | ||||
chr8:22733056-22733368 | Common:3; Rare:66 |