Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:103847568-103847687 | Rare:52 | ||||
chr14:103921451-103921720 | Common:3; Rare:86 | ||||
chr14:104138240-104138610 | Common:3; Rare:121 | ||||
chr14:104689483-104689674 | Common:1; Rare:46; Clinvar (benign):1 | ||||
chr14:104752978-104753278 | Common:2; Rare:114 | ||||
chr14:104865167-104865283 | Common:1; Rare:33 | ||||
chr14:104985629-104985822 | Common:3; Rare:78 | ||||
chr14:105021015-105021472 | Common:1; Rare:166 | ||||
chr14:105248438-105248623 | Common:4; Rare:92 | ||||
chr14:105300881-105301128 | Rare:68 | ||||
chr14:105398522-105398565 | Common:1; Rare:19 | ||||
chr14:105419748-105420057 | Rare:93 | ||||
chr15:22786483-22786783 | Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
chr15:22838477-22838780 | Common:3; Rare:118 | ||||
chr15:23039519-23039698 | Common:1; Rare:79 |