Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:100835712-100835868 | Common:2; Rare:39 | ||||
chr14:101160374-101160486 | Rare:20 | ||||
chr14:101408238-101408332 | Rare:17 | ||||
chr14:101441923-101442114 | Common:3; Rare:25 | ||||
chr14:101475782-101476053 | Rare:48 | ||||
chr14:101559916-101559983 | Rare:15 | ||||
chr14:101559991-101560034 | Rare:9 | ||||
chr14:101760469-101760711 | Common:2; Rare:77 | ||||
chr14:101834550-101834666 | Rare:17 | ||||
chr14:101948057-101948407 | Common:2; Rare:101 | ||||
chr14:102010197-102010326 | Rare:36; Clinvar (benign):5 | ||||
chr14:102066256-102066403 | Rare:23 | ||||
chr14:102088013-102088179 | Common:3; Rare:41 | ||||
chr14:102088608-102088688 | Common:1; Rare:28 | ||||
chr14:102298460-102298712 | Common:4; Rare:63 |