Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:96363369-96363552 | Common:1; Rare:62 | ||||
chr14:96502301-96502431 | Rare:50 | ||||
chr14:100375425-100375709 | Common:1; Rare:43 | ||||
chr14:100376269-100376502 | Common:3; Rare:78 | ||||
chr14:100569560-100569784 | Common:3; Rare:41 | ||||
chr14:102139667-102139916 | Rare:86 | ||||
chr14:102305071-102305369 | Common:1; Rare:86 | ||||
chr14:102362862-102363092 | Rare:103 | ||||
chr14:103528988-103529249 | Common:1; Rare:73 | ||||
chr14:103562624-103563019 | Common:6; Rare:143; Clinvar (benign):2 | ||||
chr14:105021041-105021386 | Common:1; Rare:122 | ||||
chr14:105419737-105420031 | Rare:92 | ||||
chr15:30903747-30903936 | Common:1; Rare:51 | ||||
chr15:32615156-32615571 | Common:5; Rare:104 | ||||
chr15:34101841-34102107 | Common:1; Rare:54 |