Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:101809792-101809893 | Rare:20 | ||||
chr14:101964287-101964674 | Common:4; Rare:115; Clinvar:1; Clinvar (benign):1 | ||||
chr14:102086989-102087314 | Common:4; Rare:129 | ||||
chr14:102139636-102139935 | Rare:107 | ||||
chr14:102305056-102305224 | Rare:47 | ||||
chr14:102362862-102363092 | Rare:103 | ||||
chr14:103333951-103334246 | Common:2; Rare:120 | ||||
chr14:103385255-103385431 | Rare:64 | ||||
chr14:103522818-103522975 | Rare:51 | ||||
chr14:103529058-103529233 | Common:1; Rare:51 | ||||
chr14:103562620-103563053 | Common:8; Rare:171; Clinvar (benign):5 | ||||
chr14:103629111-103629491 | Common:4; Rare:147 | ||||
chr14:103715466-103715853 | Common:1; Rare:126 | ||||
chr14:104752862-104753207 | Common:3; Rare:115 | ||||
chr14:105021044-105021440 | Common:1; Rare:141 |