Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:101809684-101809888 | Rare:41 | ||||
chr14:101810248-101810436 | Common:2; Rare:40 | ||||
chr14:102086978-102087491 | Common:6; Rare:214 | ||||
chr14:102139667-102139923 | Rare:89 | ||||
chr14:102319389-102319426 | Rare:5 | ||||
chr14:102362862-102363094 | Rare:103 | ||||
chr14:103123258-103123461 | Rare:39 | ||||
chr14:103333969-103334252 | Common:1; Rare:117 | ||||
chr14:103529070-103529229 | Common:1; Rare:48 | ||||
chr14:103562623-103563059 | Common:8; Rare:173; Clinvar (benign):5 | ||||
chr14:103629136-103629470 | Common:4; Rare:127 | ||||
chr14:104752981-104753208 | Common:2; Rare:84 | ||||
chr14:104985646-104985800 | Common:3; Rare:57 | ||||
chr14:105021053-105021396 | Common:1; Rare:122 | ||||
chr14:105419731-105420032 | Rare:97 |