Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:102086968-102087469 | Common:5; Rare:212 | ||||
chr14:102139655-102139947 | Rare:101 | ||||
chr14:102305083-102305276 | Common:1; Rare:62 | ||||
chr14:102362847-102363092 | Rare:112 | ||||
chr14:103529107-103529233 | Common:1; Rare:44 | ||||
chr14:103562231-103562376 | Rare:60 | ||||
chr14:103562623-103563048 | Common:8; Rare:166; Clinvar (benign):5 | ||||
chr14:103629123-103629397 | Common:2; Rare:107 | ||||
chr14:103715470-103715860 | Common:1; Rare:126 | ||||
chr14:105021044-105021386 | Common:1; Rare:120 | ||||
chr15:22838438-22838748 | Common:3; Rare:121 | ||||
chr15:30903617-30903936 | Common:3; Rare:84 | ||||
chr15:32615127-32615594 | Common:7; Rare:116 | ||||
chr15:32684149-32684471 | Common:1; Rare:60 | ||||
chr15:34101821-34102092 | Common:1; Rare:59 |