Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:99480731-99481185 | Common:2; Rare:150 | ||||
chr14:100376259-100376485 | Common:3; Rare:74 | ||||
chr14:102139693-102139921 | Rare:76 | ||||
chr14:102235409-102235766 | Rare:80 | ||||
chr14:102362846-102363098 | Rare:113 | ||||
chr14:103123338-103123464 | Rare:19 | ||||
chr14:103529035-103529246 | Common:1; Rare:64 | ||||
chr14:103562624-103563002 | Common:5; Rare:135; Clinvar (benign):1 | ||||
chr14:103715409-103715883 | Common:1; Rare:160 | ||||
chr14:105021044-105021413 | Common:1; Rare:133 | ||||
chr14:105248438-105248618 | Common:4; Rare:89 | ||||
chr14:105419757-105419888 | Rare:26 | ||||
chr15:22838460-22838933 | Common:4; Rare:160 | ||||
chr15:25438496-25438528 | Rare:10 | ||||
chr15:34101828-34102080 | Common:1; Rare:55 |