Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:35121941-35122822 | Common:4; Rare:245 | ||||
chr14:35404668-35404905 | Common:2; Rare:83; Clinvar (benign):2 | ||||
chr14:35826210-35826460 | Rare:62 | ||||
chr14:36320503-36320731 | Common:5; Rare:83 | ||||
chr14:39179203-39179458 | Common:1; Rare:75 | ||||
chr14:39267110-39267417 | Common:1; Rare:106 | ||||
chr14:39432402-39432618 | Common:6; Rare:73 | ||||
chr14:44897044-44897332 | Common:1; Rare:99 | ||||
chr14:44961892-44962278 | Common:3; Rare:111 | ||||
chr14:45253051-45253312 | Rare:71 | ||||
chr14:49598673-49599023 | Common:2; Rare:136 | ||||
chr14:49620570-49620855 | Common:2; Rare:115; Clinvar:4 | ||||
chr14:49892913-49893128 | Rare:86 | ||||
chr14:50231576-50231665 | Rare:23 | ||||
chr14:50312193-50312374 | Rare:70 |