Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:39970918-39971196 | Common:4; Rare:76 | ||||
chr19:39996956-39997095 | Common:4; Rare:49 | ||||
chr19:40056148-40056293 | Rare:19 | ||||
chr19:40090900-40091015 | Rare:31 | ||||
chr19:40348393-40348704 | Common:4; Rare:95 | ||||
chr19:40444294-40444517 | Common:3; Rare:67 | ||||
chr19:40750455-40750909 | Common:5; Rare:110 | ||||
chr19:40751033-40751283 | Common:3; Rare:80 | ||||
chr19:40777934-40778276 | Common:1; Rare:95 | ||||
chr19:41363801-41363992 | Common:1; Rare:66; Clinvar:1 | ||||
chr19:41397324-41397606 | Common:4; Rare:73 | ||||
chr19:41876982-41877364 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
chr19:42075855-42076186 | Rare:91 | ||||
chr19:42132383-42132670 | Rare:67 | ||||
chr19:42423569-42423803 | Common:2; Rare:75 |