Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25859355-25859580 | Common:3; Rare:94 | ||||
chr1:26234023-26234248 | Common:1; Rare:81 | ||||
chr1:26279934-26280199 | Rare:143 | ||||
chr1:26432085-26432404 | Common:5; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472288-26472624 | Common:4; Rare:124 | ||||
chr1:26695539-26695786 | Rare:80 | ||||
chr1:26695927-26696051 | Rare:40 | ||||
chr1:26826583-26826773 | Rare:67 | ||||
chr1:26900396-26900548 | Rare:63 | ||||
chr1:26921888-26921926 | Rare:8 | ||||
chr1:26993643-26994010 | Common:3; Rare:127 | ||||
chr1:27322035-27322336 | Common:1; Rare:109 | ||||
chr1:27773036-27773297 | Common:1; Rare:98 | ||||
chr1:28235958-28236254 | Common:3; Rare:95 | ||||
chr1:28259282-28259536 | Common:1; Rare:65 |