Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21864148-21864337 | Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
chr1:21890055-21890418 | Common:2; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
chr1:22025450-22025537 | Common:4; Rare:34 | ||||
chr1:22536774-22536929 | Common:2; Rare:40 | ||||
chr1:22676998-22677153 | Rare:24 | ||||
chr1:22740380-22740481 | Rare:15 | ||||
chr1:22745661-22745837 | Common:1; Rare:33 | ||||
chr1:23244361-23244535 | Rare:25 | ||||
chr1:23320101-23320314 | Rare:42 | ||||
chr1:23521616-23521972 | Common:1; Rare:88 | ||||
chr1:23554723-23555095 | Common:3; Rare:144 | ||||
chr1:24254848-24255062 | Common:2; Rare:52 | ||||
chr1:24321896-24322042 | Common:1; Rare:34 | ||||
chr1:24490407-24490683 | Common:2; Rare:65 | ||||
chr1:25207927-25208066 | Rare:17 |