Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32767901-32768080 | Rare:55 | ||||
chr1:32769688-32769956 | Rare:98 | ||||
chr1:37518883-37519082 | Common:1; Rare:64 | ||||
chr1:43119780-43120158 | Common:11; Rare:109 | ||||
chr1:44030321-44030440 | Rare:46 | ||||
chr1:45205844-45205950 | Common:1; Rare:33 | ||||
chr1:45303532-45303872 | Common:1; Rare:100 | ||||
chr1:51329536-51329669 | Rare:21 | ||||
chr1:51518164-51518308 | Rare:29 | ||||
chr1:52896591-52896816 | Rare:40 | ||||
chr1:58576029-58576166 | Common:2; Rare:25; Clinvar:2; Clinvar (benign):2 | ||||
chr1:58782931-58783008 | Rare:31 | ||||
chr1:58783048-58783125 | Rare:25 | ||||
chr1:58783548-58783681 | Rare:27 | ||||
chr1:65067711-65067825 | Rare:31 |