Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:7961481-7961723 | Common:3; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
chr1:19251525-19251798 | Common:6; Rare:81 | ||||
chr1:31296752-31296986 | Common:4; Rare:70 | ||||
chr1:37808206-37808534 | Common:1; Rare:72 | ||||
chr1:43974778-43974960 | Common:2; Rare:47 | ||||
chr1:45688059-45688202 | Common:1; Rare:34 | ||||
chr1:46303609-46303698 | Common:1; Rare:17 | ||||
chr1:74733009-74733083 | Common:2; Rare:27 | ||||
chr1:93345822-93345955 | Common:2; Rare:49 | ||||
chr1:101236635-101236922 | Common:2; Rare:50 | ||||
chr1:160343220-160343386 | Rare:60 | ||||
chr1:161117997-161118105 | Rare:53 | ||||
chr1:167935991-167936247 | Common:1; Rare:79 | ||||
chr1:224616199-224616325 | Common:1; Rare:38 | ||||
chr1:230978836-230979094 | Common:1; Rare:90 |