Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160262436-160262625 | Common:1; Rare:59 | ||||
chr1:160285120-160285313 | Common:3; Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
chr1:160343163-160343409 | Rare:97 | ||||
chr1:160400313-160400679 | Common:3; Rare:85 | ||||
chr1:161021021-161021507 | Common:6; Rare:133 | ||||
chr1:161038905-161039035 | Common:1; Rare:46 | ||||
chr1:161045878-161046077 | Common:1; Rare:52 | ||||
chr1:161117988-161118141 | Rare:81 | ||||
chr1:161132583-161132624 | Common:1; Rare:13 | ||||
chr1:161132625-161132840 | Common:1; Rare:59 | ||||
chr1:161159337-161159536 | Common:2; Rare:59 | ||||
chr1:161166299-161166430 | Rare:30 | ||||
chr1:161314201-161314414 | Common:3; Rare:77; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:162497756-162497888 | Common:2; Rare:49 | ||||
chr1:162790397-162790789 | Common:4; Rare:102 |