Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:28643061-28643181 | Rare:39 | ||||
chr1:31296638-31297101 | Common:6; Rare:166 | ||||
chr1:31644852-31644973 | Common:2; Rare:45 | ||||
chr1:31938230-31938586 | Rare:111 | ||||
chr1:32200461-32200680 | Rare:48 | ||||
chr1:32650929-32651247 | Common:2; Rare:111 | ||||
chr1:32817270-32817692 | Common:1; Rare:113; Clinvar:5; Clinvar (benign):2 | ||||
chr1:35079340-35079381 | Rare:13 | ||||
chr1:35193120-35193290 | Rare:60 | ||||
chr1:35557360-35557451 | Rare:22 | ||||
chr1:35557629-35557857 | Common:2; Rare:90 | ||||
chr1:35769941-35770153 | Rare:58 | ||||
chr1:36155854-36156210 | Rare:137 | ||||
chr1:37690477-37690757 | Common:7; Rare:81 | ||||
chr1:37692218-37692553 | Common:4; Rare:71 |