Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161118000-161118109 | Rare:53 | ||||
chr1:161132592-161132703 | Common:1; Rare:36 | ||||
chr1:161314308-161314400 | Common:2; Rare:35; Clinvar (benign):2 | ||||
chr1:162497761-162497867 | Common:1; Rare:40 | ||||
chr1:163321752-163322108 | Common:1; Rare:93 | ||||
chr1:165768772-165769042 | Common:2; Rare:110 | ||||
chr1:165827500-165827830 | Common:1; Rare:101 | ||||
chr1:166839254-166839522 | Rare:83 | ||||
chr1:168225901-168226053 | Common:1; Rare:55 | ||||
chr1:169367904-169368250 | Common:1; Rare:69 | ||||
chr1:169427410-169427517 | Rare:22 | ||||
chr1:169795001-169795094 | Common:2; Rare:28 | ||||
chr1:170532036-170532191 | Rare:67; Clinvar:1 | ||||
chr1:171741941-171742154 | Common:1; Rare:73 | ||||
chr1:173476978-173477442 | Common:5; Rare:158 |