Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:174159310-174159607 | Common:3; Rare:101 | ||||
chr1:174160039-174160259 | Common:1; Rare:50 | ||||
chr1:174999331-174999471 | Rare:39 | ||||
chr1:174999679-175000145 | Common:3; Rare:144 | ||||
chr1:176207498-176207669 | Common:1; Rare:68 | ||||
chr1:176553273-176553569 | Rare:46 | ||||
chr1:177164684-177164833 | Rare:33 | ||||
chr1:178093581-178093795 | Common:2; Rare:66 | ||||
chr1:178725090-178725335 | Common:10; Rare:92 | ||||
chr1:179877766-179877866 | Rare:22 | ||||
chr1:179882182-179882300 | Rare:23 | ||||
chr1:179882478-179882868 | Rare:183; Clinvar:8; Clinvar (benign):2 | ||||
chr1:179954669-179954827 | Common:1; Rare:35 | ||||
chr1:180502372-180502647 | Common:1; Rare:96 | ||||
chr1:180631821-180632135 | Common:6; Rare:115 |