Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19311982-19312366 | Common:8; Rare:172 | ||||
chr1:19485435-19485765 | Common:1; Rare:124 | ||||
chr1:19596829-19597063 | Common:2; Rare:98 | ||||
chr1:19799716-19799987 | Common:4; Rare:84 | ||||
chr1:20185983-20186128 | Common:1; Rare:49 | ||||
chr1:20186350-20186486 | Rare:33 | ||||
chr1:20486179-20486379 | Rare:47 | ||||
chr1:20508057-20508200 | Common:2; Rare:52 | ||||
chr1:20552458-20552669 | Common:2; Rare:41 | ||||
chr1:20660955-20661212 | Common:3; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
chr1:20661331-20661705 | Common:3; Rare:136; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786606-20786870 | Rare:99 | ||||
chr1:21176836-21177146 | Rare:92 | ||||
chr1:21279508-21279711 | Rare:36 | ||||
chr1:21290194-21290381 | Rare:38 |