Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:159102857-159103079 | Common:4; Rare:89 | ||||
chr4:162712904-162713146 | Common:1; Rare:48 | ||||
chr4:163095520-163095752 | Common:6; Rare:41 | ||||
chr4:163103915-163104087 | Common:1; Rare:36 | ||||
chr4:166717093-166717366 | Common:2; Rare:76 | ||||
chr4:167440323-167440447 | Rare:37 | ||||
chr4:168925992-168926329 | Rare:61; Clinvar:3; Clinvar (benign):2 | ||||
chr4:170679271-170679309 | Rare:5 | ||||
chr4:172959179-172959477 | Common:3; Rare:64 | ||||
chr4:173169638-173169745 | Common:1; Rare:38 | ||||
chr4:173608697-173608990 | Rare:94 | ||||
chr4:174291817-174291925 | Rare:16 | ||||
chr4:175019339-175019488 | Rare:33 | ||||
chr4:176320508-176320701 | Rare:59 | ||||
chr4:178209965-178210021 | Rare:13 |