Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:169485704-169486234 | Common:2; Rare:151; Clinvar:6; Clinvar (benign):4 | ||||
chr1:169794831-169795105 | Common:3; Rare:73 | ||||
chr1:170074448-170074717 | Common:2; Rare:89 | ||||
chr1:170532034-170532210 | Rare:82; Clinvar:1 | ||||
chr1:171485345-171485731 | Common:1; Rare:122 | ||||
chr1:171742030-171742154 | Rare:36 | ||||
chr1:171742179-171742184 | |||||
chr1:171781843-171781881 | Rare:9 | ||||
chr1:173477136-173477493 | Common:4; Rare:130 | ||||
chr1:173481064-173481327 | Common:2; Rare:36 | ||||
chr1:173714852-173715082 | Common:1; Rare:51 | ||||
chr1:173824096-173824763 | Rare:142; Clinvar:2 | ||||
chr1:173824790-173825011 | Rare:46 | ||||
chr1:173867957-173868223 | Common:1; Rare:101 | ||||
chr1:174022278-174022505 | Rare:56 |