Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:92029921-92030046 | Rare:35 | ||||
chr1:92298889-92299076 | Common:1; Rare:85; Clinvar:2; Clinvar (benign):2 | ||||
chr1:92785058-92785393 | Common:6; Rare:108 | ||||
chr1:92831871-92832113 | Common:1; Rare:109; Clinvar:6; Clinvar (benign):5 | ||||
chr1:92961425-92961804 | Common:3; Rare:115 | ||||
chr1:93079060-93079319 | Common:4; Rare:111 | ||||
chr1:93180224-93180751 | Common:2; Rare:209 | ||||
chr1:93345759-93345985 | Common:4; Rare:91 | ||||
chr1:93447976-93448170 | Common:2; Rare:71 | ||||
chr1:93847220-93847322 | Common:1; Rare:23 | ||||
chr1:93879144-93879339 | Common:3; Rare:73 | ||||
chr1:94237566-94237744 | Rare:68 | ||||
chr1:94418179-94418470 | Common:2; Rare:106 | ||||
chr1:94820140-94820391 | Common:4; Rare:61 | ||||
chr1:94925820-94926021 | Common:1; Rare:38 |