Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26432095-26432418 | Common:5; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26695615-26695747 | Rare:45 | ||||
chr1:26900408-26900548 | Rare:54 | ||||
chr1:26921574-26921874 | Common:3; Rare:92 | ||||
chr1:27772983-27773297 | Common:1; Rare:109 | ||||
chr1:28505807-28506182 | Common:5; Rare:151 | ||||
chr1:28643019-28643176 | Rare:64 | ||||
chr1:28668423-28668733 | Rare:56 | ||||
chr1:28737530-28737773 | Rare:96 | ||||
chr1:29123918-29123979 | Common:1; Rare:28 | ||||
chr1:31296720-31297111 | Common:5; Rare:131 | ||||
chr1:31798279-31798472 | Common:2; Rare:57 | ||||
chr1:31937757-31937998 | Common:1; Rare:64 | ||||
chr1:31938031-31938166 | Rare:43 | ||||
chr1:31938306-31938613 | Rare:92 |