Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:148679690-148679938 | Rare:23 | ||||
chr1:148952021-148952141 | Common:3; Rare:32 | ||||
chr1:148952213-148952596 | Common:5; Rare:109 | ||||
chr1:149811634-149811905 | Rare:73 | ||||
chr1:149812173-149812560 | Common:2; Rare:170 | ||||
chr1:149813276-149813470 | Rare:105 | ||||
chr1:149832408-149832658 | |||||
chr1:149842745-149842984 | Rare:3 | ||||
chr1:149850781-149851074 | Common:2; Rare:12 | ||||
chr1:149886612-149887172 | Common:3; Rare:221 | ||||
chr1:149887885-149888217 | Rare:102 | ||||
chr1:149927767-149927901 | Common:1; Rare:51; Clinvar (benign):4 | ||||
chr1:150010703-150010837 | Rare:33 | ||||
chr1:150067216-150067315 | Common:1; Rare:18 | ||||
chr1:150067649-150067871 | Rare:65 |