Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145996417-145996808 | Common:1; Rare:142 | ||||
chr1:147172420-147172830 | Common:1; Rare:105 | ||||
chr1:147225315-147225762 | Common:3; Rare:82 | ||||
chr1:147541213-147541501 | Common:2; Rare:43 | ||||
chr1:148952021-148952141 | Common:3; Rare:32 | ||||
chr1:148952271-148952669 | Common:5; Rare:106 | ||||
chr1:149812355-149812560 | Rare:64 | ||||
chr1:149886632-149887004 | Common:2; Rare:140 | ||||
chr1:149887904-149888215 | Rare:95 | ||||
chr1:149927760-149927900 | Common:1; Rare:58; Clinvar (benign):4 | ||||
chr1:150010540-150010919 | Common:3; Rare:96 | ||||
chr1:150067671-150067873 | Rare:62 | ||||
chr1:150236083-150236449 | Rare:81 | ||||
chr1:150272628-150272815 | Common:1; Rare:44 | ||||
chr1:150282299-150282550 | Common:2; Rare:41 |