Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145858993-145859184 | Rare:54 | ||||
chr1:145918680-145919013 | Common:2; Rare:74 | ||||
chr1:145927368-145927618 | Common:1; Rare:63; Clinvar (pathogenic):1 | ||||
chr1:145958000-145958212 | Rare:49 | ||||
chr1:145964495-145964742 | Rare:60 | ||||
chr1:145996534-145996802 | Rare:106 | ||||
chr1:147172460-147172785 | Common:1; Rare:83 | ||||
chr1:148952354-148952644 | Common:4; Rare:78 | ||||
chr1:149812283-149812532 | Common:2; Rare:113 | ||||
chr1:149850826-149851062 | Rare:1 | ||||
chr1:149886632-149887004 | Common:2; Rare:140 | ||||
chr1:149887848-149888215 | Rare:115 | ||||
chr1:149927740-149927863 | Rare:50; Clinvar (benign):4 | ||||
chr1:150067665-150067860 | Rare:61 | ||||
chr1:150235932-150236167 | Common:1; Rare:57 |