Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:93862732-93863054 | Common:1; Rare:71 | ||||
chr15:94855881-94856102 | Common:3; Rare:63 | ||||
chr15:96327346-96327383 | Rare:7 | ||||
chr15:96333716-96333801 | Rare:18 | ||||
chr15:96333923-96334209 | Rare:79; Clinvar (benign):1 | ||||
chr15:99105791-99105931 | Common:7; Rare:70 | ||||
chr15:101961544-101961640 | Rare:3 | ||||
chr16:519646-519805 | Rare:49 | ||||
chr16:1361770-1361940 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr16:1553441-1553768 | Common:4; Rare:65 | ||||
chr16:1748545-1748620 | Rare:24 | ||||
chr16:2603402-2603477 | Rare:37 | ||||
chr16:2673372-2673679 | Common:8; Rare:106 | ||||
chr16:10457832-10458060 | Rare:49 | ||||
chr16:11896613-11896908 | Common:1; Rare:78 |