Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:99546454-99546513 | Rare:19 | ||||
chr6:106702606-106703000 | Common:3; Rare:85 | ||||
chr6:106717207-106717245 | Rare:6 | ||||
chr6:106739435-106739750 | Common:3; Rare:67 | ||||
chr6:106787350-106787723 | Rare:64 | ||||
chr6:108654085-108654396 | Common:4; Rare:51 | ||||
chr6:110566608-110566735 | Rare:20 | ||||
chr6:111674507-111674726 | Rare:33; Clinvar:1 | ||||
chr6:112114661-112114862 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):3 | ||||
chr6:112115978-112116359 | Common:2; Rare:63; Clinvar:1 | ||||
chr6:113873317-113873409 | Common:2; Rare:17 | ||||
chr6:116277306-116277487 | Common:1; Rare:30 | ||||
chr6:131033789-131033811 | Rare:2 | ||||
chr6:131581136-131581490 | Common:3; Rare:96; Clinvar:2; Clinvar (pathogenic):4 | ||||
chr6:131950050-131950412 | Common:1; Rare:116 |