Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:110915011-110915208 | Common:3; Rare:84 | ||||
chr13:111153595-111153713 | Common:2; Rare:54 | ||||
chr13:113208632-113208751 | Rare:68 | ||||
chr13:113863832-113864201 | Common:3; Rare:90 | ||||
chr13:114281305-114281664 | Common:5; Rare:147 | ||||
chr14:20343212-20343644 | Common:12; Rare:251 | ||||
chr14:20455054-20455270 | Common:2; Rare:67 | ||||
chr14:20684438-20684639 | Common:2; Rare:34; Clinvar (benign):2 | ||||
chr14:21383938-21384259 | Common:8; Rare:105 | ||||
chr14:21476636-21476766 | Rare:58 | ||||
chr14:21476868-21477271 | Common:2; Rare:131 | ||||
chr14:21511263-21511555 | Rare:82 | ||||
chr14:22871669-22871886 | Rare:52 | ||||
chr14:22872038-22872168 | Common:2; Rare:25 | ||||
chr14:22929338-22929609 | Rare:68 |