Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:110615564-110615610 | Rare:21 | ||||
chr13:113208632-113208765 | Rare:77 | ||||
chr13:114281299-114281654 | Common:5; Rare:140 | ||||
chr14:20343190-20343644 | Common:12; Rare:267 | ||||
chr14:20455046-20455281 | Common:2; Rare:70 | ||||
chr14:20684471-20684629 | Common:1; Rare:25; Clinvar (benign):1 | ||||
chr14:21021104-21021430 | Common:1; Rare:74 | ||||
chr14:21025494-21025621 | Common:1; Rare:31 | ||||
chr14:21456058-21456348 | Common:3; Rare:77 | ||||
chr14:21476878-21477258 | Common:2; Rare:119 | ||||
chr14:21511289-21511519 | Rare:59 | ||||
chr14:22766554-22766699 | Common:1; Rare:77 | ||||
chr14:22815382-22815516 | Rare:23 | ||||
chr14:22871970-22872156 | Common:2; Rare:42 | ||||
chr14:22929363-22929643 | Common:1; Rare:76 |