Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:113208632-113208751 | Rare:68 | ||||
chr13:113490699-113491017 | Common:1; Rare:117 | ||||
chr13:113863850-113864180 | Common:3; Rare:81 | ||||
chr13:114281323-114281673 | Common:5; Rare:147 | ||||
chr13:114282145-114282430 | Common:4; Rare:81 | ||||
chr14:20343184-20343675 | Common:12; Rare:292 | ||||
chr14:20413420-20413531 | Common:3; Rare:31 | ||||
chr14:20454800-20455357 | Common:7; Rare:141 | ||||
chr14:20684427-20684601 | Common:2; Rare:26; Clinvar (benign):2 | ||||
chr14:20989665-20990002 | Common:7; Rare:71 | ||||
chr14:21456042-21456134 | Common:2; Rare:23 | ||||
chr14:21476950-21477271 | Common:1; Rare:96 | ||||
chr14:21511248-21511549 | Rare:90 | ||||
chr14:22588954-22589022 | Rare:13 | ||||
chr14:22589144-22589476 | Common:4; Rare:107 |