Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:112969135-112969323 | Common:2; Rare:54 | ||||
chr13:113208620-113208751 | Rare:78 | ||||
chr13:113490709-113491021 | Common:1; Rare:115 | ||||
chr13:113759147-113759275 | Rare:36 | ||||
chr13:114281315-114281675 | Common:5; Rare:151 | ||||
chr14:20343184-20343645 | Common:12; Rare:270 | ||||
chr14:20413407-20413512 | Common:2; Rare:27 | ||||
chr14:20454762-20455375 | Common:7; Rare:156 | ||||
chr14:20684471-20684595 | Common:1; Rare:19; Clinvar (benign):1 | ||||
chr14:20989665-20990011 | Common:7; Rare:78 | ||||
chr14:21383923-21384259 | Common:8; Rare:112 | ||||
chr14:21456041-21456445 | Common:4; Rare:104 | ||||
chr14:21476611-21476750 | Rare:63 | ||||
chr14:21476837-21477271 | Common:2; Rare:143 | ||||
chr14:21511257-21511553 | Rare:86 |