Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:63636053-63636149 | Rare:31 | ||||
chr6:70413195-70413545 | Common:2; Rare:102 | ||||
chr6:72622086-72622333 | Common:3; Rare:60 | ||||
chr6:73696053-73696207 | Rare:29 | ||||
chr6:75284675-75285022 | Common:1; Rare:103 | ||||
chr6:75493531-75493876 | Common:1; Rare:67 | ||||
chr6:75749112-75749262 | Common:3; Rare:42; Clinvar:2 | ||||
chr6:79537346-79537658 | Common:2; Rare:98; Clinvar:4 | ||||
chr6:83193222-83193414 | Common:3; Rare:70 | ||||
chr6:85449884-85450090 | Common:1; Rare:58 | ||||
chr6:85593812-85594115 | Common:1; Rare:86 | ||||
chr6:85643812-85643931 | Common:2; Rare:37 | ||||
chr6:87155218-87155615 | Rare:109 | ||||
chr6:87589959-87590177 | Common:3; Rare:98; Clinvar (benign):4 | ||||
chr6:88963579-88963830 | Common:2; Rare:84 |