Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:158819323-158819446 | Common:2; Rare:46 | ||||
chr6:159000141-159000209 | Common:1; Rare:17 | ||||
chr6:159693253-159693597 | Common:5; Rare:97 | ||||
chr6:159726926-159727198 | Common:1; Rare:98 | ||||
chr6:159727333-159727633 | Common:5; Rare:130 | ||||
chr6:159789538-159790014 | Common:5; Rare:160 | ||||
chr6:159790235-159790514 | Common:7; Rare:88 | ||||
chr6:160991581-160991789 | Common:2; Rare:63 | ||||
chr6:161273992-161274232 | Rare:42 | ||||
chr6:166342508-166342653 | Common:3; Rare:57 | ||||
chr6:166627950-166628127 | Rare:38 | ||||
chr6:166999061-166999412 | Common:1; Rare:119 | ||||
chr6:169701993-169702193 | Common:3; Rare:99 | ||||
chr6:169751526-169751646 | Rare:43; Clinvar (benign):2 | ||||
chr6:170554186-170554409 | Common:1; Rare:69 |