Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:85543452-85543780 | Rare:58; Clinvar (benign):1 | ||||
chr2:85549898-85550296 | Common:1; Rare:98; Clinvar:1 | ||||
chr2:85805861-85806155 | Common:5; Rare:57 | ||||
chr2:87014985-87015162 | Rare:11 | ||||
chr2:87483210-87483364 | Common:3; Rare:38 | ||||
chr2:87754756-87754982 | Rare:29 | ||||
chr2:88016536-88016817 | Common:10; Rare:122 | ||||
chr2:88137066-88137085 | Rare:2 | ||||
chr2:88138481-88138623 | Common:2; Rare:24 | ||||
chr2:88857461-88857685 | Rare:74 | ||||
chr2:91659950-91660045 | Rare:19 | ||||
chr2:94290212-94290218 | |||||
chr2:95526660-95526973 | Common:1; Rare:99 | ||||
chr2:109615913-109616200 | Rare:82 | ||||
chr2:109617927-109618248 | Common:2; Rare:55 |