Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:7799855-7800052 | Rare:49 | ||||
chr10:12195797-12196271 | Rare:135 | ||||
chr10:13099771-13100234 | Common:4; Rare:113; Clinvar:3; Clinvar (benign):5 | ||||
chr10:13300061-13300196 | Rare:46 | ||||
chr10:14838028-14838370 | Common:2; Rare:91 | ||||
chr10:14878665-14878902 | Common:2; Rare:67 | ||||
chr10:14954044-14954209 | Rare:51 | ||||
chr10:17230604-17230707 | Rare:39 | ||||
chr10:17643871-17644276 | Common:2; Rare:122 | ||||
chr10:18659245-18659643 | Common:2; Rare:138 | ||||
chr10:24466332-24466555 | Rare:34 | ||||
chr10:26438064-26438357 | Common:2; Rare:70 | ||||
chr10:27154190-27154479 | Rare:80 | ||||
chr10:27155161-27155395 | Common:4; Rare:85; Clinvar:5; Clinvar (benign):4 | ||||
chr10:27744988-27745237 | Common:1; Rare:51 |