Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:231528583-231528713 | Common:1; Rare:45 | ||||
chr1:234373398-234373554 | Common:1; Rare:79; Clinvar (benign):3 | ||||
chr1:234373666-234373768 | Rare:41; Clinvar (benign):2 | ||||
chr1:235866898-235867206 | Common:2; Rare:95 | ||||
chr1:241848073-241848243 | Common:2; Rare:40 | ||||
chr1:244451884-244452212 | Common:1; Rare:109 | ||||
chr1:244864445-244864677 | Rare:91 | ||||
chr1:246566209-246566515 | Common:1; Rare:102 | ||||
chr1:248906022-248906255 | Common:1; Rare:86 | ||||
chr10:988292-988464 | Rare:61 | ||||
chr10:1048878-1049086 | Common:2; Rare:110 | ||||
chr10:7787950-7788213 | Common:1; Rare:108 | ||||
chr10:12195810-12196234 | Rare:113 | ||||
chr10:14878671-14878882 | Common:2; Rare:57 | ||||
chr10:27154342-27154493 | Rare:42 |