Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:177337361-177337727 | Common:1; Rare:124 | ||||
chr5:178206571-178206758 | Common:2; Rare:58 | ||||
chr5:178211905-178212167 | Rare:88; Clinvar (pathogenic):1 | ||||
chr5:178338248-178338372 | Common:3; Rare:19 | ||||
chr5:179622341-179622604 | Common:1; Rare:85 | ||||
chr5:180830881-180831032 | Common:1; Rare:48 | ||||
chr5:180831596-180831718 | Common:2; Rare:48 | ||||
chr5:181207566-181207798 | Common:5; Rare:96 | ||||
chr6:3019355-3019500 | Common:2; Rare:27 | ||||
chr6:3380830-3381043 | Common:3; Rare:30 | ||||
chr6:3403284-3403590 | Rare:77 | ||||
chr6:3788839-3788965 | Common:2; Rare:22 | ||||
chr6:3872414-3872441 | Rare:4 | ||||
chr6:4018688-4018831 | Common:2; Rare:45 | ||||
chr6:5457971-5458003 | Common:1; Rare:5 |