Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:109689761-109689981 | Common:2; Rare:86 | ||||
chr5:110738906-110739124 | Common:2; Rare:88 | ||||
chr5:111512440-111512750 | Common:3; Rare:110 | ||||
chr5:112419180-112419293 | Common:1; Rare:52 | ||||
chr5:112707374-112707677 | Common:7; Rare:130; Clinvar:69; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
chr5:112737732-112737923 | Rare:47; Clinvar:1; Clinvar (benign):3 | ||||
chr5:113294640-113294749 | Rare:27 | ||||
chr5:115262800-115262898 | Common:1; Rare:46 | ||||
chr5:115544619-115545007 | Common:3; Rare:139 | ||||
chr5:115602365-115602446 | Rare:18 | ||||
chr5:115816483-115816570 | Common:1; Rare:16 | ||||
chr5:115816638-115816807 | Rare:42 | ||||
chr5:115841482-115842071 | Common:8; Rare:256 | ||||
chr5:116084693-116085067 | Common:9; Rare:128 | ||||
chr5:116085351-116085462 | Rare:29 |