Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:26347037-26347115 | Rare:16 | ||||
chr8:26353315-26353448 | Common:1; Rare:22 | ||||
chr8:26392007-26392102 | Rare:18 | ||||
chr8:30393012-30393206 | Rare:37 | ||||
chr8:30412225-30412439 | Rare:31 | ||||
chr8:30425462-30425720 | Rare:62 | ||||
chr8:30477527-30477835 | Common:2; Rare:59 | ||||
chr8:30509251-30509569 | Common:3; Rare:46 | ||||
chr8:30547088-30547432 | Common:2; Rare:66 | ||||
chr8:30553209-30553260 | Rare:8 | ||||
chr8:30555464-30555776 | Common:1; Rare:76 | ||||
chr8:30569054-30569286 | Rare:48 | ||||
chr8:30677966-30678083 | Rare:21 | ||||
chr8:31076005-31076240 | Rare:45; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr8:31131872-31131924 | Rare:11 |