Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:103396426-103396711 | Rare:102 | ||||
chr10:104338435-104338540 | Rare:26 | ||||
chr10:110006022-110006098 | Rare:14 | ||||
chr10:110007696-110008017 | Rare:94 | ||||
chr10:110919326-110919647 | Common:7; Rare:88; Clinvar:1 | ||||
chr10:112446860-112447241 | Common:3; Rare:91 | ||||
chr10:118046891-118047008 | Rare:35 | ||||
chr10:119080651-119080734 | Common:3; Rare:25 | ||||
chr10:119080868-119081159 | Common:2; Rare:84 | ||||
chr10:119872822-119873039 | Common:4; Rare:79 | ||||
chr10:119892564-119892772 | Common:2; Rare:79 | ||||
chr10:120851207-120851419 | Common:5; Rare:77 | ||||
chr10:122954186-122954456 | Rare:99 | ||||
chr10:123008722-123009021 | Common:6; Rare:79; Clinvar:4; Clinvar (benign):5 | ||||
chr10:125719450-125719723 | Rare:84 |