Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:32780770-32781201 | Common:4; Rare:202 | ||||
chr3:32794660-32795160 | Rare:122 | ||||
chr3:32795098-32795760 | Common:3; Rare:164 | ||||
chr3:32796485-32796710 | Common:4; Rare:87 | ||||
chr3:32816319-32816966 | Common:7; Rare:317 | ||||
chr3:32839981-32840601 | Common:4; Rare:189 | ||||
chr3:38347622-38347790 | Common:1; Rare:52 | ||||
chr3:39384240-39384510 | Common:13; Rare:115 | ||||
chr3:40453142-40453460 | Common:12; Rare:142 | ||||
chr3:41265877-41266240 | Common:2; Rare:110 | ||||
chr3:42179510-42179880 | Rare:114 | ||||
chr3:42846592-42847493 | Common:6; Rare:201 | ||||
chr3:44478796-44478999 | Rare:47 | ||||
chr3:45394180-45394850 | Common:4; Rare:193; Clinvar:2; Clinvar (benign):6 | ||||
chr3:47840680-47841030 | Common:1; Rare:100 |