Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:95577414-95577602 | Common:5; Rare:57 | ||||
chr6:96521685-96521876 | Common:6; Rare:91 | ||||
chr6:100881201-100881482 | Common:5; Rare:103 | ||||
chr6:106629462-106629588 | Common:1; Rare:25 | ||||
chr6:106975302-106975526 | Common:1; Rare:65 | ||||
chr6:107958142-107958428 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):2 | ||||
chr6:108260917-108261328 | Common:2; Rare:167 | ||||
chr6:108848317-108848452 | Rare:46 | ||||
chr6:109440598-109440872 | Common:2; Rare:99 | ||||
chr6:109455726-109455832 | Rare:24 | ||||
chr6:109691161-109691332 | Common:3; Rare:40; Clinvar:4; Clinvar (benign):3 | ||||
chr6:110958629-110958659 | Common:1; Rare:5 | ||||
chr6:110958681-110958788 | Common:2; Rare:46 | ||||
chr6:110981954-110982109 | Common:2; Rare:79 | ||||
chr6:112087446-112087663 | Rare:68 |