Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:109453825-109453917 | Rare:30 | ||||
chr6:111329666-111329847 | Rare:41 | ||||
chr6:111424721-111424811 | Rare:14 | ||||
chr6:112115861-112116125 | Rare:59; Clinvar:5; Clinvar (benign):3 | ||||
chr6:118895098-118895251 | Rare:42 | ||||
chr6:119350581-119350713 | Common:2; Rare:28 | ||||
chr6:129130435-129130468 | Rare:8 | ||||
chr6:129396057-129396332 | Common:3; Rare:49 | ||||
chr6:129478524-129478792 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr6:137218003-137218202 | Common:1; Rare:37 | ||||
chr6:139978228-139978395 | Common:2; Rare:27 | ||||
chr6:142945737-142946031 | Rare:80 | ||||
chr6:144284880-144284983 | Rare:22 | ||||
chr6:144702942-144703066 | Common:1; Rare:25 | ||||
chr6:148508465-148508802 | Common:1; Rare:56 |