Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:73517691-73518267 | Common:2; Rare:153 | ||||
chr6:78966850-78967058 | Common:1; Rare:33 | ||||
chr6:84139329-84139584 | Common:1; Rare:45 | ||||
chr6:85678706-85678971 | Rare:97 | ||||
chr6:87675601-87675768 | Common:1; Rare:29 | ||||
chr6:89720936-89721156 | Common:2; Rare:37 | ||||
chr6:93416756-93416955 | Common:1; Rare:53 | ||||
chr6:109454253-109454268 | Rare:1 | ||||
chr6:111689874-111690084 | Common:2; Rare:47 | ||||
chr6:113873386-113873541 | Rare:28 | ||||
chr6:113995922-113995976 | Common:1; Rare:10 | ||||
chr6:129427533-129427775 | Common:1; Rare:52; Clinvar (benign):1 | ||||
chr6:154410472-154410748 | Rare:43 | ||||
chr6:159170047-159170105 | Rare:12 | ||||
chr6:167796717-167796913 | Common:1; Rare:43 |