Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1782503-1782771 | Common:4; Rare:88 | ||||
chr16:1782810-1783012 | Rare:65 | ||||
chr16:1827147-1827225 | Common:1; Rare:33 | ||||
chr16:1943130-1943499 | Common:1; Rare:117 | ||||
chr16:1964811-1965061 | Common:6; Rare:114 | ||||
chr16:1971895-1972141 | Common:1; Rare:73 | ||||
chr16:2047724-2048034 | Rare:148; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2155354-2155657 | Rare:89 | ||||
chr16:2268059-2268210 | Common:1; Rare:69 | ||||
chr16:2268361-2268482 | Common:1; Rare:42 | ||||
chr16:2474982-2475155 | Rare:56; Clinvar (benign):2 | ||||
chr16:2752564-2752843 | Common:2; Rare:121 | ||||
chr16:2758472-2758680 | Rare:66 | ||||
chr16:2777245-2777410 | Common:3; Rare:64 | ||||
chr16:2980410-2980620 | Common:2; Rare:74 |