Chrom Start End Enhancer ID Tissues that enhancer appears More
chr16 88771579 88772211 vista23510

Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr16 88772046 rs6500489 T C 4667048
chr16 88772121 rs544088991 C T 4667049
chr16 88772298 rs116026784 C T 4667050
chr16 88772419 rs533646410 G C 4667051
chr16 88772491 rs7194105 A G 4667052
chr16 88772518 rs556630785 G T 4667053
chr16 88772746 rs112070238 C T 4667054
chr16 88772749 rs558499488 GCGCCGCC G 4667055
chr16 88772787 rs531640048 C A 4667056
chr16 88772815 rs880233 C T 4667057
chr16 88772896 rs533325268 C G 4667058
chr16 88772907 rs533608663 C T 4667059
chr16 88772928 rs880234 C T 4667060
chr16 88772936 rs570424055 C G,T 4667061
chr16 88772963 rs137933845 G A 4667062
chr16 88773026 rs554371052 C G 4667063
chr16 88773163 rs529919447 C G 4667064
chr16 88773282 rs76902342 C T 4667065
chr16 88773350 rs144162256 G A 4667066
chr16 88773396 rs2340973 G A 4667067
chr16 88773406 rs4644850 C T 4667068
chr16 88773414 rs57958330 G T 4667069
chr16 88773525 rs185353598 C A,T 4667070
chr16 88773528 rs11641194 C A,G,T 4667071
chr16 88773738 rs881633 C T 4667072
chr16 88773753 rs6500490 C A 4667073
chr16 88773809 rs192924047 T C 4667074
chr16 88773826 rs77839429 A G 4667075
chr16 88773855 rs571980186 T G 4667076
chr16 88773893 rs11641365 C T 4667077
chr16 88773984 rs28685172 C G 4667078
chr16 88774066 rs555690643 C T 4667079
chr16 88774083 rs117557103 C T 4667080
chr16 88774121 rs574628861 C T 4667081
chr16 88774195 rs576145008 G A 4667082
chr16 88774196 rs149972590 C T 4667083
chr16 88774208 rs76251716 G T 4667084
chr16 88774220 rs11395253 G GT,GTTGT,GTTGTT 4667085
chr16 88774220 rs199673451 G T 4667086
chr16 88774220 rs34760068 G GT 4667087
chr16 88774220 rs397707337 G GT 4667088
chr16 88774223 rs541143507 T G 4667089
chr16 88774275 rs376010638 A C 4667090
chr16 88774359 rs149230876 C T 4667091
chr16 88774474 rs58797132 G A 4667092
chr16 88774513 rs139276441 C T 4667093
chr16 88774525 rs11076701 A G 4667094
chr16 88774552 rs57817451 C T 4667095
chr16 88774569 rs11076702 A C 4667096
chr16 88774582 rs189524291 C G,T 4667097
chr16 88774594 rs146962609 C G 4667098
chr16 88774596 rs181795543 G T 4667099
chr16 88774708 rs117317047 G A 4667100
chr16 88774764 rs147998951 C G 4667101
chr16 88774784 rs141635211 C T 4667102
chr16 88774827 rs189815273 C T 4667103
chr16 88774828 rs561056205 G GC 4667104
chr16 88774829 rs553206121 T A,C 4667105
chr16 88774830 rs564860653 G GCCCA 4667106
chr16 88774871 rs115942789 A G 4667107
chr16 88774921 rs7404845 C A,T 4667108
chr16 88774996 rs138381960 G A 4667109
chr16 88775035 rs141896575 A G 4667110
chr16 88775036 rs117900187 C G,T 4667111
chr16 88775076 rs556822977 C T 4667112
chr16 88775109 rs115326109 G A 4667113
chr16 88775128 rs146267921 C A,T 4667114
chr16 88775199 rs74033353 T C 4667115
chr16 88775220 rs4238685 T C 4667116
chr16 88775254 rs80304559 G A 4667117
chr16 88775433 rs72811462 A C,G 4667118
chr16 88775485 rs111656785 C G 4667119
chr16 88775573 rs148521699 C G 4667120
chr16 88775581 rs115571374 C T 4667121
chr16 88775614 rs11640071 G C 4667122

Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End Strand Gene Name Ensembl ID TSS TSI of Normal tissues TSI of Cancer tissues Distance to TFBS id More
chr16 88762903 88772829 - RNF166 ENSG00000158717.6 88772829 0.81 1.0 912 15160
chr16 88772871 88781794 + CTU2 ENSG00000174177.8 88772871 0.72 1.0 954 15161


Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End strand miRNA Name miRBase ID TSS TSI of Normal tissues TSI of Cancer tissues Distance to TFBS id More

No results