Variant report

Variant	rs10912656
Chromosome Location	chr1:173603912-173603913
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:173602098..173604115-chr1:173674279..173675875,2	K562	blood:

rs_ID	r²[population]
rs10798282	0.82[CHB][hapmap]
rs10798283	0.80[AMR][1000 genomes]
rs10798295	0.91[CHB][hapmap]
rs10912632	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10912634	0.80[AMR][1000 genomes]
rs10912651	0.83[AMR][1000 genomes]
rs10912660	0.83[ASN][1000 genomes]
rs11578058	0.86[MKK][hapmap];0.91[TSI][hapmap]
rs11582670	0.81[AMR][1000 genomes]
rs12026427	0.80[AMR][1000 genomes]
rs12033623	0.80[AMR][1000 genomes]
rs12034341	0.80[AMR][1000 genomes]
rs12034533	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12035105	0.80[AMR][1000 genomes]
rs12037210	0.93[MKK][hapmap]
rs12067170	0.84[ASN][1000 genomes]
rs12075071	0.84[ASN][1000 genomes]
rs12092383	1.00[CHB][hapmap];0.80[JPT][hapmap];0.81[ASN][1000 genomes]
rs12140760	0.82[CHB][hapmap]
rs12406500	0.80[AMR][1000 genomes]
rs1461023	0.80[AMR][1000 genomes]
rs1547156	0.80[AMR][1000 genomes]
rs16846113	0.80[AMR][1000 genomes]
rs1925340	0.87[AMR][1000 genomes]
rs2901747	0.81[AMR][1000 genomes]
rs2901748	0.81[AMR][1000 genomes]
rs34906768	0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4336887	0.81[AMR][1000 genomes]
rs4382766	0.82[CHB][hapmap]
rs4916358	0.82[CHB][hapmap]
rs4916362	0.82[CHB][hapmap]
rs4916368	0.80[AMR][1000 genomes]
rs57592568	0.84[ASN][1000 genomes]
rs6675929	0.80[AMR][1000 genomes]
rs6702320	0.80[AMR][1000 genomes]
rs6702835	0.87[CHB][hapmap]
rs72709325	0.80[AMR][1000 genomes]
rs728908	0.80[AMR][1000 genomes]
rs7314	0.87[CHB][hapmap]
rs7365380	0.93[ASN][1000 genomes]
rs745573	0.80[AMR][1000 genomes]
rs745574	0.80[AMR][1000 genomes]
rs7537938	0.82[CHB][hapmap]
rs7540065	0.87[CHB][hapmap]
rs7542910	0.85[ASN][1000 genomes]
rs7552939	0.91[CHB][hapmap]
rs898657	0.81[AMR][1000 genomes]
rs9425718	0.82[CHB][hapmap]
rs969029	0.86[ASN][1000 genomes]

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:173598000-173607000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:173603000-173606200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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