Variant report

Variant	rs10071145
Chromosome Location	chr5:145224442-145224443
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1001433	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10043321	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10045188	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10050400	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10055545	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10477291	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1565437	1.00[EUR][1000 genomes]
rs28451090	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28673057	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3995495	1.00[GIH][hapmap];1.00[TSI][hapmap]
rs56410343	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59511054	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs60544283	0.96[EUR][1000 genomes]
rs60708187	0.96[EUR][1000 genomes]
rs9324996	1.00[JPT][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:145216000-145227200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr5:145221600-145225400	Weak transcription	K562	blood

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Input of quick search could be:

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

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