Variant report

Variant	rs11729344
Chromosome Location	chr4:127459568-127459569
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10002417	0.82[AFR][1000 genomes]
rs11098884	0.82[AFR][1000 genomes]
rs1511135	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1542999	0.82[AFR][1000 genomes]
rs1543000	0.82[AFR][1000 genomes]
rs192856	0.82[YRI][hapmap]
rs2202824	0.82[AFR][1000 genomes]
rs2221682	1.00[AFR][1000 genomes]
rs313090	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[YRI][hapmap];0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs313104	0.92[LWK][hapmap];0.91[YRI][hapmap]
rs667581	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6823628	0.86[AFR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127455000-127460000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr4:127456400-127459600	Strong transcription	K562	blood
3	chr4:127459400-127460400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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