Variant report

Variant	rs11732391
Chromosome Location	chr4:30807244-30807245
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10517220	1.00[JPT][hapmap];1.00[MEX][hapmap]
rs11724608	1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap]
rs11934948	1.00[JPT][hapmap];1.00[MEX][hapmap]
rs11939033	1.00[JPT][hapmap]
rs12648636	1.00[JPT][hapmap]
rs17718569	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17719504	1.00[JPT][hapmap]
rs6817721	1.00[JPT][hapmap]
rs6822389	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6833448	1.00[JPT][hapmap];1.00[MEX][hapmap]
rs6837246	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73213191	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73213192	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73213193	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73213197	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7670614	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7676204	1.00[JPT][hapmap]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30791600-30809800	Weak transcription	Fetal Lung	lung
2	chr4:30795800-30824000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:30796000-30810400	Weak transcription	Fetal Heart	heart
4	chr4:30801200-30809600	Weak transcription	Fetal Stomach	stomach
5	chr4:30803800-30817200	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr4:30804800-30819400	Weak transcription	Aorta	Aorta

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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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