Variant report

Variant	rs56286938
Chromosome Location	chr14:69738897-69738898
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11629094	0.95[ASN][1000 genomes]
rs12588610	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12590134	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1890939	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34842688	0.83[ASN][1000 genomes]
rs4902706	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62637934	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7141424	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72720292	1.00[ASN][1000 genomes]
rs7493080	0.96[ASN][1000 genomes]

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69730800-69740200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr14:69730800-69754000	Weak transcription	Brain Anterior Caudate	brain
3	chr14:69733000-69748000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr14:69735800-69771600	Weak transcription	Fetal Intestine Small	intestine
5	chr14:69736600-69740000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:69736800-69740800	Weak transcription	HSMMtube	muscle
7	chr14:69738200-69758200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr14:69738400-69739600	Weak transcription	Right Ventricle	heart
9	chr14:69738400-69740000	Weak transcription	Left Ventricle	heart
10	chr14:69738400-69740000	Weak transcription	Right Atrium	heart
11	chr14:69738600-69740400	Weak transcription	Fetal Heart	heart

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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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