Variant report

Variant	rs1565437
Chromosome Location	chr5:145226391-145226392
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1001433	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10043321	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10045188	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10050400	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10055545	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10071145	1.00[EUR][1000 genomes]
rs10477291	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28451090	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28673057	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56410343	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs59511054	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60544283	0.96[EUR][1000 genomes]
rs60708187	0.96[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:145216000-145227200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr5:145225400-145227000	Enhancers	Fetal Heart	heart
3	chr5:145225400-145234400	Weak transcription	Gastric	stomach
4	chr5:145225600-145232600	Weak transcription	Aorta	Aorta
5	chr5:145225800-145226800	Enhancers	Stomach Mucosa	stomach
6	chr5:145225800-145227000	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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