Variant report

Variant	rs4371387
Chromosome Location	chr2:21221133-21221134
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1042031	0.94[CEU][hapmap]
rs12720828	0.89[CEU][hapmap]
rs12992267	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13014683	0.82[EUR][1000 genomes]
rs1801702	0.93[YRI][hapmap]
rs34059329	0.88[AFR][1000 genomes]
rs34776010	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3749054	0.95[CEU][hapmap]
rs4665709	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56327713	0.81[AFR][1000 genomes]
rs56984418	0.80[EUR][1000 genomes]
rs62122484	0.85[EUR][1000 genomes]
rs6721844	0.83[AFR][1000 genomes]
rs6725189	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6756501	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs952274	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21216400-21225600	Weak transcription	Aorta	Aorta
2	chr2:21220200-21225600	Weak transcription	Left Ventricle	heart
3	chr2:21220600-21224200	Weak transcription	HepG2	liver
4	chr2:21221000-21224400	Weak transcription	Fetal Intestine Small	intestine

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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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