Variant report

Variant	rs2043552
Chromosome Location	chr12:43350345-43350346
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs12317369	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1520819	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1520826	1.00[AFR][1000 genomes]
rs17092544	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17513656	1.00[CEU][hapmap]
rs17585302	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17585588	1.00[CEU][hapmap]
rs4768472	1.00[CEU][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4768476	1.00[CEU][hapmap]
rs7955263	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7958072	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7967110	1.00[AFR][1000 genomes]
rs7968365	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7968724	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:43341000-43351400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:43348800-43352200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr12:43350000-43353600	Enhancers	Fetal Brain Male	brain
4	chr12:43350200-43350400	Enhancers	Fetal Muscle Leg	muscle
5	chr12:43350200-43350800	Enhancers	Fetal Brain Female	brain

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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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