Variant report

Variant	rs7586488
Chromosome Location	chr2:231513725-231513726
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs4072492	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4072493	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4072494	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4072495	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4994158	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55813008	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59447445	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59448537	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61479181	1.00[EUR][1000 genomes]
rs6436961	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6436962	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73103326	1.00[EUR][1000 genomes]
rs73103330	1.00[EUR][1000 genomes]
rs73103367	1.00[EUR][1000 genomes]
rs73106851	1.00[EUR][1000 genomes]
rs73108724	1.00[EUR][1000 genomes]
rs73992491	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7572545	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7604318	1.00[EUR][1000 genomes]

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231508800-231515400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr2:231509000-231514400	Weak transcription	K562	blood
3	chr2:231509400-231517200	Weak transcription	Placenta	Placenta
4	chr2:231509600-231519000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr2:231509600-231521600	Weak transcription	Primary B cells from peripheral blood	blood
6	chr2:231509800-231518800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr2:231509800-231521000	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr2:231510000-231518400	Weak transcription	Fetal Thymus	thymus
9	chr2:231513200-231515400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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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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