Variant report

Variant	rs7069438
Chromosome Location	chr10:44095684-44095685
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11238594	0.83[AMR][1000 genomes]
rs11238596	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11238597	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12246417	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59017094	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs61563250	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7096121	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73260732	0.83[AMR][1000 genomes]
rs7900073	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44091400-44101400	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr10:44091800-44101200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr10:44092200-44101400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr10:44093000-44101600	Weak transcription	Primary T cells from cord blood	blood
5	chr10:44094200-44095800	Weak transcription	Primary hematopoietic stem cells	blood
6	chr10:44095000-44101400	Weak transcription	Spleen	Spleen

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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