Variant report

Variant	rs7075793
Chromosome Location	chr10:22662412-22662413
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10508643	0.88[YRI][hapmap];0.81[AFR][1000 genomes]
rs11012946	0.89[YRI][hapmap]
rs11012959	0.81[YRI][hapmap];0.83[AFR][1000 genomes]
rs11012963	0.89[YRI][hapmap];0.87[AFR][1000 genomes]
rs12241581	0.88[YRI][hapmap]
rs12249265	0.89[YRI][hapmap];0.81[AFR][1000 genomes]
rs12257327	0.89[YRI][hapmap];0.83[AFR][1000 genomes]
rs2026631	1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7084298	0.83[AFR][1000 genomes]
rs7092238	0.89[YRI][hapmap];0.83[AFR][1000 genomes]
rs7904329	0.81[AFR][1000 genomes]
rs9971241	0.89[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:22659400-22663800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr10:22659600-22663200	Weak transcription	Gastric	stomach
3	chr10:22659600-22663200	Weak transcription	HUVEC	blood vessel
4	chr10:22659600-22663600	Weak transcription	GM12878-XiMat	blood
5	chr10:22660000-22663600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr10:22660400-22663800	Weak transcription	Primary hematopoietic stem cells	blood
7	chr10:22661600-22663800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr10:22662200-22663800	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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