Variant report

Variant	rs60037611
Chromosome Location	chr11:8426106-8426107
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:8410429..8412576-chr11:8424308..8426564,3	K562	blood:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs11041903	1.00[ASN][1000 genomes]
rs11826221	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11826312	1.00[ASN][1000 genomes]
rs11827424	0.94[ASN][1000 genomes]
rs11827954	1.00[ASN][1000 genomes]
rs11828529	1.00[ASN][1000 genomes]
rs12574773	1.00[ASN][1000 genomes]
rs12577458	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57125396	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57577868	1.00[ASN][1000 genomes]
rs58650381	1.00[ASN][1000 genomes]
rs58852267	0.91[EUR][1000 genomes]
rs61142266	1.00[ASN][1000 genomes]
rs61570828	0.94[ASN][1000 genomes]
rs7111218	1.00[ASN][1000 genomes]
rs7114156	1.00[ASN][1000 genomes]
rs7114460	1.00[ASN][1000 genomes]
rs7114477	1.00[ASN][1000 genomes]
rs7114977	1.00[ASN][1000 genomes]
rs7116588	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7123919	0.94[ASN][1000 genomes]
rs7124356	1.00[ASN][1000 genomes]
rs7125131	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7126521	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73402058	1.00[ASN][1000 genomes]
rs73402059	1.00[ASN][1000 genomes]
rs73402067	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73402068	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73402076	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73402080	0.89[ASN][1000 genomes]
rs73402082	1.00[ASN][1000 genomes]
rs7934876	1.00[ASN][1000 genomes]
rs7942481	1.00[ASN][1000 genomes]
rs7950148	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7950961	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1797209	chr11:8417452-8474015	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8424400-8430200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr11:8425800-8426200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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