Variant report

Variant	rs12793350
Chromosome Location	chr11:46223281-46223282
allele	C/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:17)

rs_ID	r²[population]
rs10838573	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10838578	0.88[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs10838579	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11038803	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11038811	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11038812	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11038814	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11038815	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11038816	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12221745	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs17725617	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4755349	0.93[ASN][1000 genomes]
rs4756060	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4756065	0.82[AFR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4756066	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs71474108	1.00[ASN][1000 genomes]
rs870498	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051344	chr11:46188818-46306447	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
2	nsv541028	chr11:46188818-46306447	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46222800-46224000	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr11:46223000-46224000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr11:46223000-46231400	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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