Variant report

Variant	rs11714743
Chromosome Location	chr3:46549797-46549798
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10514713	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11130093	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11130094	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11719033	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12489007	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12489117	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12490169	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12496623	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12496864	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1402151	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2037391	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2280407	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28413725	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3934896	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60986461	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs883739	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[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	nsv1013306	chr3:46469014-46698538	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46537200-46550200	Enhancers	K562	blood
2	chr3:46541000-46557600	Weak transcription	Left Ventricle	heart
3	chr3:46541000-46580200	Weak transcription	Fetal Heart	heart
4	chr3:46541200-46562200	Weak transcription	Right Ventricle	heart
5	chr3:46544800-46556000	Weak transcription	Psoas Muscle	Psoas
6	chr3:46544800-46599400	Weak transcription	Right Atrium	heart
7	chr3:46545400-46551200	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr3:46545600-46558000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr3:46545600-46559200	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr3:46547400-46552600	Weak transcription	HSMMtube	muscle
11	chr3:46548200-46553000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr3:46549200-46585400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr3:46549400-46579000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr3:46549600-46578600	Weak transcription	H1 Cell Line	embryonic stem cell

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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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