Variant report

Variant	rs10130216
Chromosome Location	chr14:79899861-79899862
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10483921	0.91[ASN][1000 genomes]
rs12888258	0.89[ASN][1000 genomes]
rs12891144	0.83[ASN][1000 genomes]
rs12894675	0.93[ASN][1000 genomes]
rs1865719	0.86[EUR][1000 genomes]
rs2011312	0.86[EUR][1000 genomes]
rs2370983	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35086482	0.90[ASN][1000 genomes]
rs4243664	0.93[ASN][1000 genomes]
rs4640109	0.82[ASN][1000 genomes]
rs4899746	0.83[EUR][1000 genomes]
rs4903860	0.93[ASN][1000 genomes]
rs56034924	0.87[ASN][1000 genomes]
rs56209900	0.90[ASN][1000 genomes]
rs61995162	0.86[ASN][1000 genomes]
rs6574507	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7140201	0.90[ASN][1000 genomes]
rs7159565	0.90[EUR][1000 genomes]
rs8003893	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931412	chr14:79420297-79928269	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv902110	chr14:79624492-79998294	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv530072	chr14:79769657-79928269	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1045241	chr14:79885361-80734201	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79884200-79901800	Weak transcription	Stomach Smooth Muscle	stomach

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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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