Variant report

Variant	rs13115151
Chromosome Location	chr4:129658732-129658733
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:16)

rs_ID	r²[population]
rs10002938	0.94[EUR][1000 genomes]
rs10006675	0.89[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12506981	0.89[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12509201	0.89[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs13128507	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1364968	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1425619	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1991237	0.96[ASN][1000 genomes]
rs2391327	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs28453786	0.90[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4282195	0.92[EUR][1000 genomes]
rs4450950	0.88[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4975246	0.87[ASN][1000 genomes]
rs57872653	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6811857	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7692380	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869258	chr4:129191619-130138148	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
2	nsv1020801	chr4:129658178-129778086	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
3	nsv537248	chr4:129658178-129778086	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:129633000-129689600	Weak transcription	Right Atrium	heart
2	chr4:129658000-129659000	Enhancers	Fetal Heart	heart
3	chr4:129658200-129658800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr4:129658200-129658800	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr4:129658200-129658800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr4:129658200-129658800	Enhancers	K562	blood
7	chr4:129658400-129658800	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr4:129658400-129658800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr4:129658400-129658800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:129658400-129658800	Enhancers	Left Ventricle	heart
11	chr4:129658600-129659800	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr4:129658600-129660000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr4:129658600-129663200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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