Variant report

Variant	rs13115289
Chromosome Location	chr4:127692711-127692712
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10518505	0.88[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs10518506	0.88[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs10518507	0.88[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs11722194	0.82[ASN][1000 genomes]
rs11724202	0.85[AFR][1000 genomes]
rs11730606	0.82[ASN][1000 genomes]
rs13101665	0.82[ASN][1000 genomes]
rs13104073	0.88[AFR][1000 genomes];0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs13111812	0.82[ASN][1000 genomes]
rs13112009	0.88[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs13120233	0.80[ASN][1000 genomes]
rs13120674	0.80[ASN][1000 genomes]
rs13121471	0.82[ASN][1000 genomes]
rs13123489	0.82[ASN][1000 genomes]
rs13129376	0.82[ASN][1000 genomes]
rs13134285	0.85[AFR][1000 genomes]
rs13138589	0.82[ASN][1000 genomes]
rs13147181	0.80[ASN][1000 genomes]
rs13147327	0.82[ASN][1000 genomes]
rs13147530	0.82[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs13150274	0.80[ASN][1000 genomes]
rs1388240	0.82[ASN][1000 genomes]
rs1503628	0.82[ASN][1000 genomes]
rs1604723	0.82[ASN][1000 genomes]
rs17011512	0.82[ASN][1000 genomes]
rs17011514	0.82[ASN][1000 genomes]
rs17011515	0.82[ASN][1000 genomes]
rs1955280	0.88[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs2391093	0.88[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs2391101	0.82[ASN][1000 genomes]
rs34078351	0.81[ASN][1000 genomes]
rs4295276	0.82[ASN][1000 genomes]
rs4413416	0.82[ASN][1000 genomes]
rs4833353	0.82[ASN][1000 genomes]
rs4833354	0.82[ASN][1000 genomes]
rs6811594	0.82[ASN][1000 genomes]
rs6839577	0.88[AFR][1000 genomes];0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7688921	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012833	chr4:127468474-127760933	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv537242	chr4:127468474-127760933	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv524850	chr4:127470903-127768849	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1007477	chr4:127561735-127726291	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv537244	chr4:127561735-127726291	Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv879907	chr4:127646765-127709859	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
7	nsv879908	chr4:127646765-127749390	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
8	nsv879909	chr4:127646765-127792639	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv879910	chr4:127646765-127805466	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv879911	chr4:127646765-127835677	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127683800-127698000	Weak transcription	HMEC	breast
2	chr4:127685200-127698000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:127685600-127693800	Weak transcription	K562	blood
4	chr4:127688400-127693200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr4:127691800-127698000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr4:127692400-127692800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin

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