Variant report

Variant	rs1155655
Chromosome Location	chr7:126566028-126566029
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	7:126085913-126088095..7:126563918-126569249	K562	blood:

Variant related genes	Relation type
ENSG00000179603	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1003037	1.00[CHB][hapmap]
rs10229548	1.00[CHB][hapmap]
rs10239010	1.00[CHB][hapmap]
rs10243157	1.00[CHB][hapmap]
rs10246394	1.00[CHB][hapmap]
rs10252394	1.00[CHB][hapmap]
rs10267279	1.00[CHB][hapmap]
rs10267858	1.00[CHB][hapmap]
rs1154326	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1154333	1.00[CHB][hapmap]
rs1155657	1.00[CHB][hapmap];0.85[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11767521	0.82[YRI][hapmap]
rs1204553	1.00[CHB][hapmap]
rs1204554	1.00[CHB][hapmap]
rs1204555	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1204556	1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1204558	1.00[CHB][hapmap]
rs1204559	1.00[CHB][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1204560	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1204561	1.00[CHB][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1204562	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1204565	1.00[CHB][hapmap]
rs1204566	1.00[CHB][hapmap]
rs1204568	1.00[CHB][hapmap]
rs1204570	1.00[CHB][hapmap]
rs1204572	1.00[CHB][hapmap]
rs1204574	1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1204582	1.00[CHB][hapmap]
rs1204585	1.00[CHB][hapmap]
rs1204589	1.00[CHB][hapmap]
rs1204595	1.00[CHB][hapmap]
rs1361970	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1419455	0.88[EUR][1000 genomes]
rs1419456	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1419457	1.00[CHB][hapmap];0.85[YRI][hapmap];0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1419463	1.00[CHB][hapmap];0.85[YRI][hapmap]
rs1419466	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1419509	1.00[CHB][hapmap]
rs17864092	1.00[CHB][hapmap]
rs2021162	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2109740	1.00[CHB][hapmap]
rs2254259	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2254260	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2518946	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2518948	1.00[CHB][hapmap];0.85[YRI][hapmap]
rs2518952	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2518956	1.00[CHB][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2518959	1.00[CHB][hapmap]
rs2535928	1.00[CHB][hapmap]
rs2535937	1.00[CHB][hapmap];0.82[YRI][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2896388	1.00[CHB][hapmap]
rs67993661	0.82[AFR][1000 genomes]
rs6946530	1.00[CHB][hapmap]
rs916614	1.00[CHB][hapmap]
rs971789	1.00[CHB][hapmap]
rs974441	1.00[CHB][hapmap]
rs994783	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529300	chr7:125669493-126587858	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1032938	chr7:126067684-126587859	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv539119	chr7:126067684-126587859	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv608376	chr7:126457779-126571077	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv2758132	chr7:126494789-126677843	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv2759562	chr7:126494789-126677843	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv427805	chr7:126494789-126677843	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv5940	chr7:126535731-126580660	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
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