Variant report

Variant	rs11563730
Chromosome Location	chr7:126717157-126717158
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	chr7:126714682..126717546-chr7:126724506..126726256,2	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10464688	0.82[CHB][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10954142	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1111183	0.88[CHB][hapmap];0.87[CHD][hapmap];0.85[JPT][hapmap];0.82[TSI][hapmap]
rs11563304	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11563358	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11563361	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11563500	1.00[CEU][hapmap]
rs11563510	1.00[CEU][hapmap]
rs11563742	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11563744	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11563745	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11563776	1.00[CEU][hapmap]
rs11563791	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11563792	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1156652	0.85[TSI][hapmap]
rs1156653	0.85[TSI][hapmap]
rs1156654	0.85[TSI][hapmap]
rs11765785	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11771611	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11971261	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12706758	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12706759	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.95[TSI][hapmap]
rs12706761	0.88[CHB][hapmap];0.85[JPT][hapmap];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13234354	0.83[GIH][hapmap]
rs13239456	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13239559	0.83[GIH][hapmap]
rs1419442	0.88[CHB][hapmap];0.87[CHD][hapmap];0.83[GIH][hapmap];0.85[JPT][hapmap];0.82[TSI][hapmap]
rs1419447	0.85[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap]
rs1468096	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs1468097	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1557644	0.88[CHB][hapmap];0.87[CHD][hapmap];0.83[GIH][hapmap];0.85[JPT][hapmap];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1557645	0.88[CHB][hapmap];0.85[JPT][hapmap];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17862281	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17863206	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2023640	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.90[TSI][hapmap]
rs2188187	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.95[TSI][hapmap];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2299524	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap]
rs2299531	0.86[CHB][hapmap];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2299532	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2299536	0.83[GIH][hapmap]
rs4728062	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4728063	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4728065	0.88[CHB][hapmap];0.85[JPT][hapmap];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs882894	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs916608	0.88[CHB][hapmap];0.82[JPT][hapmap]
rs916610	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs916611	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs916612	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs953016	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][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	nsv831121	chr7:126593363-126774413	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv889189	chr7:126699088-126963028	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv2761367	chr7:126717157-126865324	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 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
chromosomal regions: chr1:12345-34567

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