Variant report

Variant	rs11173406
Chromosome Location	chr12:60724522-60724523
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:60722184..60725266-chr12:60727493..60729736,3	K562	blood:

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs1021886	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs10784049	1.00[CHB][hapmap];0.96[ASN][1000 genomes]
rs11173425	1.00[JPT][hapmap]
rs1119985	0.92[ASN][1000 genomes]
rs1119986	0.92[ASN][1000 genomes]
rs1119987	0.92[ASN][1000 genomes]
rs12299963	0.88[AFR][1000 genomes]
rs12303899	0.95[AFR][1000 genomes]
rs12312951	0.92[ASN][1000 genomes]
rs12313027	0.92[ASN][1000 genomes]
rs12322592	0.84[AFR][1000 genomes]
rs1466939	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1472738	0.92[ASN][1000 genomes]
rs1504445	0.92[ASN][1000 genomes]
rs1504447	0.92[ASN][1000 genomes]
rs1504448	0.92[ASN][1000 genomes]
rs1504461	0.96[ASN][1000 genomes]
rs1587823	0.92[ASN][1000 genomes]
rs1604863	0.81[ASN][1000 genomes]
rs1604864	0.92[ASN][1000 genomes]
rs17123761	0.92[ASN][1000 genomes]
rs17123775	0.92[ASN][1000 genomes]
rs1827639	0.92[ASN][1000 genomes]
rs1827640	0.92[ASN][1000 genomes]
rs1910676	0.92[ASN][1000 genomes]
rs1948852	0.98[AFR][1000 genomes]
rs1960370	0.92[ASN][1000 genomes]
rs1961693	0.92[ASN][1000 genomes]
rs1967225	0.92[ASN][1000 genomes]
rs1995517	1.00[ASN][1000 genomes]
rs2047909	0.92[ASN][1000 genomes]
rs2047910	0.92[ASN][1000 genomes]
rs2047911	0.92[ASN][1000 genomes]
rs2089152	0.92[ASN][1000 genomes]
rs2089153	0.92[ASN][1000 genomes]
rs2102256	0.92[ASN][1000 genomes]
rs2134884	0.92[ASN][1000 genomes]
rs2134885	0.92[ASN][1000 genomes]
rs2134886	0.92[ASN][1000 genomes]
rs2202363	0.92[ASN][1000 genomes]
rs2202364	0.92[ASN][1000 genomes]
rs2262938	0.92[ASN][1000 genomes]
rs2262940	0.92[ASN][1000 genomes]
rs2363586	0.81[ASN][1000 genomes]
rs2455997	0.92[ASN][1000 genomes]
rs2468380	0.92[ASN][1000 genomes]
rs2468381	0.92[ASN][1000 genomes]
rs2655850	0.92[ASN][1000 genomes]
rs2655854	0.88[ASN][1000 genomes]
rs2655855	0.92[ASN][1000 genomes]
rs2655862	0.92[ASN][1000 genomes]
rs2655864	0.92[ASN][1000 genomes]
rs2655865	0.92[ASN][1000 genomes]
rs2655866	0.92[ASN][1000 genomes]
rs2655867	0.92[ASN][1000 genomes]
rs2655869	0.92[ASN][1000 genomes]
rs2655870	0.92[ASN][1000 genomes]
rs2655872	0.92[ASN][1000 genomes]
rs2655874	0.92[ASN][1000 genomes]
rs2655876	0.92[ASN][1000 genomes]
rs2655881	0.92[ASN][1000 genomes]
rs2655882	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2655883	0.92[ASN][1000 genomes]
rs2731450	0.92[ASN][1000 genomes]
rs2731452	0.92[ASN][1000 genomes]
rs2731453	0.92[ASN][1000 genomes]
rs2731454	0.92[ASN][1000 genomes]
rs2731461	0.92[ASN][1000 genomes]
rs2731463	0.92[ASN][1000 genomes]
rs2731464	0.92[ASN][1000 genomes]
rs2731466	0.92[ASN][1000 genomes]
rs2731479	0.92[ASN][1000 genomes]
rs2731480	0.92[ASN][1000 genomes]
rs2731481	0.92[ASN][1000 genomes]
rs2731483	0.92[ASN][1000 genomes]
rs2731486	0.92[ASN][1000 genomes]
rs2731493	0.92[ASN][1000 genomes]
rs2938649	0.81[ASN][1000 genomes]
rs2956516	0.92[ASN][1000 genomes]
rs4500518	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4594036	0.92[ASN][1000 genomes]
rs56915133	0.92[ASN][1000 genomes]
rs61357417	0.84[AFR][1000 genomes]
rs6581317	0.92[ASN][1000 genomes]
rs7307145	0.96[ASN][1000 genomes]
rs7307414	0.92[ASN][1000 genomes]
rs7307798	0.92[ASN][1000 genomes]
rs73368995	0.80[AFR][1000 genomes]
rs73370703	0.86[AFR][1000 genomes]
rs73370791	0.98[AFR][1000 genomes]
rs7968422	1.00[ASN][1000 genomes]
rs7974290	1.00[ASN][1000 genomes]
rs905724	0.88[ASN][1000 genomes]
rs905725	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899137	chr12:60568891-60797083	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv1054287	chr12:60601870-60861866	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv832431	chr12:60626292-60809233	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1047466	chr12:60702221-61521156	Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv983465	chr12:60721408-60752940	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 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	chr12:60722600-60726800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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