Variant report

Variant	rs9639172
Chromosome Location	chr7:14062055-14062056
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	chr7:14059044..14062154-chr7:14062708..14065783,4	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10251025	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10254238	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10254973	0.81[CEU][hapmap]
rs10262618	0.84[AMR][1000 genomes]
rs10263141	0.83[AMR][1000 genomes]
rs10268435	0.81[CEU][hapmap]
rs10271792	0.81[CEU][hapmap]
rs10275495	0.83[EUR][1000 genomes]
rs11772292	0.83[AMR][1000 genomes]
rs11971058	0.90[JPT][hapmap]
rs11972032	0.88[AMR][1000 genomes]
rs11973792	1.00[CEU][hapmap];0.84[JPT][hapmap];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11977311	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13438227	1.00[CEU][hapmap];0.82[CHB][hapmap];0.84[JPT][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17167755	0.81[CEU][hapmap]
rs17167779	0.83[ASN][1000 genomes]
rs2190065	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2190066	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28633703	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3888604	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4027217	0.85[JPT][hapmap]
rs4308625	0.94[CEU][hapmap];0.85[AMR][1000 genomes]
rs4721297	0.94[JPT][hapmap]
rs58361379	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs58447577	0.95[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62452790	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6944510	0.86[ASN][1000 genomes]
rs6954954	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6969768	1.00[CEU][hapmap];0.81[CHB][hapmap];0.89[JPT][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6970150	1.00[CEU][hapmap];0.81[CHB][hapmap];0.89[JPT][hapmap];0.89[YRI][hapmap];0.97[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7785120	0.94[CEU][hapmap]
rs7788676	0.80[EUR][1000 genomes]
rs917136	0.94[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019873	chr7:13707148-14133367	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv949467	chr7:13938464-14279074	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1030645	chr7:14015533-14078153	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv538739	chr7:14015533-14078153	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14050200-14070800	Weak transcription	K562	blood
2	chr7:14061200-14062400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr7:14061200-14062800	Weak transcription	Osteobl	bone

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