Variant report

Variant	rs321094
Chromosome Location	chrX:77565956-77565957
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10991	0.81[CHB][hapmap];0.94[JPT][hapmap]
rs167674	0.86[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap]
rs2073176	0.86[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap]
rs2073178	0.86[CHB][hapmap];0.94[JPT][hapmap]
rs2643581	0.86[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap]
rs320988	0.86[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap]
rs320990	0.93[CEU][hapmap];0.86[CHB][hapmap];0.87[JPT][hapmap]
rs320992	0.86[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap]
rs320995	0.86[CEU][hapmap];0.86[CHB][hapmap]
rs320996	0.86[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap]
rs320999	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs321005	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs321028	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs321029	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs321073	0.86[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap]
rs321074	0.86[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap]
rs321085	0.80[CEU][hapmap];0.87[CHB][hapmap];0.94[JPT][hapmap]
rs321086	0.80[CEU][hapmap];0.87[CHB][hapmap];0.94[JPT][hapmap]
rs321088	0.86[CEU][hapmap];0.94[JPT][hapmap]
rs321090	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs321091	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs321095	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs379704	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs428207	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4826248	0.86[CHB][hapmap];0.94[JPT][hapmap]

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	nsv529299	chrX:77040316-77947157	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv532880	chrX:77085352-77769755	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	nsv492122	chrX:77450503-77664330	Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 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	chrX:77558600-77576600	Weak transcription	Primary B cells from cord blood	blood
2	chrX:77558800-77566600	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chrX:77558800-77570000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chrX:77559800-77576400	Weak transcription	Primary hematopoietic stem cells	blood
5	chrX:77565600-77567000	Enhancers	Primary B cells from peripheral blood	blood
6	chrX:77565800-77566200	Enhancers	Primary T helper cells PMA-I stimulated	--

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