Variant report

Variant	rs5943047
Chromosome Location	chrX:109927567-109927568
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10047014	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs10126502	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs12012172	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs12395955	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs12396834	0.90[CEU][hapmap];1.00[CHB][hapmap]
rs12857107	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs191800	1.00[CHB][hapmap]
rs197023	1.00[CHB][hapmap]
rs197036	1.00[CHB][hapmap]
rs2016878	0.90[CEU][hapmap];1.00[CHB][hapmap]
rs2206971	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs2223782	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs2404177	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs5942660	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs5942661	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs5942674	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs5942675	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs5942676	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs5942677	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs5942678	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs5942680	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs5942681	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs5942953	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5942955	0.90[CEU][hapmap];1.00[CHB][hapmap]
rs5943019	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs5943044	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs5943045	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs5943046	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs5943048	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs5943050	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs5943051	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs5943052	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs5943053	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs5943055	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs5943056	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[YRI][hapmap]
rs5943057	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs5985302	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs5985519	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs5985544	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs5985545	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[YRI][hapmap]
rs5985546	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs7060124	0.95[CEU][hapmap];1.00[CHB][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817233	chrX:109693720-110244649	Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:109910800-109936600	Weak transcription	Primary hematopoietic stem cells	blood
2	chrX:109919400-109938200	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chrX:109919400-109948800	Weak transcription	Adipose Nuclei	Adipose
4	chrX:109922200-109927800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chrX:109925400-109931200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chrX:109926000-109928200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chrX:109926200-109928200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chrX:109926400-109928000	Enhancers	H9 Cell Line	embryonic stem cell
9	chrX:109926600-109928000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
10	chrX:109926800-109928200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chrX:109927000-109927800	Enhancers	H1 Cell Line	embryonic stem cell
12	chrX:109927400-109927600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
13	chrX:109927400-109927800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chrX:109927400-109927800	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chrX:109927400-109928000	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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