Variant report

Variant	rs5972128
Chromosome Location	chrX:29467739-29467740
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs1014721	0.80[CEU][hapmap]
rs1014723	0.81[CHB][hapmap]
rs1014724	0.81[CHB][hapmap]
rs12559505	0.91[CHB][hapmap];0.84[MEX][hapmap]
rs12832809	0.85[CEU][hapmap];0.91[CHB][hapmap];0.84[CHD][hapmap];0.92[JPT][hapmap];0.80[TSI][hapmap]
rs16988538	0.81[YRI][hapmap]
rs16988539	0.81[YRI][hapmap]
rs1883446	0.91[CHB][hapmap]
rs1983591	0.81[CHB][hapmap]
rs2050063	0.80[CEU][hapmap]
rs2206335	0.91[CHB][hapmap]
rs2206336	0.91[CHB][hapmap]
rs2340372	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs2879753	0.91[CHB][hapmap]
rs4829167	0.85[CEU][hapmap];0.91[CHB][hapmap];0.92[JPT][hapmap]
rs4829188	0.80[CEU][hapmap]
rs4829190	0.80[CEU][hapmap]
rs4829197	0.85[JPT][hapmap]
rs4829401	0.81[CHB][hapmap]
rs5927469	0.81[CHB][hapmap]
rs5927483	0.91[CHB][hapmap]
rs5928926	0.81[CHB][hapmap]
rs5971494	0.80[CEU][hapmap];0.85[JPT][hapmap]
rs5971497	0.80[CEU][hapmap]
rs5971499	0.80[CEU][hapmap]
rs5971500	0.80[CEU][hapmap]
rs5971517	0.85[CEU][hapmap]
rs5972037	0.91[CHB][hapmap]
rs5972082	0.91[CHB][hapmap]
rs5972100	0.85[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs5972125	0.85[CEU][hapmap];0.91[CHB][hapmap];0.80[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap]
rs5972176	0.80[CEU][hapmap]
rs5972233	0.85[CEU][hapmap]
rs5972234	0.84[CEU][hapmap]
rs5972238	0.85[CEU][hapmap]
rs5972241	0.84[CEU][hapmap]
rs5973678	0.91[CHB][hapmap]
rs5973811	0.85[CEU][hapmap]
rs6526854	0.91[CHB][hapmap];0.92[JPT][hapmap]
rs6526862	0.85[JPT][hapmap]
rs6526871	0.84[CEU][hapmap]
rs6628425	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap]
rs6628428	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.97[TSI][hapmap]
rs6628429	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap]
rs6630859	0.85[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs6630860	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap]
rs6630862	0.85[CEU][hapmap];0.91[CHB][hapmap];0.92[JPT][hapmap]
rs7063024	0.89[CEU][hapmap]
rs7065566	0.85[JPT][hapmap]
rs7065783	0.85[JPT][hapmap]
rs715328	0.80[CEU][hapmap];0.85[JPT][hapmap]

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	nsv432292	chrX:29109744-29845461	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
2	nsv531754	chrX:29147023-29533186	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv531766	chrX:29225499-29928832	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
4	nsv948944	chrX:29398264-29902917	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
5	nsv869450	chrX:29433295-29940875	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region lncRNA miRNA	2 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:29464200-29468400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chrX:29467200-29468000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chrX:29467200-29468000	Enhancers	Fetal Heart	heart
4	chrX:29467400-29468400	Enhancers	GM12878-XiMat	blood
5	chrX:29467600-29468000	Enhancers	Fetal Brain Male	brain
6	chrX:29467600-29468600	Enhancers	HUVEC	blood vessel

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