Variant report

Variant	rs10030057
Chromosome Location	chr4:119093532-119093533
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10002349	1.00[AMR][1000 genomes]
rs10003652	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10005659	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10007553	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10018706	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10024548	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10025029	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10025515	1.00[AMR][1000 genomes]
rs10028823	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10031402	1.00[AMR][1000 genomes]
rs11931409	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11946772	1.00[AFR][1000 genomes]
rs13434557	1.00[AMR][1000 genomes]
rs28421577	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28451256	1.00[AMR][1000 genomes]
rs28484271	1.00[AMR][1000 genomes]
rs28558085	1.00[AMR][1000 genomes]
rs28567841	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28576396	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28582030	1.00[AMR][1000 genomes]
rs28585079	1.00[AMR][1000 genomes]
rs28610040	1.00[AMR][1000 genomes]
rs28619162	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28634343	1.00[AMR][1000 genomes]
rs28665169	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28667620	1.00[AMR][1000 genomes]
rs28669076	1.00[AMR][1000 genomes]
rs28682376	1.00[AMR][1000 genomes]
rs28706008	1.00[AMR][1000 genomes]
rs28715892	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28735538	1.00[AMR][1000 genomes]
rs28740899	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28771156	1.00[AMR][1000 genomes]
rs28776305	1.00[AMR][1000 genomes]
rs28823876	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28847597	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28886020	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57461354	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9307456	1.00[AMR][1000 genomes]
rs9994181	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519017	chr4:118828807-119771481	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv1009076	chr4:118949490-119269424	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1001236	chr4:118949490-119271243	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv1008236	chr4:118989467-119154024	ZNF genes & repeats Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv999152	chr4:119001143-119138322	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	esv34038	chr4:119035124-119455391	Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119092400-119094400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr4:119092800-119094000	Weak transcription	NHLF	lung
3	chr4:119092800-119095200	Weak transcription	Thymus	Thymus
4	chr4:119093000-119094400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr4:119093000-119094400	Weak transcription	Fetal Thymus	thymus
6	chr4:119093000-119096000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:119093400-119093800	Weak transcription	Primary T cells from cord blood	blood
8	chr4:119093400-119094400	Enhancers	Dnd41	blood
9	chr4:119093400-119095200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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