Variant report

Variant	rs4749325
Chromosome Location	chr10:5866171-5866172
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	chr10:5864529..5867284-chr10:5869249..5871114,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10508297	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11257371	1.00[AFR][1000 genomes]
rs11592184	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11592260	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11592964	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11593253	1.00[EUR][1000 genomes]
rs11594153	1.00[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs11595445	0.80[ASN][1000 genomes]
rs11595457	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11595970	1.00[EUR][1000 genomes]
rs11596603	1.00[EUR][1000 genomes]
rs11597597	1.00[EUR][1000 genomes]
rs11597948	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11598319	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2137422	1.00[AFR][1000 genomes]
rs2296136	1.00[AFR][1000 genomes]
rs34249852	1.00[AFR][1000 genomes]
rs3750656	1.00[AFR][1000 genomes]
rs41306916	1.00[AFR][1000 genomes]
rs4749407	1.00[AFR][1000 genomes]
rs55718140	1.00[AFR][1000 genomes]
rs56213022	1.00[AFR][1000 genomes]
rs56296494	1.00[AFR][1000 genomes]
rs56354230	1.00[AFR][1000 genomes]
rs57034347	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs57075354	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs58782668	0.80[ASN][1000 genomes]
rs59511159	1.00[EUR][1000 genomes]
rs60255716	1.00[EUR][1000 genomes]
rs61658636	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7904512	1.00[AFR][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	esv34147	chr10:5726821-6105717	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	esv34061	chr10:5726821-6225187	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv1042286	chr10:5795129-6578445	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	nsv831775	chr10:5804335-6000849	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv515935	chr10:5820394-5869839	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv549896	chr10:5820394-5880066	Strong transcription Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5857000-5866800	Weak transcription	NHLF	lung
2	chr10:5857400-5871400	Weak transcription	Pancreas	Pancrea

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