Variant report

Variant	rs7322186
Chromosome Location	chr13:38903816-38903817
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:38903073..38904879-chr13:38922211..38923976,2	K562	blood:
2	chr13:38902336..38904691-chr13:38908487..38911212,2	K562	blood:

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1011484	1.00[CHB][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10507469	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10507470	1.00[CHB][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1590952	1.00[ASN][1000 genomes]
rs17057355	1.00[CHB][hapmap]
rs17057710	1.00[ASN][1000 genomes]
rs17057723	0.82[AFR][1000 genomes]
rs17057848	1.00[ASN][1000 genomes]
rs17057900	1.00[ASN][1000 genomes]
rs2019516	1.00[CHB][hapmap];0.82[YRI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2173948	1.00[ASN][1000 genomes]
rs2231320	1.00[ASN][1000 genomes]
rs2231335	1.00[ASN][1000 genomes]
rs2231336	1.00[ASN][1000 genomes]
rs2455408	1.00[ASN][1000 genomes]
rs2455413	1.00[ASN][1000 genomes]
rs2481887	1.00[ASN][1000 genomes]
rs2481888	1.00[ASN][1000 genomes]
rs2481892	1.00[ASN][1000 genomes]
rs2485779	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2496468	1.00[ASN][1000 genomes]
rs56306542	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73460211	0.82[AFR][1000 genomes]
rs73460212	0.82[AFR][1000 genomes]
rs73460215	0.82[AFR][1000 genomes]
rs73460283	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74047550	1.00[ASN][1000 genomes]
rs74047552	1.00[ASN][1000 genomes]
rs74047553	1.00[ASN][1000 genomes]
rs74047554	1.00[ASN][1000 genomes]
rs9532217	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9548328	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9888482	1.00[CHB][hapmap];0.82[YRI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv915901	chr13:38199035-39032633	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv869125	chr13:38550449-39132813	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv949406	chr13:38561474-39033484	Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv561512	chr13:38881318-38930893	Flanking Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv900005	chr13:38881318-38932949	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:38902800-38919600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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