Variant report

Variant	rs324624
Chromosome Location	chr7:136669236-136669237
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs324576	1.00[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap]
rs324577	0.92[CHB][hapmap];0.93[JPT][hapmap]
rs324578	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs324579	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs324580	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs324581	0.87[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs324582	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs324584	1.00[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap];0.82[AMR][1000 genomes]
rs324586	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs324587	1.00[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap]
rs324588	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs324589	0.88[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs324591	0.89[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs324592	0.89[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs324593	0.88[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs324595	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs324596	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs324611	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs324612	1.00[CEU][hapmap];0.85[CHB][hapmap];0.93[JPT][hapmap]
rs324615	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs324616	0.80[ASN][1000 genomes]
rs324617	0.92[AFR][1000 genomes]
rs324619	0.87[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs324620	0.91[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs324622	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs324623	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs324625	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs324627	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs324631	1.00[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs324632	1.00[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029192	chr7:136433278-137147566	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv831147	chr7:136583444-136755741	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	esv2753059	chr7:136633745-136893745	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv528311	chr7:136650607-136680801	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136661800-136677200	Weak transcription	Fetal Heart	heart
2	chr7:136662400-136678000	Weak transcription	Colon Smooth Muscle	Colon
3	chr7:136666400-136685400	Weak transcription	Stomach Smooth Muscle	stomach
4	chr7:136669200-136669400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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