Variant report

Variant	rs324616
Chromosome Location	chr7:136664887-136664888
allele	C/T
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	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs324577	0.83[ASN][1000 genomes]
rs324578	0.86[ASN][1000 genomes]
rs324579	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs324580	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs324581	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs324582	0.86[ASN][1000 genomes]
rs324585	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs324586	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs324587	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs324588	0.85[ASN][1000 genomes]
rs324589	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs324590	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs324591	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs324592	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs324593	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs324595	0.86[ASN][1000 genomes]
rs324596	0.86[ASN][1000 genomes]
rs324611	0.86[ASN][1000 genomes]
rs324613	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs324615	0.81[ASN][1000 genomes]
rs324617	0.88[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs324618	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs324619	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs324620	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs324624	0.80[ASN][1000 genomes]
rs324625	0.86[ASN][1000 genomes]
rs324627	0.86[ASN][1000 genomes]
rs324630	0.83[ASN][1000 genomes]
rs324632	0.83[ASN][1000 genomes]

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:2 , 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

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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