Variant report

Variant	rs6902043
Chromosome Location	chr6:121006137-121006138
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10457397	0.94[EUR][1000 genomes]
rs11153944	0.94[EUR][1000 genomes]
rs11153956	0.87[EUR][1000 genomes]
rs11153957	0.86[EUR][1000 genomes]
rs12193834	0.87[EUR][1000 genomes]
rs12193885	0.87[EUR][1000 genomes]
rs12196688	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12213687	0.87[EUR][1000 genomes]
rs1339017	0.87[EUR][1000 genomes]
rs1933820	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2358048	0.89[ASN][1000 genomes]
rs6901407	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6933679	0.91[ASN][1000 genomes]
rs6935352	0.87[EUR][1000 genomes]
rs6935477	0.87[EUR][1000 genomes]
rs7741833	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7757463	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9401327	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757191	chr6:120967277-121029949	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv2759466	chr6:120967277-121029949	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv886586	chr6:120968061-121020821	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv886587	chr6:120978943-121006814	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
5	nsv886588	chr6:120978943-121016929	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
6	nsv886589	chr6:120978943-121020821	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
7	esv2754699	chr6:120983610-121029949	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv464036	chr6:120983748-121008679	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
9	nsv604570	chr6:120983748-121008679	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:0 , 50 per page) page:

No data

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Input of quick search could be:

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

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