Variant report

Variant	rs344307
Chromosome Location	chr8:62881553-62881554
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10111776	0.80[EUR][1000 genomes]
rs1400499	0.82[EUR][1000 genomes]
rs1607124	0.82[EUR][1000 genomes]
rs1607126	0.84[EUR][1000 genomes]
rs168252	0.87[EUR][1000 genomes]
rs180751	0.95[EUR][1000 genomes]
rs1850369	0.80[EUR][1000 genomes]
rs1966106	0.82[EUR][1000 genomes]
rs237413	0.93[EUR][1000 genomes]
rs28377818	0.98[EUR][1000 genomes]
rs28379606	0.98[EUR][1000 genomes]
rs28400370	0.98[EUR][1000 genomes]
rs28558888	0.98[EUR][1000 genomes]
rs344200	0.89[EUR][1000 genomes]
rs344203	0.89[EUR][1000 genomes]
rs344204	0.91[EUR][1000 genomes]
rs344206	0.81[EUR][1000 genomes]
rs344207	0.89[EUR][1000 genomes]
rs344209	0.89[EUR][1000 genomes]
rs344210	0.89[EUR][1000 genomes]
rs344219	0.93[EUR][1000 genomes]
rs344220	0.93[EUR][1000 genomes]
rs344230	0.93[EUR][1000 genomes]
rs344231	0.93[EUR][1000 genomes]
rs344232	0.93[EUR][1000 genomes]
rs344233	0.93[EUR][1000 genomes]
rs344234	0.93[EUR][1000 genomes]
rs344236	0.93[EUR][1000 genomes]
rs344238	0.93[EUR][1000 genomes]
rs344240	0.93[EUR][1000 genomes]
rs344241	0.93[EUR][1000 genomes]
rs344242	0.93[EUR][1000 genomes]
rs344248	0.91[EUR][1000 genomes]
rs344251	0.89[EUR][1000 genomes]
rs344252	0.87[EUR][1000 genomes]
rs344254	0.89[EUR][1000 genomes]
rs344270	0.89[EUR][1000 genomes]
rs344272	0.87[EUR][1000 genomes]
rs344273	0.89[EUR][1000 genomes]
rs344274	0.89[EUR][1000 genomes]
rs344281	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs344310	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35594910	0.80[EUR][1000 genomes]
rs58080416	0.82[EUR][1000 genomes]
rs58710029	0.82[EUR][1000 genomes]
rs60520860	0.82[EUR][1000 genomes]
rs62135	0.89[EUR][1000 genomes]
rs6471975	0.82[EUR][1000 genomes]
rs679344	0.89[EUR][1000 genomes]
rs681078	0.89[EUR][1000 genomes]
rs73255128	0.80[EUR][1000 genomes]
rs73255147	0.82[EUR][1000 genomes]
rs73255155	0.82[EUR][1000 genomes]
rs73255157	0.82[EUR][1000 genomes]
rs73255189	0.98[EUR][1000 genomes]
rs73682603	0.82[EUR][1000 genomes]
rs73685158	0.82[EUR][1000 genomes]
rs73685159	0.82[EUR][1000 genomes]
rs7821502	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024432	chr8:62086247-62898782	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv932198	chr8:62336705-62914562	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv831338	chr8:62736394-62913048	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr8:62881200-62881600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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