Variant report

Variant	rs4735346
Chromosome Location	chr8:96118840-96118841
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10808672	0.82[EUR][1000 genomes]
rs11781181	0.81[EUR][1000 genomes]
rs1561714	0.81[EUR][1000 genomes]
rs1561715	0.81[EUR][1000 genomes]
rs1975425	0.81[EUR][1000 genomes]
rs2044034	0.81[EUR][1000 genomes]
rs2583365	0.81[EUR][1000 genomes]
rs2599726	0.81[EUR][1000 genomes]
rs4392868	0.81[EUR][1000 genomes]
rs4735345	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4735347	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4735350	0.81[EUR][1000 genomes]
rs6983365	0.81[EUR][1000 genomes]
rs7000734	0.81[EUR][1000 genomes]
rs7002233	0.81[EUR][1000 genomes]
rs7822998	0.81[EUR][1000 genomes]
rs7845016	0.81[EUR][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	nsv1017301	chr8:95273503-96248352	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv539680	chr8:95273503-96248352	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv508520	chr8:95939373-96140068	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
4	nsv891207	chr8:96106037-96160914	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96113800-96122400	Weak transcription	Gastric	stomach
2	chr8:96113800-96122400	Weak transcription	Pancreas	Pancrea
3	chr8:96113800-96127800	Weak transcription	Right Ventricle	heart
4	chr8:96115600-96122400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:96115600-96122600	Weak transcription	Osteobl	bone
6	chr8:96115800-96123200	Weak transcription	K562	blood
7	chr8:96116200-96121800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr8:96117600-96122400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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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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