Variant report

Variant	rs6676768
Chromosome Location	chr1:10081782-10081783
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11801988	0.84[EUR][1000 genomes]
rs11803995	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11808311	0.84[EUR][1000 genomes]
rs28671063	0.84[EUR][1000 genomes]
rs41280788	0.84[EUR][1000 genomes]
rs56682893	0.84[EUR][1000 genomes]
rs56760324	0.84[EUR][1000 genomes]
rs57216908	0.84[EUR][1000 genomes]
rs61134758	0.89[EUR][1000 genomes]
rs61462323	0.84[EUR][1000 genomes]
rs6693686	0.84[EUR][1000 genomes]
rs6701103	0.84[EUR][1000 genomes]
rs72859590	0.84[EUR][1000 genomes]
rs72861431	0.84[EUR][1000 genomes]
rs72861447	0.84[EUR][1000 genomes]
rs72861453	0.84[EUR][1000 genomes]
rs9661116	0.84[EUR][1000 genomes]
rs9661131	0.85[AFR][1000 genomes];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3385337	chr1:9105242-10082223	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	549 gene(s)	inside rSNPs	diseases
2	esv3417409	chr1:9683992-10241703	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv1012469	chr1:9925714-10147796	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv1012301	chr1:9963962-10118393	Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	nsv534853	chr1:9963962-10118393	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
6	nsv1001742	chr1:9971776-10116767	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10074600-10092400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr1:10076400-10081800	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr1:10076400-10082200	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr1:10080400-10092400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:10080600-10082000	Weak transcription	NHDF-Ad	bronchial
6	chr1:10081000-10081800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr1:10081600-10083600	Enhancers	Primary monocytes fromperipheralblood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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