Variant report

Variant	rs4140441
Chromosome Location	chr6:144218979-144218980
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs12527718	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12527740	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs35274932	1.00[ASN][1000 genomes]
rs4895623	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4896684	1.00[JPT][hapmap]
rs4896685	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4896686	0.82[CHB][hapmap];0.96[ASN][1000 genomes]
rs6570586	1.00[JPT][hapmap]
rs761540	0.96[ASN][1000 genomes]
rs761541	0.82[CHB][hapmap];0.96[ASN][1000 genomes]
rs764667	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7742707	0.82[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7755147	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9484827	1.00[JPT][hapmap]
rs9496799	1.00[CHB][hapmap]

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	esv3408554	chr6:144106707-144369589	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	esv3522138	chr6:144174685-144367463	Enhancers Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	esv3522139	chr6:144174685-144367463	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv830830	chr6:144177942-144380870	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144186000-144223000	Weak transcription	Primary B cells from peripheral blood	blood
2	chr6:144204800-144220800	Weak transcription	Primary B cells from cord blood	blood
3	chr6:144205800-144222600	Weak transcription	Fetal Stomach	stomach
4	chr6:144207200-144222800	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr6:144217400-144219800	Weak transcription	Fetal Muscle Trunk	muscle
6	chr6:144217600-144222000	Weak transcription	Fetal Lung	lung
7	chr6:144217800-144222800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr6:144218200-144222200	Weak transcription	Fetal Muscle Leg	muscle
9	chr6:144218400-144222800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr6:144218400-144224000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr6:144218800-144221800	Weak transcription	GM12878-XiMat	blood
12	chr6:144218800-144222800	Weak transcription	Placenta	Placenta

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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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