Variant report

Variant	rs71634907
Chromosome Location	chr1:161690593-161690594
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs35287180	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7520519	1.00[AFR][1000 genomes]
rs905591	1.00[AFR][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	nsv428257	chr1:161406315-161868263	Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	esv33393	chr1:161478681-162080327	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
3	nsv464184	chr1:161646807-161885352	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	nsv548075	chr1:161646807-161885352	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:161676200-161692000	Weak transcription	Spleen	Spleen
2	chr1:161688800-161690600	Enhancers	Primary B cells from peripheral blood	blood
3	chr1:161688800-161691400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:161689000-161690800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr1:161689000-161692400	Enhancers	Primary B cells from cord blood	blood
6	chr1:161689000-161692600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
7	chr1:161689000-161695400	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr1:161689000-161695600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr1:161689400-161691400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
10	chr1:161689400-161692600	Enhancers	GM12878-XiMat	blood
11	chr1:161689400-161692800	Enhancers	NHDF-Ad	bronchial
12	chr1:161689600-161691400	Enhancers	K562	blood
13	chr1:161689600-161691600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr1:161689800-161692600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:161690200-161690600	Bivalent Enhancer	Fetal Heart	heart

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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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