Variant report

Variant	rs7042262
Chromosome Location	chr9:21567651-21567652
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10757226	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13283078	1.00[ASN][1000 genomes]
rs1377192	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1377193	0.86[ASN][1000 genomes]
rs1452653	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1452654	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1551919	0.95[ASN][1000 genomes]
rs1562996	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1869207	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4141713	0.83[ASN][1000 genomes]
rs4978124	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6475539	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7046179	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7046475	1.00[ASN][1000 genomes]
rs71504796	1.00[ASN][1000 genomes]
rs9298816	1.00[CHB][hapmap];1.00[JPT][hapmap]

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	nsv1031432	chr9:21472601-21608774	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	122 gene(s)	inside rSNPs	diseases
2	nsv540085	chr9:21472601-21608774	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	122 gene(s)	inside rSNPs	diseases
3	nsv1029634	chr9:21542970-21765286	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7042262	IFNW1	cis	parietal	SCAN

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21564600-21570400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr9:21564800-21568000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr9:21565200-21568600	Flanking Active TSS	A549	lung
4	chr9:21565600-21576000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr9:21565800-21567800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr9:21565800-21568200	Enhancers	NHEK	skin
7	chr9:21565800-21570400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:21565800-21570400	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr9:21566400-21570200	Weak transcription	Hela-S3	cervix
10	chr9:21566400-21570200	Weak transcription	HMEC	breast
11	chr9:21566600-21570600	Weak transcription	NH-A	brain
12	chr9:21567200-21570400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr9:21567200-21570400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr9:21567400-21568000	Enhancers	NHDF-Ad	bronchial
15	chr9:21567400-21570400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr9:21567600-21567800	Enhancers	HUES64 Cell Line	embryonic stem cell

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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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