Variant report

Variant	rs1156954
Chromosome Location	chr7:117594838-117594839
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	7:116434729-116454408..7:117586475-117595620	Hela-S3	cervix:
2	7:116754962-116765597..7:117586475-117595620	Hela-S3	cervix:

Variant related genes	Relation type
ENSG00000198898	Chromatin interaction
ENSG00000004866	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1024432	0.98[ASN][1000 genomes]
rs1024433	0.98[ASN][1000 genomes]
rs1024434	0.98[ASN][1000 genomes]
rs10250850	0.88[ASN][1000 genomes]
rs10252771	0.84[CEU][hapmap]
rs10259910	0.83[CEU][hapmap]
rs10266994	0.90[ASN][1000 genomes]
rs10272923	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10276758	0.89[EUR][1000 genomes]
rs10487380	0.89[EUR][1000 genomes]
rs11978052	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12668510	0.93[ASN][1000 genomes]
rs12706159	0.90[ASN][1000 genomes]
rs13221302	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1477114	0.90[ASN][1000 genomes]
rs1548460	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1548461	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs17488728	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1989880	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2158050	0.98[ASN][1000 genomes]
rs2214227	0.96[ASN][1000 genomes]
rs34729439	0.89[EUR][1000 genomes]
rs35582707	0.91[EUR][1000 genomes]
rs62471815	0.96[ASN][1000 genomes]
rs6943120	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6950622	1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs6950716	0.98[ASN][1000 genomes]
rs6959314	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6961907	0.88[EUR][1000 genomes]
rs6965740	0.95[JPT][hapmap]
rs6966339	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6969783	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7782815	0.89[EUR][1000 genomes]
rs7789130	0.90[ASN][1000 genomes]
rs7807019	0.90[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs7807677	0.95[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869971	chr7:117420583-118274149	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh 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	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117587000-117601000	Weak transcription	Fetal Lung	lung
2	chr7:117592200-117596200	Weak transcription	Fetal Kidney	kidney

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