Variant report

Variant	rs35263530
Chromosome Location	chr9:117949288-117949289
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10120799	0.96[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs10122188	0.82[EUR][1000 genomes]
rs10124924	0.82[EUR][1000 genomes]
rs10125919	0.82[EUR][1000 genomes]
rs10125923	0.82[EUR][1000 genomes]
rs10125938	0.82[EUR][1000 genomes]
rs10817719	0.96[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs10817720	0.96[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs10817724	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10817726	0.96[AFR][1000 genomes]
rs10982578	0.96[AFR][1000 genomes]
rs10982583	0.96[AFR][1000 genomes]
rs10982589	0.96[AFR][1000 genomes]
rs10982590	0.96[AFR][1000 genomes]
rs10982596	0.85[EUR][1000 genomes]
rs10982597	0.85[EUR][1000 genomes]
rs10982600	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12115362	0.82[EUR][1000 genomes]
rs12339665	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12346640	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12350544	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12350563	0.85[EUR][1000 genomes]
rs13289510	0.82[EUR][1000 genomes]
rs16932349	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34459511	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4607691	0.96[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs60715510	0.96[AFR][1000 genomes]
rs71505533	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7357687	0.88[AFR][1000 genomes]
rs9886855	0.96[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	nsv615250	chr9:117768021-118012841	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv916912	chr9:117770039-118014140	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv831697	chr9:117860416-118023927	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv893769	chr9:117936903-117985886	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117930000-117964400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr9:117945600-117959400	Weak transcription	Fetal Kidney	kidney
3	chr9:117945800-117959600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr9:117947000-117954200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr9:117947200-117949600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr9:117947200-117953000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr9:117947200-117954400	Weak transcription	Colon Smooth Muscle	Colon

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