Variant report

Variant	rs35166393
Chromosome Location	chr9:103145288-103145289
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs11998985	1.00[EUR][1000 genomes]
rs13284374	1.00[EUR][1000 genomes]
rs13286077	1.00[EUR][1000 genomes]
rs13286964	0.83[EUR][1000 genomes]
rs13287099	0.91[EUR][1000 genomes]
rs13290328	0.91[EUR][1000 genomes]
rs13290330	0.91[EUR][1000 genomes]
rs13290800	1.00[EUR][1000 genomes]
rs13293829	0.91[EUR][1000 genomes]
rs13294600	0.91[EUR][1000 genomes]
rs13296977	0.91[EUR][1000 genomes]
rs13297769	0.91[EUR][1000 genomes]
rs13298673	1.00[EUR][1000 genomes]
rs13301192	0.91[EUR][1000 genomes]
rs13302253	1.00[EUR][1000 genomes]
rs13302469	0.91[EUR][1000 genomes]
rs34069247	1.00[EUR][1000 genomes]
rs34089428	0.91[EUR][1000 genomes]
rs34092424	0.91[EUR][1000 genomes]
rs34104764	1.00[EUR][1000 genomes]
rs34169614	0.83[EUR][1000 genomes]
rs34179958	1.00[EUR][1000 genomes]
rs34304209	0.83[EUR][1000 genomes]
rs34314753	0.91[EUR][1000 genomes]
rs34332248	1.00[EUR][1000 genomes]
rs34407044	1.00[EUR][1000 genomes]
rs34553251	0.91[EUR][1000 genomes]
rs34622900	0.91[EUR][1000 genomes]
rs34696628	0.91[EUR][1000 genomes]
rs34727324	0.91[EUR][1000 genomes]
rs34821647	1.00[EUR][1000 genomes]
rs34831686	0.91[EUR][1000 genomes]
rs34872449	1.00[EUR][1000 genomes]
rs34919065	0.91[EUR][1000 genomes]
rs35051712	0.91[EUR][1000 genomes]
rs35123004	0.91[EUR][1000 genomes]
rs35415036	0.91[EUR][1000 genomes]
rs35427402	0.91[EUR][1000 genomes]
rs35439180	0.91[EUR][1000 genomes]
rs35550115	1.00[EUR][1000 genomes]
rs35563956	1.00[EUR][1000 genomes]
rs35575118	0.91[EUR][1000 genomes]
rs35747178	0.91[EUR][1000 genomes]
rs35747546	0.91[EUR][1000 genomes]
rs35801424	0.91[EUR][1000 genomes]
rs35970442	0.91[EUR][1000 genomes]
rs35982519	0.91[EUR][1000 genomes]
rs35998454	1.00[EUR][1000 genomes]
rs36068962	1.00[EUR][1000 genomes]
rs36082352	1.00[EUR][1000 genomes]
rs36148968	0.91[EUR][1000 genomes]
rs71507670	0.91[EUR][1000 genomes]
rs71507673	0.91[EUR][1000 genomes]
rs71507674	0.91[EUR][1000 genomes]
rs71507676	0.91[EUR][1000 genomes]
rs71507677	0.91[EUR][1000 genomes]
rs71507679	1.00[EUR][1000 genomes]
rs71507680	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531599	chr9:102227922-103156864	Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv893623	chr9:102648036-103405197	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:103134400-103152600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr9:103140200-103145400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr9:103142800-103145400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr9:103142800-103145600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr9:103142800-103145600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr9:103142800-103145800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr9:103145200-103145600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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