Variant report

Variant	rs17536318
Chromosome Location	chr9:96625560-96625561
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10992914	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10992916	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10992925	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10992926	0.85[CHB][hapmap]
rs10992927	0.85[CHB][hapmap]
rs10992928	1.00[CHB][hapmap];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10992929	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10992930	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62574261	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62574262	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62575578	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62575579	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62575608	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62575609	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62575610	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62575611	0.97[AMR][1000 genomes];0.92[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	nsv893588	chr9:96620419-96668352	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv893589	chr9:96624645-96884544	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96619800-96626000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr9:96623400-96626800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr9:96623600-96626000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr9:96624400-96631400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr9:96624600-96625600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr9:96624600-96626000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr9:96625000-96626000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr9:96625400-96627000	Enhancers	Fetal Brain Male	brain

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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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