Variant report

Variant	rs16924826
Chromosome Location	chr9:108431971-108431972
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12348555	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16924823	0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs16924827	1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[ASN][1000 genomes]
rs57574693	1.00[ASN][1000 genomes]
rs58612454	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60923669	1.00[ASN][1000 genomes]
rs73504012	1.00[EUR][1000 genomes]
rs73516093	1.00[EUR][1000 genomes]
rs73518122	1.00[EUR][1000 genomes]
rs73520076	1.00[EUR][1000 genomes]
rs9696805	1.00[ASN][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	nsv519023	chr9:108371549-108454745	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	n/a
2	nsv893693	chr9:108427062-108683134	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:108419800-108432800	Weak transcription	Brain Germinal Matrix	brain
2	chr9:108423600-108451600	Weak transcription	Psoas Muscle	Psoas
3	chr9:108425400-108433000	Weak transcription	GM12878-XiMat	blood
4	chr9:108430600-108432000	Weak transcription	Liver	Liver
5	chr9:108431800-108432200	Enhancers	K562	blood
6	chr9:108431800-108433400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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