Variant report

Variant	rs4736929
Chromosome Location	chr8:39846489-39846490
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1362847	0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs16888491	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2032723	0.83[ASN][1000 genomes]
rs4736794	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4736961	0.92[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs4736962	0.92[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs56767874	0.93[ASN][1000 genomes]
rs57804443	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62511373	0.84[ASN][1000 genomes]
rs62511374	0.82[ASN][1000 genomes]
rs62511375	0.92[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs62511376	0.92[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs62513785	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7820968	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7837357	0.81[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	nsv539555	chr8:39683857-40673606	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1033371	chr8:39749437-39899540	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39835200-39853600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:39836200-39847400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr8:39837000-39847200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:39837600-39847600	Weak transcription	Right Atrium	heart
5	chr8:39840400-39847800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:39842400-39847800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr8:39843000-39847600	Weak transcription	Liver	Liver
8	chr8:39843000-39847600	Weak transcription	Hela-S3	cervix
9	chr8:39843000-39853000	Weak transcription	Lung	lung
10	chr8:39843400-39847600	Weak transcription	Fetal Heart	heart
11	chr8:39845200-39848800	Weak transcription	Pancreas	Pancrea
12	chr8:39845400-39847600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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