Variant report

Variant	rs72643908
Chromosome Location	chr8:39786932-39786933
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10216703	0.82[EUR][1000 genomes]
rs10958575	0.82[EUR][1000 genomes]
rs41324645	0.89[AFR][1000 genomes]
rs66694577	0.84[EUR][1000 genomes]
rs6983467	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7008770	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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	nsv508505	chr8:39730094-39791331	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	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:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39771600-39797200	Weak transcription	Right Atrium	heart
2	chr8:39782400-39787000	Weak transcription	HUVEC	blood vessel
3	chr8:39782800-39790000	Weak transcription	Fetal Lung	lung
4	chr8:39783000-39787200	Weak transcription	K562	blood
5	chr8:39783000-39792000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr8:39783200-39790800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr8:39785600-39787400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr8:39785600-39792000	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr8:39785600-39805800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr8:39785800-39790600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr8:39785800-39791000	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr8:39785800-39791000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr8:39785800-39792000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr8:39786000-39790400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr8:39786000-39790800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr8:39786000-39790800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr8:39786000-39791000	Weak transcription	H1 Cell Line	embryonic stem cell

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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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