Variant report

Variant	rs9321755
Chromosome Location	chr6:140169474-140169475
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12111348	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3015436	0.93[CHB][hapmap]
rs62432085	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62432086	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62432087	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62432089	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62432092	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73557442	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7753070	0.81[ASN][1000 genomes]
rs9373252	0.94[ASN][1000 genomes]
rs9376471	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs9376472	0.95[ASN][1000 genomes]
rs9376473	0.88[ASN][1000 genomes]
rs9484317	0.98[ASN][1000 genomes]
rs9495586	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869066	chr6:139777114-140639695	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
2	nsv830820	chr6:140059279-140255292	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a
3	nsv1017015	chr6:140084137-140300565	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1019407	chr6:140087307-140304334	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1022881	chr6:140098646-140172570	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:140167400-140169600	Enhancers	Colon Smooth Muscle	Colon
2	chr6:140167800-140169600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:140168200-140169800	Enhancers	Fetal Intestine Small	intestine
4	chr6:140168400-140170000	Enhancers	Fetal Intestine Large	intestine
5	chr6:140168400-140174000	Weak transcription	Fetal Lung	lung
6	chr6:140168600-140170200	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr6:140168800-140173400	Weak transcription	Duodenum Mucosa	Duodenum
8	chr6:140168800-140177000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr6:140169000-140169600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr6:140169000-140177000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr6:140169200-140169600	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr6:140169200-140173400	Weak transcription	Rectal Smooth Muscle	rectum
13	chr6:140169400-140170000	Enhancers	Primary monocytes fromperipheralblood	blood

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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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