Variant report

Variant	rs7755091
Chromosome Location	chr6:100906662-100906663
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs17060629	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17060659	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs241814	1.00[CEU][hapmap];0.92[YRI][hapmap]
rs3798484	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58927095	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6907007	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6907169	0.92[YRI][hapmap];0.91[AFR][1000 genomes]
rs6928357	0.90[AFR][1000 genomes]
rs6934173	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6942018	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7755275	0.84[ASN][1000 genomes]
rs7766553	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9322060	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9485075	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9485089	0.82[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9485091	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9485097	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9485098	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9497479	1.00[JPT][hapmap];0.91[YRI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9497547	0.90[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9497562	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9497585	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949535	chr6:100740293-101469052	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1028122	chr6:100774245-100964347	Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv1023710	chr6:100810738-101001115	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv538388	chr6:100810738-101001115	Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv515895	chr6:100868779-100910798	Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
6	nsv533053	chr6:100883636-100911512	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:100897400-100908600	Weak transcription	HSMMtube	muscle
2	chr6:100901600-100906800	ZNF genes & repeats	Spleen	Spleen
3	chr6:100901600-100907200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr6:100901800-100907600	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr6:100902000-100913600	Active TSS	Psoas Muscle	Psoas
6	chr6:100905200-100906800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
7	chr6:100905200-100906800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
8	chr6:100905200-100906800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr6:100905400-100906800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
10	chr6:100905400-100906800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
11	chr6:100905400-100906800	ZNF genes & repeats	Lung	lung
12	chr6:100905600-100906800	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr6:100905800-100906800	Bivalent Enhancer	Fetal Stomach	stomach
14	chr6:100906000-100906800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:100906000-100906800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
16	chr6:100906000-100906800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr6:100906000-100906800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:100906000-100906800	Flanking Active TSS	Pancreas	Pancrea
19	chr6:100906200-100906800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
20	chr6:100906200-100907000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr6:100906400-100906800	Bivalent Enhancer	HUVEC	blood vessel
22	chr6:100906400-100907600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:100906400-100908400	Enhancers	Muscle Satellite Cultured Cells	--
24	chr6:100906600-100906800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
25	chr6:100906600-100906800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
26	chr6:100906600-100906800	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
27	chr6:100906600-100907000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
28	chr6:100906600-100907000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
29	chr6:100906600-100907000	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr6:100906600-100907000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
31	chr6:100906600-100907000	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr6:100906600-100914200	Bivalent/Poised TSS	Fetal Kidney	kidney

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links