Variant report

Variant	rs9467699
Chromosome Location	chr6:26294677-26294678
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11962660	1.00[CHB][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1883215	1.00[ASN][1000 genomes]
rs6456710	1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs6902389	1.00[ASN][1000 genomes]
rs6902392	1.00[ASN][1000 genomes]
rs6903015	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6908156	1.00[ASN][1000 genomes]
rs6910374	0.89[ASN][1000 genomes]
rs6923139	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6939799	1.00[ASN][1000 genomes]
rs6939978	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7745232	0.89[ASN][1000 genomes]
rs7769926	1.00[CHB][hapmap]
rs9467700	1.00[CHB][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9467701	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs9467704	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs9467707	1.00[ASN][1000 genomes]
rs9467708	1.00[ASN][1000 genomes]
rs9467709	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
6	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
7	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases
8	nsv1015782	chr6:26026870-26323895	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1114 gene(s)	inside rSNPs	diseases
9	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
10	nsv601173	chr6:26239404-26322524	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	184 gene(s)	inside rSNPs	diseases
11	nsv482729	chr6:26291011-26470898	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26286800-26295400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:26287200-26295600	Weak transcription	A549	lung
3	chr6:26293800-26296400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr6:26294400-26294800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:26294400-26294800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:26294400-26294800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr6:26294400-26294800	Enhancers	Placenta Amnion	Placenta Amnion
8	chr6:26294400-26294800	Enhancers	Psoas Muscle	Psoas
9	chr6:26294400-26294800	Bivalent Enhancer	HepG2	liver
10	chr6:26294400-26295000	Enhancers	H1 Cell Line	embryonic stem cell
11	chr6:26294400-26295600	Enhancers	Fetal Intestine Large	intestine
12	chr6:26294400-26295600	ZNF genes & repeats	K562	blood
13	chr6:26294400-26296800	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr6:26294600-26294800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr6:26294600-26294800	Enhancers	Fetal Kidney	kidney
16	chr6:26294600-26294800	Enhancers	Fetal Muscle Leg	muscle
17	chr6:26294600-26295800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:26294600-26295800	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr6:26294600-26299200	Weak transcription	H9 Cell Line	embryonic stem cell

Quick Search:

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

what's new

Quick links