Variant report

Variant	rs6833176
Chromosome Location	chr4:100131163-100131164
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10000357	0.92[ASN][1000 genomes]
rs10015824	0.85[ASN][1000 genomes]
rs10020052	0.92[ASN][1000 genomes]
rs10030920	1.00[ASN][1000 genomes]
rs1154404	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1154415	0.89[CEU][hapmap];1.00[JPT][hapmap]
rs11724783	0.92[ASN][1000 genomes]
rs1311621	0.89[CEU][hapmap];1.00[JPT][hapmap]
rs13121905	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13148577	0.89[CEU][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs17595102	0.89[CEU][hapmap];1.00[JPT][hapmap]
rs1800760	0.83[ASN][1000 genomes]
rs1869458	0.89[CEU][hapmap];1.00[JPT][hapmap]
rs1893883	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2000864	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2187483	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2851275	0.89[CEU][hapmap];1.00[JPT][hapmap]
rs2851301	0.89[CEU][hapmap];1.00[JPT][hapmap]
rs28720150	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28762430	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28805070	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28848249	0.85[ASN][1000 genomes]
rs2903166	1.00[ASN][1000 genomes]
rs34195655	0.85[ASN][1000 genomes]
rs34511427	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3857224	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4147544	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4147545	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4147547	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4148886	0.83[ASN][1000 genomes]
rs4333190	1.00[ASN][1000 genomes]
rs4577585	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4585310	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4699733	1.00[CHB][hapmap]
rs62325498	0.92[ASN][1000 genomes]
rs6830685	0.80[YRI][hapmap]
rs7684914	0.82[YRI][hapmap]
rs9307238	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9994326	0.88[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	nsv1009017	chr4:99669441-100406394	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	nsv1002927	chr4:99952472-100148690	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv879656	chr4:99976646-100533722	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	nsv1002574	chr4:100023999-100133693	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	esv3355763	chr4:100070566-100376814	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv879657	chr4:100082154-100139366	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1014237	chr4:100102701-100365700	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv1010988	chr4:100105463-100444445	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv1000659	chr4:100117276-100444445	Enhancers Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	nsv999549	chr4:100121609-100351749	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
11	nsv879658	chr4:100123776-100131163	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100108400-100141600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:100127000-100131200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:100127000-100139000	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr4:100127000-100139400	Weak transcription	Ovary	ovary
5	chr4:100127000-100140200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr4:100127000-100142600	Weak transcription	Small Intestine	intestine
7	chr4:100127400-100139000	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr4:100127600-100138800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr4:100128400-100131400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr4:100128600-100131400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:100128800-100131400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr4:100129000-100143200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr4:100129400-100133800	Genic enhancers	Liver	Liver
14	chr4:100129800-100131400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr4:100129800-100131600	Enhancers	NHLF	lung
16	chr4:100130000-100131400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr4:100130000-100131400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:100130000-100131400	Enhancers	NHDF-Ad	bronchial
19	chr4:100130200-100131200	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr4:100130200-100131200	Weak transcription	Fetal Kidney	kidney
21	chr4:100130200-100131400	Enhancers	Aorta	Aorta
22	chr4:100130200-100134600	Weak transcription	Pancreas	Pancrea
23	chr4:100130600-100131400	Enhancers	Osteobl	bone
24	chr4:100130600-100132200	Enhancers	HSMMtube	muscle
25	chr4:100130800-100132000	Strong transcription	HepG2	liver
26	chr4:100131000-100131200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:100131000-100131200	Enhancers	Esophagus	oesophagus
28	chr4:100131000-100131200	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr4:100131000-100131400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr4:100131000-100131400	Enhancers	Placenta Amnion	Placenta Amnion
31	chr4:100131000-100132800	Weak transcription	Fetal Lung	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links