Variant report

Variant	rs3127573
Chromosome Location	chr6:160681393-160681394
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs2279463	1.00[CHB][hapmap];0.80[CHD][hapmap];0.85[JPT][hapmap]
rs3119309	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.94[TSI][hapmap];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3119310	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3119311	1.00[CEU][hapmap];0.87[GIH][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3127572	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[JPT][hapmap];0.82[MEX][hapmap];0.94[TSI][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3127578	1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3127579	0.80[AMR][1000 genomes]
rs3798156	1.00[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.80[AMR][1000 genomes]
rs7756836	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7757336	0.80[CEU][hapmap];0.87[GIH][hapmap];0.85[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758089	chr6:160372244-161234665	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	esv2759484	chr6:160372244-161234665	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	esv35098	chr6:160422589-161070870	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	esv2757197	chr6:160432331-161070870	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv818463	chr6:160435569-161025547	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv1030746	chr6:160592321-160867031	Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv538493	chr6:160592321-160867031	Weak transcription Bivalent/Poised TSS Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1030171	chr6:160648469-161091864	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
9	nsv886809	chr6:160670494-160979275	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Creatinine levels	20383145	GWAS catalog

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:160676400-160682000	Weak transcription	Pancreas	Pancrea
2	chr6:160676400-160683200	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr6:160676600-160683000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:160677000-160681800	Weak transcription	Duodenum Mucosa	Duodenum
5	chr6:160677800-160681800	Weak transcription	A549	lung
6	chr6:160678200-160681800	Enhancers	Colon Smooth Muscle	Colon
7	chr6:160678400-160681800	Weak transcription	HMEC	breast
8	chr6:160679000-160681600	Enhancers	Fetal Stomach	stomach
9	chr6:160679000-160682200	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr6:160679000-160683200	Enhancers	Placenta Amnion	Placenta Amnion
11	chr6:160679400-160681800	Enhancers	Rectal Smooth Muscle	rectum
12	chr6:160679400-160682200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr6:160679600-160682600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr6:160679800-160681400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:160680000-160681800	Enhancers	H1 Cell Line	embryonic stem cell
16	chr6:160680000-160682000	Enhancers	Fetal Muscle Leg	muscle
17	chr6:160680000-160685800	Enhancers	Fetal Intestine Large	intestine
18	chr6:160680200-160682200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr6:160680200-160686000	Enhancers	Fetal Intestine Small	intestine
20	chr6:160680400-160681400	Enhancers	H9 Cell Line	embryonic stem cell
21	chr6:160680400-160681600	Weak transcription	Placenta	Placenta
22	chr6:160680400-160681800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr6:160680400-160682000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr6:160680600-160681400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr6:160680600-160682400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr6:160680600-160682800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr6:160680800-160681400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr6:160680800-160682000	Enhancers	NHEK	skin
29	chr6:160681000-160681400	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr6:160681000-160681400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr6:160681000-160682000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr6:160681200-160681600	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr6:160681200-160681600	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr6:160681200-160681800	Weak transcription	Fetal Kidney	kidney
35	chr6:160681200-160682000	Enhancers	Stomach Smooth Muscle	stomach
36	chr6:160681200-160683200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr6:160681200-160683400	Enhancers	Hela-S3	cervix

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links