Variant report

Variant	rs11741476
Chromosome Location	chr5:177380624-177380625
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10060376	0.90[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10794706	0.90[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11739986	0.84[ASN][1000 genomes]
rs11742117	0.90[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12186510	0.90[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12187456	0.90[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs13166313	0.81[AMR][1000 genomes]
rs13178333	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4077204	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4077205	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4077206	0.85[ASN][1000 genomes]
rs4959001	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4959002	0.90[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4959003	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs56268665	0.85[ASN][1000 genomes]
rs60355061	0.90[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7341034	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024444	chr5:176751921-177427715	Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	142 gene(s)	inside rSNPs	diseases
2	esv2752795	chr5:176898619-177488281	Active TSS Strong transcription Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer 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	78 gene(s)	inside rSNPs	diseases
3	nsv1033211	chr5:177133646-177383386	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv1030383	chr5:177310325-177571254	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
5	nsv883184	chr5:177311043-177488281	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv883185	chr5:177357964-177401509	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv521629	chr5:177364884-177396200	Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv883186	chr5:177376317-177549491	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
9	nsv883187	chr5:177377400-177419967	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	esv3447343	chr5:177378396-177382794	Weak transcription Strong transcription ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
11	esv2760946	chr5:177379490-177401509	Weak transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv432821	chr5:177380624-177400868	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177368200-177396400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr5:177371000-177381800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr5:177371000-177393000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr5:177371600-177383800	Weak transcription	Liver	Liver
5	chr5:177371600-177385200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr5:177371600-177389600	Weak transcription	Brain Germinal Matrix	brain
7	chr5:177371800-177384200	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr5:177371800-177387400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr5:177371800-177387600	Weak transcription	Pancreas	Pancrea
10	chr5:177371800-177387800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr5:177371800-177388200	Weak transcription	Gastric	stomach
12	chr5:177371800-177390200	Weak transcription	Primary T cells from cord blood	blood
13	chr5:177371800-177390800	Weak transcription	Ovary	ovary
14	chr5:177371800-177392800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr5:177371800-177394200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr5:177371800-177394200	Weak transcription	Right Ventricle	heart
17	chr5:177372000-177381800	Weak transcription	Lung	lung
18	chr5:177372000-177382800	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr5:177372000-177385200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr5:177372000-177385400	Weak transcription	NHDF-Ad	bronchial
21	chr5:177372200-177390000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr5:177372400-177385600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr5:177372600-177385600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr5:177372600-177388200	Weak transcription	Esophagus	oesophagus
25	chr5:177374200-177384400	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr5:177374400-177385200	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr5:177375200-177387600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr5:177375400-177385200	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr5:177375400-177385200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr5:177375600-177381000	Weak transcription	Thymus	Thymus
31	chr5:177378000-177388400	Weak transcription	Primary B cells from peripheral blood	blood
32	chr5:177378600-177385200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr5:177378600-177387600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr5:177379000-177383000	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr5:177379000-177383200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr5:177379200-177382600	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr5:177379200-177383000	Weak transcription	Fetal Stomach	stomach
38	chr5:177379200-177385800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr5:177379200-177386000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr5:177379200-177387600	Weak transcription	NHLF	lung
41	chr5:177379200-177392400	Weak transcription	Primary T cells fromperipheralblood	blood

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