Variant report

Variant	rs55915216
Chromosome Location	chr7:38232139-38232140
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1014136	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10224886	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10234310	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10254082	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10282163	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10464362	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11766931	0.99[ASN][1000 genomes]
rs11773477	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12669726	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12670582	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17410426	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2270165	0.99[ASN][1000 genomes]
rs2392540	0.99[ASN][1000 genomes]
rs28664954	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3778894	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56147907	0.99[ASN][1000 genomes]
rs56228793	0.98[ASN][1000 genomes]
rs60713125	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62443299	0.91[ASN][1000 genomes]
rs62443315	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9638935	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9639788	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9986766	0.84[AFR][1000 genomes];0.97[AMR][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	nsv1016355	chr7:38168232-38372719	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
2	nsv830963	chr7:38172988-38344779	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	esv2758112	chr7:38218703-38523455	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
4	esv2759524	chr7:38218703-38523455	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer 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	37 gene(s)	inside rSNPs	diseases
5	nsv427776	chr7:38218703-38523455	Genic enhancers Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
6	nsv830964	chr7:38218708-38390518	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
7	nsv1030349	chr7:38227528-38372719	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
8	nsv538818	chr7:38227528-38372719	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
9	nsv1025974	chr7:38227528-38503472	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
10	nsv538819	chr7:38227528-38503472	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
11	nsv433041	chr7:38229107-38358728	Strong transcription Genic enhancers Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38218600-38259200	Weak transcription	Colonic Mucosa	Colon
2	chr7:38219600-38241400	Weak transcription	Fetal Intestine Large	intestine
3	chr7:38219800-38234600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:38220200-38235400	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr7:38220200-38235400	Weak transcription	Thymus	Thymus
6	chr7:38220200-38236800	Weak transcription	Fetal Stomach	stomach
7	chr7:38220200-38246600	Weak transcription	Fetal Thymus	thymus
8	chr7:38220200-38254800	Weak transcription	Brain Hippocampus Middle	brain
9	chr7:38220400-38232400	Weak transcription	Fetal Brain Male	brain
10	chr7:38220400-38247000	Weak transcription	Fetal Intestine Small	intestine
11	chr7:38221000-38236400	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr7:38221000-38246800	Weak transcription	Primary T cells from cord blood	blood
13	chr7:38223600-38255600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr7:38224200-38235800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr7:38224200-38235800	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr7:38224200-38235800	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr7:38225000-38247000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr7:38225600-38235800	Weak transcription	Ovary	ovary
19	chr7:38225800-38235800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr7:38227000-38235400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr7:38227000-38235400	Weak transcription	NHLF	lung
22	chr7:38227000-38237400	Weak transcription	Aorta	Aorta
23	chr7:38227600-38238400	Weak transcription	Rectal Smooth Muscle	rectum
24	chr7:38228000-38235400	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr7:38228000-38236800	Weak transcription	Left Ventricle	heart
26	chr7:38228000-38256600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr7:38228200-38237400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr7:38228200-38237400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr7:38228200-38239400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr7:38228200-38241400	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr7:38228200-38254400	Weak transcription	Duodenum Mucosa	Duodenum
32	chr7:38228800-38235800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr7:38228800-38239600	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr7:38228800-38247200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr7:38229000-38236800	Weak transcription	Fetal Heart	heart
36	chr7:38229200-38249200	Weak transcription	Primary B cells from peripheral blood	blood
37	chr7:38229600-38246600	Weak transcription	Primary B cells from cord blood	blood
38	chr7:38229800-38233800	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr7:38229800-38237400	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr7:38229800-38246400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr7:38230200-38232200	ZNF genes & repeats	GM12878-XiMat	blood
42	chr7:38230200-38235000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr7:38230200-38235200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr7:38230200-38235200	Weak transcription	HSMMtube	muscle
45	chr7:38230200-38235400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr7:38230200-38235400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr7:38230200-38235400	Weak transcription	NH-A	brain
48	chr7:38230200-38235400	Weak transcription	NHEK	skin
49	chr7:38230200-38235400	Weak transcription	Osteobl	bone
50	chr7:38230200-38259200	Weak transcription	K562	blood

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