Variant report

Variant	rs395561
Chromosome Location	chr5:106861975-106861976
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs153189	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs163895	1.00[CHB][hapmap]
rs1966892	1.00[CHB][hapmap]
rs250251	0.96[ASN][1000 genomes]
rs250253	1.00[CHD][hapmap];0.96[ASN][1000 genomes]
rs352605	1.00[CHB][hapmap]
rs388016	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs446774	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6879279	1.00[CHB][hapmap]
rs7443170	1.00[CHB][hapmap]
rs848827	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs848828	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034276	chr5:106461538-106944163	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv537851	chr5:106461538-106944163	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	esv34018	chr5:106720912-107110506	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:106842400-106880000	Weak transcription	Gastric	stomach
2	chr5:106848800-106865000	Weak transcription	Right Atrium	heart
3	chr5:106856000-106865000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:106856000-106868600	Weak transcription	Right Ventricle	heart
5	chr5:106856400-106865000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr5:106856600-106865000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr5:106856600-106865000	Weak transcription	Aorta	Aorta
8	chr5:106856800-106862000	Weak transcription	Fetal Heart	heart
9	chr5:106857400-106868000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr5:106857800-106867200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:106859200-106862000	Weak transcription	Pancreas	Pancrea
12	chr5:106859400-106862200	Weak transcription	Fetal Lung	lung
13	chr5:106859400-106865000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr5:106859600-106863800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr5:106859600-106865000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr5:106859600-106873600	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr5:106860000-106862000	Weak transcription	HSMMtube	muscle
18	chr5:106860000-106864800	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr5:106860000-106865000	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr5:106860200-106862000	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr5:106860200-106862000	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr5:106860200-106862000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr5:106860200-106865000	Weak transcription	Left Ventricle	heart
24	chr5:106860400-106864800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr5:106860600-106862000	Weak transcription	NHEK	skin
26	chr5:106860600-106865200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr5:106860600-106867000	Weak transcription	Fetal Kidney	kidney
28	chr5:106860600-106874600	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr5:106860800-106862000	Weak transcription	HMEC	breast
30	chr5:106860800-106864600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr5:106861000-106862000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr5:106861000-106862000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr5:106861400-106862400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr5:106861600-106862000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr5:106861600-106862400	Enhancers	Stomach Mucosa	stomach
36	chr5:106861600-106864200	Enhancers	A549	lung
37	chr5:106861800-106862200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr5:106861800-106862200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr5:106861800-106862200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr5:106861800-106862200	Enhancers	Placenta Amnion	Placenta Amnion
41	chr5:106861800-106862400	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr5:106861800-106862400	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:106861800-106862800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr5:106861800-106862800	Enhancers	HSMM	muscle
45	chr5:106861800-106863000	Enhancers	Muscle Satellite Cultured Cells	--

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