Variant report

Variant	rs7674173
Chromosome Location	chr4:20288024-20288025
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10516347	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10516348	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10516350	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs10516354	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11942988	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16867613	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16867614	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs16869447	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16869450	0.89[AMR][1000 genomes]
rs16869454	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16869455	1.00[EUR][1000 genomes]
rs16869457	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16869461	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16869465	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs16869475	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16869481	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1951740	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2296014	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56967065	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57013929	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61114792	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6832019	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6833323	1.00[EUR][1000 genomes]
rs715214	1.00[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73803832	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7661055	0.89[AMR][1000 genomes]
rs7668570	0.85[AMR][1000 genomes]
rs7668724	0.94[AMR][1000 genomes]
rs7668969	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7668991	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7673645	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv878738	chr4:20255306-20300192	Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv878739	chr4:20255306-20307922	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv461287	chr4:20261786-20292239	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv593791	chr4:20261786-20292239	Genic enhancers Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv593792	chr4:20275477-20362716	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv593793	chr4:20282334-20333722	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20258200-20299400	Weak transcription	Fetal Stomach	stomach
2	chr4:20274600-20288600	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr4:20278800-20290400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:20278800-20298000	Weak transcription	Colon Smooth Muscle	Colon
5	chr4:20281800-20294000	Enhancers	Placenta Amnion	Placenta Amnion
6	chr4:20283600-20288400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:20284600-20290400	Strong transcription	Fetal Lung	lung
8	chr4:20285400-20290400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:20285400-20290600	Enhancers	NHEK	skin
10	chr4:20285800-20288600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr4:20285800-20289000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr4:20286000-20288600	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr4:20286200-20292400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr4:20286400-20288600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr4:20286400-20288800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr4:20286600-20288800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr4:20286600-20291800	Enhancers	HMEC	breast
18	chr4:20286800-20289800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr4:20286800-20291800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr4:20287000-20288600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr4:20287000-20288600	Weak transcription	NHDF-Ad	bronchial
22	chr4:20287000-20288800	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr4:20287200-20288600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr4:20287200-20288600	Weak transcription	Osteobl	bone
25	chr4:20287200-20288800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr4:20287400-20298200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr4:20287600-20288600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr4:20287600-20288800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr4:20288000-20288200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr4:20288000-20288800	Weak transcription	HUES64 Cell Line	embryonic stem cell

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