Variant report

Variant	rs7668570
Chromosome Location	chr4:20281795-20281796
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	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10516348	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10516350	0.87[AFR][1000 genomes]
rs10516354	1.00[ASN][1000 genomes]
rs11942988	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs16867613	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16867614	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs16869447	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs16869450	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs16869454	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16869455	0.94[ASN][1000 genomes]
rs16869457	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs16869461	0.94[ASN][1000 genomes]
rs16869465	0.96[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs16869475	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16869481	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1951740	0.94[ASN][1000 genomes]
rs2296014	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56967065	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs57013929	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61114792	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6832019	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6833323	0.83[AFR][1000 genomes]
rs715214	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73803832	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7661055	1.00[ASN][1000 genomes]
rs7668724	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7668969	0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7668991	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7673645	0.85[AMR][1000 genomes]
rs7674173	0.85[AMR][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	nsv878737	chr4:20233035-20282334	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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
5	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
6	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

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20258200-20299400	Weak transcription	Fetal Stomach	stomach
2	chr4:20268800-20283200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr4:20269200-20284600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr4:20273800-20286600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr4:20274400-20282200	Weak transcription	Fetal Kidney	kidney
6	chr4:20274600-20285600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr4:20274600-20286800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr4:20274600-20288600	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr4:20276400-20283000	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr4:20276400-20286000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr4:20277400-20283000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr4:20277400-20286400	Weak transcription	Osteobl	bone
13	chr4:20278400-20284400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr4:20278600-20283000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:20278600-20283400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr4:20278600-20283400	Weak transcription	Rectal Smooth Muscle	rectum
17	chr4:20278800-20282200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr4:20278800-20283200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr4:20278800-20290400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr4:20278800-20298000	Weak transcription	Colon Smooth Muscle	Colon
21	chr4:20280800-20281800	Enhancers	NHEK	skin
22	chr4:20281000-20282800	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr4:20281400-20281800	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr4:20281400-20282600	Enhancers	Fetal Lung	lung
25	chr4:20281400-20282800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:20281400-20283200	Weak transcription	NHDF-Ad	bronchial
27	chr4:20281400-20285600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr4:20281600-20283000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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