Variant report

Variant	rs28735796
Chromosome Location	chr4:20284532-20284533
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1323066	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17535770	0.97[ASN][1000 genomes]
rs2025287	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28642776	0.89[AMR][1000 genomes]
rs500869	0.86[ASN][1000 genomes]
rs505954	0.97[ASN][1000 genomes]
rs587032	0.86[ASN][1000 genomes]
rs668592	0.97[ASN][1000 genomes]
rs7655084	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7682397	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7685284	0.91[EUR][1000 genomes];0.90[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:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20258200-20299400	Weak transcription	Fetal Stomach	stomach
2	chr4:20269200-20284600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr4:20273800-20286600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:20274600-20285600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr4:20274600-20286800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr4:20274600-20288600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr4:20276400-20286000	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr4:20277400-20286400	Weak transcription	Osteobl	bone
9	chr4:20278800-20290400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr4:20278800-20298000	Weak transcription	Colon Smooth Muscle	Colon
11	chr4:20281400-20285600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr4:20281800-20294000	Enhancers	Placenta Amnion	Placenta Amnion
13	chr4:20282200-20286000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr4:20282800-20284600	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr4:20282800-20285800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr4:20283000-20284600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr4:20283000-20286800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:20283000-20287200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:20283000-20287400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr4:20283200-20284600	Weak transcription	Fetal Lung	lung
21	chr4:20283200-20284800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr4:20283200-20285800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr4:20283400-20284800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:20283400-20285000	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr4:20283400-20285000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr4:20283400-20285600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:20283400-20286400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr4:20283400-20286600	Weak transcription	HMEC	breast
29	chr4:20283600-20286200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:20283600-20288400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr4:20283800-20284800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr4:20283800-20284800	Weak transcription	NHEK	skin
33	chr4:20284000-20286000	Weak transcription	NHDF-Ad	bronchial
34	chr4:20284400-20285000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr4:20284400-20285800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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