Variant report

Variant	rs28479832
Chromosome Location	chr4:152332872-152332873
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10155290	0.81[AMR][1000 genomes]
rs12510777	0.85[AMR][1000 genomes]
rs17027640	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17591223	1.00[EUR][1000 genomes]
rs17690873	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2709835	0.80[ASN][1000 genomes]
rs28378042	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28501688	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28505227	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28513809	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28866051	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4336208	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7685383	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880262	chr4:151712054-152519899	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv881526	chr4:151968295-152489087	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv1025192	chr4:152202627-152498890	Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv537307	chr4:152202627-152498890	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv880624	chr4:152280646-152549112	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152329000-152333000	Active TSS	Breast Myoepithelial Primary Cells	Breast
2	chr4:152331200-152333000	Flanking Active TSS	NHEK	skin
3	chr4:152331200-152336000	Weak transcription	HUVEC	blood vessel
4	chr4:152331600-152338000	Weak transcription	Psoas Muscle	Psoas
5	chr4:152331600-152339200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:152331800-152333200	Enhancers	HepG2	liver
7	chr4:152331800-152336400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr4:152331800-152338000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr4:152331800-152338000	Weak transcription	Pancreas	Pancrea
10	chr4:152331800-152338400	Weak transcription	Stomach Mucosa	stomach
11	chr4:152332000-152333000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:152332000-152337000	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr4:152332000-152337200	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr4:152332000-152340400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr4:152332000-152347600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr4:152332200-152333000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr4:152332200-152333000	Weak transcription	Duodenum Mucosa	Duodenum
18	chr4:152332200-152333000	Enhancers	HMEC	breast
19	chr4:152332200-152336600	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr4:152332200-152338000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr4:152332200-152338000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:152332400-152336600	Weak transcription	Hela-S3	cervix
23	chr4:152332400-152338000	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr4:152332600-152333000	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr4:152332800-152333000	Weak transcription	Fetal Intestine Large	intestine
26	chr4:152332800-152333400	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr4:152332800-152336800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:152332800-152337200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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