Variant report

Variant	rs1502734
Chromosome Location	chr4:160607175-160607176
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:160606063..160608102-chr4:160627902..160629687,2	MCF-7	breast:
2	chr4:160581437..160584184-chr4:160604611..160607448,2	MCF-7	breast:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10000541	0.97[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11100248	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11100250	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1119663	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1304931	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13143749	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13151214	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1476297	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1502727	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1502729	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1502730	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1502738	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17038655	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2047794	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2134425	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4358345	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4358346	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6536451	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6536454	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6536455	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6845876	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6846319	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7699838	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs974590	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv1015469	chr4:160389277-160841619	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv537316	chr4:160389277-160841619	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv881205	chr4:160516090-160628006	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	esv2755953	chr4:160557413-160626250	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv595813	chr4:160574450-160665365	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160605400-160607600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:160606200-160607200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr4:160606200-160607400	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr4:160606200-160607600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr4:160606200-160608400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:160606400-160607400	Enhancers	Brain Substantia Nigra	brain
7	chr4:160606400-160607600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr4:160606600-160607200	Enhancers	H1 Cell Line	embryonic stem cell
9	chr4:160606600-160607200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:160606600-160607200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr4:160606600-160607400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr4:160606600-160607400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr4:160606800-160607200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr4:160606800-160607200	Enhancers	Brain Anterior Caudate	brain
15	chr4:160606800-160607200	Enhancers	Brain Hippocampus Middle	brain
16	chr4:160606800-160607400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
17	chr4:160606800-160607400	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr4:160606800-160607400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr4:160606800-160607400	Enhancers	Brain Angular Gyrus	brain
20	chr4:160606800-160607400	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr4:160606800-160607800	Enhancers	Colon Smooth Muscle	Colon
22	chr4:160606800-160608000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr4:160606800-160613000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr4:160607000-160607400	Weak transcription	Rectal Smooth Muscle	rectum

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