Variant report

Variant	rs60581845
Chromosome Location	chr3:23477816-23477817
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:23477379..23479456-chr3:23479836..23482736,2	MCF-7	breast:
2	chr3:23477632..23480027-chr3:23493781..23495810,2	MCF-7	breast:

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs11129119	0.85[AFR][1000 genomes]
rs11916411	0.83[EUR][1000 genomes]
rs12715047	0.85[EUR][1000 genomes]
rs13064035	0.84[EUR][1000 genomes]
rs13321359	0.89[EUR][1000 genomes]
rs13326048	0.88[EUR][1000 genomes]
rs1498809	0.85[EUR][1000 genomes]
rs1498811	0.84[EUR][1000 genomes]
rs1692612	0.88[EUR][1000 genomes]
rs1692617	0.87[EUR][1000 genomes]
rs1692620	0.88[EUR][1000 genomes]
rs1692622	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1692650	0.85[EUR][1000 genomes]
rs1692651	0.89[EUR][1000 genomes]
rs1692652	0.89[EUR][1000 genomes]
rs1695171	0.89[EUR][1000 genomes]
rs1695181	0.85[EUR][1000 genomes]
rs1695200	0.88[EUR][1000 genomes]
rs17194786	0.83[EUR][1000 genomes]
rs1874235	0.84[EUR][1000 genomes]
rs1908773	0.88[EUR][1000 genomes]
rs2359759	0.86[EUR][1000 genomes]
rs2359763	0.87[EUR][1000 genomes]
rs3104243	0.87[EUR][1000 genomes]
rs3104244	0.82[EUR][1000 genomes]
rs4858077	0.89[EUR][1000 genomes]
rs4858504	0.83[EUR][1000 genomes]
rs4858506	0.84[EUR][1000 genomes]
rs4858508	0.83[EUR][1000 genomes]
rs6550756	0.84[EUR][1000 genomes]
rs66649889	0.95[ASN][1000 genomes]
rs6763329	0.84[EUR][1000 genomes]
rs6763535	0.84[EUR][1000 genomes]
rs6769173	0.86[EUR][1000 genomes]
rs6770091	0.90[ASN][1000 genomes]
rs6775232	0.84[EUR][1000 genomes]
rs6776424	0.84[EUR][1000 genomes]
rs6784195	0.89[EUR][1000 genomes]
rs6796840	0.89[EUR][1000 genomes]
rs704533	0.85[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs704534	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs716457	0.84[EUR][1000 genomes]
rs7631334	0.87[EUR][1000 genomes]
rs778459	0.89[EUR][1000 genomes]
rs778460	0.85[EUR][1000 genomes]
rs778461	0.87[EUR][1000 genomes]
rs778462	0.88[EUR][1000 genomes]
rs778467	0.89[EUR][1000 genomes]
rs778468	0.89[EUR][1000 genomes]
rs778470	0.89[EUR][1000 genomes]
rs778475	0.88[EUR][1000 genomes]
rs778476	0.88[EUR][1000 genomes]
rs778480	0.89[EUR][1000 genomes]
rs778484	0.89[EUR][1000 genomes]
rs778485	0.89[EUR][1000 genomes]
rs778486	0.84[EUR][1000 genomes]
rs778487	0.89[EUR][1000 genomes]
rs778488	0.89[EUR][1000 genomes]
rs778494	0.87[EUR][1000 genomes]
rs778496	0.85[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs778499	0.81[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs778500	0.83[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs778501	0.81[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs778503	0.87[EUR][1000 genomes]
rs778506	0.89[EUR][1000 genomes]
rs778507	0.89[EUR][1000 genomes]
rs778508	0.89[EUR][1000 genomes]
rs778510	0.84[EUR][1000 genomes]
rs778514	0.84[EUR][1000 genomes]
rs778521	0.94[ASN][1000 genomes]
rs778523	0.87[EUR][1000 genomes]
rs778526	0.88[EUR][1000 genomes]
rs9824359	0.81[EUR][1000 genomes]
rs9825778	0.86[EUR][1000 genomes]
rs9826089	0.83[EUR][1000 genomes]
rs9826647	0.86[EUR][1000 genomes]
rs9830392	0.91[ASN][1000 genomes]
rs9836574	0.93[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs9840820	0.87[EUR][1000 genomes]
rs9849424	0.83[EUR][1000 genomes]
rs9859515	0.84[EUR][1000 genomes]
rs9859651	0.89[EUR][1000 genomes]
rs9873317	0.84[EUR][1000 genomes]
rs9874519	0.82[EUR][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	nsv1002823	chr3:23277838-23623083	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1007373	chr3:23367952-23710331	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv876624	chr3:23385877-23483536	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv876625	chr3:23390301-23509597	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv533980	chr3:23445901-24311972	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23447000-23479600	Weak transcription	Primary B cells from cord blood	blood
2	chr3:23467600-23478400	Weak transcription	Fetal Heart	heart
3	chr3:23472400-23478400	Weak transcription	Left Ventricle	heart
4	chr3:23472800-23484400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr3:23472800-23488000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr3:23473000-23480600	Weak transcription	Primary B cells from peripheral blood	blood
7	chr3:23473200-23478200	Weak transcription	Brain Substantia Nigra	brain
8	chr3:23473400-23478600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:23473800-23494000	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr3:23475600-23478800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr3:23476200-23478600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr3:23476400-23478400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr3:23476400-23479600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr3:23476600-23478000	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr3:23476600-23478600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr3:23476600-23479400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr3:23476800-23478600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr3:23476800-23481800	Weak transcription	Primary hematopoietic stem cells	blood
19	chr3:23477000-23478000	Enhancers	H1 Cell Line	embryonic stem cell
20	chr3:23477000-23478000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr3:23477000-23478800	Enhancers	Psoas Muscle	Psoas
22	chr3:23477000-23480000	Weak transcription	GM12878-XiMat	blood
23	chr3:23477200-23478200	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr3:23477200-23481400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr3:23477400-23479200	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr3:23477400-23480800	Weak transcription	Dnd41	blood
27	chr3:23477400-23482600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr3:23477800-23478800	Enhancers	HSMMtube	muscle
29	chr3:23477800-23487800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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