Variant report

Variant	rs1565035
Chromosome Location	chr8:122361772-122361773
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	chr8:122357699..122359685-chr8:122361092..122363691,2	MCF-7	breast:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10094084	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10102395	0.83[ASN][1000 genomes]
rs10107573	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10481070	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10481147	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10956033	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10956035	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10956038	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10956039	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10956040	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12545486	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13265234	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13265478	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13274258	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1487162	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1487168	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1487169	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1487170	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16892957	0.89[ASN][1000 genomes]
rs1843789	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1843790	0.98[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1906216	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2046570	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2385927	0.83[ASN][1000 genomes]
rs2386122	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2891939	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4144692	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4460379	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4871187	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6469998	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6470000	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6985415	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6988724	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7000174	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7004666	0.89[ASN][1000 genomes]
rs7006642	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7006650	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7008446	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7008769	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7015873	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7017097	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7824421	1.00[CEU][hapmap];0.87[CHB][hapmap];0.90[JPT][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7824450	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7829217	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7838314	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891424	chr8:121873345-122393258	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv3330574	chr8:122039099-122386130	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv891426	chr8:122078334-122393258	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1025365	chr8:122323246-122394774	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv465792	chr8:122329373-122398867	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv612131	chr8:122329373-122398867	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv831445	chr8:122336877-122509300	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:122359800-122362400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr8:122360400-122362600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr8:122360600-122361800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:122360600-122361800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr8:122360600-122361800	Enhancers	HMEC	breast
6	chr8:122360600-122361800	Enhancers	NHDF-Ad	bronchial
7	chr8:122360600-122361800	Enhancers	NHLF	lung
8	chr8:122360600-122362000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr8:122360800-122361800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr8:122360800-122361800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr8:122360800-122361800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr8:122360800-122361800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr8:122360800-122361800	Enhancers	HSMM	muscle
14	chr8:122360800-122361800	Enhancers	HUVEC	blood vessel
15	chr8:122360800-122361800	Enhancers	NH-A	brain
16	chr8:122360800-122361800	Enhancers	NHEK	skin
17	chr8:122360800-122362000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr8:122360800-122362200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr8:122361000-122361800	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr8:122361000-122361800	Enhancers	Fetal Thymus	thymus
21	chr8:122361000-122362000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr8:122361200-122361800	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr8:122361200-122362200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr8:122361400-122361800	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr8:122361400-122361800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr8:122361400-122361800	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr8:122361400-122361800	Enhancers	Thymus	Thymus
28	chr8:122361400-122361800	Flanking Active TSS	HepG2	liver
29	chr8:122361400-122362000	Enhancers	Primary T cells from cord blood	blood
30	chr8:122361600-122361800	Enhancers	Muscle Satellite Cultured Cells	--
31	chr8:122361600-122362000	Enhancers	A549	lung

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