Variant report

Variant	rs1597389
Chromosome Location	chr3:142853433-142853434
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	chr3:142851820..142854133-chr3:142856452..142858967,2	MCF-7	breast:
2	chr3:142850270..142855258-chr3:142857254..142859835,5	K562	blood:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10084718	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1056360	0.99[EUR][1000 genomes]
rs1134685	0.99[EUR][1000 genomes]
rs11710763	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11711866	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11719768	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16853045	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1900994	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1900995	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4683448	0.81[EUR][1000 genomes]
rs4683449	0.82[EUR][1000 genomes]
rs4683450	0.89[ASN][1000 genomes]
rs4683451	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4683452	0.84[ASN][1000 genomes]
rs4683454	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4683455	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4683741	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4683743	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4683744	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4683745	0.94[EUR][1000 genomes]
rs4683746	0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4683747	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4683748	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56367421	0.81[EUR][1000 genomes]
rs56405449	0.81[EUR][1000 genomes]
rs6440136	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6440137	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6440141	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6440142	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs66726727	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs67496487	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs67627912	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6770489	0.81[EUR][1000 genomes]
rs6789472	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6801537	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6801610	0.85[ASN][1000 genomes]
rs6805732	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs68171708	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs726737	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73159623	0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs735564	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9829651	0.86[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	esv2757893	chr3:142720230-142962932	Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	esv2759183	chr3:142720230-142964373	Strong transcription Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv949288	chr3:142793323-143585882	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv1007164	chr3:142837004-142891719	Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv508250	chr3:142842454-142943722	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142840600-142854600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr3:142841200-142858000	Weak transcription	Spleen	Spleen
3	chr3:142844800-142858200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr3:142845800-142858200	Weak transcription	Fetal Brain Male	brain
5	chr3:142849200-142854200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr3:142851800-142853800	Enhancers	K562	blood
7	chr3:142852000-142856600	Weak transcription	Dnd41	blood
8	chr3:142852200-142855000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr3:142852400-142854400	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr3:142852600-142855400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr3:142852600-142855600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr3:142852800-142855000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr3:142853000-142855600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr3:142853200-142853600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr3:142853200-142854200	Enhancers	H1 Cell Line	embryonic stem cell
16	chr3:142853200-142854400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr3:142853200-142854800	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr3:142853200-142854800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr3:142853200-142855000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr3:142853200-142855000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr3:142853200-142855000	Enhancers	Fetal Lung	lung
22	chr3:142853200-142855000	Enhancers	HMEC	breast
23	chr3:142853200-142855000	Enhancers	NHDF-Ad	bronchial
24	chr3:142853200-142855000	Enhancers	NHEK	skin
25	chr3:142853200-142855000	Enhancers	Osteobl	bone
26	chr3:142853200-142855600	Enhancers	HUVEC	blood vessel
27	chr3:142853200-142855600	Enhancers	NHLF	lung
28	chr3:142853400-142853600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr3:142853400-142853600	Enhancers	Fetal Thymus	thymus
30	chr3:142853400-142854200	Flanking Active TSS	NH-A	brain
31	chr3:142853400-142854600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr3:142853400-142854600	Enhancers	GM12878-XiMat	blood
33	chr3:142853400-142854800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr3:142853400-142854800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr3:142853400-142854800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr3:142853400-142854800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr3:142853400-142854800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr3:142853400-142854800	Enhancers	Fetal Brain Female	brain
39	chr3:142853400-142855000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr3:142853400-142855000	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr3:142853400-142855000	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr3:142853400-142855000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr3:142853400-142855000	Enhancers	Muscle Satellite Cultured Cells	--
44	chr3:142853400-142855000	Enhancers	HSMM	muscle
45	chr3:142853400-142855000	Enhancers	HSMMtube	muscle
46	chr3:142853400-142870600	Weak transcription	Primary T cells from cord blood	blood

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