Variant report

Variant	rs7629926
Chromosome Location	chr3:138679826-138679827
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:138671344..138677284-chr3:138678243..138683566,6	K562	blood:
2	chr3:138672783..138675327-chr3:138678243..138680215,2	K562	blood:
3	chr3:138678001..138680024-chr3:138682116..138684203,2	K562	blood:
4	chr3:138659774..138660703-chr3:138679825..138680699,2	MCF-7	breast:
5	chr3:138660724..138663201-chr3:138679791..138682336,2	K562	blood:
6	chr3:138660095..138660771-chr3:138679788..138680398,3	K562	blood:

Variant related genes	Relation type
ENSG00000244578	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs12493711	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12497789	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2018794	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs360709	0.87[ASN][1000 genomes]
rs360711	0.90[ASN][1000 genomes]
rs56679446	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs57084332	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs57106095	0.84[EUR][1000 genomes]
rs57908668	0.84[EUR][1000 genomes]
rs58880010	0.80[AFR][1000 genomes]
rs58908753	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs59081321	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs60291969	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs60515064	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60650442	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60838328	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61408596	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6439830	0.84[EUR][1000 genomes]
rs6439831	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs66475108	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs67626684	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6780823	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72976944	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72976956	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7617892	0.84[EUR][1000 genomes]
rs7620461	0.84[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs7626152	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs7639044	0.82[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs7639122	0.93[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7644875	0.89[EUR][1000 genomes]
rs7649365	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs931250	0.80[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530057	chr3:138014877-138734390	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv1013074	chr3:138213166-138737688	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv1002612	chr3:138213274-138831792	Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	nsv536726	chr3:138213274-138831792	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	nsv1009726	chr3:138219923-138737688	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh 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 miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv869205	chr3:138248190-138775288	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv868955	chr3:138248190-138848947	Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv591854	chr3:138348081-138764229	Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
9	nsv1010514	chr3:138365640-138737688	Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
10	nsv917964	chr3:138440701-138699084	Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
11	nsv877542	chr3:138645013-138750904	Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138673400-138683200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:138679200-138680000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:138679200-138680000	Flanking Active TSS	Primary hematopoietic stem cells	blood
4	chr3:138679200-138680000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr3:138679200-138680000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr3:138679200-138680000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr3:138679400-138680000	Bivalent/Poised TSS	Primary T cells from cord blood	blood
8	chr3:138679400-138680000	Bivalent Enhancer	Fetal Thymus	thymus
9	chr3:138679400-138680400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
10	chr3:138679400-138680400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
11	chr3:138679400-138680400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
12	chr3:138679400-138680400	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
13	chr3:138679400-138680600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
14	chr3:138679400-138680600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
15	chr3:138679600-138680000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
16	chr3:138679600-138680000	Flanking Active TSS	Ovary	ovary
17	chr3:138679600-138680200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr3:138679600-138680200	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
19	chr3:138679600-138680400	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
20	chr3:138679800-138680000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
21	chr3:138679800-138680000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
22	chr3:138679800-138680000	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
23	chr3:138679800-138680000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr3:138679800-138680000	Bivalent Enhancer	Fetal Brain Female	brain
25	chr3:138679800-138680400	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood

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