Variant report

Variant	rs13357786
Chromosome Location	chr5:43047361-43047362
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:43045206..43050609-chr5:43062079..43064977,5	K562	blood:
2	chr5:43045693..43047655-chr5:43065213..43067765,2	K562	blood:
3	chr5:43006809..43009457-chr5:43045449..43048396,2	K562	blood:
4	chr5:43034726..43053192-chr5:43061725..43074206,66	K562	blood:
5	chr5:43036901..43050217-chr5:43060442..43069391,53	MCF-7	breast:
6	chr5:43038662..43048059-chr5:43059399..43070773,40	MCF-7	breast:

Variant related genes	Relation type
ENSG00000272144	Chromatin interaction
ENSG00000271788	Chromatin interaction
ENSG00000172262	Chromatin interaction
ENSG00000177738	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10051990	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10052644	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10054331	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10056822	0.90[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs10057416	0.92[AMR][1000 genomes]
rs10064210	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10071791	0.92[EUR][1000 genomes]
rs10077219	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1122510	0.92[EUR][1000 genomes]
rs13357845	0.84[EUR][1000 genomes]
rs13360205	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28490330	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28573681	0.82[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs28609175	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28628732	0.92[EUR][1000 genomes]
rs56917209	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs56962140	0.92[AMR][1000 genomes]
rs585302	0.80[EUR][1000 genomes]
rs58980582	1.00[EUR][1000 genomes]
rs60608708	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6451664	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6451666	1.00[EUR][1000 genomes]
rs6451670	0.88[EUR][1000 genomes]
rs673855	0.84[EUR][1000 genomes]
rs6858989	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6859319	0.85[AMR][1000 genomes]
rs6867941	0.92[AMR][1000 genomes]
rs6881467	0.93[AMR][1000 genomes]
rs6886503	0.92[EUR][1000 genomes]
rs6890021	0.92[AMR][1000 genomes]
rs6895961	0.92[AMR][1000 genomes]
rs73090747	0.85[AMR][1000 genomes]
rs7720810	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7728625	0.96[EUR][1000 genomes]
rs7730865	0.81[AMR][1000 genomes]
rs9292865	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv993554	chr5:42720939-43251863	Bivalent/Poised TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	298 gene(s)	inside rSNPs	diseases
2	nsv462126	chr5:42728831-43237188	Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	297 gene(s)	inside rSNPs	diseases
3	nsv597925	chr5:42728831-43237188	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	297 gene(s)	inside rSNPs	diseases
4	nsv1023741	chr5:42768215-43348145	Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	309 gene(s)	inside rSNPs	diseases
5	nsv537737	chr5:42768215-43348145	Genic enhancers Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	309 gene(s)	inside rSNPs	diseases
6	nsv534185	chr5:42804840-43067088	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	165 gene(s)	inside rSNPs	diseases
7	nsv1024636	chr5:42959979-43295782	Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	283 gene(s)	inside rSNPs	diseases
8	nsv537739	chr5:42959979-43295782	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	283 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:43043600-43050600	Weak transcription	GM12878-XiMat	blood
2	chr5:43043600-43052600	Weak transcription	A549	lung
3	chr5:43043600-43058200	Weak transcription	Gastric	stomach
4	chr5:43043600-43058200	Weak transcription	HSMMtube	muscle
5	chr5:43043600-43061600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:43043600-43063800	Weak transcription	Aorta	Aorta
7	chr5:43043600-43064000	Weak transcription	NHEK	skin
8	chr5:43043800-43050600	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr5:43043800-43054400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr5:43043800-43057400	Weak transcription	Primary B cells from cord blood	blood
11	chr5:43043800-43058000	Weak transcription	HepG2	liver
12	chr5:43043800-43061200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr5:43043800-43064000	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr5:43044600-43052800	Weak transcription	Primary hematopoietic stem cells	blood
15	chr5:43044800-43047600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr5:43044800-43049000	Weak transcription	HSMM	muscle
17	chr5:43044800-43050600	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr5:43044800-43051200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr5:43044800-43052600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr5:43044800-43052600	Weak transcription	Placenta	Placenta
21	chr5:43044800-43058200	Weak transcription	Lung	lung
22	chr5:43044800-43059400	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr5:43044800-43064000	Weak transcription	Right Ventricle	heart
24	chr5:43044800-43064200	Weak transcription	Duodenum Mucosa	Duodenum
25	chr5:43044800-43064400	Weak transcription	Brain Substantia Nigra	brain
26	chr5:43045000-43048200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr5:43045000-43052400	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr5:43045000-43061400	Weak transcription	NHLF	lung
29	chr5:43045000-43063800	Weak transcription	Adipose Nuclei	Adipose
30	chr5:43045000-43064200	Weak transcription	Primary B cells from peripheral blood	blood
31	chr5:43045000-43064400	Weak transcription	Esophagus	oesophagus
32	chr5:43045200-43048200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr5:43045200-43049800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr5:43045200-43053400	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr5:43045200-43053400	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr5:43045400-43047600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr5:43045400-43047600	Weak transcription	Osteobl	bone
38	chr5:43045400-43048800	Weak transcription	HUVEC	blood vessel
39	chr5:43045400-43051200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr5:43045400-43053400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr5:43045400-43058600	Weak transcription	Pancreas	Pancrea
42	chr5:43045400-43061400	Weak transcription	Hela-S3	cervix
43	chr5:43045400-43064200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr5:43045400-43066000	Weak transcription	Spleen	Spleen
45	chr5:43045600-43048000	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr5:43045600-43049000	Weak transcription	NH-A	brain
47	chr5:43045600-43051000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr5:43045600-43058800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr5:43045600-43061000	Weak transcription	Brain Cingulate Gyrus	brain
50	chr5:43045600-43063600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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