Variant report

Variant	rs1824194
Chromosome Location	chr8:103241893-103241894
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:103241352..103244052-chr8:103875043..103877128,2	K562	blood:
2	chr8:103241583..103244347-chr8:103821474..103823149,2	K562	blood:
3	chr8:103240120..103242197-chr8:103818124..103819971,2	K562	blood:
4	chr8:103241777..103245132-chr8:103247970..103252049,6	MCF-7	breast:
5	chr8:103233367..103236328-chr8:103240756..103243276,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000048392	Chromatin interaction
ENSG00000155096	Chromatin interaction
ENSG00000253669	Chromatin interaction
ENSG00000253320	Chromatin interaction
ENSG00000246263	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1037698	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10505023	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10505026	1.00[ASN][1000 genomes]
rs11575866	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11783533	1.00[ASN][1000 genomes]
rs16869246	1.00[ASN][1000 genomes]
rs17185155	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17185245	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17432015	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17433890	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17509673	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17512347	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17512821	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs28927372	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28928568	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28928570	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28928575	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28928577	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28928583	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28928584	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28928588	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28928589	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28928594	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28928595	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28928599	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28928601	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28928602	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28928606	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28999688	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28999709	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs29000269	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs29000275	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs29000279	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs29000280	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs29000281	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs29000284	0.97[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3204695	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34739767	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs35066978	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4102401	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56273032	1.00[ASN][1000 genomes]
rs58160045	1.00[ASN][1000 genomes]
rs73285249	1.00[ASN][1000 genomes]
rs73285260	1.00[ASN][1000 genomes]
rs7836803	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1020359	chr8:103109921-103318415	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1033829	chr8:103110057-103525696	Strong transcription Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv1021459	chr8:103163436-103401754	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv539701	chr8:103163436-103401754	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	nsv1025935	chr8:103199207-103468322	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
6	nsv1018990	chr8:103207922-103357742	Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv539702	chr8:103207922-103357742	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
8	nsv1028890	chr8:103207922-103401754	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
9	nsv891242	chr8:103210971-103282418	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
10	nsv891243	chr8:103219629-103292724	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103209800-103244800	Weak transcription	Stomach Mucosa	stomach
2	chr8:103215600-103248400	Weak transcription	Psoas Muscle	Psoas
3	chr8:103216200-103247400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:103216400-103245200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr8:103216400-103246600	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr8:103217000-103248400	Weak transcription	Small Intestine	intestine
7	chr8:103217800-103246400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr8:103218000-103246200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr8:103218600-103244200	Weak transcription	Fetal Heart	heart
10	chr8:103219200-103247600	Weak transcription	Fetal Brain Male	brain
11	chr8:103220400-103248800	Weak transcription	Hela-S3	cervix
12	chr8:103222600-103246000	Strong transcription	Osteobl	bone
13	chr8:103227600-103246800	Strong transcription	Primary B cells from cord blood	blood
14	chr8:103228000-103242200	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr8:103229600-103246800	Strong transcription	Primary hematopoietic stem cells	blood
16	chr8:103229800-103245000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr8:103230000-103242200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr8:103231600-103249800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr8:103232000-103242600	Weak transcription	HepG2	liver
20	chr8:103234600-103250000	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr8:103234800-103242400	Weak transcription	NHLF	lung
22	chr8:103234800-103242800	Weak transcription	Brain Germinal Matrix	brain
23	chr8:103236600-103245800	Strong transcription	HSMMtube	muscle
24	chr8:103237200-103248400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr8:103237400-103242200	Weak transcription	NHDF-Ad	bronchial
26	chr8:103237400-103245400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr8:103238200-103248800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr8:103238400-103248200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr8:103238400-103248800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr8:103239200-103244000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr8:103239400-103242200	Strong transcription	HUES48 Cell Line	embryonic stem cell
32	chr8:103239400-103242800	Strong transcription	HUES6 Cell Line	embryonic stem cell
33	chr8:103239400-103242800	Strong transcription	Primary T cells from cord blood	blood
34	chr8:103239400-103244600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr8:103239400-103246800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr8:103239600-103242000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr8:103239600-103243800	Strong transcription	Duodenum Mucosa	Duodenum
38	chr8:103239600-103244600	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr8:103239800-103242200	Strong transcription	Colon Smooth Muscle	Colon
40	chr8:103239800-103243000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr8:103239800-103244400	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr8:103239800-103244400	Strong transcription	Liver	Liver
43	chr8:103240000-103242000	Strong transcription	Brain Anterior Caudate	brain
44	chr8:103240000-103244000	Strong transcription	Primary T helper cells PMA-I stimulated	--
45	chr8:103240000-103244400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr8:103240000-103245400	Strong transcription	NH-A	brain
47	chr8:103240000-103246800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr8:103240200-103243000	Weak transcription	K562	blood
49	chr8:103240200-103243800	Strong transcription	Brain Angular Gyrus	brain
50	chr8:103240400-103242600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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