Variant report

Variant	rs8037446
Chromosome Location	chr15:50744180-50744181
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:50658523..50661516-chr15:50743007..50745833,2	MCF-7	breast:
2	chr15:50737403..50740009-chr15:50742579..50744249,2	K562	blood:
3	chr15:50743302..50746301-chr15:51199824..51201736,2	MCF-7	breast:
4	chr15:50743195..50745548-chr15:50749068..50751032,2	MCF-7	breast:
5	chr15:50646452..50649147-chr15:50743736..50746031,3	K562	blood:

Variant related genes	Relation type
ENSG00000104064	Chromatin interaction
ENSG00000081014	Chromatin interaction
ENSG00000244879	Chromatin interaction
ENSG00000138592	Chromatin interaction

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs10519276	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10519278	0.94[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11070774	1.00[CEU][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11070775	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11070777	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11070778	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11070779	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11070780	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11070781	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11070785	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11070786	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11070787	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11070788	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11630309	1.00[CEU][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11631351	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11631398	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11632697	1.00[CEU][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11632708	1.00[CEU][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11632823	1.00[CEU][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11633608	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11633624	1.00[CEU][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11633765	1.00[CEU][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11634832	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11637031	0.93[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11637104	1.00[CEU][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11637111	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11638198	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11638390	1.00[CEU][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12439248	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12440152	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17519466	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17519536	1.00[CEU][hapmap];0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17597852	1.00[CEU][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17597915	1.00[CEU][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17598061	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2414044	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2414045	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs34659874	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4380013	0.84[EUR][1000 genomes]
rs4774569	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4774570	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4774571	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4774572	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4775883	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4775884	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4775885	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4775886	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4775888	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4775889	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62016938	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62016939	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62016940	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62016942	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62016943	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62016944	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62016945	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62016947	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62019074	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62019075	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62019076	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62019077	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62019078	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62019079	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62019080	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62019082	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62019084	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62019085	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62019087	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62019112	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62019113	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62019115	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62019116	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62019117	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7165464	0.94[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7168783	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7169778	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7170114	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7181536	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7182569	1.00[CEU][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7182980	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7494907	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8030373	1.00[CEU][hapmap];0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8037553	0.93[CEU][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs934636	1.00[CEU][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045456	chr15:50592472-51019873	Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
2	nsv948579	chr15:50645530-51045564	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
3	nsv524613	chr15:50656449-50868779	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv904210	chr15:50702058-50786024	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	nsv1040717	chr15:50715572-50846521	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking 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	27 gene(s)	inside rSNPs	diseases
6	nsv1053966	chr15:50715572-51133186	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats 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	65 gene(s)	inside rSNPs	diseases
7	nsv542383	chr15:50715572-51133186	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
8	nsv1043805	chr15:50715572-51208891	Genic enhancers Enhancers Weak transcription Active TSS 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	82 gene(s)	inside rSNPs	diseases
9	nsv542384	chr15:50715572-51208891	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic 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	82 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	chr15:50717400-50747000	Weak transcription	Aorta	Aorta
2	chr15:50717600-50764600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:50717600-50774800	Weak transcription	Stomach Mucosa	stomach
4	chr15:50717800-50758800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr15:50718000-50755400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr15:50718000-50757000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr15:50722800-50764600	Weak transcription	Esophagus	oesophagus
8	chr15:50724600-50755800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr15:50724800-50764600	Weak transcription	Pancreas	Pancrea
10	chr15:50728200-50750200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr15:50730400-50744400	Strong transcription	Fetal Intestine Small	intestine
12	chr15:50730800-50754200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr15:50731000-50748800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr15:50731200-50748400	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr15:50731600-50748800	Strong transcription	Fetal Intestine Large	intestine
16	chr15:50732200-50749000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr15:50732800-50744600	Weak transcription	K562	blood
18	chr15:50733000-50747000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr15:50733400-50744400	Weak transcription	HSMMtube	muscle
20	chr15:50733400-50744800	Weak transcription	Fetal Kidney	kidney
21	chr15:50733400-50745000	Weak transcription	NHLF	lung
22	chr15:50733400-50747000	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr15:50733400-50747000	Weak transcription	Fetal Lung	lung
24	chr15:50733400-50747000	Weak transcription	Small Intestine	intestine
25	chr15:50733400-50747400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr15:50733400-50785200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr15:50733600-50758200	Weak transcription	HMEC	breast
28	chr15:50733600-50758800	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr15:50733800-50746800	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr15:50733800-50747000	Weak transcription	Rectal Smooth Muscle	rectum
31	chr15:50733800-50752800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr15:50733800-50755800	Weak transcription	Brain Cingulate Gyrus	brain
33	chr15:50734000-50746400	Weak transcription	Brain Angular Gyrus	brain
34	chr15:50734000-50747000	Weak transcription	Fetal Brain Female	brain
35	chr15:50734000-50763200	Weak transcription	Brain Anterior Caudate	brain
36	chr15:50734000-50776400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr15:50734000-50785600	Weak transcription	Fetal Brain Male	brain
38	chr15:50734600-50752800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr15:50734600-50772600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr15:50734800-50747200	Weak transcription	Brain Hippocampus Middle	brain
41	chr15:50734800-50748000	Weak transcription	Colonic Mucosa	Colon
42	chr15:50735400-50764600	Weak transcription	Psoas Muscle	Psoas
43	chr15:50735600-50746200	Weak transcription	Gastric	stomach
44	chr15:50735600-50746200	Weak transcription	Ovary	ovary
45	chr15:50735600-50773000	Weak transcription	Brain Substantia Nigra	brain
46	chr15:50736000-50746600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr15:50736200-50758600	Weak transcription	Right Ventricle	heart
48	chr15:50737200-50744600	Weak transcription	Primary hematopoietic stem cells	blood
49	chr15:50737200-50745800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr15:50737200-50746800	Weak transcription	Spleen	Spleen

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