Variant report

Variant	rs12976812
Chromosome Location	chr19:36519347-36519348
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:36515922..36517591-chr19:36519314..36521673,2	K562	blood:
2	chr19:36518073..36521044-chr19:36525057..36527255,2	K562	blood:
3	chr19:36499646..36502624-chr19:36517798..36521500,4	MCF-7	breast:
4	chr19:36512890..36520143-chr19:36521963..36527491,9	K562	blood:
5	chr19:36518180..36521030-chr19:36528618..36530229,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000181392	Chromatin interaction
ENSG00000105270	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10407011	0.87[EUR][1000 genomes]
rs10414877	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10418015	0.95[JPT][hapmap]
rs10420353	0.89[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.86[YRI][hapmap];0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10421966	0.90[CEU][hapmap];0.88[CHB][hapmap];0.95[JPT][hapmap];0.87[YRI][hapmap];0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10423651	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10425692	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10426582	1.00[CHB][hapmap];0.90[JPT][hapmap];0.95[ASN][1000 genomes]
rs12462432	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12462632	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12462674	0.90[CEU][hapmap];0.81[CHB][hapmap];0.87[YRI][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12972490	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12976505	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12977814	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12978482	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12979093	0.95[ASN][1000 genomes]
rs12981654	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17639286	0.89[CEU][hapmap];0.96[EUR][1000 genomes]
rs2023865	0.90[CEU][hapmap];0.86[CHB][hapmap];0.87[YRI][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2239510	0.85[CEU][hapmap];0.91[YRI][hapmap];0.87[EUR][1000 genomes]
rs34906485	0.87[ASN][1000 genomes]
rs35125548	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35875194	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3826995	0.90[CEU][hapmap];0.86[CHB][hapmap];0.87[YRI][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4461192	0.86[CHB][hapmap];0.90[YRI][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4805154	1.00[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs4805155	0.95[ASN][1000 genomes]
rs4806252	0.98[ASN][1000 genomes]
rs4806253	0.96[ASN][1000 genomes]
rs71337524	0.87[AFR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs721542	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7245762	0.86[CHB][hapmap]
rs7247057	0.95[JPT][hapmap]
rs7250448	1.00[CHB][hapmap];0.90[JPT][hapmap];0.93[ASN][1000 genomes]
rs7257383	0.86[CHB][hapmap]
rs7259592	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7260609	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs8103569	0.90[CEU][hapmap];0.86[CHB][hapmap];0.87[YRI][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432045	chr19:35556260-36520760	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv911638	chr19:36265508-36537959	Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	esv3526489	chr19:36306483-36741945	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh 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	114 gene(s)	inside rSNPs	diseases
4	esv3526490	chr19:36306483-36741945	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
5	esv1831737	chr19:36324324-36690874	Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
6	nsv911641	chr19:36473677-36536938	Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Weak transcription Genic enhancers Enhancers 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	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36505600-36521000	Weak transcription	Fetal Brain Male	brain
2	chr19:36505800-36522000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr19:36505800-36522200	Weak transcription	Fetal Kidney	kidney
4	chr19:36505800-36522800	Weak transcription	Small Intestine	intestine
5	chr19:36506000-36522400	Weak transcription	NH-A	brain
6	chr19:36506000-36522800	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr19:36506000-36523000	Weak transcription	HSMM	muscle
8	chr19:36506000-36523200	Weak transcription	Left Ventricle	heart
9	chr19:36506000-36523600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr19:36506200-36519400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr19:36506200-36519400	Strong transcription	Fetal Brain Female	brain
12	chr19:36506200-36522400	Strong transcription	Fetal Stomach	stomach
13	chr19:36506200-36522800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr19:36506200-36523000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr19:36506200-36523200	Weak transcription	HUVEC	blood vessel
16	chr19:36506200-36523400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr19:36506200-36523400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr19:36506400-36519600	Strong transcription	Fetal Muscle Leg	muscle
19	chr19:36506400-36519800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr19:36506400-36519800	Strong transcription	Stomach Smooth Muscle	stomach
21	chr19:36506400-36520400	Strong transcription	Brain Germinal Matrix	brain
22	chr19:36506400-36521600	Strong transcription	Cortex derived primary cultured neurospheres	brain
23	chr19:36506400-36521800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr19:36506400-36523000	Weak transcription	Primary hematopoietic stem cells	blood
25	chr19:36506400-36544400	Weak transcription	GM12878-XiMat	blood
26	chr19:36506600-36519600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr19:36506800-36519800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr19:36506800-36532400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr19:36507000-36532200	Weak transcription	Hela-S3	cervix
30	chr19:36507600-36521800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr19:36507800-36519800	Strong transcription	Fetal Intestine Small	intestine
32	chr19:36508800-36519800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr19:36508800-36532400	Weak transcription	NHEK	skin
34	chr19:36511400-36519600	Strong transcription	Brain Angular Gyrus	brain
35	chr19:36511400-36519600	Strong transcription	Brain Inferior Temporal Lobe	brain
36	chr19:36511400-36519600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr19:36511400-36519800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr19:36511400-36519800	Strong transcription	Fetal Muscle Trunk	muscle
39	chr19:36511400-36521800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr19:36511800-36519600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr19:36511800-36519800	Strong transcription	Ovary	ovary
42	chr19:36512200-36519600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr19:36513000-36519800	Strong transcription	Muscle Satellite Cultured Cells	--
44	chr19:36513400-36523600	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr19:36513600-36523000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr19:36513600-36525600	Weak transcription	K562	blood
47	chr19:36514400-36522400	Weak transcription	Liver	Liver
48	chr19:36514400-36523200	Weak transcription	Primary B cells from peripheral blood	blood
49	chr19:36514600-36519800	Strong transcription	Aorta	Aorta
50	chr19:36514600-36519800	Strong transcription	NHLF	lung

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