Variant report

Variant	rs61583185
Chromosome Location	chr12:65051859-65051860
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RUNX3	chr12:65051664-65052010	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:65047034..65048625-chr12:65050187..65053133,2	K562	blood:
2	chr12:64989952..64991972-chr12:65050682..65053342,2	K562	blood:
3	chr12:65029173..65030793-chr12:65051618..65053248,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000256314	TF binding region

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs55655091	1.00[AFR][1000 genomes]
rs55837927	1.00[AFR][1000 genomes]
rs56210002	1.00[AFR][1000 genomes]
rs56361026	0.95[AFR][1000 genomes]
rs57591736	0.91[AFR][1000 genomes]
rs57892940	0.91[AFR][1000 genomes]
rs58815475	1.00[AFR][1000 genomes]
rs60504329	1.00[AFR][1000 genomes]
rs60961957	0.84[AFR][1000 genomes]
rs61043338	0.91[AFR][1000 genomes]
rs61603142	1.00[AFR][1000 genomes]
rs61611512	1.00[AFR][1000 genomes]
rs73319681	0.91[AFR][1000 genomes]
rs73319695	0.91[AFR][1000 genomes]
rs73319699	1.00[AFR][1000 genomes]
rs73321717	1.00[AFR][1000 genomes]
rs73321729	1.00[AFR][1000 genomes]
rs73321732	1.00[AFR][1000 genomes]
rs73321736	1.00[AFR][1000 genomes]
rs73321741	1.00[AFR][1000 genomes]
rs73321744	1.00[AFR][1000 genomes]
rs73321748	1.00[AFR][1000 genomes]
rs73321754	1.00[AFR][1000 genomes]
rs73321759	1.00[AFR][1000 genomes]
rs73321764	1.00[AFR][1000 genomes]
rs73321766	1.00[AFR][1000 genomes]
rs73321767	1.00[AFR][1000 genomes]
rs73321779	1.00[AFR][1000 genomes]
rs74100723	1.00[AFR][1000 genomes]
rs74100755	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832443	chr12:64878856-65057265	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv832444	chr12:64981484-65168472	Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv559203	chr12:65002969-65199922	Genic enhancers Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv1045216	chr12:65009102-65176894	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv541513	chr12:65009102-65176894	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	nsv469457	chr12:65009243-65195977	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv559204	chr12:65009243-65195977	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:65025000-65059600	Weak transcription	Thymus	Thymus
2	chr12:65028600-65056400	Weak transcription	NHEK	skin
3	chr12:65033000-65052600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr12:65033600-65059400	Weak transcription	Primary hematopoietic stem cells	blood
5	chr12:65041600-65052200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr12:65043600-65059600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
7	chr12:65044000-65059400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr12:65045600-65054600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr12:65045800-65056400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr12:65046400-65058600	Weak transcription	Ovary	ovary
11	chr12:65047000-65056400	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr12:65047000-65059400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr12:65047200-65059400	Weak transcription	Fetal Stomach	stomach
14	chr12:65047400-65059400	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr12:65047800-65052600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr12:65047800-65056000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr12:65047800-65056400	Weak transcription	Hela-S3	cervix
18	chr12:65047800-65056600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr12:65047800-65059400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:65047800-65059400	Weak transcription	NHLF	lung
21	chr12:65047800-65063000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr12:65048000-65052400	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr12:65048000-65060400	Weak transcription	Dnd41	blood
24	chr12:65048000-65063000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr12:65048400-65062200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr12:65048600-65053400	Enhancers	HepG2	liver
27	chr12:65048600-65054600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr12:65048600-65059400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr12:65048800-65060200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr12:65049000-65052000	Weak transcription	Adipose Nuclei	Adipose
31	chr12:65049000-65059600	Enhancers	Primary T cells fromperipheralblood	blood
32	chr12:65049200-65052600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr12:65049200-65053600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr12:65049200-65058800	Weak transcription	K562	blood
35	chr12:65049200-65062200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr12:65049400-65052800	Weak transcription	Fetal Intestine Large	intestine
37	chr12:65049400-65055800	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr12:65049400-65059000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr12:65049800-65059600	Weak transcription	Placenta	Placenta
40	chr12:65050000-65053200	Genic enhancers	Primary B cells from peripheral blood	blood
41	chr12:65050000-65053200	Enhancers	Stomach Mucosa	stomach
42	chr12:65050000-65053400	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr12:65050000-65053600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr12:65050200-65052600	Weak transcription	Small Intestine	intestine
45	chr12:65050200-65053000	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
46	chr12:65050400-65052200	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr12:65050400-65052800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
48	chr12:65050400-65052800	Weak transcription	HUVEC	blood vessel
49	chr12:65050400-65059400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr12:65050400-65059400	Weak transcription	NH-A	brain

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