Variant report

Variant	rs7956056
Chromosome Location	chr12:47428290-47428291
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:47426514..47428986-chr12:47432819..47435080,2	K562	blood:
2	chr12:47427484..47430448-chr12:47461043..47464291,4	MCF-7	breast:
3	chr12:47424715..47431022-chr12:47469878..47476557,9	MCF-7	breast:
4	chr12:47423549..47426668-chr12:47427215..47430937,3	K562	blood:

Variant related genes	Relation type
ENSG00000139211	Chromatin interaction
ENSG00000179715	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10736030	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10748457	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10748458	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10748460	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10785649	0.99[ASN][1000 genomes]
rs10785650	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10785653	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10881023	0.98[ASN][1000 genomes]
rs10881024	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10881026	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10881027	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10881029	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10881030	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10881031	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10881033	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1557781	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1859112	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2158133	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2214335	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2408711	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2711698	0.94[EUR][1000 genomes]
rs2711713	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7133990	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7136412	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7139043	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7311552	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs757149	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs757150	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7956758	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7958499	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7961460	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7976595	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7978006	0.98[ASN][1000 genomes]
rs7979771	0.99[ASN][1000 genomes]
rs8181633	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs886315	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs886317	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1845143	chr12:47051076-47431496	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv469368	chr12:47374908-47675680	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv558784	chr12:47374908-47675680	Genic enhancers Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:47418000-47428400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:47426200-47428800	Enhancers	Primary T helper cells PMA-I stimulated	--
3	chr12:47426600-47428400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr12:47426600-47428600	Enhancers	Muscle Satellite Cultured Cells	--
5	chr12:47426600-47428800	Enhancers	HSMMtube	muscle
6	chr12:47426600-47429000	Enhancers	HMEC	breast
7	chr12:47426600-47429000	Enhancers	HSMM	muscle
8	chr12:47426600-47429000	Enhancers	NH-A	brain
9	chr12:47426600-47429200	Enhancers	Colon Smooth Muscle	Colon
10	chr12:47426600-47429200	Flanking Active TSS	A549	lung
11	chr12:47426600-47429600	Enhancers	Hela-S3	cervix
12	chr12:47426600-47429800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr12:47426800-47428600	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr12:47426800-47428800	Enhancers	NHEK	skin
15	chr12:47426800-47429000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr12:47426800-47429000	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr12:47426800-47429000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr12:47426800-47429400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr12:47426800-47429400	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr12:47426800-47429400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr12:47426800-47429800	Enhancers	Placenta Amnion	Placenta Amnion
22	chr12:47427000-47429000	Enhancers	Ovary	ovary
23	chr12:47427000-47429400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:47427000-47429600	Enhancers	Fetal Intestine Large	intestine
25	chr12:47427200-47428400	Weak transcription	Fetal Kidney	kidney
26	chr12:47427200-47428400	Weak transcription	Pancreas	Pancrea
27	chr12:47427200-47428600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr12:47427200-47428600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr12:47427200-47429400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr12:47427400-47428800	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr12:47427400-47429000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr12:47427400-47429200	Enhancers	Fetal Intestine Small	intestine
33	chr12:47427600-47428800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr12:47427600-47429000	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr12:47427800-47428600	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr12:47427800-47428600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr12:47427800-47429200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr12:47427800-47431800	Weak transcription	Liver	Liver
39	chr12:47428000-47428600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr12:47428000-47428800	Enhancers	Stomach Smooth Muscle	stomach
41	chr12:47428200-47428600	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr12:47428200-47428800	Enhancers	Osteobl	bone
43	chr12:47428200-47429000	Enhancers	H9 Cell Line	embryonic stem cell

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