Variant report

Variant	rs56132728
Chromosome Location	chr11:107717908-107717909
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:107715556..107718513-chr11:107720703..107722662,2	K562	blood:
2	chr11:107716345..107718524-chr11:107728424..107730206,2	K562	blood:
3	chr11:107717688..107720633-chr11:107727875..107730541,3	MCF-7	breast:
4	chr11:107711394..107713234-chr11:107715059..107718295,3	K562	blood:
5	chr11:107716345..107719089-chr11:107728424..107730844,2	K562	blood:

Variant related genes	Relation type
ENSG00000110660	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10890771	0.94[AFR][1000 genomes]
rs11212463	1.00[EUR][1000 genomes]
rs12274618	0.91[AFR][1000 genomes]
rs12282665	0.98[AFR][1000 genomes]
rs12289394	1.00[EUR][1000 genomes]
rs12296042	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1242711	1.00[EUR][1000 genomes]
rs17107554	1.00[EUR][1000 genomes]
rs28414916	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4028256	1.00[EUR][1000 genomes]
rs471794	1.00[EUR][1000 genomes]
rs507416	1.00[EUR][1000 genomes]
rs515624	1.00[EUR][1000 genomes]
rs59048491	1.00[EUR][1000 genomes]
rs600815	1.00[EUR][1000 genomes]
rs61473755	1.00[EUR][1000 genomes]
rs73546814	1.00[EUR][1000 genomes]
rs73546826	1.00[EUR][1000 genomes]
rs73555308	1.00[EUR][1000 genomes]
rs73555311	1.00[EUR][1000 genomes]
rs73555346	1.00[EUR][1000 genomes]
rs73555364	1.00[EUR][1000 genomes]
rs73555373	1.00[EUR][1000 genomes]
rs73555376	1.00[EUR][1000 genomes]
rs73555378	1.00[EUR][1000 genomes]
rs9804577	1.00[EUR][1000 genomes]
rs9804666	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533794	chr11:107349817-108093259	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv1039425	chr11:107468681-107895836	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv427899	chr11:107471544-107805894	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv1049524	chr11:107540937-107954011	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS 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	22 gene(s)	inside rSNPs	diseases
5	nsv1038581	chr11:107564274-107838386	Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	12 gene(s)	inside rSNPs	diseases
6	nsv898378	chr11:107580985-107847983	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv521771	chr11:107590335-107904646	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	18 gene(s)	inside rSNPs	diseases
8	nsv1048938	chr11:107604473-107929950	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	18 gene(s)	inside rSNPs	diseases
9	nsv1052829	chr11:107686808-107725297	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv1045388	chr11:107686808-107733498	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
11	esv3417743	chr11:107699670-107725103	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107673400-107727800	Weak transcription	Primary B cells from cord blood	blood
2	chr11:107705200-107718600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr11:107711600-107719400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:107711600-107720600	Weak transcription	Pancreas	Pancrea
5	chr11:107711800-107719200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr11:107711800-107722400	Weak transcription	Duodenum Mucosa	Duodenum
7	chr11:107712000-107718400	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr11:107712000-107719200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr11:107712000-107719200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr11:107712000-107720600	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr11:107712200-107720800	Weak transcription	Esophagus	oesophagus
12	chr11:107712200-107723000	Weak transcription	HSMM	muscle
13	chr11:107712200-107728400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr11:107712400-107718400	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr11:107712400-107720800	Weak transcription	Primary hematopoietic stem cells	blood
16	chr11:107712400-107727200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr11:107712400-107727800	Weak transcription	Primary B cells from peripheral blood	blood
18	chr11:107712400-107728000	Weak transcription	NHDF-Ad	bronchial
19	chr11:107712600-107718000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr11:107712600-107723600	Weak transcription	K562	blood
21	chr11:107712600-107727000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr11:107712600-107727000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr11:107712600-107728200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr11:107712600-107728600	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr11:107712800-107720400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr11:107712800-107720400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr11:107712800-107727000	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr11:107713000-107728400	Weak transcription	Fetal Intestine Small	intestine
29	chr11:107713400-107727200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr11:107713600-107725000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr11:107713800-107718400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr11:107714000-107719000	Weak transcription	A549	lung
33	chr11:107715000-107719800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr11:107715000-107725400	Weak transcription	HUVEC	blood vessel
35	chr11:107715000-107727800	Weak transcription	HMEC	breast
36	chr11:107715200-107719200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr11:107715200-107719200	Weak transcription	Hela-S3	cervix
38	chr11:107716200-107719200	Weak transcription	Placenta	Placenta
39	chr11:107716200-107719400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr11:107716400-107718200	Weak transcription	NHEK	skin
41	chr11:107716600-107727600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr11:107717800-107718600	Weak transcription	Small Intestine	intestine
43	chr11:107717800-107718600	Enhancers	GM12878-XiMat	blood
44	chr11:107717800-107719600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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