Variant report

Variant	rs557814460
Chromosome Location	chr11:63529937-63529938
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:63526116..63528464-chr11:63528882..63530638,2	K562	blood:
2	chr11:63527527..63531451-chr11:63579707..63582153,3	MCF-7	breast:
3	chr11:63522435..63525089-chr11:63529331..63531365,3	K562	blood:
4	chr11:63528210..63531118-chr11:63540362..63542813,2	MCF-7	breast:
5	chr11:63520245..63522926-chr11:63528476..63531329,2	MCF-7	breast:
6	chr11:63515783..63518081-chr11:63529282..63531993,2	K562	blood:
7	chr11:63438066..63440126-chr11:63528980..63530613,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000168005	Chromatin interaction
ENSG00000184743	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

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	nsv1051171	chr11:62987064-63835715	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer 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	100 gene(s)	inside rSNPs	diseases
2	nsv832183	chr11:63416678-63564565	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv468589	chr11:63515752-63713239	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv555180	chr11:63515752-63713239	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	esv3427424	chr11:63529176-63532974	Strong transcription Bivalent Enhancer Flanking Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv3401646	chr11:63529601-63532149	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63501800-63530000	Weak transcription	Psoas Muscle	Psoas
2	chr11:63509000-63534800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr11:63511000-63534800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr11:63516000-63534800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr11:63516400-63533400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr11:63516400-63534200	Weak transcription	Primary B cells from peripheral blood	blood
7	chr11:63516600-63533800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
8	chr11:63516800-63530000	Weak transcription	Esophagus	oesophagus
9	chr11:63517400-63530000	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr11:63518800-63530000	Weak transcription	Aorta	Aorta
11	chr11:63519400-63534800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr11:63520400-63533400	Weak transcription	GM12878-XiMat	blood
13	chr11:63521200-63534600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr11:63521400-63534400	Weak transcription	Primary B cells from cord blood	blood
15	chr11:63521400-63534800	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr11:63523400-63532600	Strong transcription	Fetal Thymus	thymus
17	chr11:63523400-63533600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr11:63523600-63533400	Strong transcription	Dnd41	blood
19	chr11:63523800-63530600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr11:63525000-63534400	Weak transcription	HSMMtube	muscle
21	chr11:63525400-63530200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr11:63525400-63532000	Weak transcription	Spleen	Spleen
23	chr11:63525600-63530000	Weak transcription	Lung	lung
24	chr11:63525600-63532200	Weak transcription	HepG2	liver
25	chr11:63525800-63534600	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr11:63526200-63534600	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr11:63526400-63530000	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr11:63526600-63530600	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr11:63526600-63534800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr11:63526600-63534800	Weak transcription	Small Intestine	intestine
31	chr11:63527400-63530200	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr11:63527400-63530200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr11:63527400-63530200	Strong transcription	Thymus	Thymus
34	chr11:63527600-63530000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr11:63527600-63533600	Weak transcription	Primary hematopoietic stem cells	blood
36	chr11:63527800-63530000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr11:63528000-63530200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr11:63528000-63530200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr11:63528000-63534200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr11:63528000-63534200	Weak transcription	Fetal Kidney	kidney
41	chr11:63528200-63532400	Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr11:63528400-63533800	Weak transcription	HMEC	breast
43	chr11:63528400-63534000	Weak transcription	HSMM	muscle
44	chr11:63528400-63534600	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr11:63528600-63530000	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:63528600-63530000	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr11:63528600-63530000	Weak transcription	Left Ventricle	heart
48	chr11:63528600-63532000	Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr11:63528600-63532400	Active TSS	HUES48 Cell Line	embryonic stem cell
50	chr11:63528600-63533000	Active TSS	iPS-20b Cell Line	embryonic stem cell

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