Variant report

Variant	rs186217864
Chromosome Location	chr11:71142472-71142473
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:71137647..71140040-chr11:71141812..71145984,4	K562	blood:
2	chr11:71138540..71142714-chr11:71144455..71147360,4	K562	blood:
3	chr11:71140807..71143299-chr11:71274419..71277304,2	MCF-7	breast:
4	chr11:71141203..71142816-chr11:71167410..71170126,2	K562	blood:
5	chr11:70982645..70985292-chr11:71142311..71143975,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000204572	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

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	nsv1048123	chr11:70795222-71231382	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
2	nsv526973	chr11:71088949-71215880	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
3	nsv897897	chr11:71088949-71217571	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
4	nsv530623	chr11:71088949-72020418	Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	134 gene(s)	inside rSNPs	diseases
5	nsv897898	chr11:71103143-71211654	Weak transcription ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
6	nsv519224	chr11:71108341-71215880	Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
7	nsv518163	chr11:71142350-71155153	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71132600-71144000	Weak transcription	Spleen	Spleen
2	chr11:71135000-71150600	Weak transcription	NH-A	brain
3	chr11:71135400-71145000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr11:71137000-71144800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:71137200-71144000	Weak transcription	Hela-S3	cervix
6	chr11:71137200-71145000	Weak transcription	Brain Germinal Matrix	brain
7	chr11:71137200-71149600	Weak transcription	Primary B cells from peripheral blood	blood
8	chr11:71137600-71146000	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr11:71138000-71144800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:71138000-71145200	Weak transcription	HMEC	breast
11	chr11:71139200-71145000	Weak transcription	GM12878-XiMat	blood
12	chr11:71139200-71145800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr11:71139400-71145000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr11:71139600-71145200	Enhancers	Ovary	ovary
15	chr11:71139800-71142800	Enhancers	HepG2	liver
16	chr11:71140000-71144000	Weak transcription	Fetal Brain Female	brain
17	chr11:71140400-71142600	Weak transcription	Fetal Intestine Small	intestine
18	chr11:71140400-71145000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr11:71140600-71143000	Weak transcription	Brain Anterior Caudate	brain
20	chr11:71140600-71143200	Weak transcription	Brain Cingulate Gyrus	brain
21	chr11:71140600-71144000	Weak transcription	Left Ventricle	heart
22	chr11:71140600-71144000	Weak transcription	Lung	lung
23	chr11:71140600-71144600	Weak transcription	Right Ventricle	heart
24	chr11:71140600-71158200	Weak transcription	Fetal Brain Male	brain
25	chr11:71140800-71143200	Weak transcription	Brain Angular Gyrus	brain
26	chr11:71140800-71143200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr11:71140800-71144000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr11:71140800-71144000	Weak transcription	Gastric	stomach
29	chr11:71140800-71144800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr11:71140800-71145800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr11:71140800-71154000	Weak transcription	Fetal Lung	lung
32	chr11:71140800-71154000	Weak transcription	HSMM	muscle
33	chr11:71141000-71143800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr11:71141000-71145800	Weak transcription	HSMMtube	muscle
35	chr11:71141200-71143800	Weak transcription	Stomach Mucosa	stomach
36	chr11:71141200-71148200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr11:71141600-71142800	Enhancers	Placenta	Placenta
38	chr11:71141600-71143000	Weak transcription	Adipose Nuclei	Adipose
39	chr11:71141600-71144600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr11:71141600-71144800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr11:71141600-71145000	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr11:71141600-71145200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr11:71141800-71144400	Weak transcription	Primary T cells from cord blood	blood
44	chr11:71141800-71144800	Weak transcription	Fetal Stomach	stomach
45	chr11:71141800-71145800	Enhancers	Liver	Liver
46	chr11:71142000-71144800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr11:71142200-71144200	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr11:71142400-71142600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr11:71142400-71142800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr11:71142400-71144800	Enhancers	Brain Inferior Temporal Lobe	brain

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