Variant report

Variant	rs11604864
Chromosome Location	chr11:75055107-75055108
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:75052872..75055185-chr11:75109817..75111998,3	K562	blood:
2	chr11:75053704..75056779-chr11:75098443..75101386,3	MCF-7	breast:
3	chr11:75040463..75042023-chr11:75053067..75055611,2	MCF-7	breast:
4	chr11:75053225..75057197-chr11:75082707..75085103,4	MCF-7	breast:
5	chr11:75018656..75020776-chr11:75054796..75056696,2	K562	blood:
6	chr11:75052872..75055185-chr11:75110340..75111998,2	K562	blood:
7	chr11:74995398..74998082-chr11:75052769..75055576,2	MCF-7	breast:
8	chr11:75047858..75058236-chr11:75058819..75065197,25	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000206941	Chromatin interaction
ENSG00000149273	Chromatin interaction
ENSG00000137486	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11236405	1.00[ASN][1000 genomes]
rs11236416	1.00[ASN][1000 genomes]
rs11602383	1.00[ASN][1000 genomes]
rs11605734	1.00[ASN][1000 genomes]
rs12270766	1.00[ASN][1000 genomes]
rs12271945	1.00[ASN][1000 genomes]
rs12283536	1.00[ASN][1000 genomes]
rs12291595	1.00[ASN][1000 genomes]
rs12790302	1.00[ASN][1000 genomes]
rs12794577	1.00[ASN][1000 genomes]
rs34775308	1.00[ASN][1000 genomes]
rs34990111	1.00[ASN][1000 genomes]
rs35242615	1.00[ASN][1000 genomes]
rs35257045	1.00[ASN][1000 genomes]
rs36089315	1.00[ASN][1000 genomes]
rs56386203	1.00[ASN][1000 genomes]
rs67965584	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7101921	1.00[ASN][1000 genomes]
rs7116977	1.00[ASN][1000 genomes]
rs7120396	1.00[ASN][1000 genomes]
rs7131065	1.00[ASN][1000 genomes]
rs73004237	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036292	chr11:74937977-75059496	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
2	nsv1041640	chr11:74945824-75174688	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	94 gene(s)	inside rSNPs	diseases
3	nsv832211	chr11:74945839-75106125	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
4	nsv522447	chr11:74982939-75068767	Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	57 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75039400-75060800	Enhancers	Placenta	Placenta
2	chr11:75044200-75055400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr11:75044200-75055600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr11:75044200-75055800	Enhancers	Brain Hippocampus Middle	brain
5	chr11:75044200-75056600	Enhancers	Esophagus	oesophagus
6	chr11:75044200-75056800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
7	chr11:75044200-75060400	Genic enhancers	Fetal Stomach	stomach
8	chr11:75044400-75055200	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr11:75044400-75056400	Enhancers	Placenta Amnion	Placenta Amnion
10	chr11:75044400-75057200	Enhancers	Fetal Muscle Trunk	muscle
11	chr11:75046400-75061200	Enhancers	Fetal Thymus	thymus
12	chr11:75046800-75060200	Enhancers	Brain Anterior Caudate	brain
13	chr11:75046800-75061600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr11:75047000-75059600	Enhancers	Pancreas	Pancrea
15	chr11:75047000-75061200	Enhancers	Left Ventricle	heart
16	chr11:75047000-75061200	Enhancers	Stomach Mucosa	stomach
17	chr11:75047200-75060400	Enhancers	Brain Angular Gyrus	brain
18	chr11:75047400-75055400	Enhancers	Fetal Intestine Large	intestine
19	chr11:75047600-75056000	Enhancers	Fetal Muscle Leg	muscle
20	chr11:75047600-75060600	Enhancers	Right Atrium	heart
21	chr11:75047800-75060600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr11:75047800-75060800	Genic enhancers	Fetal Intestine Small	intestine
23	chr11:75048000-75055600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr11:75048000-75055800	Enhancers	Lung	lung
25	chr11:75048000-75058200	Enhancers	Primary B cells from cord blood	blood
26	chr11:75048000-75061600	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr11:75048400-75061000	Enhancers	Liver	Liver
28	chr11:75048600-75058400	Enhancers	Small Intestine	intestine
29	chr11:75049000-75056000	Enhancers	Ovary	ovary
30	chr11:75049200-75055400	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr11:75049400-75055800	Enhancers	Fetal Brain Female	brain
32	chr11:75049800-75056600	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr11:75050400-75056200	Enhancers	NHLF	lung
34	chr11:75050400-75057600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr11:75050600-75056200	Enhancers	NHDF-Ad	bronchial
36	chr11:75050800-75059200	Enhancers	Fetal Lung	lung
37	chr11:75051000-75056400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr11:75051000-75057600	Enhancers	H1 Cell Line	embryonic stem cell
39	chr11:75051400-75056000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr11:75051600-75055200	Enhancers	Colon Smooth Muscle	Colon
41	chr11:75051600-75056000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr11:75051600-75058800	Enhancers	Fetal Brain Male	brain
43	chr11:75051600-75060400	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr11:75051800-75060600	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr11:75052000-75055600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr11:75052000-75056000	Enhancers	HUVEC	blood vessel
47	chr11:75052000-75058000	Weak transcription	Psoas Muscle	Psoas
48	chr11:75052000-75058200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr11:75052200-75055400	Weak transcription	Thymus	Thymus
50	chr11:75052200-75055600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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