Variant report

Variant	rs10437691
Chromosome Location	chr11:120323022-120323023
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:120322636..120325614-chr11:120329269..120331112,2	K562	blood:
2	chr11:120205411..120207219-chr11:120322379..120324809,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000269601	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10466597	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11217780	1.00[AMR][1000 genomes]
rs11217784	1.00[AMR][1000 genomes]
rs11217894	1.00[AMR][1000 genomes]
rs12272851	1.00[AMR][1000 genomes]
rs12273736	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12278707	1.00[AMR][1000 genomes]
rs12279381	1.00[AMR][1000 genomes]
rs12280403	1.00[AMR][1000 genomes]
rs12281995	1.00[YRI][hapmap]
rs12283229	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12285146	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12286309	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs12288495	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12288854	1.00[AMR][1000 genomes]
rs12288900	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12290756	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12291269	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12294024	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12294303	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17123749	1.00[AMR][1000 genomes]
rs28739499	1.00[AMR][1000 genomes]
rs7943655	1.00[AMR][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	nsv1054057	chr11:119781953-120519770	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv541178	chr11:119781953-120519770	Weak transcription Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv529003	chr11:120209386-120355230	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120301400-120355200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:120303600-120355600	Weak transcription	Stomach Mucosa	stomach
3	chr11:120303800-120328000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr11:120304400-120323200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr11:120304600-120329800	Strong transcription	HSMM	muscle
6	chr11:120304800-120359400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr11:120306600-120341200	Strong transcription	Osteobl	bone
8	chr11:120306800-120341600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:120307000-120335800	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr11:120307000-120341200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr11:120307600-120334600	Strong transcription	Skeletal Muscle Female	skeletal muscle
12	chr11:120308000-120341800	Strong transcription	Fetal Intestine Large	intestine
13	chr11:120308000-120352600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr11:120308000-120359000	Strong transcription	Placenta	Placenta
15	chr11:120308200-120330600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr11:120308200-120336400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr11:120308400-120333200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr11:120308400-120334600	Strong transcription	Rectal Mucosa Donor 31	rectum
19	chr11:120308400-120339000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr11:120308400-120339000	Strong transcription	Muscle Satellite Cultured Cells	--
21	chr11:120308400-120357800	Strong transcription	Adipose Nuclei	Adipose
22	chr11:120309800-120333800	Strong transcription	HUES64 Cell Line	embryonic stem cell
23	chr11:120310000-120336000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr11:120310200-120350600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:120310400-120358000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr11:120310800-120333800	Strong transcription	HUES48 Cell Line	embryonic stem cell
27	chr11:120311200-120357200	Strong transcription	Duodenum Smooth Muscle	Duodenum
28	chr11:120312000-120328800	Strong transcription	Fetal Muscle Trunk	muscle
29	chr11:120312000-120333800	Strong transcription	Skeletal Muscle Male	skeletal muscle
30	chr11:120312200-120323600	Strong transcription	Fetal Lung	lung
31	chr11:120312200-120333000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr11:120312200-120339000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr11:120312400-120326800	Strong transcription	HSMMtube	muscle
34	chr11:120312400-120328400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr11:120312400-120329800	Strong transcription	Rectal Mucosa Donor 29	rectum
36	chr11:120312400-120341800	Strong transcription	Fetal Muscle Leg	muscle
37	chr11:120312400-120351800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr11:120312400-120354000	Strong transcription	Duodenum Mucosa	Duodenum
39	chr11:120312800-120334000	Strong transcription	Stomach Smooth Muscle	stomach
40	chr11:120312800-120357800	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr11:120313000-120325800	Strong transcription	Colon Smooth Muscle	Colon
42	chr11:120314200-120362200	Strong transcription	Liver	Liver
43	chr11:120314800-120342000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr11:120315000-120323600	Strong transcription	NH-A	brain
45	chr11:120315200-120353000	Strong transcription	Fetal Brain Female	brain
46	chr11:120315400-120329000	Strong transcription	Brain Cingulate Gyrus	brain
47	chr11:120315400-120342400	Strong transcription	HUES6 Cell Line	embryonic stem cell
48	chr11:120315600-120328400	Strong transcription	Brain Germinal Matrix	brain
49	chr11:120315800-120325600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr11:120315800-120325600	Strong transcription	Sigmoid Colon	Sigmoid Colon

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