Variant report

Variant	rs11704156
Chromosome Location	chr22:31796563-31796564
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:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:31686527..31689345-chr22:31795585..31798136,2	MCF-7	breast:
2	chr22:31686029..31689751-chr22:31793811..31797004,3	K562	blood:
3	chr22:31739411..31743940-chr22:31792561..31797746,12	K562	blood:
4	chr22:31685604..31688964-chr22:31794244..31796594,4	MCF-7	breast:
5	chr22:31784063..31789675-chr22:31793262..31796684,7	MCF-7	breast:
6	chr22:31793990..31796986-chr22:31884678..31887767,3	K562	blood:
7	chr22:31738670..31747056-chr22:31790500..31799012,36	MCF-7	breast:
8	chr22:31737798..31746418-chr22:31793074..31801662,34	MCF-7	breast:
9	chr22:31795193..31796801-chr22:32026385..32029380,2	MCF-7	breast:
10	chr22:31795756..31797975-chr6:82164220..82166358,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000206615	Chromatin interaction
ENSG00000100105	Chromatin interaction
ENSG00000100100	Chromatin interaction
ENSG00000241878	Chromatin interaction
ENSG00000213888	Chromatin interaction
ENSG00000184708	Chromatin interaction
ENSG00000228839	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11089495	1.00[CHD][hapmap];0.81[MEX][hapmap]
rs11556237	0.86[MEX][hapmap]
rs11703005	1.00[CHD][hapmap];0.86[MEX][hapmap]
rs11703847	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs11704523	1.00[CHD][hapmap];0.86[MEX][hapmap]
rs16989291	1.00[GIH][hapmap];0.92[MEX][hapmap];0.82[TSI][hapmap]
rs16989459	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.82[EUR][1000 genomes]
rs2413054	1.00[GIH][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap]
rs3091392	0.86[MEX][hapmap]
rs4820972	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55661998	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5749277	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5753682	1.00[GIH][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap]
rs5997917	1.00[CHD][hapmap];0.81[MEX][hapmap]
rs5997937	1.00[CHD][hapmap];0.81[MEX][hapmap]
rs5997942	1.00[CHD][hapmap];0.81[MEX][hapmap]
rs5998023	0.81[AMR][1000 genomes]
rs60389972	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs695413	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs695455	0.86[MEX][hapmap]
rs695582	0.94[AMR][1000 genomes]
rs7287715	1.00[CHD][hapmap];0.86[MEX][hapmap]
rs73158543	0.82[EUR][1000 genomes]
rs73158567	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73158578	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73158585	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73158592	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73160605	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73160624	0.83[ASN][1000 genomes]
rs738658	0.86[MEX][hapmap]
rs8136792	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8143159	1.00[CHD][hapmap];0.86[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834176	chr22:31682426-31864701	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
2	esv1816779	chr22:31743711-31797094	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:31794800-31796800	Active TSS	H1 Cell Line	embryonic stem cell
2	chr22:31794800-31796800	Active TSS	HUES48 Cell Line	embryonic stem cell
3	chr22:31794800-31797000	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr22:31794800-31797000	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr22:31794800-31797000	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr22:31794800-31797000	Active TSS	GM12878-XiMat	blood
7	chr22:31794800-31797000	Active TSS	K562	blood
8	chr22:31795000-31796600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr22:31795000-31796600	Active TSS	Esophagus	oesophagus
10	chr22:31795000-31796600	Active TSS	Fetal Muscle Trunk	muscle
11	chr22:31795000-31796600	Active TSS	Left Ventricle	heart
12	chr22:31795000-31796600	Active TSS	Ovary	ovary
13	chr22:31795000-31796600	Active TSS	Pancreas	Pancrea
14	chr22:31795000-31796600	Active TSS	Psoas Muscle	Psoas
15	chr22:31795000-31796600	Active TSS	Right Atrium	heart
16	chr22:31795000-31796600	Active TSS	Sigmoid Colon	Sigmoid Colon
17	chr22:31795000-31796800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr22:31795000-31796800	Active TSS	H9 Cell Line	embryonic stem cell
19	chr22:31795000-31796800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr22:31795000-31796800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
21	chr22:31795000-31796800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr22:31795000-31796800	Flanking Active TSS	Primary hematopoietic stem cells	blood
23	chr22:31795000-31796800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr22:31795000-31796800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr22:31795000-31796800	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr22:31795000-31796800	Active TSS	Lung	lung
27	chr22:31795000-31796800	Active TSS	Small Intestine	intestine
28	chr22:31795000-31796800	Active TSS	A549	lung
29	chr22:31795000-31797000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr22:31795000-31797000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr22:31795000-31797000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr22:31795000-31797000	Active TSS	Right Ventricle	heart
33	chr22:31795000-31797000	Active TSS	Hela-S3	cervix
34	chr22:31795000-31797000	Active TSS	HSMM	muscle
35	chr22:31795000-31797000	Active TSS	HSMMtube	muscle
36	chr22:31795000-31797000	Active TSS	NHDF-Ad	bronchial
37	chr22:31795000-31797000	Active TSS	NHLF	lung
38	chr22:31795200-31796600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
39	chr22:31795200-31796600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr22:31795200-31796600	ZNF genes & repeats	Fetal Brain Male	brain
41	chr22:31795200-31796800	Active TSS	iPS-15b Cell Line	embryonic stem cell
42	chr22:31795200-31796800	Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr22:31795200-31796800	Active TSS	Gastric	stomach
44	chr22:31795200-31797000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr22:31795200-31797000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr22:31795400-31796600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr22:31795400-31796800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr22:31795400-31797000	Active TSS	HMEC	breast
49	chr22:31795600-31796600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
50	chr22:31795800-31796600	Flanking Active TSS	Primary B cells from cord blood	blood

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