Variant report

Variant	rs7157314
Chromosome Location	chr14:64381040-64381041
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11158512	0.83[AMR][1000 genomes]
rs11158516	0.84[CEU][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12587472	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12588087	0.81[AMR][1000 genomes]
rs12894053	0.88[CEU][hapmap];0.86[CHB][hapmap];0.82[JPT][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12894864	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1959034	0.87[CEU][hapmap];0.81[JPT][hapmap];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1959035	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2210650	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2275018	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2357002	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2357003	0.95[CEU][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34780876	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4902247	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4902248	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6573534	0.81[AMR][1000 genomes]
rs6573535	0.80[CHB][hapmap]
rs7145302	0.82[CHB][hapmap]
rs7146821	0.87[CEU][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7149766	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7153101	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7157323	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7160127	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7493416	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8005899	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8015158	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8015354	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8022917	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs945030	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs951250	0.80[CHB][hapmap]
rs954730	0.84[CEU][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9707224	0.83[AMR][1000 genomes]
rs998241	0.84[CEU][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]

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	nsv915909	chr14:63620440-64560369	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv1038825	chr14:64109441-64491720	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv1037140	chr14:64248421-64442980	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv542119	chr14:64248421-64442980	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv564904	chr14:64346190-64416898	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	esv1793389	chr14:64346190-64457224	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64337800-64403800	Weak transcription	Thymus	Thymus
2	chr14:64360600-64382200	Weak transcription	Psoas Muscle	Psoas
3	chr14:64364400-64385200	Weak transcription	Pancreas	Pancrea
4	chr14:64364600-64387800	Weak transcription	HMEC	breast
5	chr14:64365000-64430200	Weak transcription	Fetal Brain Male	brain
6	chr14:64365200-64386200	Weak transcription	Gastric	stomach
7	chr14:64365400-64393600	Weak transcription	Right Ventricle	heart
8	chr14:64369800-64386200	Weak transcription	Esophagus	oesophagus
9	chr14:64374600-64399600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr14:64375200-64385000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr14:64375200-64395000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr14:64375200-64395200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr14:64375800-64384000	Weak transcription	Fetal Intestine Large	intestine
14	chr14:64375800-64384800	Weak transcription	Fetal Kidney	kidney
15	chr14:64375800-64386200	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr14:64375800-64388600	Weak transcription	Hela-S3	cervix
17	chr14:64375800-64389000	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr14:64375800-64393200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr14:64376000-64383400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr14:64376000-64385400	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr14:64376000-64386200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr14:64376000-64386200	Weak transcription	Left Ventricle	heart
23	chr14:64376000-64389000	Weak transcription	Adipose Nuclei	Adipose
24	chr14:64376000-64389600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr14:64376000-64389600	Weak transcription	Duodenum Mucosa	Duodenum
26	chr14:64376000-64389600	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr14:64376000-64391200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr14:64376000-64399200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr14:64376000-64399600	Weak transcription	Small Intestine	intestine
30	chr14:64376000-64399800	Weak transcription	Primary T cells from cord blood	blood
31	chr14:64376000-64416200	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr14:64376200-64399400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr14:64376400-64394000	Weak transcription	Lung	lung
34	chr14:64377600-64386200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr14:64377600-64388000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr14:64377600-64389400	Weak transcription	Fetal Intestine Small	intestine
37	chr14:64378000-64383600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr14:64378000-64384600	Weak transcription	Stomach Mucosa	stomach
39	chr14:64378000-64385200	Weak transcription	Ovary	ovary
40	chr14:64378000-64386000	Weak transcription	Fetal Stomach	stomach
41	chr14:64378000-64386200	Weak transcription	Fetal Muscle Leg	muscle
42	chr14:64378000-64389400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr14:64378000-64394800	Weak transcription	Fetal Heart	heart
44	chr14:64378000-64404800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr14:64378000-64416200	Weak transcription	Fetal Lung	lung
46	chr14:64378200-64385800	Weak transcription	Aorta	Aorta
47	chr14:64378200-64389200	Weak transcription	Brain Germinal Matrix	brain
48	chr14:64378400-64383200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr14:64378400-64416000	Weak transcription	Primary B cells from cord blood	blood
50	chr14:64378600-64383200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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