Variant report

Variant	rs7152445
Chromosome Location	chr14:68313198-68313199
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 114 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:111)

rs_ID	r²[population]
rs10130605	0.84[EUR][1000 genomes]
rs10130837	0.84[EUR][1000 genomes]
rs10133485	0.84[EUR][1000 genomes]
rs10133652	0.84[EUR][1000 genomes]
rs10134988	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10135925	0.84[EUR][1000 genomes]
rs10137712	0.84[EUR][1000 genomes]
rs10142687	0.92[EUR][1000 genomes]
rs10142929	0.92[EUR][1000 genomes]
rs10144128	0.84[EUR][1000 genomes]
rs10145884	0.84[EUR][1000 genomes]
rs10146766	0.84[EUR][1000 genomes]
rs10146831	0.84[EUR][1000 genomes]
rs10148893	0.84[EUR][1000 genomes]
rs10150330	0.84[EUR][1000 genomes]
rs10450891	0.84[EUR][1000 genomes]
rs10467819	0.84[EUR][1000 genomes]
rs1073025	0.84[EUR][1000 genomes]
rs1073026	0.84[EUR][1000 genomes]
rs1118397	0.84[EUR][1000 genomes]
rs17104663	0.92[ASN][1000 genomes]
rs17104681	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17104689	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17104700	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17104758	0.84[EUR][1000 genomes]
rs17104774	0.84[EUR][1000 genomes]
rs17104783	0.84[EUR][1000 genomes]
rs17104786	0.84[EUR][1000 genomes]
rs17104793	0.84[EUR][1000 genomes]
rs17104796	0.84[EUR][1000 genomes]
rs17104799	0.84[EUR][1000 genomes]
rs17783202	0.84[EUR][1000 genomes]
rs2180537	0.84[EUR][1000 genomes]
rs28396172	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28405326	0.84[EUR][1000 genomes]
rs28434770	0.84[EUR][1000 genomes]
rs28444090	0.84[EUR][1000 genomes]
rs28473357	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28516665	0.84[EUR][1000 genomes]
rs28697984	0.85[ASN][1000 genomes]
rs28701947	0.84[EUR][1000 genomes]
rs28751961	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28757308	0.84[EUR][1000 genomes]
rs28816808	0.84[EUR][1000 genomes]
rs28833913	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28835585	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28847917	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28896907	0.84[EUR][1000 genomes]
rs34663731	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34700596	0.84[EUR][1000 genomes]
rs34768780	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34787467	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34935709	0.82[EUR][1000 genomes]
rs35588855	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35608268	1.00[EUR][1000 genomes]
rs35927243	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3742884	0.92[ASN][1000 genomes]
rs4899226	0.92[EUR][1000 genomes]
rs4899228	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4899229	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4902523	0.92[EUR][1000 genomes]
rs4902525	0.96[ASN][1000 genomes]
rs4902529	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4902530	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4902531	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4902532	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4902534	0.84[EUR][1000 genomes]
rs4902537	0.84[EUR][1000 genomes]
rs4902541	0.84[EUR][1000 genomes]
rs4902543	0.84[EUR][1000 genomes]
rs58159602	0.92[ASN][1000 genomes]
rs60014063	0.84[EUR][1000 genomes]
rs6573802	0.84[EUR][1000 genomes]
rs7140987	0.84[EUR][1000 genomes]
rs7141203	0.90[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7143377	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7143521	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7147296	0.84[EUR][1000 genomes]
rs7149122	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7149351	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7149356	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7149360	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7149460	0.84[EUR][1000 genomes]
rs7149796	0.92[EUR][1000 genomes]
rs7150467	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7150860	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7151035	0.92[EUR][1000 genomes]
rs7152727	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7153470	0.84[EUR][1000 genomes]
rs7156492	0.92[ASN][1000 genomes]
rs7159786	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8003181	0.84[EUR][1000 genomes]
rs8006175	0.84[EUR][1000 genomes]
rs8007989	0.92[EUR][1000 genomes]
rs8008791	0.84[EUR][1000 genomes]
rs8012665	0.92[ASN][1000 genomes]
rs8014844	0.84[EUR][1000 genomes]
rs8015520	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8015595	0.92[EUR][1000 genomes]
rs8015741	0.84[EUR][1000 genomes]
rs8016246	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8016563	0.84[EUR][1000 genomes]
rs8017718	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8017930	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8018883	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8019420	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8020512	0.84[EUR][1000 genomes]
rs9652362	0.84[EUR][1000 genomes]
rs9652364	0.84[EUR][1000 genomes]
rs9788517	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9796374	0.84[EUR][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	nsv1042536	chr14:68136913-68343198	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv542122	chr14:68136913-68343198	Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv1054697	chr14:68202004-68345982	Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:68287400-68315200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr14:68287600-68317800	Weak transcription	Spleen	Spleen
3	chr14:68287800-68318200	Weak transcription	Duodenum Mucosa	Duodenum
4	chr14:68294200-68315000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr14:68294200-68316600	Weak transcription	Placenta	Placenta
6	chr14:68294600-68318200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr14:68300600-68336200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr14:68303000-68315000	Weak transcription	Primary B cells from peripheral blood	blood
9	chr14:68303200-68315000	Weak transcription	Primary B cells from cord blood	blood
10	chr14:68303200-68318200	Weak transcription	Ovary	ovary
11	chr14:68303200-68331800	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr14:68311000-68316000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr14:68311400-68325800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr14:68312000-68313400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr14:68312000-68313800	ZNF genes & repeats	Fetal Intestine Small	intestine
16	chr14:68312000-68313800	ZNF genes & repeats	Fetal Stomach	stomach
17	chr14:68312400-68313200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
18	chr14:68312600-68313200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr14:68312600-68313800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr14:68312600-68314000	ZNF genes & repeats	Dnd41	blood
21	chr14:68312800-68313200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr14:68312800-68313200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr14:68312800-68313200	Strong transcription	Primary T cells from cord blood	blood
24	chr14:68312800-68313200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
25	chr14:68312800-68313200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr14:68312800-68313200	ZNF genes & repeats	Aorta	Aorta
27	chr14:68312800-68313200	Enhancers	Gastric	stomach
28	chr14:68312800-68313200	ZNF genes & repeats	Pancreas	Pancrea
29	chr14:68312800-68313800	ZNF genes & repeats	Esophagus	oesophagus
30	chr14:68312800-68315800	ZNF genes & repeats	Primary hematopoietic stem cells	blood

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