Variant report

Variant	rs7151198
Chromosome Location	chr14:32149430-32149431
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 120 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:112)

rs_ID	r²[population]
rs10047861	1.00[EUR][1000 genomes]
rs10132862	1.00[EUR][1000 genomes]
rs10137974	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10139914	0.85[EUR][1000 genomes]
rs10142679	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10143144	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs10148038	1.00[CEU][hapmap];0.80[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10149668	1.00[CEU][hapmap];0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10150831	1.00[CEU][hapmap];0.80[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10151156	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10151379	1.00[CEU][hapmap]
rs10162515	1.00[CEU][hapmap]
rs11156681	1.00[ASN][1000 genomes]
rs11846852	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11847014	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11847815	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11848462	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11850880	1.00[EUR][1000 genomes]
rs12884784	1.00[ASN][1000 genomes]
rs12894985	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13379320	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1430424	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17098019	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17098168	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17098171	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs17098197	1.00[CEU][hapmap]
rs17098211	1.00[CEU][hapmap]
rs1982013	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs1982014	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2034070	0.86[EUR][1000 genomes]
rs2115957	1.00[EUR][1000 genomes]
rs2120135	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2120137	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2120138	0.93[EUR][1000 genomes]
rs2163302	1.00[EUR][1000 genomes]
rs2378899	1.00[CEU][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2378900	1.00[EUR][1000 genomes]
rs2378934	1.00[CEU][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28446445	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28532719	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28580449	0.93[EUR][1000 genomes]
rs28637268	0.82[AFR][1000 genomes]
rs28806946	1.00[EUR][1000 genomes]
rs28862034	1.00[EUR][1000 genomes]
rs28864375	0.93[EUR][1000 genomes]
rs4981882	1.00[ASN][1000 genomes]
rs55674235	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58097888	1.00[EUR][1000 genomes]
rs58213271	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58280106	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58900150	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59002501	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs59679301	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60654485	0.93[EUR][1000 genomes]
rs6571449	1.00[CEU][hapmap];0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6571451	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6571455	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6571456	1.00[CEU][hapmap];0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6571460	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6571465	1.00[EUR][1000 genomes]
rs6571466	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs6571467	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs6571471	1.00[CEU][hapmap]
rs7140146	1.00[CEU][hapmap]
rs7140277	1.00[CEU][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7140603	1.00[CEU][hapmap]
rs7141267	1.00[EUR][1000 genomes]
rs7141477	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7141722	1.00[EUR][1000 genomes]
rs7143532	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7144178	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7145785	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7146383	1.00[CEU][hapmap]
rs7147779	1.00[EUR][1000 genomes]
rs7148248	1.00[EUR][1000 genomes]
rs7148746	1.00[CEU][hapmap]
rs7149861	1.00[CEU][hapmap]
rs7150042	1.00[EUR][1000 genomes]
rs7150488	1.00[EUR][1000 genomes]
rs7150851	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7153885	1.00[CEU][hapmap];0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7154277	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7156676	1.00[EUR][1000 genomes]
rs7156907	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7158443	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7158652	1.00[EUR][1000 genomes]
rs7158693	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7159193	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7159319	0.93[EUR][1000 genomes]
rs7161592	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7161628	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs73253213	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73253245	1.00[ASN][1000 genomes]
rs73255199	1.00[EUR][1000 genomes]
rs74043606	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8003033	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8004616	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs8005763	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs8005857	0.82[EUR][1000 genomes]
rs8009012	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs8010697	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8015179	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8015245	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8015640	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8018137	1.00[CEU][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8018529	0.86[EUR][1000 genomes]
rs8020874	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs8021182	1.00[CEU][hapmap];0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8022324	1.00[EUR][1000 genomes]
rs970489	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs9743593	1.00[EUR][1000 genomes]
rs9743878	1.00[CEU][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934206	chr14:31887749-32257097	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv564180	chr14:31958566-32368934	Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv564181	chr14:31958761-32363980	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv901591	chr14:32093548-32202677	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv901592	chr14:32093548-32267323	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv564182	chr14:32110519-32584337	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv1046526	chr14:32110537-32567426	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
8	esv3414517	chr14:32144250-32168719	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32135800-32170800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr14:32140600-32153200	Weak transcription	Primary T cells from cord blood	blood
3	chr14:32141400-32175800	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr14:32141800-32151200	Weak transcription	Gastric	stomach
5	chr14:32142200-32166200	Weak transcription	Primary B cells from cord blood	blood
6	chr14:32144600-32150800	Weak transcription	Primary hematopoietic stem cells	blood
7	chr14:32145000-32150200	Weak transcription	Adipose Nuclei	Adipose
8	chr14:32145400-32150400	Weak transcription	Fetal Intestine Large	intestine
9	chr14:32145600-32170600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr14:32147600-32158600	Weak transcription	Left Ventricle	heart
11	chr14:32147800-32150000	Weak transcription	Thymus	Thymus
12	chr14:32148000-32149600	Weak transcription	Fetal Stomach	stomach
13	chr14:32148000-32150800	Weak transcription	Fetal Intestine Small	intestine
14	chr14:32148000-32151400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr14:32148000-32152000	Weak transcription	Ovary	ovary
16	chr14:32148000-32183600	Weak transcription	Stomach Smooth Muscle	stomach
17	chr14:32148200-32150800	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr14:32148200-32151000	Weak transcription	Fetal Muscle Trunk	muscle
19	chr14:32148400-32150000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr14:32148400-32150000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr14:32148400-32150000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr14:32148400-32150800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr14:32148400-32155400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr14:32148400-32165400	Weak transcription	HepG2	liver
25	chr14:32149400-32149600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr14:32149400-32151200	Enhancers	Muscle Satellite Cultured Cells	--

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