Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10144720	0.85[CEU][hapmap]
rs1038239	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11158584	0.82[CEU][hapmap]
rs11158590	0.83[GIH][hapmap]
rs11846705	0.86[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs1256541	0.87[CEU][hapmap];0.84[YRI][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1256542	0.82[CEU][hapmap];0.90[YRI][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1256544	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17180994	0.86[EUR][1000 genomes]
rs2101084	0.85[CEU][hapmap];0.83[GIH][hapmap]
rs2411915	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3986780	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4299072	0.83[GIH][hapmap]
rs4899175	0.84[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs7141874	0.83[GIH][hapmap];0.84[MKK][hapmap]
rs7144530	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs8015222	0.85[CEU][hapmap];0.86[EUR][1000 genomes]
rs8020305	0.87[CEU][hapmap]
rs8021946	0.86[EUR][1000 genomes]
rs8023016	0.86[EUR][1000 genomes]
rs899960	0.87[CEU][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832817	chr14:65637069-65810406	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
2	nsv832818	chr14:65706859-65882320	Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1036403	chr14:65724229-66208114	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
4	nsv515522	chr14:65746566-65771110	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65754600-65768600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:65754800-65764400	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr14:65758600-65763000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr14:65758600-65763000	Weak transcription	NHDF-Ad	bronchial
5	chr14:65758800-65763600	Weak transcription	Pancreas	Pancrea
6	chr14:65758800-65764400	Weak transcription	Duodenum Mucosa	Duodenum
7	chr14:65758800-65770000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr14:65758800-65773400	Weak transcription	Spleen	Spleen
9	chr14:65759000-65764600	Weak transcription	Colonic Mucosa	Colon
10	chr14:65759000-65766000	Weak transcription	Fetal Thymus	thymus
11	chr14:65759000-65766000	Weak transcription	Thymus	Thymus
12	chr14:65759400-65763000	Weak transcription	GM12878-XiMat	blood
13	chr14:65759600-65763600	Weak transcription	Stomach Mucosa	stomach
14	chr14:65759800-65766000	Weak transcription	Primary T cells from cord blood	blood
15	chr14:65759800-65766200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr14:65760000-65763200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr14:65760000-65781000	Weak transcription	Primary B cells from cord blood	blood
18	chr14:65760200-65763200	Weak transcription	Primary B cells from peripheral blood	blood

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