Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1280079	0.81[AFR][1000 genomes]
rs1280082	0.87[AFR][1000 genomes]
rs1385553	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1385554	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1683106	0.81[AFR][1000 genomes]
rs2062386	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2220192	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4900355	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4905565	0.87[AFR][1000 genomes]
rs4905569	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6575602	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs710264	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8022166	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs856223	0.95[YRI][hapmap]
rs856224	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs856226	1.00[YRI][hapmap]
rs856227	0.82[AFR][1000 genomes]
rs856255	1.00[YRI][hapmap]
rs856258	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs856260	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs856272	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs864121	0.95[YRI][hapmap];0.82[AFR][1000 genomes]
rs936784	0.95[YRI][hapmap]

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	nsv1044202	chr14:97155291-97683983	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv542179	chr14:97155291-97683983	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv948620	chr14:97334444-98133191	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv832867	chr14:97365919-97541763	Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97368600-97391400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:97379400-97411800	Weak transcription	Primary T cells from cord blood	blood
3	chr14:97387000-97391400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr14:97387200-97395200	Weak transcription	Fetal Brain Male	brain
5	chr14:97388000-97391600	Weak transcription	K562	blood
6	chr14:97388400-97397400	Weak transcription	Dnd41	blood
7	chr14:97389600-97391400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr14:97390200-97391200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr14:97390400-97390800	Active TSS	Spleen	Spleen
10	chr14:97390400-97391000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr14:97390600-97391200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr14:97390600-97391400	Weak transcription	Fetal Brain Female	brain

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