Variant report

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

rs_ID	r²[population]
rs10483663	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10483664	0.85[EUR][1000 genomes]
rs1383395	0.85[EUR][1000 genomes]
rs17090926	1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17090962	0.85[EUR][1000 genomes]
rs17090964	0.85[EUR][1000 genomes]
rs17093198	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55941817	0.83[AMR][1000 genomes]
rs57701314	0.83[EUR][1000 genomes]
rs6573080	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7143395	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7157348	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73287035	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73287042	0.85[EUR][1000 genomes]
rs8007410	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8013624	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs8014396	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8017757	0.85[EUR][1000 genomes]
rs8018061	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8019044	0.85[EUR][1000 genomes]
rs8019376	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34106	chr14:56346245-56550642	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56541000-56554200	Weak transcription	Gastric	stomach
2	chr14:56547800-56550400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr14:56548600-56550000	Enhancers	Fetal Intestine Small	intestine
4	chr14:56549200-56550400	Enhancers	Fetal Intestine Large	intestine
5	chr14:56549400-56554200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr14:56549400-56554200	Weak transcription	Dnd41	blood
7	chr14:56549400-56554600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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