Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11076560	1.00[GIH][hapmap]
rs13334798	1.00[GIH][hapmap]
rs17743708	1.00[CEU][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs17822052	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs41280941	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55978876	1.00[EUR][1000 genomes]
rs58219806	0.87[AFR][1000 genomes]
rs60297142	0.90[AFR][1000 genomes]
rs61739606	1.00[EUR][1000 genomes]
rs62058520	1.00[EUR][1000 genomes]
rs62058523	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62058524	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62058525	1.00[EUR][1000 genomes]
rs62058527	1.00[EUR][1000 genomes]
rs62058529	1.00[EUR][1000 genomes]
rs62058530	1.00[EUR][1000 genomes]
rs62058531	1.00[EUR][1000 genomes]
rs7187887	0.88[AFR][1000 genomes]
rs7194667	1.00[GIH][hapmap]
rs74018297	0.90[AFR][1000 genomes]
rs8050306	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8058886	0.91[YRI][hapmap];0.90[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1059259	chr16:48113396-48304404	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv542916	chr16:48113396-48304404	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17821664	LRRIQ3	trans	cerebellum	SCAN

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:48192800-48204000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr16:48198800-48204800	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr16:48199200-48226600	Weak transcription	Spleen	Spleen
4	chr16:48200200-48209000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr16:48201200-48202800	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr16:48201400-48202800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr16:48201600-48206000	Weak transcription	HepG2	liver
8	chr16:48201800-48204600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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