Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs41279582	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs55873909	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55886441	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs56046664	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56156710	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73118200	1.00[AMR][1000 genomes]
rs73120213	1.00[AMR][1000 genomes]
rs73120220	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73120230	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73120241	0.85[EUR][1000 genomes]
rs73120243	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73120259	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73120268	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73120282	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73120287	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73122226	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73122288	0.85[AMR][1000 genomes]
rs73122296	0.85[AMR][1000 genomes]
rs740066	1.00[AMR][1000 genomes]
rs741265	1.00[AMR][1000 genomes]
rs7776921	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7778313	1.00[AMR][1000 genomes]
rs7803476	1.00[AMR][1000 genomes]
rs7811443	0.84[AMR][1000 genomes];0.85[EUR][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	nsv932229	chr7:38248340-38727527	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
2	nsv830966	chr7:38393663-38602553	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38502600-38549400	Weak transcription	Fetal Stomach	stomach
2	chr7:38502800-38533800	Weak transcription	Aorta	Aorta
3	chr7:38524000-38543400	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr7:38524200-38545000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr7:38528600-38553000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:38531400-38544600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:38531800-38543800	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr7:38532000-38540200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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