Variant report

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

rs_ID	r²[population]
rs10951189	0.81[ASN][1000 genomes]
rs12216542	0.83[ASN][1000 genomes]
rs12671866	0.80[AMR][1000 genomes]
rs192254	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2107821	0.86[ASN][1000 genomes]
rs2107822	0.85[ASN][1000 genomes]
rs253310	0.81[AMR][1000 genomes]
rs38500	0.85[AMR][1000 genomes]
rs38502	0.94[ASN][1000 genomes]
rs38504	0.86[ASN][1000 genomes]
rs38507	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs38510	0.84[ASN][1000 genomes]
rs38513	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs38514	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs38515	0.97[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs38516	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs38517	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4365989	0.81[ASN][1000 genomes]
rs4422694	0.81[ASN][1000 genomes]
rs57551874	0.81[ASN][1000 genomes]
rs72598569	0.80[AMR][1000 genomes]
rs72598573	0.83[AMR][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	nsv949025	chr7:27578167-28075172	Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1030685	chr7:27844038-28177301	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:28002800-28034600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr7:28006200-28024800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr7:28006400-28031800	Weak transcription	NHDF-Ad	bronchial
4	chr7:28012400-28028000	Weak transcription	Primary B cells from peripheral blood	blood
5	chr7:28013400-28034200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr7:28015600-28032400	Weak transcription	Ovary	ovary
7	chr7:28017600-28042400	Weak transcription	Aorta	Aorta
8	chr7:28017800-28028000	Weak transcription	Fetal Muscle Leg	muscle
9	chr7:28018000-28026200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:28020000-28032400	Weak transcription	Primary B cells from cord blood	blood
11	chr7:28022400-28026200	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr7:28022400-28026400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr7:28022400-28028000	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr7:28022400-28031000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr7:28022400-28036200	Weak transcription	Lung	lung

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