Variant report

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

rs_ID	r²[population]
rs10002442	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1112880	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1112881	0.85[EUR][1000 genomes]
rs11723025	0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11724815	0.92[AMR][1000 genomes]
rs13130117	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17005046	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17005047	0.85[EUR][1000 genomes]
rs28454856	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2868131	0.85[EUR][1000 genomes]
rs28685252	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs28754452	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2903748	0.85[EUR][1000 genomes]
rs34281791	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3796804	0.85[EUR][1000 genomes]
rs4565072	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6833113	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7657739	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7671128	0.85[EUR][1000 genomes]
rs7679480	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7695150	0.85[EUR][1000 genomes]
rs7700247	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999729	chr4:81802554-82627820	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537156	chr4:81802554-82627820	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers 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 miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv829984	chr4:81979988-82113977	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:81998200-82030000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:82004000-82017200	Weak transcription	Fetal Intestine Small	intestine
3	chr4:82005800-82019000	Weak transcription	Fetal Intestine Large	intestine
4	chr4:82006200-82024800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr4:82006600-82014400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr4:82006800-82024800	Weak transcription	NHDF-Ad	bronchial
7	chr4:82012800-82014800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr4:82013000-82033200	Weak transcription	NHLF	lung
9	chr4:82013600-82015600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:82014000-82017200	Enhancers	Fetal Heart	heart

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