Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10002442	0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1112880	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1112881	0.81[EUR][1000 genomes]
rs1113771	1.00[CEU][hapmap]
rs11723025	1.00[CEU][hapmap];0.88[CHB][hapmap];0.82[ASN][1000 genomes]
rs11724815	0.90[ASN][1000 genomes]
rs13125120	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13130117	0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1443545	1.00[CEU][hapmap]
rs17005046	0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17005047	0.89[EUR][1000 genomes]
rs28454856	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2868131	0.89[EUR][1000 genomes]
rs2868133	0.81[EUR][1000 genomes]
rs2868134	1.00[CEU][hapmap]
rs28685252	0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28754452	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2903748	0.89[EUR][1000 genomes]
rs34281791	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3796804	0.89[EUR][1000 genomes]
rs6833113	0.88[ASN][1000 genomes]
rs7671128	0.89[EUR][1000 genomes]
rs7679480	0.85[CEU][hapmap]
rs7695150	0.89[EUR][1000 genomes]
rs7700247	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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	nsv1006466	chr4:81888983-82009675	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	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:8 , 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	chr4:82006800-82012000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr4:82006800-82024800	Weak transcription	NHDF-Ad	bronchial
8	chr4:82007600-82010400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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