Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10010581	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12498851	0.91[ASN][1000 genomes]
rs12511208	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13109231	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs13111654	0.80[ASN][1000 genomes]
rs13114428	0.90[ASN][1000 genomes]
rs13124084	0.81[ASN][1000 genomes]
rs1500458	0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs1500465	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1587491	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1587492	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1827239	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs1827240	0.80[ASN][1000 genomes]
rs1983021	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2202025	0.84[EUR][1000 genomes]
rs36079959	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4697293	0.84[EUR][1000 genomes]
rs56717131	0.91[ASN][1000 genomes]
rs6448153	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7683451	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv817467	chr4:21602921-22422816	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv428756	chr4:22239826-22406106	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:22329000-22389400	Weak transcription	Pancreas	Pancrea
2	chr4:22336600-22385400	Weak transcription	Fetal Intestine Large	intestine
3	chr4:22354000-22378200	Weak transcription	Aorta	Aorta
4	chr4:22365600-22386800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:22365800-22384600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:22366000-22385000	Weak transcription	NHEK	skin
7	chr4:22368800-22418600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:22371600-22449800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr4:22371800-22377200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:22372000-22400400	Weak transcription	Gastric	stomach
11	chr4:22374000-22376000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr4:22374400-22375600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:22374800-22383600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:22375000-22376000	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr4:22375000-22385000	Weak transcription	HUES64 Cell Line	embryonic stem cell

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