Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10016792	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10030489	0.96[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10866423	0.96[AFR][1000 genomes]
rs11133363	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11133364	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12645088	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13115127	0.93[AFR][1000 genomes]
rs13143119	0.93[AFR][1000 genomes]
rs13143543	0.93[AFR][1000 genomes]
rs1993584	0.92[AFR][1000 genomes]
rs1993585	0.88[AFR][1000 genomes]
rs1993586	0.92[AFR][1000 genomes]
rs2899030	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34364773	0.94[AFR][1000 genomes]
rs4304028	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4864960	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62306569	0.91[AFR][1000 genomes]
rs6810735	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6812621	0.97[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6852640	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6853855	0.95[AFR][1000 genomes];0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7435539	0.92[AFR][1000 genomes]
rs7440118	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526344	chr4:55522488-56231119	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56035800-56042200	Weak transcription	Right Atrium	heart
2	chr4:56036000-56050600	Weak transcription	Pancreas	Pancrea
3	chr4:56036200-56038600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:56036200-56039000	Weak transcription	NHLF	lung
5	chr4:56036200-56039200	Weak transcription	Adipose Nuclei	Adipose
6	chr4:56036200-56041800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr4:56036200-56044400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr4:56036400-56038200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr4:56036400-56038200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:56036400-56038600	Weak transcription	NH-A	brain
11	chr4:56036600-56038000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr4:56036600-56038200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr4:56036800-56038200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr4:56036800-56038600	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr4:56036800-56038800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr4:56036800-56044600	Weak transcription	Stomach Mucosa	stomach

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