Variant report

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

rs_ID	r²[population]
rs1026006	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11241314	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11241315	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11951180	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12186657	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12188014	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12188143	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12189322	0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2974503	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2974511	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2974513	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55638352	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55799813	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55898517	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55927006	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56250025	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62380016	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62380051	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62380053	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6859538	0.94[ASN][1000 genomes]
rs6881197	0.94[ASN][1000 genomes]
rs72811756	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7706928	0.84[EUR][1000 genomes];0.97[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	nsv882729	chr5:113743628-114497708	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv830453	chr5:114277261-114546536	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114424400-114428200	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr5:114424400-114428200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr5:114425000-114431000	Weak transcription	Fetal Brain Male	brain
4	chr5:114425200-114428200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr5:114425800-114430600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:114426000-114428600	Enhancers	H1 Cell Line	embryonic stem cell
7	chr5:114427000-114432000	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr5:114427200-114428600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr5:114427600-114429000	Enhancers	H9 Cell Line	embryonic stem cell
10	chr5:114428000-114431200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr5:114428000-114431600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr5:114428000-114434000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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