Variant report

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

rs_ID	r²[population]
rs12506993	0.88[EUR][1000 genomes]
rs2866904	0.92[EUR][1000 genomes]
rs2866905	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2949624	0.80[EUR][1000 genomes]
rs2949632	0.83[CHB][hapmap];0.81[CHD][hapmap];0.92[TSI][hapmap];0.80[EUR][1000 genomes]
rs2949633	0.80[EUR][1000 genomes]
rs2949634	0.80[EUR][1000 genomes]
rs2949635	0.80[EUR][1000 genomes]
rs3018056	0.92[EUR][1000 genomes]
rs3018073	0.80[EUR][1000 genomes]
rs3018074	0.80[EUR][1000 genomes]
rs3018075	0.83[CHB][hapmap];0.80[EUR][1000 genomes]
rs3018076	0.83[CHB][hapmap];0.82[CHD][hapmap];0.84[GIH][hapmap];0.92[TSI][hapmap];0.80[EUR][1000 genomes]
rs3108137	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3108139	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3108140	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3108141	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3108143	0.96[EUR][1000 genomes]
rs3108148	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4383690	0.90[EUR][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	nsv830029	chr4:107203096-107353483	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv1008963	chr4:107282656-107384924	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	12 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	chr4:107331000-107333600	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr4:107331200-107335600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:107331200-107335600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr4:107331400-107333400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr4:107331600-107333200	Weak transcription	Fetal Kidney	kidney
6	chr4:107331600-107335600	Weak transcription	Osteobl	bone
7	chr4:107331800-107332800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:107332400-107335600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr4:107332600-107335600	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr4:107332600-107339200	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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