Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs17175238	1.00[AMR][1000 genomes]
rs17175245	1.00[AMR][1000 genomes]
rs17253787	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17253794	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34546989	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9516383	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9516384	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9516387	1.00[AMR][1000 genomes]
rs9516390	1.00[AMR][1000 genomes]
rs9524407	0.89[ASN][1000 genomes]
rs9524408	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9524409	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9524411	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9524412	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9524413	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9524415	0.89[ASN][1000 genomes]
rs9524416	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9524417	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9524418	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9524419	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9524420	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9524422	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9524423	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9524425	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9524432	1.00[AMR][1000 genomes]
rs9524434	1.00[AMR][1000 genomes]
rs9524438	1.00[AMR][1000 genomes]
rs9645929	1.00[AMR][1000 genomes];0.87[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	nsv948455	chr13:94451368-94988900	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv916640	chr13:94521959-95101443	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv533063	chr13:94560362-95101443	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv34004	chr13:94906537-95392644	Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 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	chr13:94936600-94956000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr13:94947800-94949800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr13:94947800-94954800	Weak transcription	HepG2	liver
4	chr13:94948400-94950000	Enhancers	Liver	Liver
5	chr13:94948600-94950800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr13:94948800-94949600	Enhancers	Fetal Muscle Leg	muscle
7	chr13:94948800-94949600	Enhancers	Pancreas	Pancrea
8	chr13:94949000-94950600	Weak transcription	Fetal Thymus	thymus
9	chr13:94949400-94949800	Enhancers	Fetal Lung	lung
10	chr13:94949400-94950000	Enhancers	Colon Smooth Muscle	Colon

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