Variant report

Variant	rs73091745
Chromosome Location	chr12:44457857-44457858
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10880616	0.80[AMR][1000 genomes]
rs10880617	0.80[AMR][1000 genomes]
rs11182375	1.00[ASN][1000 genomes]
rs11182384	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182385	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182402	0.80[AMR][1000 genomes]
rs11182404	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11182405	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12099769	1.00[ASN][1000 genomes]
rs12230287	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12296857	0.80[AMR][1000 genomes]
rs12301507	0.83[AMR][1000 genomes]
rs1532218	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1565620	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17093973	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17093993	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17094007	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17121301	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1976211	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2407791	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3929354	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55641600	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55657021	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55756710	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55773976	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55834309	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55917469	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56011342	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56081380	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56114967	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56122564	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56198335	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56227915	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56337317	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56355753	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6582495	1.00[ASN][1000 genomes]
rs7132451	0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7136217	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7303909	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73085758	0.95[EUR][1000 genomes]
rs73085764	0.98[EUR][1000 genomes]
rs73085767	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73085788	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73087603	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73087605	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73087610	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73087626	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73087664	1.00[EUR][1000 genomes]
rs73087684	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73087687	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73087696	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73087700	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73087702	1.00[EUR][1000 genomes]
rs73089723	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73089727	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73089730	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73089734	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73089739	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73089744	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73089748	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73089752	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73089753	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73089761	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73091736	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73091741	1.00[EUR][1000 genomes]
rs7311778	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7959226	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7960478	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7980005	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9783422	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9783507	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9919676	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9919711	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9919742	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832390	chr12:44318071-44512114	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1041188	chr12:44331098-44528712	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv832391	chr12:44394137-44552555	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44439200-44464400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:44447000-44459800	Weak transcription	Gastric	stomach
3	chr12:44454000-44470400	Weak transcription	Fetal Brain Female	brain
4	chr12:44456400-44458200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:44456600-44458600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr12:44457000-44470600	Weak transcription	Psoas Muscle	Psoas

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