Variant report

Variant	rs13136054
Chromosome Location	chr4:96596412-96596413
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10005387	0.87[AMR][1000 genomes]
rs10006440	0.87[AMR][1000 genomes]
rs10012383	0.87[AMR][1000 genomes]
rs10016746	0.90[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs10023027	0.90[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs10024142	0.82[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs10024303	0.87[AMR][1000 genomes]
rs10024516	0.87[AMR][1000 genomes]
rs1025629	0.84[ASN][1000 genomes]
rs11097481	0.87[AMR][1000 genomes]
rs1117212	0.85[AMR][1000 genomes]
rs12498523	0.87[AMR][1000 genomes]
rs12502460	0.87[AMR][1000 genomes]
rs12508146	0.87[AMR][1000 genomes]
rs12640394	0.84[AMR][1000 genomes]
rs12643258	0.87[AMR][1000 genomes]
rs12643863	0.80[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs12646632	0.87[AMR][1000 genomes]
rs12649375	0.87[AMR][1000 genomes]
rs12649816	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12650006	0.81[AMR][1000 genomes]
rs13108901	0.90[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs13114915	0.87[AMR][1000 genomes]
rs13121624	0.81[ASN][1000 genomes]
rs13122865	0.81[AMR][1000 genomes]
rs13136351	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13139338	0.87[AMR][1000 genomes]
rs13139501	0.87[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs13147649	0.92[AMR][1000 genomes]
rs1369996	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1370002	0.87[AMR][1000 genomes]
rs1370004	0.90[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs1436580	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1436586	0.80[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs1579618	0.87[AMR][1000 genomes]
rs1579619	0.87[AMR][1000 genomes]
rs1579622	0.85[AMR][1000 genomes]
rs1579623	0.85[AMR][1000 genomes]
rs1579625	0.84[ASN][1000 genomes]
rs1579626	0.87[AMR][1000 genomes]
rs1583546	0.84[ASN][1000 genomes]
rs1595205	0.85[AMR][1000 genomes]
rs1821738	0.87[AMR][1000 genomes]
rs1821739	0.87[AMR][1000 genomes]
rs1836907	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1865850	0.87[AMR][1000 genomes]
rs1865851	0.87[AMR][1000 genomes]
rs1898251	0.84[ASN][1000 genomes]
rs2118052	0.87[AMR][1000 genomes]
rs2164544	0.87[AMR][1000 genomes]
rs2164545	0.87[AMR][1000 genomes]
rs2865468	0.81[AMR][1000 genomes]
rs2865710	0.86[AMR][1000 genomes]
rs2903012	0.81[AMR][1000 genomes]
rs3975035	0.87[AMR][1000 genomes]
rs4305518	0.81[AMR][1000 genomes]
rs4422420	0.88[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs4590043	0.87[AMR][1000 genomes]
rs4699275	0.87[AMR][1000 genomes]
rs4699450	0.87[AMR][1000 genomes]
rs4699451	0.87[AMR][1000 genomes]
rs6821135	0.87[AMR][1000 genomes]
rs6821324	0.87[AMR][1000 genomes]
rs6843996	0.86[AMR][1000 genomes]
rs6844205	0.87[AMR][1000 genomes]
rs6853495	0.87[AMR][1000 genomes]
rs6854333	0.90[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs6854348	0.87[AMR][1000 genomes]
rs6854512	0.87[ASN][1000 genomes]
rs7438910	0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs7654532	0.84[AMR][1000 genomes]
rs7654785	0.83[AMR][1000 genomes]
rs7655804	0.81[AMR][1000 genomes]
rs7658878	0.87[AMR][1000 genomes]
rs7667706	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7680769	0.87[AMR][1000 genomes]
rs7680812	0.87[AMR][1000 genomes]
rs7680962	0.90[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs7681281	0.87[AMR][1000 genomes]
rs9993422	0.87[AMR][1000 genomes]
rs9993596	0.87[AMR][1000 genomes]
rs9994206	0.87[AMR][1000 genomes]
rs9994390	0.87[AMR][1000 genomes]
rs9996557	0.81[ASN][1000 genomes]
rs9997433	0.80[AFR][1000 genomes];0.84[ASN][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	nsv830012	chr4:96547783-96746163	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv1844506	chr4:96554889-96704333	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1007133	chr4:96556072-96614235	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv997304	chr4:96575198-96861349	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:96593600-96597800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:96594000-96596800	Enhancers	Fetal Kidney	kidney
3	chr4:96594200-96596800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:96595000-96597000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:96595800-96597000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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