Variant report

Variant	rs58232472
Chromosome Location	chr13:94449840-94449841
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10492636	0.84[AFR][1000 genomes]
rs10492638	1.00[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs12427786	0.86[ASN][1000 genomes]
rs12427803	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs12428209	0.86[ASN][1000 genomes]
rs12428875	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12429608	0.86[ASN][1000 genomes]
rs12429856	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs17174721	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs17174735	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs17253234	0.86[ASN][1000 genomes]
rs17253241	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs17253255	0.86[ASN][1000 genomes]
rs17253262	0.86[ASN][1000 genomes]
rs17253269	0.86[ASN][1000 genomes]
rs2389052	0.87[ASN][1000 genomes]
rs2892668	0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs56003695	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56118807	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs56396732	0.86[ASN][1000 genomes]
rs56970055	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs57002007	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs57310418	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57433205	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs57605778	1.00[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs57800923	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs58794076	0.84[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs59283174	0.86[ASN][1000 genomes]
rs60257121	0.86[ASN][1000 genomes]
rs60393268	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61462500	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs61506126	0.86[ASN][1000 genomes]
rs74108858	0.89[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs74108860	0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs74108861	0.89[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs74108875	0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs74108888	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs74108889	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs74108892	0.86[ASN][1000 genomes]
rs74108894	0.86[ASN][1000 genomes]
rs74108896	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs74108897	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs74108898	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs74108901	0.86[ASN][1000 genomes]
rs74108902	0.86[ASN][1000 genomes]
rs74110903	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs74110907	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74111004	0.86[ASN][1000 genomes]
rs74111005	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs74111006	0.86[ASN][1000 genomes]
rs74111008	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs74111010	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs74111011	0.86[ASN][1000 genomes]
rs74111015	0.86[ASN][1000 genomes]
rs74111033	0.84[AFR][1000 genomes]
rs74111035	0.84[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948714	chr13:94100104-94699435	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv933807	chr13:94187158-94845505	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1045230	chr13:94277683-94764671	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv832684	chr13:94379507-94550853	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1130	chr13:94410849-94455628	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:94445200-94453400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:94447400-94450200	Weak transcription	GM12878-XiMat	blood
3	chr13:94448400-94456200	Weak transcription	Right Atrium	heart
4	chr13:94448800-94450600	Enhancers	Pancreatic Islets	Pancreatic Islet

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