Variant report

Variant	rs7962840
Chromosome Location	chr12:87743358-87743359
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs10735256	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10735257	1.00[ASN][1000 genomes]
rs10735258	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10735261	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10735262	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10735264	0.88[EUR][1000 genomes]
rs10745442	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10745444	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10745446	0.92[AMR][1000 genomes]
rs10745448	0.88[EUR][1000 genomes]
rs10745449	0.88[EUR][1000 genomes]
rs10777031	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10777032	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10777033	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10777034	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10777035	1.00[ASN][1000 genomes]
rs10777040	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10777042	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10777043	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10777048	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10858592	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10858598	0.85[AMR][1000 genomes]
rs10858599	0.86[EUR][1000 genomes]
rs11104443	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11104470	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1353484	0.88[EUR][1000 genomes]
rs1353486	0.88[EUR][1000 genomes]
rs1353487	0.88[EUR][1000 genomes]
rs1353488	0.88[EUR][1000 genomes]
rs1390604	0.88[EUR][1000 genomes]
rs1390605	0.88[EUR][1000 genomes]
rs1496320	0.88[EUR][1000 genomes]
rs1496321	0.88[EUR][1000 genomes]
rs2047306	0.88[EUR][1000 genomes]
rs2406753	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2406754	1.00[ASN][1000 genomes]
rs2897518	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4147490	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4240740	1.00[ASN][1000 genomes]
rs4254148	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4258454	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4269999	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4284481	1.00[ASN][1000 genomes]
rs4300469	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4300470	1.00[ASN][1000 genomes]
rs4303307	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4310691	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4319586	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4326883	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4338623	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4372533	0.88[EUR][1000 genomes]
rs4402386	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4442619	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4456347	1.00[ASN][1000 genomes]
rs4460889	1.00[ASN][1000 genomes]
rs4466916	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4502057	1.00[ASN][1000 genomes]
rs4561282	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4564410	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4576908	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4590963	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4597138	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4625561	1.00[ASN][1000 genomes]
rs4635161	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4842455	1.00[ASN][1000 genomes]
rs4842462	0.88[EUR][1000 genomes]
rs4842556	1.00[ASN][1000 genomes]
rs4842559	1.00[ASN][1000 genomes]
rs4842570	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4842576	0.88[EUR][1000 genomes]
rs5005936	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6538078	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6538079	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6538082	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6538083	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6538084	0.86[EUR][1000 genomes]
rs6538086	1.00[ASN][1000 genomes]
rs6538087	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6538088	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6538104	0.88[EUR][1000 genomes]
rs6538105	0.88[EUR][1000 genomes]
rs6538106	0.88[EUR][1000 genomes]
rs7305305	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7310810	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7311170	0.88[EUR][1000 genomes]
rs7959041	0.88[EUR][1000 genomes]
rs7967687	0.88[EUR][1000 genomes]
rs7969510	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7969855	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7970683	1.00[ASN][1000 genomes]
rs7970729	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7970832	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7970866	1.00[ASN][1000 genomes]
rs7971055	1.00[ASN][1000 genomes]
rs7971424	1.00[ASN][1000 genomes]
rs7974679	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7980176	1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427918	chr12:87647585-87786660	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:87742000-87751800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:87742200-87743800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:87743200-87743800	Enhancers	Fetal Brain Female	brain

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