Variant report

Variant	rs983989
Chromosome Location	chr10:23806687-23806688
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10741030	0.82[EUR][1000 genomes]
rs10828465	0.88[EUR][1000 genomes]
rs10828466	0.88[EUR][1000 genomes]
rs10828467	0.90[EUR][1000 genomes]
rs10828469	0.98[EUR][1000 genomes]
rs10828470	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10828474	0.81[EUR][1000 genomes]
rs10828475	0.81[EUR][1000 genomes]
rs11013531	0.92[EUR][1000 genomes]
rs11013540	0.92[EUR][1000 genomes]
rs11013541	0.93[EUR][1000 genomes]
rs11013543	0.98[EUR][1000 genomes]
rs11013545	0.95[EUR][1000 genomes]
rs11013557	0.81[EUR][1000 genomes]
rs12244668	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12254275	0.90[EUR][1000 genomes]
rs12261799	0.90[EUR][1000 genomes]
rs12263327	0.89[EUR][1000 genomes]
rs12266577	0.98[EUR][1000 genomes]
rs12266853	0.89[EUR][1000 genomes]
rs1337324	0.99[EUR][1000 genomes]
rs1337325	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1415418	0.82[EUR][1000 genomes]
rs1856113	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1877325	0.92[EUR][1000 genomes]
rs1877326	0.92[EUR][1000 genomes]
rs1877327	0.92[EUR][1000 genomes]
rs1877328	0.92[EUR][1000 genomes]
rs1984173	0.83[EUR][1000 genomes]
rs1985697	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2366162	0.80[EUR][1000 genomes]
rs4008949	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4359093	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4564227	0.84[EUR][1000 genomes]
rs4748902	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6482290	0.84[EUR][1000 genomes]
rs6482291	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6482292	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6482293	0.92[EUR][1000 genomes]
rs7071059	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7097155	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7899130	0.91[EUR][1000 genomes]
rs7901238	0.88[EUR][1000 genomes]
rs7904301	0.84[EUR][1000 genomes]
rs7907290	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7908703	0.92[EUR][1000 genomes]
rs7908715	0.91[EUR][1000 genomes]
rs7913401	0.99[EUR][1000 genomes]
rs7921141	0.80[EUR][1000 genomes]
rs983990	0.82[AMR][1000 genomes];0.99[EUR][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	nsv831811	chr10:23734326-23913370	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv466835	chr10:23801555-23869175	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
3	nsv550215	chr10:23801555-23869175	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23805600-23806800	Enhancers	Liver	Liver
2	chr10:23805600-23806800	Enhancers	HepG2	liver
3	chr10:23806200-23807000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr10:23806400-23807000	Enhancers	Monocytes-CD14+_RO01746	blood

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