Variant report

Variant	rs10011982
Chromosome Location	chr4:171571515-171571516
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10008486	0.83[ASN][1000 genomes]
rs10008580	0.83[ASN][1000 genomes]
rs10016504	0.85[ASN][1000 genomes]
rs10018573	0.85[ASN][1000 genomes]
rs10030592	0.85[ASN][1000 genomes]
rs13119766	0.81[ASN][1000 genomes]
rs13147483	0.85[ASN][1000 genomes]
rs1442911	0.85[ASN][1000 genomes]
rs1596248	0.86[EUR][1000 genomes]
rs1596249	0.82[EUR][1000 genomes]
rs17055995	0.81[ASN][1000 genomes]
rs2030542	0.86[EUR][1000 genomes]
rs28413006	0.85[ASN][1000 genomes]
rs28594344	0.81[ASN][1000 genomes]
rs34348601	0.85[ASN][1000 genomes]
rs34704211	0.81[ASN][1000 genomes]
rs34733312	0.90[ASN][1000 genomes]
rs34764144	0.85[ASN][1000 genomes]
rs34877800	0.85[ASN][1000 genomes]
rs34998985	0.95[ASN][1000 genomes]
rs35199694	0.85[ASN][1000 genomes]
rs35270214	0.90[ASN][1000 genomes]
rs35432171	0.90[ASN][1000 genomes]
rs35735782	0.90[ASN][1000 genomes]
rs35838289	0.85[ASN][1000 genomes]
rs35978308	0.85[ASN][1000 genomes]
rs35988152	0.90[ASN][1000 genomes]
rs3927277	0.84[ASN][1000 genomes]
rs4123378	0.81[ASN][1000 genomes]
rs4339170	0.85[ASN][1000 genomes]
rs4368570	0.85[ASN][1000 genomes]
rs4591556	0.81[ASN][1000 genomes]
rs4593092	0.85[ASN][1000 genomes]
rs4607176	0.81[ASN][1000 genomes]
rs57901929	0.85[ASN][1000 genomes]
rs59988282	0.85[ASN][1000 genomes]
rs6553537	0.85[ASN][1000 genomes]
rs6828724	0.83[ASN][1000 genomes]
rs6853295	0.81[ASN][1000 genomes]
rs6855350	0.81[ASN][1000 genomes]
rs6855380	0.85[ASN][1000 genomes]
rs6855386	0.81[ASN][1000 genomes]
rs71607810	0.81[ASN][1000 genomes]
rs71607811	0.85[ASN][1000 genomes]
rs71607812	0.84[ASN][1000 genomes]
rs73866043	0.85[ASN][1000 genomes]
rs73866044	0.85[ASN][1000 genomes]
rs73866045	0.85[ASN][1000 genomes]
rs73866069	0.85[ASN][1000 genomes]
rs73866098	0.85[ASN][1000 genomes]
rs7667249	0.81[ASN][1000 genomes]
rs7667290	0.81[ASN][1000 genomes]
rs7669074	0.85[ASN][1000 genomes]
rs7670495	0.85[ASN][1000 genomes]
rs7670523	0.85[ASN][1000 genomes]
rs7672244	0.90[ASN][1000 genomes]
rs7676680	0.85[ASN][1000 genomes]
rs7694510	0.85[ASN][1000 genomes]
rs9994841	0.85[ASN][1000 genomes]
rs9996819	0.83[ASN][1000 genomes]
rs9996914	0.83[ASN][1000 genomes]
rs9997039	0.83[ASN][1000 genomes]
rs9997272	0.80[EUR][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	nsv830151	chr4:171423566-171577867	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:171571200-171573000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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