Variant report

Variant	rs10025010
Chromosome Location	chr4:174918693-174918694
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:174918419..174920333-chr4:174922806..174925607,2	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10050239	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11723453	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11724561	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11734841	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11930283	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11932516	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4285061	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4289426	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4290874	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4299560	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4331760	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4501199	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4627836	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55801980	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60891530	0.81[EUR][1000 genomes]
rs62336579	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62336581	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62336609	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6814121	0.83[EUR][1000 genomes]
rs6815176	0.83[EUR][1000 genomes]
rs6818208	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6818217	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6830884	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6833109	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6845317	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6856702	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6858266	0.83[EUR][1000 genomes]
rs9998241	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[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	nsv830154	chr4:174781983-174940640	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:174914800-174922400	Weak transcription	Rectal Smooth Muscle	rectum
2	chr4:174918200-174920000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr4:174918400-174919600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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