Variant report

Variant	rs10131119
Chromosome Location	chr14:63203085-63203086
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10137751	0.93[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs10144027	0.99[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs10146714	0.99[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs10149875	0.85[AFR][1000 genomes]
rs1032306	0.90[EUR][1000 genomes]
rs10483755	0.87[ASN][1000 genomes]
rs1387756	0.87[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs2101552	0.87[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2130445	0.87[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2171878	0.87[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2355061	0.90[EUR][1000 genomes]
rs28754390	0.92[AFR][1000 genomes]
rs4899094	0.87[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs4902178	0.86[AFR][1000 genomes]
rs4902182	0.87[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs61472478	0.96[ASN][1000 genomes]
rs6573459	0.81[AFR][1000 genomes]
rs7141855	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7141868	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7154700	0.99[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7157416	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7157560	0.82[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7158523	0.86[AFR][1000 genomes]
rs73271163	0.83[ASN][1000 genomes]
rs73271176	0.83[ASN][1000 genomes]
rs73271181	0.81[ASN][1000 genomes]
rs73271182	0.85[ASN][1000 genomes]
rs73271187	0.83[ASN][1000 genomes]
rs73271188	0.83[ASN][1000 genomes]
rs73271190	0.81[ASN][1000 genomes]
rs73271194	0.83[ASN][1000 genomes]
rs74058950	0.97[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs8003224	0.82[AFR][1000 genomes]
rs8010787	0.81[ASN][1000 genomes]
rs8010814	0.93[ASN][1000 genomes]
rs915064	0.90[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	nsv527675	chr14:63168547-63211280	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63201000-63203400	Enhancers	HMEC	breast
2	chr14:63201800-63206200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr14:63202400-63203800	Flanking Active TSS	Hela-S3	cervix
4	chr14:63202600-63203200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr14:63202800-63203200	Enhancers	A549	lung
6	chr14:63202800-63212000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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