Variant report

Variant	rs4903927
Chromosome Location	chr14:81079765-81079766
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:81075319..81077418-chr14:81079123..81081073,2	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10498547	0.81[ASN][1000 genomes]
rs11159470	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11159471	0.81[ASN][1000 genomes]
rs12589019	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12589109	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17519	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1871458	0.86[ASN][1000 genomes]
rs34201956	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4903930	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4903931	0.83[EUR][1000 genomes]
rs6574592	0.95[ASN][1000 genomes]
rs66523962	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7141390	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7142417	0.90[ASN][1000 genomes]
rs71430713	0.82[ASN][1000 genomes]
rs7144036	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7144975	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7145447	0.86[ASN][1000 genomes]
rs7152126	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7156452	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7158869	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7159302	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8003492	0.95[ASN][1000 genomes]
rs8006458	0.81[EUR][1000 genomes]
rs8007955	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8008167	0.81[EUR][1000 genomes]
rs8013202	0.83[ASN][1000 genomes]
rs8013610	0.84[ASN][1000 genomes]
rs8018031	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv902116	chr14:81018237-81082400	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81062200-81082200	Weak transcription	Dnd41	blood
2	chr14:81076200-81086600	Weak transcription	A549	lung

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