Variant report

Variant	rs10055063
Chromosome Location	chr5:80622004-80622005
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	chr5:80621145..80622665-chr5:80622960..80624684,2	K562	blood:
2	chr5:80619315..80622153-chr5:80629970..80632926,2	K562	blood:

Variant related genes	Relation type
ENSG00000172497	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 13 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10038684	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10041063	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10053706	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10066296	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10078279	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10474656	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10514213	0.82[EUR][1000 genomes]
rs1055383	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10942945	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11950033	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13362314	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1566432	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2270823	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28464111	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28650401	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4703827	0.82[EUR][1000 genomes]
rs4704707	0.82[EUR][1000 genomes]
rs4704708	0.82[EUR][1000 genomes]
rs4704710	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4704712	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4704715	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4704720	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59132806	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs60488995	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs60904680	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61244991	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6893467	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73130869	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7381116	0.81[AMR][1000 genomes]
rs7720009	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7728465	0.80[AMR][1000 genomes]
rs9293841	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[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	nsv1024844	chr5:79862428-80860430	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases

mRNA abundance (count:13)

SNP	Gene	Cis/trans	Tissue	Source
rs10055063	CTD-2248H3.1	cis	Esophagus Muscularis	GTEx
rs10055063	CTC-281B15.1	cis	Nerve Tibial	GTEx
rs10055063	CTC-281B15.1	cis	Artery Aorta	GTEx
rs10055063	CTD-2248H3.1	cis	Adipose Subcutaneous	GTEx
rs10055063	CTC-281B15.1	cis	Esophagus Muscularis	GTEx
rs10055063	CTD-2248H3.1	cis	Thyroid	GTEx
rs10055063	CTC-281B15.1	cis	Stomach	GTEx
rs10055063	CTC-281B15.1	cis	Thyroid	GTEx
rs10055063	CTC-281B15.1	cis	Esophagus Mucosa	GTEx
rs10055063	CTC-281B15.1	cis	Artery Tibial	GTEx
rs10055063	CTD-2248H3.1	cis	lung	GTEx
rs10055063	CTC-281B15.1	cis	lung	GTEx
rs10055063	CTD-2248H3.1	cis	Artery Aorta	GTEx

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:80608600-80623000	Weak transcription	Psoas Muscle	Psoas
2	chr5:80611600-80623600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr5:80612200-80623600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr5:80619600-80622400	Weak transcription	Liver	Liver
5	chr5:80621800-80622400	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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