Variant report

Variant	rs10836110
Chromosome Location	chr11:33802866-33802867
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:33796395..33799145-chr11:33801691..33803227,2	MCF-7	breast:
2	chr11:33802470..33804969-chr11:33808877..33811819,2	K562	blood:
3	chr11:33793454..33797702-chr11:33802064..33806582,4	K562	blood:
4	chr11:33800180..33801974-chr11:33802206..33805134,2	K562	blood:

Variant related genes	Relation type
ENSG00000110429	Chromatin interaction
ENSG00000255272	Chromatin interaction
ENSG00000254508	Chromatin interaction
ENSG00000255161	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10742306	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs10768028	0.94[CHB][hapmap];0.89[JPT][hapmap];0.91[ASN][1000 genomes]
rs10768029	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10836111	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11032383	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11032397	0.90[CEU][hapmap];0.90[CHB][hapmap];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1112841	0.82[CEU][hapmap]
rs12223394	0.84[CHB][hapmap]
rs12224154	0.86[CEU][hapmap]
rs12806824	0.87[CEU][hapmap]
rs12807373	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1522084	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1522085	0.86[CEU][hapmap]
rs1718067	0.87[CEU][hapmap]
rs2272064	0.86[CEU][hapmap]
rs2746602	0.87[CEU][hapmap]
rs4348870	0.87[CEU][hapmap]
rs4756002	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7107237	0.92[ASN][1000 genomes]
rs7115489	0.91[CEU][hapmap]
rs7937643	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs831592	0.86[CEU][hapmap]
rs831595	0.87[CEU][hapmap]
rs884710	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs953142	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs999479	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs10836110	CD59	cis	Thyroid	GTEx
rs10836110	CD59	cis	Esophagus Muscularis	GTEx
rs10836110	CD59	Cis_1M	lymphoblastoid	RTeQTL
rs10836110	CD59	cis	Artery Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33802200-33818200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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