Variant report

Variant	rs10792942
Chromosome Location	chr11:87043832-87043833
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:87043141-87044798	HepG2	liver:	n/a	n/a
2	POLR2A	chr11:87043812-87044091	HepG2	liver:	n/a	n/a
3	POLR2A	chr11:87035892-87046208	K562	blood:	n/a	n/a

Variant related genes	Relation type
PSMA2P1	TF binding region

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10501636	0.84[ASN][1000 genomes]
rs10792943	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10792944	0.92[ASN][1000 genomes]
rs10898667	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10898669	0.83[EUR][1000 genomes]
rs10898673	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10898674	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10898675	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10898677	0.92[ASN][1000 genomes]
rs10898682	0.89[ASN][1000 genomes]
rs10898686	0.84[ASN][1000 genomes]
rs11235088	0.86[CEU][hapmap]
rs11235104	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235105	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235106	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235107	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235109	0.95[ASN][1000 genomes]
rs11235110	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11235122	0.92[ASN][1000 genomes]
rs11235130	0.89[ASN][1000 genomes]
rs11501862	0.89[ASN][1000 genomes]
rs11501863	0.89[ASN][1000 genomes]
rs11604458	0.95[ASN][1000 genomes]
rs12276145	0.86[CEU][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12281655	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12294015	0.95[ASN][1000 genomes]
rs12295057	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12295490	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12361047	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12363623	0.89[ASN][1000 genomes]
rs12363892	0.90[ASN][1000 genomes]
rs12790362	0.86[CEU][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2186727	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28395418	0.92[ASN][1000 genomes]
rs4245431	0.84[ASN][1000 genomes]
rs4453264	0.89[ASN][1000 genomes]
rs4471448	0.89[ASN][1000 genomes]
rs4536247	1.00[ASN][1000 genomes]
rs4943983	0.84[ASN][1000 genomes]
rs4944700	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4944701	0.95[ASN][1000 genomes]
rs7122267	0.89[ASN][1000 genomes]
rs7125169	0.89[ASN][1000 genomes]
rs7125381	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7938135	0.89[ASN][1000 genomes]
rs7951257	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043562	chr11:86755535-87547185	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv541120	chr11:86755535-87547185	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv1046288	chr11:86757573-87158571	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:87012800-87044200	Weak transcription	Brain Hippocampus Middle	brain
2	chr11:87014400-87047400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr11:87033600-87044200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr11:87036800-87046400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:87041600-87046600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr11:87042800-87047800	Weak transcription	Aorta	Aorta

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