Variant report

Variant	rs932914
Chromosome Location	chr13:52441175-52441176
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	chr13:52433253..52437139-chr13:52439387..52442312,3	MCF-7	breast:
2	chr13:52438903..52441827-chr13:52476688..52479504,2	K562	blood:

Variant related genes	Relation type
ENSG00000123171	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1748124	0.84[EUR][1000 genomes]
rs17601275	0.83[EUR][1000 genomes]
rs1886322	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34944966	0.89[AMR][1000 genomes]
rs4310756	0.82[EUR][1000 genomes]
rs4941714	0.85[AMR][1000 genomes]
rs4943033	0.86[AMR][1000 genomes]
rs4943034	0.83[AMR][1000 genomes]
rs4943036	0.84[AMR][1000 genomes]
rs7324123	0.85[AMR][1000 genomes]
rs7325195	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7326982	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7350659	0.96[ASN][1000 genomes]
rs7490241	0.83[EUR][1000 genomes]
rs913900	0.85[AMR][1000 genomes]
rs932913	0.80[ASW][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs9526797	0.91[ASN][1000 genomes]
rs9526802	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9526803	0.83[EUR][1000 genomes]
rs9535776	1.00[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs9535779	0.82[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.89[TSI][hapmap];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9535780	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9535781	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9535782	0.83[EUR][1000 genomes]
rs9535783	0.83[EUR][1000 genomes]
rs9568670	0.90[AMR][1000 genomes]
rs9568671	0.83[AMR][1000 genomes]
rs9591437	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9596596	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9596598	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9596607	0.81[AMR][1000 genomes]
rs9634847	0.85[AMR][1000 genomes]
rs9634848	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9989110	0.89[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530718	chr13:52291802-52832752	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv933424	chr13:52293482-52507732	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1044310	chr13:52321564-52643924	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1050117	chr13:52325116-52643924	Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
5	nsv934070	chr13:52362588-53174923	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs932914	THSD1	cis	cerebellum	SCAN
rs932914	NCRNA00282	cis	cerebellum	SCAN
rs932914	CKAP2	cis	parietal	SCAN
rs932914	CKAP2	cis	cerebellum	SCAN

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52433800-52479400	Weak transcription	HepG2	liver
2	chr13:52438000-52441200	Weak transcription	Fetal Thymus	thymus
3	chr13:52438200-52446000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr13:52438200-52455400	Weak transcription	Fetal Intestine Small	intestine

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