Variant report

Variant	rs1388244
Chromosome Location	chr6:45650154-45650155
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:45388238..45390141-chr6:45649008..45651079,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RUNX2-3	chr6:45649094-45651012	l_3186_chr6:45649093-45652486_testes

Variant related genes	Relation type
ENSG00000124813	Chromatin interaction
ENSG00000271857	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs12175323	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12661654	0.81[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs12663985	0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs12665728	0.83[ASN][1000 genomes]
rs1388242	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1491139	0.90[ASN][1000 genomes]
rs1491144	0.99[ASN][1000 genomes]
rs1491145	0.97[ASN][1000 genomes]
rs1994682	0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs2035791	0.97[ASN][1000 genomes]
rs2396505	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2782658	0.81[CHB][hapmap]
rs2782660	0.81[CHB][hapmap];0.84[GIH][hapmap]
rs321324	0.91[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs321325	0.91[CHB][hapmap];0.90[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs4326224	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs4714864	0.89[ASN][1000 genomes]
rs6458457	0.83[ASN][1000 genomes]
rs6458458	0.90[ASN][1000 genomes]
rs6919919	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6935044	0.91[CEU][hapmap]
rs7761790	0.83[ASN][1000 genomes]
rs7762915	0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs7774097	0.84[ASN][1000 genomes]
rs9349324	0.90[ASN][1000 genomes]
rs9357489	0.97[ASN][1000 genomes]
rs9369572	0.96[ASN][1000 genomes]
rs9395110	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9395111	0.96[ASN][1000 genomes]
rs9472541	0.90[JPT][hapmap];0.81[ASN][1000 genomes]
rs9472547	0.87[ASN][1000 genomes]
rs9472548	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9472552	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs9472555	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9472557	0.91[CHB][hapmap];0.90[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap];0.88[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	nsv1028393	chr6:44875558-45822335	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv538211	chr6:44875558-45822335	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv532024	chr6:45475088-45982640	Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45646800-45650400	ZNF genes & repeats	GM12878-XiMat	blood
2	chr6:45647800-45650800	ZNF genes & repeats	Primary B cells from peripheral blood	blood
3	chr6:45649400-45650400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:45649800-45650400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood

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