Variant report

Variant	rs6914299
Chromosome Location	chr6:88149176-88149177
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:88144877..88146719-chr6:88147665..88149814,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000213204	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1051131	0.91[CHB][hapmap]
rs1051148	0.91[CHB][hapmap]
rs10755484	0.91[CHB][hapmap]
rs13214153	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1753154	0.81[CHB][hapmap]
rs2103764	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2207144	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2207146	0.95[CHB][hapmap];0.86[ASN][1000 genomes]
rs2268993	0.95[CHB][hapmap];0.85[ASN][1000 genomes]
rs2268994	0.96[CHB][hapmap];0.85[ASN][1000 genomes]
rs2273129	0.95[CHB][hapmap];0.86[ASN][1000 genomes]
rs2284908	0.91[CHB][hapmap];0.81[ASN][1000 genomes]
rs2300906	0.91[CHB][hapmap]
rs2300909	0.91[CHB][hapmap]
rs3757368	0.91[CHB][hapmap]
rs381782	0.81[CHB][hapmap]
rs3918467	0.95[CHB][hapmap]
rs3934838	0.91[CHB][hapmap]
rs4334949	0.91[CHB][hapmap]
rs4464759	0.91[CHB][hapmap]
rs4587143	0.91[CHB][hapmap]
rs6454630	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6454631	0.86[CHB][hapmap]
rs6903219	0.86[JPT][hapmap]
rs6905947	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6912958	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6916732	0.95[CHB][hapmap]
rs6921504	0.80[CHB][hapmap]
rs6933587	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7741825	0.82[CHB][hapmap]
rs7761814	0.96[CHB][hapmap];0.83[ASN][1000 genomes]
rs7773906	0.91[CHB][hapmap]
rs9294379	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9294380	1.00[CEU][hapmap];0.93[YRI][hapmap]
rs9294381	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9359748	0.85[JPT][hapmap]
rs9444504	0.95[CHB][hapmap];0.86[ASN][1000 genomes]
rs9444519	0.82[CEU][hapmap];0.91[CHB][hapmap]
rs9444522	0.90[CHB][hapmap]
rs9450688	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9450701	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9450704	0.96[CHB][hapmap];0.86[ASN][1000 genomes]
rs9450712	0.95[CHB][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs9450723	0.91[CHB][hapmap]
rs9450732	0.91[CHB][hapmap]
rs9450752	0.91[CHB][hapmap]
rs985764	0.91[CHB][hapmap]

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	nsv1018155	chr6:88049729-88272862	Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv830722	chr6:88054186-88223625	Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1031961	chr6:88110401-88367006	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs6914299	C6orf163	Cis_1M	lymphoblastoid	RTeQTL
rs6914299	C6orf164	cis	Whole Blood	GTEx
rs6914299	SLC35A1	cis	multi-tissue	Pritchard
rs6914299	C6orf164	cis	Thyroid	GTEx
rs6914299	C6orf164	cis	Esophagus Muscularis	GTEx
rs6914299	SLC35A1	Cis_1M	lymphoblastoid	RTeQTL
rs6914299	C6orf162	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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