Variant report

Variant	rs1517044
Chromosome Location	chr6:70894059-70894060
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1212491	0.90[EUR][1000 genomes]
rs12192985	0.88[EUR][1000 genomes]
rs12201251	0.92[CEU][hapmap]
rs1474044	0.91[CEU][hapmap];0.90[EUR][1000 genomes]
rs1517041	0.88[EUR][1000 genomes]
rs1517045	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1616745	0.91[EUR][1000 genomes]
rs16868775	0.88[EUR][1000 genomes]
rs1753258	0.91[CEU][hapmap];0.91[EUR][1000 genomes]
rs3806053	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3806066	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs4707705	0.87[EUR][1000 genomes]
rs4707706	0.87[EUR][1000 genomes]
rs540152	0.91[CEU][hapmap];0.91[EUR][1000 genomes]
rs595957	0.91[CEU][hapmap];0.90[EUR][1000 genomes]
rs627540	0.91[EUR][1000 genomes]
rs671910	0.91[CEU][hapmap];0.91[EUR][1000 genomes]
rs6909142	0.92[CEU][hapmap];0.84[EUR][1000 genomes]
rs7739562	0.88[EUR][1000 genomes]
rs7744579	0.91[CEU][hapmap];0.88[EUR][1000 genomes]
rs802172	0.91[CEU][hapmap];0.92[EUR][1000 genomes]
rs802174	0.91[CEU][hapmap];0.92[EUR][1000 genomes]
rs802175	0.92[CEU][hapmap];0.92[EUR][1000 genomes]
rs802178	0.92[CEU][hapmap];0.92[EUR][1000 genomes]
rs802180	0.90[CEU][hapmap];0.92[EUR][1000 genomes]
rs802182	0.91[CEU][hapmap];0.92[EUR][1000 genomes]
rs802184	0.92[CEU][hapmap];0.92[EUR][1000 genomes]
rs802185	0.92[EUR][1000 genomes]
rs802187	0.92[CEU][hapmap];0.91[EUR][1000 genomes]
rs802188	0.91[EUR][1000 genomes]
rs802189	0.91[CEU][hapmap];0.91[EUR][1000 genomes]
rs9346371	0.91[CEU][hapmap];0.89[EUR][1000 genomes]
rs9346372	0.88[CEU][hapmap];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026151	chr6:70621616-70946967	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv933674	chr6:70663616-70973112	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv932111	chr6:70736835-71633094	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer 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	31 gene(s)	inside rSNPs	diseases
4	nsv886142	chr6:70741209-71251421	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv830683	chr6:70743422-70941190	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1015807	chr6:70874416-70913489	Strong transcription Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70856200-70899400	Weak transcription	Left Ventricle	heart
2	chr6:70875600-70919800	Weak transcription	GM12878-XiMat	blood
3	chr6:70885800-70901400	Strong transcription	Primary B cells from cord blood	blood
4	chr6:70886000-70904600	Strong transcription	Primary B cells from peripheral blood	blood
5	chr6:70889600-70901800	Weak transcription	Fetal Muscle Trunk	muscle

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