Variant report

Variant	rs6969042
Chromosome Location	chr7:146072196-146072197
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs1358077	1.00[EUR][1000 genomes]
rs1405170	1.00[EUR][1000 genomes]
rs1405171	1.00[EUR][1000 genomes]
rs1526160	1.00[EUR][1000 genomes]
rs1631820	1.00[EUR][1000 genomes]
rs1639436	1.00[EUR][1000 genomes]
rs1639439	1.00[EUR][1000 genomes]
rs1639442	1.00[EUR][1000 genomes]
rs1639444	1.00[TSI][hapmap]
rs1639461	1.00[TSI][hapmap]
rs1639497	1.00[EUR][1000 genomes]
rs1639498	1.00[EUR][1000 genomes]
rs1639499	1.00[EUR][1000 genomes]
rs1639500	1.00[EUR][1000 genomes]
rs1639502	1.00[EUR][1000 genomes]
rs1639503	1.00[EUR][1000 genomes]
rs1718072	1.00[EUR][1000 genomes]
rs1718085	1.00[EUR][1000 genomes]
rs1718094	1.00[EUR][1000 genomes]
rs1718095	1.00[EUR][1000 genomes]
rs1718098	1.00[EUR][1000 genomes]
rs1724499	1.00[EUR][1000 genomes]
rs1724501	1.00[EUR][1000 genomes]
rs1724502	1.00[EUR][1000 genomes]
rs1724503	1.00[EUR][1000 genomes]
rs1724504	1.00[EUR][1000 genomes]
rs1724505	1.00[EUR][1000 genomes]
rs1724514	1.00[EUR][1000 genomes]
rs1724518	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs1724519	1.00[EUR][1000 genomes]
rs1724520	1.00[EUR][1000 genomes]
rs1724521	1.00[EUR][1000 genomes]
rs1724522	1.00[EUR][1000 genomes]
rs1724523	1.00[EUR][1000 genomes]
rs1724524	1.00[EUR][1000 genomes]
rs6947836	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7782691	0.92[YRI][hapmap]
rs7804084	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs802193	1.00[EUR][1000 genomes]
rs802197	1.00[EUR][1000 genomes]
rs802199	1.00[EUR][1000 genomes]
rs802201	1.00[EUR][1000 genomes]
rs802202	1.00[EUR][1000 genomes]
rs802204	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs802526	1.00[MEX][hapmap]
rs940958	1.00[EUR][1000 genomes]
rs940959	1.00[EUR][1000 genomes]
rs940960	1.00[EUR][1000 genomes]
rs940961	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs940962	1.00[EUR][1000 genomes]
rs940963	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889384	chr7:145541783-146239545	Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1020950	chr7:145683419-146264304	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv889387	chr7:145903862-146239545	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv533345	chr7:145934546-146134958	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv933136	chr7:145995920-146076835	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv889388	chr7:145998111-146082957	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv524528	chr7:145998111-146086322	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv889389	chr7:145998111-146121539	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv934010	chr7:146006146-146076835	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv933530	chr7:146016273-146076835	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv608929	chr7:146020936-146082957	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv608930	chr7:146025509-146081452	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv917027	chr7:146069317-146194011	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:146068800-146072800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:146071400-146072800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:146071600-146072600	Enhancers	Fetal Brain Female	brain

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