Variant report

Variant	rs17768440
Chromosome Location	chr14:38050944-38050945
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:38049811..38051883-chr14:38056230..38058824,2	K562	blood:
2	chr14:38013794..38017816-chr14:38049871..38055560,6	MCF-7	breast:
3	chr14:38050621..38053581-chr14:38135495..38137848,2	MCF-7	breast:
4	chr14:38018016..38020323-chr14:38050834..38052652,3	MCF-7	breast:
5	chr14:38006457..38009317-chr14:38049847..38052544,2	MCF-7	breast:
6	chr14:37709149..37730989-chr14:38048141..38067789,135	MCF-7	breast:
7	chr14:38010426..38020494-chr14:38050537..38062032,33	MCF-7	breast:
8	chr14:37708906..37733371-chr14:38048131..38068843,170	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000151338	Chromatin interaction

Extended variants
information (count: 132 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:126)

rs_ID	r²[population]
rs12147674	1.00[AFR][1000 genomes]
rs12878124	1.00[AFR][1000 genomes]
rs12878633	1.00[AFR][1000 genomes]
rs12878710	1.00[AFR][1000 genomes]
rs12878846	1.00[AFR][1000 genomes]
rs12879149	1.00[AFR][1000 genomes]
rs12879319	1.00[AFR][1000 genomes]
rs12882123	1.00[AFR][1000 genomes]
rs12882687	1.00[AFR][1000 genomes]
rs12882773	1.00[AFR][1000 genomes]
rs12887471	1.00[AFR][1000 genomes]
rs12888451	1.00[AFR][1000 genomes]
rs12889687	1.00[AFR][1000 genomes]
rs12889859	1.00[AFR][1000 genomes]
rs12890074	1.00[AFR][1000 genomes]
rs12890845	1.00[AFR][1000 genomes]
rs12893402	1.00[AFR][1000 genomes]
rs12894394	1.00[AFR][1000 genomes]
rs12896790	1.00[AFR][1000 genomes]
rs12897309	1.00[AFR][1000 genomes]
rs17106861	1.00[CEU][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17179274	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17179281	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17768411	0.80[AMR][1000 genomes]
rs17768417	0.80[AMR][1000 genomes]
rs17768423	0.80[AMR][1000 genomes]
rs17768434	0.80[AMR][1000 genomes]
rs17768654	1.00[AFR][1000 genomes]
rs33984772	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34025516	1.00[AFR][1000 genomes]
rs34043056	1.00[AFR][1000 genomes]
rs34069628	1.00[AFR][1000 genomes]
rs34184341	1.00[AFR][1000 genomes]
rs34242177	1.00[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs34256053	1.00[AFR][1000 genomes]
rs34265999	1.00[AFR][1000 genomes]
rs34273412	1.00[AFR][1000 genomes]
rs34306117	1.00[AFR][1000 genomes]
rs34338696	1.00[AFR][1000 genomes]
rs34434018	1.00[AFR][1000 genomes]
rs34450997	1.00[AFR][1000 genomes]
rs34469876	1.00[AFR][1000 genomes]
rs34496783	1.00[AFR][1000 genomes]
rs34516219	1.00[AFR][1000 genomes]
rs34543736	1.00[AFR][1000 genomes]
rs34548330	1.00[AFR][1000 genomes]
rs34567961	1.00[AFR][1000 genomes]
rs34586390	1.00[AFR][1000 genomes]
rs34680819	1.00[AFR][1000 genomes]
rs34747911	1.00[AFR][1000 genomes]
rs34813864	1.00[AFR][1000 genomes]
rs34830744	1.00[AFR][1000 genomes]
rs34886614	1.00[AFR][1000 genomes]
rs35030337	1.00[AFR][1000 genomes]
rs35074434	1.00[AFR][1000 genomes]
rs35082276	1.00[AFR][1000 genomes]
rs35110244	1.00[AFR][1000 genomes]
rs35111962	1.00[AFR][1000 genomes]
rs35141852	1.00[AFR][1000 genomes]
rs35169093	1.00[AFR][1000 genomes]
rs35190835	1.00[AFR][1000 genomes]
rs35294705	1.00[AFR][1000 genomes]
rs35310265	1.00[AFR][1000 genomes]
rs35319231	1.00[AFR][1000 genomes]
rs35330350	1.00[AFR][1000 genomes]
rs35333548	1.00[AFR][1000 genomes]
rs35347282	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35350493	1.00[AFR][1000 genomes]
rs35383091	1.00[AFR][1000 genomes]
rs35393462	1.00[AFR][1000 genomes]
rs35413274	1.00[AFR][1000 genomes]
rs35427651	1.00[AFR][1000 genomes]
rs35435404	1.00[AFR][1000 genomes]
rs35438963	1.00[AFR][1000 genomes]
rs35441075	1.00[AFR][1000 genomes]
rs35470726	1.00[AFR][1000 genomes]
rs35505269	1.00[AFR][1000 genomes]
rs35536208	1.00[AFR][1000 genomes]
rs35610918	1.00[AFR][1000 genomes]
rs35699962	1.00[AFR][1000 genomes]
rs35706871	1.00[AFR][1000 genomes]
rs35748911	1.00[AFR][1000 genomes]
rs35791659	1.00[AFR][1000 genomes]
rs35802121	1.00[AFR][1000 genomes]
rs35852338	1.00[AFR][1000 genomes]
rs35891950	1.00[AFR][1000 genomes]
rs35926829	1.00[AFR][1000 genomes]
rs35926928	1.00[AFR][1000 genomes]
rs35942161	1.00[AFR][1000 genomes]
rs36004540	1.00[AFR][1000 genomes]
rs36044547	1.00[AFR][1000 genomes]
rs36074427	1.00[AFR][1000 genomes]
rs36189403	1.00[AFR][1000 genomes]
rs36194865	1.00[AFR][1000 genomes]
rs55734217	1.00[AFR][1000 genomes]
rs55751336	0.80[AMR][1000 genomes]
rs55972477	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56223359	1.00[AFR][1000 genomes]
rs56374777	0.80[AMR][1000 genomes]
rs71405800	1.00[AFR][1000 genomes]
rs71407707	1.00[AFR][1000 genomes]
rs71407708	1.00[AFR][1000 genomes]
rs71407709	1.00[AFR][1000 genomes]
rs71407710	1.00[AFR][1000 genomes]
rs71407711	1.00[AFR][1000 genomes]
rs71407712	1.00[AFR][1000 genomes]
rs71407716	1.00[AFR][1000 genomes]
rs71407717	1.00[AFR][1000 genomes]
rs71407718	1.00[AFR][1000 genomes]
rs71407720	1.00[AFR][1000 genomes]
rs71407721	1.00[AFR][1000 genomes]
rs71407722	1.00[AFR][1000 genomes]
rs71407723	1.00[AFR][1000 genomes]
rs71407724	1.00[AFR][1000 genomes]
rs71407725	1.00[AFR][1000 genomes]
rs71407726	1.00[AFR][1000 genomes]
rs71407727	1.00[AFR][1000 genomes]
rs71407728	1.00[AFR][1000 genomes]
rs71407729	1.00[AFR][1000 genomes]
rs71407730	1.00[AFR][1000 genomes]
rs71407731	1.00[AFR][1000 genomes]
rs71407732	1.00[AFR][1000 genomes]
rs71407733	1.00[AFR][1000 genomes]
rs71407734	1.00[AFR][1000 genomes]
rs71407741	1.00[AFR][1000 genomes]
rs719022	0.80[AMR][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	nsv530038	chr14:37590543-38336191	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv826923	chr14:38017619-38108645	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
3	nsv832772	chr14:38030300-38225921	Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
4	nsv901642	chr14:38041870-38081005	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
5	nsv901643	chr14:38047789-38081005	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
6	nsv901644	chr14:38049107-38064738	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38037200-38052400	Weak transcription	Liver	Liver
2	chr14:38048200-38051800	Weak transcription	HepG2	liver
3	chr14:38050000-38051800	Weak transcription	A549	lung
4	chr14:38050800-38051000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr14:38050800-38052400	Weak transcription	Hela-S3	cervix

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