Variant report

Variant	rs4714203
Chromosome Location	chr6:38940796-38940797
allele	A/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:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:38940697..38941572-chr6:39270556..39271601,4	K562	blood:
2	chr6:38940785..38941562-chr6:39059873..39060576,3	MCF-7	breast:
3	chr6:38940756..38941516-chr6:39125200..39125963,2	MCF-7	breast:
4	chr6:38934741..38936465-chr6:38939691..38941854,2	K562	blood:
5	chr6:38940416..38941559-chr6:39059453..39060636,4	K562	blood:
6	chr6:38940690..38941643-chr6:39133929..39134512,2	MCF-7	breast:
7	chr6:38940723..38941491-chr6:39055376..39056317,2	MCF-7	breast:
8	chr6:38939668..38941967-chr6:39077128..39080057,2	K562	blood:
9	chr6:38939906..38942695-chr6:38942827..38945177,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000217165	Chromatin interaction
ENSG00000112167	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11753074	0.90[CEU][hapmap]
rs11753138	0.90[CEU][hapmap]
rs1332012	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.94[GIH][hapmap];0.83[MKK][hapmap];0.89[TSI][hapmap];0.85[YRI][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1332014	0.90[CEU][hapmap]
rs1537231	0.90[CEU][hapmap]
rs2235871	0.90[CEU][hapmap]
rs2273093	0.90[CEU][hapmap]
rs2281340	0.90[CEU][hapmap]
rs2281346	0.90[CEU][hapmap]
rs2395710	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs2894418	0.90[CEU][hapmap]
rs3857575	0.90[CEU][hapmap]
rs4714202	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs4714204	0.89[CEU][hapmap]
rs4714208	0.90[CEU][hapmap]
rs506672	1.00[CEU][hapmap]
rs6458088	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs761384	0.90[CEU][hapmap]
rs761385	0.89[CEU][hapmap]
rs7766930	0.90[CEU][hapmap]
rs926674	0.85[MEX][hapmap]
rs9296273	0.90[CEU][hapmap]
rs9366992	0.89[CEU][hapmap]
rs9369100	0.90[CEU][hapmap]
rs9380815	0.89[CEU][hapmap]
rs9380817	0.90[CEU][hapmap]
rs9380818	1.00[CEU][hapmap]
rs9462460	0.90[CEU][hapmap]
rs9462464	0.90[CEU][hapmap]
rs9462466	0.90[CEU][hapmap]
rs9462469	0.90[CEU][hapmap]
rs9470949	0.90[CEU][hapmap]
rs9470950	0.90[CEU][hapmap]
rs9470961	0.89[CEU][hapmap]
rs9470962	0.90[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv885817	chr6:38036420-39019503	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1028088	chr6:38821047-39163549	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv538205	chr6:38821047-39163549	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv885821	chr6:38843970-39039503	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv948357	chr6:38920998-39035836	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38938200-38942200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr6:38939200-38941400	Weak transcription	Fetal Intestine Large	intestine
3	chr6:38939800-38941400	Weak transcription	Fetal Intestine Small	intestine

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