Variant report

Variant	rs2036740
Chromosome Location	chr15:56290020-56290021
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr15:56289909-56290109	MCF10A-Er-Src	breast:	n/a	n/a
2	POLR2A	chr15:56289897-56290087	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:56284668..56287599-chr15:56288074..56291098,3	K562	blood:
2	chr15:56281891..56284127-chr15:56288031..56290159,2	K562	blood:
3	chr15:56289959..56291765-chr15:56293575..56295875,2	K562	blood:
4	chr15:56288413..56291274-chr15:56330655..56333525,2	MCF-7	breast:

Variant related genes	Relation type
NEDD4	TF binding region
ENSG00000069869	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10162645	1.00[CEU][hapmap];0.81[CHB][hapmap];0.92[JPT][hapmap];0.86[YRI][hapmap]
rs1112535	0.92[JPT][hapmap];0.92[ASN][1000 genomes]
rs12441706	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12911653	0.92[JPT][hapmap];0.92[ASN][1000 genomes]
rs12911833	0.86[ASN][1000 genomes]
rs12913147	0.92[JPT][hapmap];0.88[ASN][1000 genomes]
rs12913423	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12915953	0.92[JPT][hapmap];0.92[ASN][1000 genomes]
rs16976674	0.92[ASN][1000 genomes]
rs2036738	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34077395	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34330530	0.92[ASN][1000 genomes]
rs34841076	0.92[ASN][1000 genomes]
rs35301686	0.90[ASN][1000 genomes]
rs35460567	0.87[ASN][1000 genomes]
rs35662811	0.92[ASN][1000 genomes]
rs35710039	0.91[ASN][1000 genomes]
rs35836088	0.92[ASN][1000 genomes]
rs35911067	0.92[ASN][1000 genomes]
rs35967908	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62046376	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71476762	0.87[ASN][1000 genomes]
rs71476763	0.92[ASN][1000 genomes]
rs71476768	0.92[ASN][1000 genomes]
rs7161742	0.91[ASN][1000 genomes]
rs7179929	0.92[ASN][1000 genomes]
rs9652429	1.00[CEU][hapmap];0.86[YRI][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761872	chr15:56211065-56426501	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv904245	chr15:56229760-56324451	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv457159	chr15:56255774-56321854	Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv569543	chr15:56255774-56321854	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv457160	chr15:56273446-56320235	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	n/a
6	nsv569544	chr15:56273446-56320235	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	n/a
7	nsv457161	chr15:56274443-56324451	Flanking Active TSS Enhancers Active TSS Strong transcription Weak 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	17 gene(s)	inside rSNPs	n/a
8	nsv569545	chr15:56274443-56324451	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	n/a
9	nsv569546	chr15:56274443-56337527	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56286600-56292000	Weak transcription	Esophagus	oesophagus
2	chr15:56286800-56290400	Weak transcription	Psoas Muscle	Psoas
3	chr15:56287000-56291600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr15:56287000-56291800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr15:56287200-56290200	Weak transcription	Fetal Intestine Large	intestine
6	chr15:56287200-56290400	Weak transcription	Placenta	Placenta
7	chr15:56287400-56291600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr15:56287600-56291800	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr15:56288000-56291600	Weak transcription	A549	lung
10	chr15:56288400-56291800	Enhancers	Hela-S3	cervix
11	chr15:56288800-56292800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr15:56289000-56295000	Enhancers	HMEC	breast
13	chr15:56289200-56295000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr15:56289400-56290600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr15:56289400-56291800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr15:56289400-56291800	Enhancers	NHEK	skin

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