Variant report

Variant	rs986201
Chromosome Location	chr14:66536914-66536915
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:66427400..66429193-chr14:66535777..66538129,25	MCF-7	breast:
2	chr14:66414502..66416771-chr14:66536392..66538001,2	MCF-7	breast:
3	chr14:66425922..66427142-chr14:66536724..66537891,6	MCF-7	breast:

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10150157	0.87[ASN][1000 genomes]
rs10150794	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1036980	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12433502	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1444168	0.83[JPT][hapmap]
rs17103222	0.84[JPT][hapmap]
rs2318844	0.81[ASN][1000 genomes]
rs4144665	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4902442	0.83[JPT][hapmap];0.82[MEX][hapmap]
rs6573645	0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7144103	0.83[ASN][1000 genomes]
rs7154776	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9323468	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043943	chr14:65782466-66698411	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
2	nsv542120	chr14:65782466-66698411	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
3	nsv817409	chr14:66220075-66990168	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
4	nsv564953	chr14:66287921-67046960	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
5	nsv1050485	chr14:66308283-67109270	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
6	nsv530775	chr14:66316836-67079049	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
7	nsv530793	chr14:66317036-67078908	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
8	nsv1046455	chr14:66345369-66848234	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
9	nsv1043864	chr14:66372458-66845503	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
10	nsv917338	chr14:66376591-66841403	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
11	esv3385263	chr14:66514718-67511481	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66532200-66537000	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr14:66532800-66537400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr14:66534800-66543400	Weak transcription	Fetal Brain Female	brain
4	chr14:66535000-66537400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr14:66535400-66537400	Enhancers	HMEC	breast
6	chr14:66535400-66537600	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr14:66536000-66537600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr14:66536000-66547000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr14:66536200-66537600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr14:66536200-66537600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr14:66536200-66541400	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr14:66536600-66537000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr14:66536600-66537000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr14:66536600-66537000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr14:66536600-66537000	Enhancers	Brain Substantia Nigra	brain
16	chr14:66536600-66537200	Enhancers	Placenta Amnion	Placenta Amnion
17	chr14:66536800-66537000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr14:66536800-66537000	Bivalent Enhancer	Fetal Stomach	stomach
19	chr14:66536800-66537400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr14:66536800-66537400	Enhancers	Brain Germinal Matrix	brain
21	chr14:66536800-66537600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr14:66536800-66537600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
23	chr14:66536800-66537600	Enhancers	Placenta	Placenta

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