Variant report

Variant	rs7158965
Chromosome Location	chr14:70394139-70394140
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:70389062..70391123-chr14:70393251..70396818,3	MCF-7	breast:

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1276119	0.80[ASN][1000 genomes]
rs227432	0.80[ASN][1000 genomes]
rs35906492	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7142820	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7148010	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7159801	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs8003679	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8016072	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs927414	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv456336	chr14:70081956-70574149	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv565007	chr14:70081956-70574149	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
3	nsv832824	chr14:70320639-70511401	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70377800-70394400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:70384800-70394400	Weak transcription	HepG2	liver
3	chr14:70389000-70396800	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr14:70389200-70394400	Weak transcription	Brain Germinal Matrix	brain
5	chr14:70389400-70394400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr14:70389400-70394400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr14:70391000-70397400	Weak transcription	Brain Substantia Nigra	brain
8	chr14:70391200-70394600	Weak transcription	NH-A	brain
9	chr14:70391400-70394600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr14:70391400-70394600	Weak transcription	Osteobl	bone
11	chr14:70391800-70395600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr14:70392000-70396800	Genic enhancers	Cortex derived primary cultured neurospheres	brain
13	chr14:70392800-70395200	Genic enhancers	Hela-S3	cervix
14	chr14:70392800-70395400	Enhancers	Fetal Stomach	stomach
15	chr14:70393000-70396000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr14:70393200-70398000	Weak transcription	Liver	Liver
17	chr14:70393400-70395200	Enhancers	Placenta	Placenta
18	chr14:70393600-70394200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr14:70393600-70394400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr14:70393800-70395200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr14:70393800-70395200	Enhancers	Spleen	Spleen
22	chr14:70393800-70395600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr14:70394000-70394800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr14:70394000-70395200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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