Variant report

Variant	rs206350
Chromosome Location	chr15:93226310-93226311
allele	C/T
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	chr15:93186486..93189076-chr15:93224544..93226997,2	MCF-7	breast:
2	chr15:93197096..93198076-chr15:93225951..93227103,4	MCF-7	breast:
3	chr15:93179649..93182992-chr15:93225341..93228473,3	MCF-7	breast:
4	chr15:93222087..93224907-chr15:93225321..93227678,2	MCF-7	breast:
5	chr15:93153824..93155691-chr15:93224962..93227625,2	MCF-7	breast:
6	chr15:93186791..93189169-chr15:93226083..93228824,3	MCF-7	breast:
7	chr15:93224785..93226821-chr15:93245528..93247882,2	MCF-7	breast:
8	chr15:93198078..93199856-chr15:93225325..93228145,2	MCF-7	breast:
9	chr15:93180560..93183388-chr15:93224923..93226823,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000185442	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs12917366	1.00[CHB][hapmap]
rs16947186	1.00[CHB][hapmap]
rs184047	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs206355	0.89[AMR][1000 genomes]
rs2132615	0.83[CEU][hapmap];1.00[CHB][hapmap]
rs285720	0.84[EUR][1000 genomes]
rs285723	0.86[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs285728	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs285737	1.00[CHB][hapmap];0.91[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];0.83[TSI][hapmap];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs285738	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs285739	0.84[CEU][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs285741	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs285743	0.87[CEU][hapmap];1.00[CHB][hapmap];0.85[GIH][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];0.83[TSI][hapmap];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs285744	0.86[CEU][hapmap];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs285764	1.00[CHB][hapmap]
rs285766	1.00[CHB][hapmap]
rs285767	1.00[CHB][hapmap]
rs99521	0.87[CEU][hapmap];1.00[CHB][hapmap];0.88[GIH][hapmap];0.83[TSI][hapmap];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][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	nsv1037972	chr15:92804908-93270761	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
2	nsv904499	chr15:92914795-93472582	Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	163 gene(s)	inside rSNPs	diseases
3	nsv948738	chr15:93070742-93728147	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
4	nsv1049490	chr15:93134405-93591660	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	151 gene(s)	inside rSNPs	diseases
5	nsv1040501	chr15:93177153-93286393	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1036897	chr15:93211991-93239388	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs206350	LOC400451	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:93214800-93232200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:93224000-93226800	Enhancers	HSMM	muscle
3	chr15:93224200-93226600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr15:93224200-93226600	Enhancers	Adipose Nuclei	Adipose
5	chr15:93224200-93226800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr15:93224200-93226800	Enhancers	Fetal Stomach	stomach
7	chr15:93224400-93226600	Enhancers	Muscle Satellite Cultured Cells	--
8	chr15:93224400-93226600	Enhancers	HSMMtube	muscle
9	chr15:93224400-93226800	Enhancers	Fetal Muscle Leg	muscle
10	chr15:93224400-93227200	Enhancers	Fetal Lung	lung
11	chr15:93224800-93227000	Enhancers	Fetal Muscle Trunk	muscle
12	chr15:93225000-93227000	Enhancers	NHDF-Ad	bronchial
13	chr15:93225000-93231800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr15:93225000-93232000	Weak transcription	Ovary	ovary
15	chr15:93225800-93226800	Enhancers	Placenta	Placenta
16	chr15:93226000-93234000	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr15:93226200-93226600	Enhancers	Lung	lung
18	chr15:93226200-93226800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr15:93226200-93226800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr15:93226200-93226800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr15:93226200-93226800	Enhancers	Left Ventricle	heart
22	chr15:93226200-93226800	Enhancers	Skeletal Muscle Male	skeletal muscle

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