Variant report

Variant	rs10953715
Chromosome Location	chr7:112136286-112136287
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:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:111381523..111382478-chr7:112135251..112136853,11	K562	blood:
2	chr7:112131612..112134582-chr7:112135231..112138012,2	K562	blood:
3	chr7:111381542..111382436-chr7:112135847..112136539,2	MCF-7	breast:
4	chr7:112090285..112091878-chr7:112134715..112136966,2	K562	blood:
5	chr7:112091872..112092453-chr7:112136033..112136757,2	MCF-7	breast:
6	chr7:112089150..112090788-chr7:112134779..112137087,2	MCF-7	breast:
7	chr7:112136223..112138120-chr7:112152281..112154931,2	K562	blood:
8	chr7:112134757..112136693-chr7:112137784..112140752,2	K562	blood:
9	chr7:112135974..112137750-chr7:112147907..112149600,2	MCF-7	breast:
10	chr7:112025626..112027691-chr7:112134133..112136855,2	K562	blood:
11	chr7:112121406..112122230-chr7:112135636..112136388,2	MCF-7	breast:
12	chr7:112134584..112136693-chr7:112137323..112139687,3	K562	blood:
13	chr7:112128634..112130975-chr7:112134554..112137012,2	MCF-7	breast:
14	chr7:112120089..112121280-chr7:112135851..112136600,6	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000181016	Chromatin interaction
ENSG00000006652	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1006536	0.84[CEU][hapmap];0.93[CHB][hapmap];0.88[CHD][hapmap];0.93[GIH][hapmap];0.82[ASN][1000 genomes]
rs10953714	0.84[CEU][hapmap]
rs11767398	0.84[CEU][hapmap]
rs13232911	0.88[JPT][hapmap]
rs2396550	0.87[CHB][hapmap];0.82[CHD][hapmap]
rs2396551	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2906789	0.80[CHD][hapmap];0.88[JPT][hapmap];0.81[ASN][1000 genomes]
rs3095031	0.87[CHB][hapmap];0.80[CHD][hapmap]
rs3095034	0.87[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs3128378	0.87[CHB][hapmap];0.83[CHD][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531436	chr7:111856171-112585407	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	105 gene(s)	inside rSNPs	diseases
2	nsv1030033	chr7:112092709-112140430	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112118800-112141600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr7:112125200-112138200	Weak transcription	Pancreas	Pancrea
3	chr7:112125400-112142200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:112125400-112143200	Weak transcription	Fetal Muscle Trunk	muscle
5	chr7:112126000-112143600	Weak transcription	Right Ventricle	heart
6	chr7:112128400-112145600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr7:112130200-112142200	Weak transcription	Adipose Nuclei	Adipose
8	chr7:112132800-112141800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr7:112133800-112137400	Weak transcription	Fetal Heart	heart
10	chr7:112134400-112136400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr7:112134800-112136400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr7:112135000-112136400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr7:112135000-112136400	Enhancers	Stomach Smooth Muscle	stomach
14	chr7:112135000-112136400	Enhancers	NHDF-Ad	bronchial
15	chr7:112135200-112137200	Weak transcription	GM12878-XiMat	blood
16	chr7:112135400-112136400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr7:112135600-112136400	Enhancers	Liver	Liver
18	chr7:112136200-112136400	Enhancers	Brain Substantia Nigra	brain
19	chr7:112136200-112136400	Enhancers	Duodenum Smooth Muscle	Duodenum
20	chr7:112136200-112136400	Enhancers	Sigmoid Colon	Sigmoid Colon
21	chr7:112136200-112136400	Enhancers	HepG2	liver

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