Variant report

Variant	rs894150
Chromosome Location	chr8:96240985-96240986
allele	A/G
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:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:96145964..96148025-chr8:96239692..96241242,2	MCF-7	breast:
2	chr8:96239351..96241151-chr8:96247805..96249381,2	MCF-7	breast:
3	chr8:96239016..96241801-chr8:96243185..96245921,2	MCF-7	breast:
4	chr8:96240965..96243166-chr8:96252025..96254042,3	K562	blood:
5	chr8:96240789..96242805-chr8:96252372..96254385,3	K562	blood:
6	chr8:96233041..96235359-chr8:96238288..96241007,3	K562	blood:
7	chr8:96084881..96087733-chr8:96239867..96242215,3	MCF-7	breast:
8	chr8:96222215..96224892-chr8:96239784..96242279,2	MCF-7	breast:
9	chr8:96224814..96227323-chr8:96239460..96241166,3	MCF-7	breast:
10	chr8:96239240..96241215-chr8:96244914..96248459,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000175895	Chromatin interaction
ENSG00000245080	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10110956	1.00[EUR][1000 genomes]
rs11984713	1.00[EUR][1000 genomes]
rs16917498	1.00[EUR][1000 genomes]
rs16917547	1.00[EUR][1000 genomes]
rs2514575	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28663698	1.00[EUR][1000 genomes]
rs56037611	1.00[EUR][1000 genomes]
rs56102903	1.00[EUR][1000 genomes]
rs73266459	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73695208	1.00[EUR][1000 genomes]
rs7839243	1.00[EUR][1000 genomes]
rs7840518	1.00[EUR][1000 genomes]
rs7845866	1.00[EUR][1000 genomes]
rs894148	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	nsv1017301	chr8:95273503-96248352	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv539680	chr8:95273503-96248352	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	esv16466	chr8:96206151-96243934	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv6315	chr8:96216465-96261671	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv465741	chr8:96221122-96247835	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv611759	chr8:96221122-96247835	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96219800-96251800	Enhancers	Primary B cells from peripheral blood	blood
2	chr8:96231600-96241600	Enhancers	Fetal Thymus	thymus
3	chr8:96235000-96242200	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr8:96235200-96249200	Enhancers	Primary B cells from cord blood	blood
5	chr8:96238600-96241000	Enhancers	HepG2	liver
6	chr8:96238600-96242000	Weak transcription	HSMMtube	muscle
7	chr8:96238600-96244800	Weak transcription	Left Ventricle	heart
8	chr8:96238600-96246600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr8:96238800-96241000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr8:96238800-96241000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr8:96238800-96241000	Weak transcription	HMEC	breast
12	chr8:96238800-96243800	Weak transcription	Fetal Heart	heart
13	chr8:96238800-96250200	Weak transcription	Stomach Smooth Muscle	stomach
14	chr8:96239000-96241000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr8:96239000-96241000	Weak transcription	Primary hematopoietic stem cells	blood
16	chr8:96239000-96241000	Weak transcription	NHEK	skin
17	chr8:96239000-96241200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr8:96239000-96243000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr8:96239000-96244000	Weak transcription	Right Atrium	heart
20	chr8:96239000-96244800	Weak transcription	Right Ventricle	heart
21	chr8:96239200-96246400	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr8:96239400-96241000	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr8:96239400-96241000	Weak transcription	Spleen	Spleen
24	chr8:96239400-96241200	Weak transcription	Esophagus	oesophagus
25	chr8:96239400-96242000	Weak transcription	Fetal Muscle Leg	muscle
26	chr8:96239600-96241000	Enhancers	Thymus	Thymus
27	chr8:96239600-96244600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr8:96239800-96244400	Weak transcription	Fetal Stomach	stomach
29	chr8:96240000-96241400	Enhancers	Primary T cells from cord blood	blood
30	chr8:96240200-96241800	Enhancers	Fetal Muscle Trunk	muscle
31	chr8:96240400-96241200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr8:96240400-96244200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr8:96240600-96241400	Enhancers	Primary T cells fromperipheralblood	blood
34	chr8:96240800-96241200	Weak transcription	Lung	lung
35	chr8:96240800-96241400	Flanking Active TSS	K562	blood
36	chr8:96240800-96241800	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr8:96240800-96241800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr8:96240800-96241800	Enhancers	Placenta	Placenta
39	chr8:96240800-96241800	Flanking Active TSS	GM12878-XiMat	blood
40	chr8:96240800-96242000	Enhancers	Fetal Intestine Large	intestine
41	chr8:96240800-96242000	Enhancers	Fetal Intestine Small	intestine

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