Variant report

Variant	rs17310732
Chromosome Location	chr8:99415437-99415438
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:99399092..99403051-chr8:99412315..99417483,4	K562	blood:
2	chr8:99410069..99412825-chr8:99413112..99416320,3	MCF-7	breast:
3	chr8:99407529..99410363-chr8:99413128..99417283,3	MCF-7	breast:
4	chr8:99404529..99406381-chr8:99414494..99416109,2	K562	blood:
5	chr8:99413566..99415958-chr8:99440640..99443091,2	MCF-7	breast:
6	chr8:99305293..99307105-chr8:99413175..99415820,2	MCF-7	breast:
7	chr8:99411379..99414219-chr8:99414803..99416412,2	K562	blood:
8	chr8:99405535..99409022-chr8:99413535..99417090,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000254267	Chromatin interaction
ENSG00000104361	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10098761	1.00[JPT][hapmap]
rs11778073	1.00[JPT][hapmap]
rs12115160	1.00[JPT][hapmap]
rs17310578	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17370425	1.00[CEU][hapmap];0.82[CHB][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs28756269	0.93[ASN][1000 genomes]
rs4130404	1.00[JPT][hapmap]
rs7005586	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7005600	0.85[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7843191	1.00[JPT][hapmap]
rs9297284	0.93[ASN][1000 genomes]
rs9642952	1.00[JPT][hapmap]

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	nsv1032904	chr8:98756076-99476925	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv539687	chr8:98756076-99476925	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv831406	chr8:99290745-99482076	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99408600-99416600	Enhancers	Ovary	ovary
2	chr8:99410000-99415600	Enhancers	Fetal Stomach	stomach
3	chr8:99410000-99416000	Enhancers	Fetal Lung	lung
4	chr8:99410600-99415600	Enhancers	Fetal Muscle Leg	muscle
5	chr8:99410800-99421400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr8:99411600-99416200	Enhancers	Left Ventricle	heart
7	chr8:99412000-99416200	Enhancers	Right Atrium	heart
8	chr8:99412600-99415600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr8:99412600-99415800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:99412600-99415800	Enhancers	Muscle Satellite Cultured Cells	--
11	chr8:99412600-99415800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr8:99412600-99415800	Enhancers	HSMM	muscle
13	chr8:99412600-99416000	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr8:99412800-99415800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr8:99412800-99415800	Weak transcription	Lung	lung
16	chr8:99414400-99415600	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr8:99414400-99416000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr8:99414600-99415600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr8:99414600-99415600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr8:99414600-99415600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr8:99414600-99416000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr8:99414600-99416000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr8:99414800-99415800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr8:99414800-99416000	Enhancers	Stomach Smooth Muscle	stomach
25	chr8:99415000-99415600	Enhancers	Placenta	Placenta
26	chr8:99415000-99416200	Enhancers	Spleen	Spleen
27	chr8:99415200-99419600	Weak transcription	Fetal Heart	heart
28	chr8:99415400-99415800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr8:99415400-99418800	Weak transcription	NHDF-Ad	bronchial

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