Variant report

Variant	rs73283932
Chromosome Location	chr8:104280928-104280929
allele	C/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:1)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:104279333..104281935-chr8:104310595..104312938,3	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf56-1	chr8:104280920-104281071	ENSG00000247081
2	lnc-C8orf56-1	chr8:104280920-104281071	ENSG00000247081
3	lnc-C8orf56-1	chr8:104280920-104281071	NONHSAT128160
4	lnc-C8orf56-1	chr8:104280920-104281071	NONHSAT128172
5	lnc-C8orf56-1	chr8:104280920-104281071	NONHSAT128173
6	lnc-C8orf56-1	chr8:104280920-104281071	NONHSAT128175
7	lnc-C8orf56-1	chr8:104280920-104281071	NONHSAT128169

No data

Variant related genes	Relation type
ENSG00000164930	Chromatin interaction
ENSG00000247081	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs34542607	1.00[AMR][1000 genomes]
rs55855345	1.00[AMR][1000 genomes]
rs61185155	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73282154	0.81[AFR][1000 genomes]
rs73282162	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73282174	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73282188	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73282194	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73282197	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73283903	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73283913	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73283915	1.00[AMR][1000 genomes]
rs73283918	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73283922	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73701722	1.00[AMR][1000 genomes]
rs73701724	1.00[AMR][1000 genomes]
rs73701730	1.00[AMR][1000 genomes]
rs73701733	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429931	chr8:104097396-104878014	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	esv1848810	chr8:104128496-104369288	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	esv1844303	chr8:104128696-104369090	Genic enhancers Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	nsv1015965	chr8:104192086-104361108	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv1017326	chr8:104236193-104313235	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104268200-104283400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:104268800-104281200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr8:104269000-104283400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:104269800-104283200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:104269800-104283600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:104279000-104281000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr8:104279200-104282600	Enhancers	NHDF-Ad	bronchial
8	chr8:104279400-104282000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:104279400-104282400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr8:104279400-104282600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr8:104279400-104282800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr8:104279600-104281200	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr8:104279600-104282600	Enhancers	Osteobl	bone
14	chr8:104279600-104282800	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr8:104279600-104282800	Enhancers	NHLF	lung
16	chr8:104279800-104281200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr8:104279800-104281800	Enhancers	HSMM	muscle
18	chr8:104280000-104283400	Weak transcription	Aorta	Aorta
19	chr8:104280200-104283400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr8:104280400-104281000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr8:104280600-104281200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr8:104280600-104281800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr8:104280600-104281800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr8:104280800-104281800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr8:104280800-104283000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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