Variant report

Variant	rs10089123
Chromosome Location	chr8:96097613-96097614
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: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	chr8:96095732..96098927-chr8:96100479..96105447,7	K562	blood:
2	chr8:96035298..96037639-chr8:96096701..96099172,2	MCF-7	breast:
3	chr8:96095758..96103345-chr8:96144049..96152228,17	MCF-7	breast:
4	chr8:96036624..96038754-chr8:96097409..96099751,2	MCF-7	breast:
5	chr8:95960634..95962626-chr8:96095689..96098105,2	MCF-7	breast:
6	chr1:149858166..149859995-chr8:96096320..96099010,2	MCF-7	breast:
7	chr8:96096428..96097966-chr8:96125843..96128409,2	K562	blood:
8	chr8:96096993..96099961-chr8:96235932..96238973,3	MCF-7	breast:
9	chr8:96096089..96098113-chr8:96363999..96366342,2	MCF-7	breast:
10	chr8:96095701..96099568-chr8:96099629..96105496,9	K562	blood:
11	chr8:96096484..96101537-chr8:96142870..96147410,9	MCF-7	breast:
12	chr8:96086982..96089497-chr8:96096571..96099137,3	K562	blood:
13	chr8:96097174..96099699-chr8:96151326..96153504,2	MCF-7	breast:
14	chr8:96087997..96090482-chr8:96096727..96098708,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000184260	Chromatin interaction
ENSG00000184678	Chromatin interaction
ENSG00000156170	Chromatin interaction
ENSG00000253878	Chromatin interaction
ENSG00000164938	Chromatin interaction
ENSG00000254248	Chromatin interaction
ENSG00000175895	Chromatin interaction
ENSG00000178096	Chromatin interaction
ENSG00000184270	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10086541	0.87[GIH][hapmap]
rs10087402	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10092003	0.87[GIH][hapmap]
rs10093594	0.87[GIH][hapmap]
rs10097930	0.87[GIH][hapmap]
rs10098453	0.87[GIH][hapmap]
rs10111154	0.87[GIH][hapmap]
rs11776189	0.87[GIH][hapmap]
rs11779506	0.83[GIH][hapmap]
rs11780931	0.87[GIH][hapmap]
rs12544717	0.91[ASN][1000 genomes]
rs13261505	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs13279040	0.83[GIH][hapmap]
rs16917233	0.87[GIH][hapmap]
rs2678823	0.83[GIH][hapmap]
rs2678829	0.83[GIH][hapmap]
rs6471511	1.00[ASN][1000 genomes]
rs6651272	0.87[GIH][hapmap]
rs71504377	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs71504378	0.93[ASN][1000 genomes]
rs7812312	0.87[GIH][hapmap]
rs7826196	0.87[GIH][hapmap]
rs9297951	0.87[GIH][hapmap]

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	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	nsv508520	chr8:95939373-96140068	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
4	nsv891205	chr8:96062601-96115476	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
5	nsv891206	chr8:96092251-96115476	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96080200-96101800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:96085600-96098200	Weak transcription	Gastric	stomach
3	chr8:96086000-96098200	Weak transcription	Thymus	Thymus
4	chr8:96088200-96098000	Weak transcription	Fetal Kidney	kidney
5	chr8:96088600-96098000	Weak transcription	K562	blood
6	chr8:96088800-96098000	Weak transcription	HepG2	liver
7	chr8:96090600-96098200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr8:96094800-96098000	Weak transcription	Primary hematopoietic stem cells	blood
9	chr8:96096200-96098000	Weak transcription	Primary B cells from peripheral blood	blood
10	chr8:96097000-96098000	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr8:96097200-96097800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr8:96097200-96098800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr8:96097200-96099200	Enhancers	Primary B cells from cord blood	blood
14	chr8:96097200-96099600	Enhancers	NHEK	skin
15	chr8:96097400-96100000	Weak transcription	Esophagus	oesophagus
16	chr8:96097600-96098000	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr8:96097600-96098400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr8:96097600-96098600	Enhancers	Pancreas	Pancrea
19	chr8:96097600-96098800	Enhancers	H1 Cell Line	embryonic stem cell
20	chr8:96097600-96098800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr8:96097600-96099200	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr8:96097600-96100800	Enhancers	Placenta	Placenta

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