Variant report

Variant	rs7085330
Chromosome Location	chr10:21548595-21548596
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:21461521..21464243-chr10:21547978..21550972,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000078114	Chromatin interaction
ENSG00000231920	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10400156	1.00[ASN][1000 genomes]
rs10828225	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10828226	1.00[ASN][1000 genomes]
rs12262659	1.00[CHB][hapmap]
rs1482899	1.00[ASN][1000 genomes]
rs2359929	1.00[ASN][1000 genomes]
rs3847375	1.00[CHB][hapmap]
rs60959763	0.90[ASN][1000 genomes]
rs6482170	0.83[ASN][1000 genomes]
rs7076532	1.00[ASN][1000 genomes]
rs7090954	1.00[ASN][1000 genomes]
rs7905100	0.90[ASN][1000 genomes]
rs7905278	1.00[ASN][1000 genomes]
rs7910610	1.00[CHB][hapmap];1.00[ASN][1000 genomes]

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	nsv530148	chr10:21065080-21724565	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv971871	chr10:21460392-21579987	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv831807	chr10:21509185-21688043	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21522000-21549600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr10:21522200-21549200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr10:21524000-21549000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr10:21524000-21549400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr10:21530600-21549600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr10:21539600-21549400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr10:21543200-21550800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr10:21546000-21550000	Weak transcription	Brain Cingulate Gyrus	brain
9	chr10:21547400-21548600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr10:21547400-21554600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr10:21547600-21549000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr10:21548000-21548600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr10:21548000-21549200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr10:21548200-21548600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr10:21548200-21549200	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr10:21548400-21548600	Enhancers	K562	blood
17	chr10:21548400-21549400	Enhancers	Brain Anterior Caudate	brain
18	chr10:21548400-21550000	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr10:21548400-21550600	Enhancers	Ovary	ovary
20	chr10:21548400-21551200	Enhancers	Fetal Lung	lung

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