Variant report

Variant	rs11595146
Chromosome Location	chr10:21554557-21554558
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:21461649..21464762-chr10:21553018..21558600,10	MCF-7	breast:
2	chr10:21460277..21462905-chr10:21553045..21556120,3	MCF-7	breast:
3	chr10:21549133..21551540-chr10:21553150..21555361,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000231920	Chromatin interaction
ENSG00000078114	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs10828230	1.00[CHB][hapmap]
rs11012626	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11012632	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 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
4	esv2761579	chr10:21554557-21612760	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	7 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	chr10:21547400-21554600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:21550200-21559800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr10:21550200-21560200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr10:21550400-21556400	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr10:21550400-21559800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr10:21550400-21560200	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr10:21551200-21564000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr10:21551800-21555200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr10:21552800-21554800	Enhancers	NHEK	skin
10	chr10:21552800-21555200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr10:21552800-21555200	Enhancers	HMEC	breast
12	chr10:21553400-21567000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr10:21554000-21555000	Enhancers	Fetal Lung	lung
14	chr10:21554200-21554800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr10:21554200-21554800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr10:21554200-21555000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr10:21554200-21555000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr10:21554200-21555000	Enhancers	Muscle Satellite Cultured Cells	--
19	chr10:21554200-21555000	Enhancers	HSMMtube	muscle
20	chr10:21554200-21555600	Enhancers	A549	lung
21	chr10:21554400-21554800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr10:21554400-21554800	Enhancers	Hela-S3	cervix
23	chr10:21554400-21554800	Enhancers	K562	blood
24	chr10:21554400-21555000	Enhancers	NH-A	brain
25	chr10:21554400-21555000	Enhancers	NHLF	lung

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