Variant report

Variant	rs10963773
Chromosome Location	chr9:18805813-18805814
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs11788996	0.84[CHB][hapmap]
rs12353154	0.84[CEU][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491807	chr9:18243672-19009770	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised 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	9 gene(s)	inside rSNPs	diseases
2	nsv525659	chr9:18288212-19009041	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1019127	chr9:18288271-18996288	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised 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	9 gene(s)	inside rSNPs	diseases
4	nsv1029449	chr9:18414752-18829127	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv540077	chr9:18414752-18829127	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv1030931	chr9:18414752-18903530	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised 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	6 gene(s)	inside rSNPs	diseases
7	nsv892692	chr9:18519699-19045502	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
8	nsv949111	chr9:18758205-18994588	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	2 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	chr9:18778400-18817000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:18788000-18825200	Weak transcription	HUVEC	blood vessel
3	chr9:18788800-18806200	Weak transcription	Colon Smooth Muscle	Colon
4	chr9:18796800-18817400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr9:18798800-18811200	Weak transcription	Aorta	Aorta
6	chr9:18800000-18824200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr9:18801200-18809000	Strong transcription	HSMM	muscle
8	chr9:18801200-18817600	Weak transcription	HSMMtube	muscle
9	chr9:18802000-18811400	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr9:18802200-18806600	Weak transcription	Fetal Stomach	stomach
11	chr9:18802200-18811200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr9:18802400-18817000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr9:18803000-18806400	Weak transcription	Fetal Muscle Leg	muscle
14	chr9:18803200-18817000	Weak transcription	NH-A	brain
15	chr9:18804200-18806000	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr9:18804200-18806400	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr9:18804800-18809400	Strong transcription	Osteobl	bone
18	chr9:18805200-18806000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr9:18805200-18806200	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr9:18805400-18806000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr9:18805400-18807200	Enhancers	Stomach Smooth Muscle	stomach
22	chr9:18805600-18806000	Enhancers	H1 Cell Line	embryonic stem cell
23	chr9:18805600-18806000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:18805600-18806000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr9:18805800-18806000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr9:18805800-18806400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr9:18805800-18807000	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr9:18805800-18807600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr9:18805800-18808400	Strong transcription	NHDF-Ad	bronchial

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