Variant report

Variant	rs10120505
Chromosome Location	chr9:18805483-18805484
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10963769	0.85[MEX][hapmap]
rs12006553	1.00[JPT][hapmap]
rs7874108	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 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	nsv892691	chr9:18519699-18805483	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
8	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
9	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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10120505	PSIP1	cis	cerebellum	SCAN

Chromatin state (count:28 , 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	chr9:18800200-18805800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr9:18801200-18809000	Strong transcription	HSMM	muscle
9	chr9:18801200-18817600	Weak transcription	HSMMtube	muscle
10	chr9:18802000-18811400	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr9:18802200-18806600	Weak transcription	Fetal Stomach	stomach
12	chr9:18802200-18811200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr9:18802400-18817000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr9:18803000-18806400	Weak transcription	Fetal Muscle Leg	muscle
15	chr9:18803200-18817000	Weak transcription	NH-A	brain
16	chr9:18803600-18805800	Weak transcription	NHDF-Ad	bronchial
17	chr9:18804200-18806000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr9:18804200-18806400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr9:18804600-18805800	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr9:18804800-18805800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr9:18804800-18809400	Strong transcription	Osteobl	bone
22	chr9:18805200-18805600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:18805200-18805800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr9:18805200-18806000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr9:18805200-18806200	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr9:18805400-18805800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr9:18805400-18806000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr9:18805400-18807200	Enhancers	Stomach Smooth Muscle	stomach

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