Variant report

Variant	rs181451664
Chromosome Location	chr9:21593326-21593327
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

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	nsv1031432	chr9:21472601-21608774	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats 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	122 gene(s)	inside rSNPs	diseases
2	nsv540085	chr9:21472601-21608774	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	122 gene(s)	inside rSNPs	diseases
3	nsv1029634	chr9:21542970-21765286	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1015623	chr9:21579110-21694039	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
5	nsv892742	chr9:21589041-21707372	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	esv3482993	chr9:21592184-21594742	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv3482994	chr9:21592184-21594742	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv824876	chr9:21592356-21594024	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21580000-21594800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr9:21591200-21593600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr9:21591400-21593600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr9:21591400-21593600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr9:21591800-21593600	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr9:21592200-21593400	Enhancers	NHEK	skin
7	chr9:21592200-21593600	Enhancers	NH-A	brain
8	chr9:21592200-21594000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr9:21592200-21596400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr9:21592400-21593400	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr9:21592400-21593400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr9:21592400-21593400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr9:21592400-21593400	Enhancers	Osteobl	bone
14	chr9:21592400-21603800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr9:21592800-21593800	Weak transcription	Hela-S3	cervix
16	chr9:21592800-21597400	Weak transcription	HUVEC	blood vessel
17	chr9:21593000-21593400	Enhancers	A549	lung
18	chr9:21593000-21596200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr9:21593000-21597400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr9:21593200-21593400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr9:21593200-21597400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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