Variant report

Variant	rs573131301
Chromosome Location	chr9:117857377-117857378
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr9:117853634-117857758	U87	brain:	n/a	n/a
2	POLR2A	chr9:117851943-117857764	U87	brain:	n/a	n/a
3	FOS	chr9:117857334-117857390	MCF10A-Er-Src	breast:	n/a	n/a
4	FOS	chr9:117857334-117857422	MCF10A-Er-Src	breast:	n/a	n/a

Variant related genes	Relation type
TNC	TF binding region

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831696	chr9:117701582-117874150	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv615250	chr9:117768021-118012841	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv916912	chr9:117770039-118014140	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv893768	chr9:117853103-117903975	Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv3376226	chr9:117856981-117859104	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region	1 gene(s)	inside rSNPs	diseases
6	esv2422541	chr9:117857050-117858665	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117815400-117859200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:117841200-117860600	Weak transcription	Fetal Kidney	kidney
3	chr9:117849400-117876200	Weak transcription	Aorta	Aorta
4	chr9:117849400-117877600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:117849600-117864600	Weak transcription	HMEC	breast
6	chr9:117849800-117860400	Weak transcription	Fetal Muscle Leg	muscle
7	chr9:117849800-117860600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr9:117851200-117867200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr9:117853400-117858800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr9:117853400-117861200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr9:117853400-117874000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr9:117854000-117860600	Weak transcription	NHDF-Ad	bronchial
13	chr9:117854400-117860600	Weak transcription	Osteobl	bone
14	chr9:117855200-117857600	Enhancers	Rectal Smooth Muscle	rectum
15	chr9:117855200-117861000	Weak transcription	NH-A	brain
16	chr9:117855400-117857400	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr9:117855400-117857600	Genic enhancers	Cortex derived primary cultured neurospheres	brain
18	chr9:117855600-117857600	Enhancers	Colon Smooth Muscle	Colon
19	chr9:117856200-117857400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr9:117856400-117857400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr9:117856600-117857400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
22	chr9:117856800-117857400	Genic enhancers	NHEK	skin
23	chr9:117856800-117860400	Weak transcription	Fetal Stomach	stomach
24	chr9:117857000-117857600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr9:117857000-117857600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr9:117857000-117857600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr9:117857200-117857400	Enhancers	Stomach Smooth Muscle	stomach
28	chr9:117857200-117857400	Genic enhancers	NHLF	lung
29	chr9:117857200-117857600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr9:117857200-117857600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr9:117857200-117857600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr9:117857200-117858200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr9:117857200-117858200	Weak transcription	Spleen	Spleen
34	chr9:117857200-117859400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr9:117857200-117859600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr9:117857200-117860000	Weak transcription	Fetal Lung	lung
37	chr9:117857200-117860400	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr9:117857200-117861000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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