Variant report

Variant	rs567310818
Chromosome Location	chr5:96515165-96515166
allele	A/G
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	GATA3	chr5:96515013-96515213	SH-SY5Y	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:96513502..96516317-chr5:96517939..96521183,3	K562	blood:
2	chr5:96508014..96513294-chr5:96513654..96520413,9	K562	blood:
3	chr5:96513279..96516622-chr5:96517923..96519975,3	MCF-7	breast:

Variant related genes	Relation type
RNU1-73P	TF binding region
ENSG00000251513	TF binding region
ENSG00000058729	Chromatin interaction
ENSG00000206698	Chromatin interaction
ENSG00000251513	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

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	nsv432755	chr5:95987984-96657483	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv598962	chr5:96057891-96893164	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv830412	chr5:96427305-96606619	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv1019790	chr5:96471680-96980633	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	nsv537812	chr5:96471680-96980633	ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
6	nsv882391	chr5:96496189-96533469	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv882392	chr5:96496189-96546238	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
8	nsv882393	chr5:96496189-96567950	Flanking Bivalent TSS/Enh Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
9	esv3348846	chr5:96514946-96516894	Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96494400-96515200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr5:96494400-96518000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:96494600-96516600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr5:96494800-96515200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr5:96494800-96516400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr5:96494800-96516400	Strong transcription	Fetal Muscle Trunk	muscle
7	chr5:96494800-96516400	Strong transcription	Fetal Thymus	thymus
8	chr5:96494800-96516600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr5:96495000-96516000	Strong transcription	Dnd41	blood
10	chr5:96495000-96516200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr5:96495200-96515200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
12	chr5:96495200-96515400	Strong transcription	H1 Cell Line	embryonic stem cell
13	chr5:96495200-96516000	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr5:96495200-96516800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr5:96495200-96518000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr5:96495400-96516600	Strong transcription	HUES48 Cell Line	embryonic stem cell
17	chr5:96495600-96515600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr5:96495600-96515800	Strong transcription	Osteobl	bone
19	chr5:96495600-96517800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr5:96495800-96517400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr5:96496000-96516800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr5:96496200-96515200	Strong transcription	NH-A	brain
23	chr5:96496600-96515600	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr5:96496600-96516400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:96497800-96516400	Strong transcription	HUES6 Cell Line	embryonic stem cell
26	chr5:96498000-96516400	Strong transcription	Placenta	Placenta
27	chr5:96499400-96515200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:96500000-96515400	Strong transcription	HMEC	breast
29	chr5:96500400-96516000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr5:96501400-96515200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr5:96501800-96515200	Strong transcription	Liver	Liver
32	chr5:96502000-96515200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr5:96502400-96516000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr5:96502600-96515400	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr5:96502600-96516000	Strong transcription	Duodenum Mucosa	Duodenum
36	chr5:96503000-96515400	Strong transcription	HSMM	muscle
37	chr5:96503000-96516600	Strong transcription	Primary T cells fromperipheralblood	blood
38	chr5:96503200-96515200	Strong transcription	Skeletal Muscle Female	skeletal muscle
39	chr5:96503200-96516000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr5:96503600-96515200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr5:96503600-96515600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr5:96503600-96515800	Strong transcription	Primary T helper cells PMA-I stimulated	--
43	chr5:96503600-96516000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr5:96503800-96515200	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr5:96504000-96516000	Strong transcription	Primary T helper cells fromperipheralblood	blood
46	chr5:96504000-96516000	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr5:96504400-96515200	Strong transcription	NHDF-Ad	bronchial
48	chr5:96504400-96516200	Strong transcription	Primary B cells from cord blood	blood
49	chr5:96504800-96515200	Strong transcription	Primary T cells from cord blood	blood
50	chr5:96504800-96515200	Strong transcription	Fetal Intestine Large	intestine

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