Variant report

Variant	rs533228509
Chromosome Location	chr9:2033191-2033192
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:2027542..2030484-chr9:2031269..2033941,3	K562	blood:
2	chr9:2016568..2019114-chr9:2030660..2033552,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000080503	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016148	chr9:1457605-2361750	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv539916	chr9:1457605-2361750	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1021712	chr9:1647840-2216839	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv539921	chr9:1647840-2216839	Bivalent Enhancer Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS 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	14 gene(s)	inside rSNPs	diseases
5	nsv1020530	chr9:1870197-2658587	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	nsv831493	chr9:1885733-2074135	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv892048	chr9:1888703-2177391	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv1021158	chr9:1963930-2040728	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv892052	chr9:1980819-2072470	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	esv2830420	chr9:1998911-2119702	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	nsv530929	chr9:1998911-2925112	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
12	nsv613079	chr9:2012767-2059341	Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
13	nsv466069	chr9:2018825-2066493	Strong transcription Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv613080	chr9:2018825-2066493	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
15	nsv466070	chr9:2024639-2044721	Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
16	nsv613081	chr9:2024639-2044721	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
17	nsv892053	chr9:2024639-2062014	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
18	nsv466071	chr9:2028757-2065892	Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
19	nsv613082	chr9:2028757-2065892	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
20	nsv466073	chr9:2029018-2069765	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
21	nsv613083	chr9:2029018-2069765	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
22	nsv466074	chr9:2032845-2074070	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
23	nsv613084	chr9:2032845-2074070	Transcr. at gene 5' and 3' Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
24	nsv466075	chr9:2033182-2067918	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
25	nsv613085	chr9:2033182-2067918	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2018200-2033400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:2019000-2033200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr9:2019200-2039400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr9:2019400-2033200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr9:2024000-2039400	Weak transcription	Stomach Mucosa	stomach
6	chr9:2025200-2044600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr9:2025400-2044000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr9:2025600-2040000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr9:2025600-2041200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr9:2025800-2043600	Weak transcription	Fetal Heart	heart
11	chr9:2026000-2037400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr9:2026000-2047400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr9:2028000-2040000	Weak transcription	HMEC	breast
14	chr9:2028200-2033400	Weak transcription	Esophagus	oesophagus
15	chr9:2028400-2033200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr9:2028600-2033200	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr9:2029000-2125200	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr9:2029200-2039600	Weak transcription	Psoas Muscle	Psoas
19	chr9:2029200-2042600	Strong transcription	Primary B cells from peripheral blood	blood
20	chr9:2029200-2053000	Weak transcription	Small Intestine	intestine
21	chr9:2029400-2043800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr9:2029600-2033200	Weak transcription	NH-A	brain
23	chr9:2029600-2051800	Strong transcription	Liver	Liver
24	chr9:2030000-2040800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr9:2031400-2048400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr9:2031400-2052200	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr9:2031600-2035000	Strong transcription	HUVEC	blood vessel
28	chr9:2031600-2039600	Strong transcription	GM12878-XiMat	blood
29	chr9:2031800-2033200	Weak transcription	Brain Germinal Matrix	brain
30	chr9:2031800-2035000	Strong transcription	Primary T cells from cord blood	blood
31	chr9:2031800-2043600	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr9:2031800-2043800	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr9:2032000-2035200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr9:2032000-2044200	Strong transcription	Dnd41	blood
35	chr9:2032200-2033200	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr9:2032200-2033800	Strong transcription	NHEK	skin
37	chr9:2032200-2034600	Strong transcription	Fetal Brain Male	brain
38	chr9:2032200-2035000	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr9:2032200-2035200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr9:2032200-2036200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr9:2032200-2042400	Strong transcription	Primary B cells from cord blood	blood
42	chr9:2032200-2044200	Strong transcription	Rectal Mucosa Donor 31	rectum
43	chr9:2032400-2033600	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr9:2032400-2033800	Strong transcription	Fetal Kidney	kidney
45	chr9:2032400-2034000	Strong transcription	Rectal Smooth Muscle	rectum
46	chr9:2032400-2034200	Strong transcription	Spleen	Spleen
47	chr9:2032400-2034400	Strong transcription	Skeletal Muscle Male	skeletal muscle
48	chr9:2032400-2034800	Strong transcription	Cortex derived primary cultured neurospheres	brain
49	chr9:2032400-2034800	Strong transcription	Duodenum Mucosa	Duodenum
50	chr9:2032400-2034800	Strong transcription	Fetal Muscle Leg	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links