Variant report

Variant	rs533024404
Chromosome Location	chr10:28505209-28505210
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	chr10:28503327..28506252-chr10:28507179..28508857,2	MCF-7	breast:

Extended variants
information (count: 22 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917149	chr10:28018919-28688694	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1042524	chr10:28290149-28506812	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv525448	chr10:28337570-28563732	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv831817	chr10:28369836-28539930	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1041555	chr10:28419399-29304934	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
6	nsv1037863	chr10:28419399-29378871	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
7	nsv540521	chr10:28419399-29378871	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
8	nsv6188	chr10:28489076-28514068	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv3494702	chr10:28502096-28512894	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3494704	chr10:28502496-28512794	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3494700	chr10:28502799-28512747	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3314296	chr10:28502956-28512061	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3314308	chr10:28502956-28512061	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3514591	chr10:28503047-28511888	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv3494699	chr10:28503097-28511918	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv3494701	chr10:28503107-28511884	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv3494705	chr10:28503162-28511857	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv3514592	chr10:28503162-28511857	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv3494703	chr10:28503269-28511812	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv498723	chr10:28503272-28511810	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
21	esv3494706	chr10:28503273-28511810	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
22	esv14688	chr10:28504295-28511827	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28467600-28525600	Weak transcription	Aorta	Aorta
2	chr10:28487600-28529000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr10:28491200-28523200	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr10:28492200-28506800	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr10:28492600-28506400	Weak transcription	Colon Smooth Muscle	Colon
6	chr10:28492600-28507200	Weak transcription	Rectal Smooth Muscle	rectum
7	chr10:28497400-28506600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr10:28498000-28505600	Weak transcription	HSMMtube	muscle
9	chr10:28498000-28506600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr10:28498200-28506600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr10:28498200-28531200	Weak transcription	Primary B cells from cord blood	blood
12	chr10:28498200-28537000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr10:28499000-28506800	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr10:28499000-28507000	Weak transcription	Ovary	ovary
15	chr10:28500400-28506800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr10:28501800-28506200	Weak transcription	Stomach Smooth Muscle	stomach
17	chr10:28502000-28506400	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr10:28502000-28531600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr10:28502400-28506600	Weak transcription	Primary T cells from cord blood	blood
20	chr10:28502400-28523000	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr10:28502400-28525000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr10:28502600-28506600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr10:28502600-28507000	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr10:28503000-28506000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr10:28503400-28505400	Enhancers	Placenta	Placenta
26	chr10:28503400-28506200	Enhancers	Placenta Amnion	Placenta Amnion
27	chr10:28503400-28506600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr10:28503800-28515600	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr10:28504200-28506600	Enhancers	Hela-S3	cervix
30	chr10:28504200-28506800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr10:28504400-28506600	Enhancers	HSMM	muscle
32	chr10:28504600-28509400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr10:28505000-28505600	Enhancers	HepG2	liver
34	chr10:28505000-28506600	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr10:28505000-28506600	Enhancers	Muscle Satellite Cultured Cells	--
36	chr10:28505000-28506800	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr10:28505000-28506800	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr10:28505200-28506200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr10:28505200-28506200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr10:28505200-28506200	Weak transcription	Psoas Muscle	Psoas
41	chr10:28505200-28506800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr10:28505200-28506800	Weak transcription	Lung	lung
43	chr10:28505200-28507000	Weak transcription	Esophagus	oesophagus
44	chr10:28505200-28507000	Weak transcription	Stomach Mucosa	stomach
45	chr10:28505200-28507200	Weak transcription	Gastric	stomach
46	chr10:28505200-28507200	Weak transcription	Pancreas	Pancrea
47	chr10:28505200-28508800	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr10:28505200-28512000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links