Variant report

Variant	nsv575474
Chromosome Location	chr17:46400536-46406546
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:46401524..46403183-chr17:46407797..46409461,2	K562	blood:
2	chr17:46403779..46407902-chr17:46408216..46412684,4	K562	blood:
3	chr17:46385991..46388677-chr17:46406157..46408894,2	K562	blood:
4	chr17:46394167..46397926-chr17:46405990..46408451,3	K562	blood:
5	chr17:46402150..46403911-chr17:46405862..46407499,2	K562	blood:
6	chr17:46402150..46403911-chr17:46405862..46407499,2	K562	blood:
7	chr17:46393909..46396723-chr17:46401139..46403154,2	K562	blood:
8	chr17:46405993..46408762-chr17:46409966..46411975,2	K562	blood:
9	chr17:46399623..46402614-chr17:46666348..46668783,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000120093	chromatin interactions
ENSG00000233101	chromatin interactions

Extended variants
information (count: 176 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:176 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201388375	chr17:46400568-46400569	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs112017193	chr17:46400569-46400570	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs147640939	chr17:46400570-46400571	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs386386199	chr17:46400576-46400577	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs5820695	chr17:46400582-46400583	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs140536122	chr17:46400586-46400587	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs111278414	chr17:46400652-46400653	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs4451990	chr17:46400653-46400654	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs530808087	chr17:46400715-46400716	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs550947870	chr17:46400733-46400734	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs570868985	chr17:46400803-46400804	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs538641697	chr17:46400838-46400839	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs539438756	chr17:46400858-46400859	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs553740644	chr17:46400874-46400875	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs369659701	chr17:46400876-46400877	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs188732144	chr17:46400946-46400947	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs9911663	chr17:46400970-46400971	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs534857461	chr17:46401047-46401048	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs193186848	chr17:46401084-46401085	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs144393927	chr17:46401116-46401117	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs151173606	chr17:46401146-46401147	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs542599759	chr17:46401181-46401182	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs560740475	chr17:46401218-46401219	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs536485162	chr17:46401240-46401241	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs7210445	chr17:46401318-46401319	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs7214589	chr17:46401400-46401401	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs140166700	chr17:46401429-46401430	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs373722397	chr17:46401467-46401468	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs184257756	chr17:46401538-46401539	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs573349062	chr17:46401555-46401556	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs542457473	chr17:46401672-46401673	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs376052013	chr17:46401684-46401685	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs562146918	chr17:46401700-46401701	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs187086150	chr17:46401726-46401727	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs149879132	chr17:46401787-46401788	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs564447232	chr17:46401788-46401789	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs144871338	chr17:46401935-46401936	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs547101753	chr17:46401979-46401980	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs140790259	chr17:46402176-46402177	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs191540582	chr17:46402215-46402216	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs548322831	chr17:46402234-46402235	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs577341216	chr17:46402308-46402309	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs547773192	chr17:46402329-46402330	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs568174756	chr17:46402351-46402352	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs536920322	chr17:46402353-46402354	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs370405900	chr17:46402407-46402408	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs556864430	chr17:46402439-46402440	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs570097529	chr17:46402474-46402475	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs539086337	chr17:46402480-46402481	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs552790760	chr17:46402484-46402485	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:46373200-46415000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr17:46375800-46415800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr17:46377200-46421000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr17:46386200-46407800	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr17:46390200-46429400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr17:46391000-46410400	Weak transcription	GM12878-XiMat	blood
7	chr17:46391000-46420200	Weak transcription	Primary B cells from peripheral blood	blood
8	chr17:46391200-46421200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr17:46391400-46405800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr17:46394000-46400800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr17:46394600-46405400	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr17:46395200-46402800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr17:46396200-46406200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr17:46396200-46421200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr17:46396800-46414400	Weak transcription	Primary T cells from cord blood	blood
16	chr17:46398600-46407600	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr17:46399800-46405800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr17:46400800-46405600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr17:46402600-46403800	Enhancers	Fetal Intestine Large	intestine
20	chr17:46402600-46404000	Enhancers	Fetal Intestine Small	intestine
21	chr17:46402800-46403600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr17:46403600-46403800	Bivalent Enhancer	Fetal Lung	lung
23	chr17:46403600-46406200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr17:46405000-46405400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
25	chr17:46405400-46406200	Strong transcription	Primary T helper cells PMA-I stimulated	--
26	chr17:46405400-46406200	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr17:46405600-46407200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr17:46405800-46406200	Enhancers	A549	lung
29	chr17:46405800-46406600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr17:46405800-46406800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr17:46406000-46406200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr17:46406000-46406200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr17:46406000-46406200	Enhancers	Fetal Kidney	kidney
34	chr17:46406200-46406400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr17:46406200-46406600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr17:46406200-46407200	Weak transcription	A549	lung
37	chr17:46406200-46410800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr17:46406200-46411000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr17:46406200-46413200	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr17:46406400-46421800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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