Variant report

Variant	nsv908565
Chromosome Location	chr17:45446158-45494645
allele	n/a
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	CBX3	chr17:45450397-45450796	HCT-116	colon:	n/a	n/a
2	CBX3	chr17:45450369-45450751	K562	blood:	n/a	n/a
3	CBX3	chr17:45450400-45450697	K562	blood:	n/a	n/a
4	CEBPB	chr17:45482271-45482609	K562	blood:	n/a	chr17:45482429-45482440 chr17:45482429-45482442 chr17:45482429-45482442 chr17:45482431-45482440 chr17:45482431-45482442
5	CEBPB	chr17:45482316-45482557	A549	lung:	n/a	chr17:45482429-45482440 chr17:45482429-45482442 chr17:45482429-45482442 chr17:45482431-45482440 chr17:45482431-45482442
6	CEBPB	chr17:45482269-45482596	HepG2	liver:	n/a	chr17:45482429-45482440 chr17:45482429-45482442 chr17:45482429-45482442 chr17:45482431-45482440 chr17:45482431-45482442
7	CEBPB	chr17:45491776-45491931	K562	blood:	n/a	n/a
8	CEBPB	chr17:45482340-45482579	IMR90	lung:	n/a	chr17:45482429-45482440 chr17:45482429-45482442 chr17:45482429-45482442 chr17:45482431-45482440 chr17:45482431-45482442
9	CEBPB	chr17:45493466-45493668	HepG2	liver:	n/a	chr17:45493564-45493575
10	CEBPB	chr17:45493468-45493688	K562	blood:	n/a	chr17:45493564-45493575
11	CEBPB	chr17:45453915-45454146	K562	blood:	n/a	chr17:45454038-45454049
12	CEBPB	chr17:45493445-45493683	A549	lung:	n/a	chr17:45493564-45493575
13	CEBPB	chr17:45453922-45454159	HepG2	liver:	n/a	chr17:45454038-45454049
14	CTCF	chr17:45480860-45481010	HCT-116	colon:	n/a	n/a
15	CTCF	chr17:45452673-45452731	GM13976	blood:	n/a	n/a
16	CTCF	chr17:45482723-45482749	GM10248	blood:	n/a	n/a
17	CTCF	chr17:45480700-45480850	AG09309	skin:	n/a	n/a
18	CTCF	chr17:45480680-45480830	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr17:45480800-45480950	AG09319	gingival:	n/a	n/a
20	CTCF	chr17:45480700-45480850	HCT-116	colon:	n/a	n/a
21	CTCF	chr17:45454666-45454686	GM10248	blood:	n/a	n/a
22	CTCF	chr17:45480760-45480910	HCT-116	colon:	n/a	n/a
23	CTCF	chr17:45491577-45491639	Fibrobl	skin:	n/a	n/a
24	CTCF	chr17:45480800-45480950	NHDF-neo	bronchial:	n/a	n/a
25	CTCF	chr17:45454572-45454639	MCF-7	breast:	n/a	n/a
26	CTCF	chr17:45450107-45450140	Lung_OC	lung:	n/a	n/a
27	CTCF	chr17:45480760-45480910	A549	lung:	n/a	n/a
28	CUX1	chr17:45477260-45477262	GM12878	blood:	n/a	n/a
29	CUX1	chr17:45490875-45491044	GM12878	blood:	n/a	n/a
30	E2F4	chr17:45456700-45456892	MCF10A-Er-Src	breast:	n/a	chr17:45456834-45456851
31	E2F4	chr17:45453392-45453442	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr17:45482292-45482492	MCF10A-Er-Src	breast:	n/a	n/a
33	EP300	chr17:45445484-45446186	ECC-1	luminal epithelium:	n/a	n/a
34	EP300	chr17:45492009-45492099	GM12878	blood:	n/a	n/a
35	GATA2	chr17:45475909-45476156	K562	blood:	n/a	n/a
36	GATA3	chr17:45472581-45472767	SH-SY5Y	brain:	n/a	n/a
37	GATA3	chr17:45450266-45450287	SH-SY5Y	brain:	n/a	n/a
38	GATA3	chr17:45488625-45488791	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr17:45477589-45477864	SH-SY5Y	brain:	n/a	n/a
40	GATA3	chr17:45484716-45485115	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr17:45465228-45465370	SH-SY5Y	brain:	n/a	n/a
42	IRF1	chr17:45492228-45492262	K562	blood:	n/a	n/a
43	IRF1	chr17:45476995-45476998	K562	blood:	n/a	n/a
44	JUN	chr17:45453645-45454040	HepG2	liver:	n/a	chr17:45453798-45453807 chr17:45453794-45453807
45	JUN	chr17:45450495-45450638	K562	blood:	n/a	n/a
46	JUND	chr17:45453615-45453970	HepG2	liver:	n/a	chr17:45453798-45453807
47	KAP1	chr17:45449871-45450896	K562	blood:	n/a	n/a
48	KAP1	chr17:45451403-45452067	K562	blood:	n/a	n/a
49	KAP1	chr17:45472097-45472297	K562	blood:	n/a	n/a
50	MAFF	chr17:45487462-45487639	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:45474211..45476724-chr17:45477326..45478919,2	MCF-7	breast:
2	chr17:45445857..45448249-chr17:45449955..45451934,2	MCF-7	breast:
3	chr17:45485568..45487998-chr17:45490186..45492096,2	K562	blood:
4	chr17:45443966..45446911-chr17:45490626..45492639,2	K562	blood:
5	chr17:45443966..45446911-chr17:45490507..45492639,3	K562	blood:
6	chr17:45443966..45446911-chr17:45490507..45492639,3	K562	blood:
7	chr17:45469114..45472029-chr17:45476038..45478353,2	K562	blood:
8	chr17:45469114..45472029-chr17:45476038..45478353,2	K562	blood:
9	chr17:45474211..45476724-chr17:45477326..45478919,2	MCF-7	breast:
10	chr17:45450399..45452853-chr17:45453985..45455878,3	K562	blood:
11	chr17:45489885..45492541-chr17:45494163..45496455,2	MCF-7	breast:
12	chr17:45443966..45446911-chr17:45490626..45492639,2	K562	blood:
13	chr17:45468184..45470293-chr17:45471127..45473354,2	MCF-7	breast:
14	chr17:45450230..45451965-chr17:45515633..45517209,2	K562	blood:
15	chr17:45463722..45466707-chr17:45470914..45473396,3	K562	blood:
16	chr17:45485568..45487998-chr17:45490186..45492096,2	K562	blood:
17	chr17:45468184..45470293-chr17:45471127..45473354,2	MCF-7	breast:
18	chr17:45463722..45466707-chr17:45470914..45473396,3	K562	blood:
19	chr17:45489885..45492541-chr17:45494163..45496455,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ITGB3-1	chr17:45446982-45447290	NONHSAT054302
2	lnc-ITGB3-1	chr17:45451838-45452004	NONHSAT054302
3	lnc-ITGB3-1	chr17:45447803-45447874	NONHSAT054302
4	lnc-AC040934.1-1	chr17:45486688-45487035	ENSG00000253347.1

Variant related genes	Relation type
EFCAB13	TF binding region
ENSG00000178852	chromatin interactions

Extended variants
information (count: 1635 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:1635 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16941928	chr17:45446158-45446159	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566203852	chr17:45446165-45446166	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs372200917	chr17:45446230-45446231	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs138392943	chr17:45446252-45446253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs1128517	chr17:45446292-45446293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554960214	chr17:45446310-45446311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574698385	chr17:45446315-45446316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183795628	chr17:45446332-45446333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373670502	chr17:45446417-45446418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557410815	chr17:45446424-45446425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577106864	chr17:45446450-45446451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546016838	chr17:45446479-45446480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559494165	chr17:45446494-45446495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs114987596	chr17:45446503-45446504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112788441	chr17:45446529-45446530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529701686	chr17:45446532-45446533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549738308	chr17:45446646-45446647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569997036	chr17:45446654-45446655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs532424185	chr17:45446702-45446703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs16941932	chr17:45446713-45446714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565840719	chr17:45446723-45446724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111389844	chr17:45446724-45446725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554814605	chr17:45446746-45446747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78669686	chr17:45446758-45446759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs368786125	chr17:45446761-45446762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537085004	chr17:45446945-45446946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142478784	chr17:45446981-45446982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375476885	chr17:45446992-45446993	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs146571979	chr17:45447028-45447029	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs148287166	chr17:45447060-45447061	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs553159766	chr17:45447204-45447205	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs535894626	chr17:45447208-45447209	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs573054238	chr17:45447275-45447276	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs373395376	chr17:45447304-45447305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113011233	chr17:45447333-45447334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542404729	chr17:45447439-45447440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560858099	chr17:45447445-45447446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs529778076	chr17:45447468-45447469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543077833	chr17:45447476-45447477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375411211	chr17:45447489-45447490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563245378	chr17:45447534-45447535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532459579	chr17:45447535-45447536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552455379	chr17:45447538-45447539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559686283	chr17:45447539-45447540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528317843	chr17:45447540-45447541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189254575	chr17:45447604-45447605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs55756546	chr17:45447634-45447635	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs192888133	chr17:45447658-45447659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550577600	chr17:45447724-45447725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs56380058	chr17:45447734-45447735	Weak transcription Enhancers	n/a	n/a	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
Chronic lymphocytic leukemia	21546498	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
Urothelial carcinoma	21177765	CNVD
Breast cancer	17142309	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
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:169 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45402200-45446400	Weak transcription	Colon Smooth Muscle	Colon
2	chr17:45402200-45500800	Weak transcription	Aorta	Aorta
3	chr17:45411600-45468200	Weak transcription	Left Ventricle	heart
4	chr17:45412400-45463400	Weak transcription	Gastric	stomach
5	chr17:45413400-45463800	Weak transcription	Ovary	ovary
6	chr17:45421800-45449800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr17:45423000-45450000	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr17:45423000-45465400	Weak transcription	Adipose Nuclei	Adipose
9	chr17:45423200-45450000	Weak transcription	Primary B cells from cord blood	blood
10	chr17:45435000-45463200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr17:45435200-45447600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr17:45435400-45449600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr17:45440600-45457200	Weak transcription	Fetal Intestine Small	intestine
14	chr17:45440800-45449400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr17:45440800-45449800	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr17:45442600-45449400	Weak transcription	Primary B cells from peripheral blood	blood
17	chr17:45442800-45449800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr17:45445600-45447800	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr17:45449400-45451000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
20	chr17:45449400-45451600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr17:45449600-45451000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr17:45449800-45450800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
23	chr17:45449800-45451000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
24	chr17:45450000-45450400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
25	chr17:45450000-45451000	ZNF genes & repeats	Primary B cells from cord blood	blood
26	chr17:45450400-45461000	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr17:45450800-45470400	Weak transcription	Liver	Liver
28	chr17:45451000-45455400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr17:45451000-45460000	Weak transcription	Primary hematopoietic stem cells	blood
30	chr17:45451000-45463000	Weak transcription	Primary B cells from peripheral blood	blood
31	chr17:45451000-45463400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr17:45451000-45464600	Weak transcription	Primary B cells from cord blood	blood
33	chr17:45451600-45453200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr17:45453200-45454000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr17:45454000-45454400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr17:45454400-45458800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr17:45455400-45456200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr17:45456200-45459200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr17:45458800-45459200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr17:45459200-45460200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr17:45460000-45460400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
42	chr17:45460200-45460400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr17:45460400-45462800	Weak transcription	Primary hematopoietic stem cells	blood
44	chr17:45460600-45467400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr17:45460800-45463200	Weak transcription	Lung	lung
46	chr17:45460800-45466600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr17:45461000-45461400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
48	chr17:45461000-45461600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr17:45461400-45463200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr17:45461400-45466800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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