Variant report

Variant	nsv908568
Chromosome Location	chr17:45506682-45590420
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1137)
CpG islands
(count:366)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1137 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:45569946-45569952	K562	blood:	n/a	n/a
2	ARID3A	chr17:45569945-45570183	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:45570956-45571035	HepG2	liver:	n/a	n/a
4	ATF1	chr17:45569891-45570104	K562	blood:	n/a	n/a
5	ATF2	chr17:45569649-45570147	GM12878	blood:	n/a	n/a
6	ATF3	chr17:45569908-45570164	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr17:45569734-45570294	A549	lung:	n/a	n/a
8	ATF3	chr17:45569636-45570283	A549	lung:	n/a	n/a
9	ATF3	chr17:45569872-45570174	K562	blood:	n/a	n/a
10	BACH1	chr17:45569861-45570142	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr17:45579872-45580148	GM12878	blood:	n/a	chr17:45580000-45580010
12	BATF	chr17:45579678-45580209	GM12878	blood:	n/a	chr17:45580000-45580010
13	BATF	chr17:45569645-45570111	GM12878	blood:	n/a	n/a
14	BATF	chr17:45578032-45578241	GM12878	blood:	n/a	n/a
15	BCL11A	chr17:45579757-45579928	GM12878	blood:	n/a	n/a
16	BCL11A	chr17:45579668-45580125	GM12878	blood:	n/a	chr17:45579999-45580008
17	BCLAF1	chr17:45569636-45570116	GM12878	blood:	n/a	chr17:45569672-45569681
18	BHLHE40	chr17:45569785-45570156	A549	lung:	n/a	n/a
19	BHLHE40	chr17:45569770-45570296	HepG2	liver:	n/a	n/a
20	BHLHE40	chr17:45569774-45570248	HepG2	liver:	n/a	n/a
21	BHLHE40	chr17:45569767-45570239	GM12878	blood:	n/a	n/a
22	BHLHE40	chr17:45569762-45570255	K562	blood:	n/a	n/a
23	BRCA1	chr17:45569743-45570065	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr17:45579916-45580110	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr17:45569445-45570802	K562	blood:	n/a	n/a
26	CBX3	chr17:45569612-45570280	K562	blood:	n/a	n/a
27	CBX3	chr17:45577979-45578350	K562	blood:	n/a	n/a
28	CCNT2	chr17:45569865-45570079	K562	blood:	n/a	n/a
29	CEBPB	chr17:45569865-45570260	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr17:45579926-45580036	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr17:45570637-45571182	HepG2	liver:	n/a	chr17:45571024-45571035 chr17:45571024-45571035 chr17:45571024-45571037 chr17:45571025-45571036
32	CEBPB	chr17:45569746-45570250	K562	blood:	n/a	n/a
33	CEBPB	chr17:45569930-45570084	HepG2	liver:	n/a	n/a
34	CEBPB	chr17:45589310-45589646	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr17:45569945-45570228	A549	lung:	n/a	n/a
36	CEBPB	chr17:45570633-45571101	K562	blood:	n/a	chr17:45571024-45571035 chr17:45571024-45571035 chr17:45571024-45571037 chr17:45571025-45571036
37	CEBPB	chr17:45570649-45571036	A549	lung:	n/a	chr17:45571024-45571035 chr17:45571024-45571035 chr17:45571025-45571036
38	CEBPB	chr17:45589395-45589618	K562	blood:	n/a	n/a
39	CEBPB	chr17:45549562-45549781	HepG2	liver:	n/a	n/a
40	CEBPB	chr17:45569950-45569994	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr17:45569940-45570140	HepG2	liver:	n/a	n/a
42	CEBPB	chr17:45569419-45570032	GM12878	blood:	n/a	n/a
43	CEBPB	chr17:45569950-45570239	IMR90	lung:	n/a	n/a
44	CEBPB	chr17:45579500-45579717	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr17:45580366-45580376	Hela-S3	cervix:	n/a	n/a
46	CEBPD	chr17:45569533-45570107	K562	blood:	n/a	n/a
47	CEBPD	chr17:45580257-45580571	K562	blood:	n/a	n/a
48	CEBPD	chr17:45569936-45570114	HepG2	liver:	n/a	n/a
49	CEBPD	chr17:45569673-45569842	HepG2	liver:	n/a	n/a
50	CEBPD	chr17:45569615-45569858	HepG2	liver:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45573695-45573745	HPAEpiC	pulmonary alveolar:	n/a
2	chr17:45566670-45566720	PFSK-1	brain:	n/a
3	chr17:45570168-45570218	CMK	blood:	n/a
4	chr17:45570048-45570098	SAEC	small airway:	n/a
5	chr17:45570168-45570218	NHBE	bronchial:	n/a
6	chr17:45573695-45573745	AG10803	skin:	n/a
7	chr17:45570133-45570183	AG04450	lung:	fetal
8	chr17:45570168-45570218	NHDF-neo	bronchial:	n/a
9	chr17:45566670-45566720	NHBE	bronchial:	n/a
10	chr17:45570168-45570218	SK-N-MC	brain:	n/a
11	chr17:45570168-45570218	HNPCEpiC	eye:	n/a
12	chr17:45573695-45573745	SK-N-SH	brain:	n/a
13	chr17:45569959-45570009	Jurkat	blood:	n/a
14	chr17:45570048-45570098	Caco-2	colon:	n/a
15	chr17:45570168-45570218	H1-hESC	embryonic stem cell:	embryo
16	chr17:45566670-45566720	HUVEC	blood vessel:	n/a
17	chr17:45570048-45570098	NT2-D1	testis:	n/a
18	chr17:45570168-45570218	AG10803	skin:	n/a
19	chr17:45570048-45570098	PANC-1	pancreas:	n/a
20	chr17:45569959-45570009	HRPEpiC	eye:	n/a
21	chr17:45570168-45570218	MCF-7	breast:	n/a
22	chr17:45570133-45570183	NHDF-neo	bronchial:	n/a
23	chr17:45566670-45566720	ProgFib	skin:	n/a
24	chr17:45570048-45570098	ovcar-3	ovarian:	n/a
25	chr17:45566670-45566720	HCPEpiC	choroid plexus:	n/a
26	chr17:45569959-45570009	NT2-D1	testis:	n/a
27	chr17:45570048-45570098	MCF-7	breast:	n/a
28	chr17:45570048-45570098	HIPEpiC	eye:	n/a
29	chr17:45566670-45566720	GM12891	blood:	n/a
30	chr17:45570133-45570183	HNPCEpiC	eye:	n/a
31	chr17:45570133-45570183	PrEC	prostate:	n/a
32	chr17:45566670-45566720	PrEC	prostate:	n/a
33	chr17:45566670-45566720	IMR90	lung:	fetal
34	chr17:45569959-45570009	PFSK-1	brain:	n/a
35	chr17:45570133-45570183	HCF	heart:	n/a
36	chr17:45573695-45573745	HepG2	liver:	n/a
37	chr17:45573695-45573745	HEK293	kidney:	embryo
38	chr17:45569959-45570009	AG10803	skin:	n/a
39	chr17:45573695-45573745	Jurkat	blood:	n/a
40	chr17:45566670-45566720	LNCaP	prostate:	n/a
41	chr17:45570048-45570098	AG09309	skin:	n/a
42	chr17:45566670-45566720	HRCEpiC	kidney:	n/a
43	chr17:45573695-45573745	HRPEpiC	eye:	n/a
44	chr17:45570133-45570183	H1-hESC	embryonic stem cell:	embryo
45	chr17:45569959-45570009	HCPEpiC	choroid plexus:	n/a
46	chr17:45566670-45566720	NHDF-neo	bronchial:	n/a
47	chr17:45569959-45570009	HCF	heart:	n/a
48	chr17:45573695-45573745	SK-N-MC	brain:	n/a
49	chr17:45573695-45573745	U87	brain:	n/a
50	chr17:45570048-45570098	NHDF-neo	bronchial:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45568465..45570063-chr17:45725230..45727294,2	K562	blood:
2	chr17:45569553..45571642-chr17:45608535..45610078,2	MCF-7	breast:
3	chr17:45567844..45569771-chr17:45694216..45696585,2	K562	blood:
4	chr17:45450230..45451965-chr17:45515633..45517209,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C17orf57-1	chr17:45522601-45522883	NONHSAT054305

No data

Variant related genes	Relation type
MRPL45P2	TF binding region
MRPL45P2	CpG island
ENSG00000263766	chromatin interactions
ENSG00000141279	chromatin interactions
ENSG00000108424	chromatin interactions

Extended variants
information (count: 2824 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:2824 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9893901	chr17:45506682-45506683	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs527853920	chr17:45506780-45506781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564405785	chr17:45506801-45506802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs77961757	chr17:45506830-45506831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs566523278	chr17:45506840-45506841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs112252397	chr17:45506912-45506913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535192106	chr17:45506930-45506931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549012018	chr17:45507003-45507004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187778024	chr17:45507036-45507037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs192509752	chr17:45507063-45507064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576966354	chr17:45507114-45507115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374918506	chr17:45507172-45507173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs371828953	chr17:45507205-45507206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs373554380	chr17:45507231-45507232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368074976	chr17:45507249-45507250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375239377	chr17:45507258-45507259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370963342	chr17:45507271-45507272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577933451	chr17:45507273-45507274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150782686	chr17:45507325-45507326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138665214	chr17:45507344-45507345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs149297512	chr17:45507368-45507369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372215001	chr17:45507384-45507385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542750743	chr17:45507457-45507458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs113442766	chr17:45507497-45507498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146255267	chr17:45507551-45507552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs11869487	chr17:45507586-45507587	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs189159567	chr17:45507589-45507590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs139315452	chr17:45507622-45507623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529241202	chr17:45507625-45507626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs113524317	chr17:45507722-45507723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142410264	chr17:45507770-45507771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561322167	chr17:45507783-45507784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529013776	chr17:45507880-45507881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548789717	chr17:45507900-45507901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs568850932	chr17:45507913-45507914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs537813454	chr17:45508017-45508018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551703910	chr17:45508094-45508095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368375715	chr17:45508124-45508125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181883260	chr17:45508167-45508168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs72829641	chr17:45508216-45508217	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs114587269	chr17:45508294-45508295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562635670	chr17:45508296-45508297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs72829642	chr17:45508314-45508315	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs536785488	chr17:45508323-45508324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372169770	chr17:45508363-45508364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145976343	chr17:45508489-45508490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576032560	chr17:45508606-45508607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372514099	chr17:45508621-45508622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544963801	chr17:45508623-45508624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558521465	chr17:45508642-45508643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:119)

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	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD

Chromatin state (count:1056 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45500600-45511200	Weak transcription	K562	blood
2	chr17:45500800-45506800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr17:45501400-45514600	Weak transcription	Primary T cells from cord blood	blood
4	chr17:45501400-45554200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr17:45501400-45554400	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr17:45501600-45509800	Weak transcription	Pancreas	Pancrea
7	chr17:45501600-45511400	Weak transcription	Esophagus	oesophagus
8	chr17:45501600-45511800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr17:45501600-45511800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr17:45501600-45515600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr17:45501600-45520200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr17:45501600-45555400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr17:45501600-45556400	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr17:45501800-45507800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr17:45501800-45508800	Weak transcription	Rectal Smooth Muscle	rectum
16	chr17:45501800-45511800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr17:45501800-45511800	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr17:45501800-45512400	Weak transcription	Primary B cells from cord blood	blood
19	chr17:45501800-45533400	Weak transcription	Gastric	stomach
20	chr17:45501800-45547400	Weak transcription	Fetal Muscle Trunk	muscle
21	chr17:45501800-45550200	Weak transcription	Ovary	ovary
22	chr17:45502200-45513600	Weak transcription	Fetal Brain Male	brain
23	chr17:45502200-45548000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr17:45502800-45548600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr17:45503000-45512000	Weak transcription	Primary hematopoietic stem cells	blood
26	chr17:45503200-45510200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr17:45503200-45511800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr17:45503200-45511800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr17:45503200-45512200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr17:45503200-45545400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr17:45503600-45509200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr17:45504600-45507400	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr17:45504800-45507600	Enhancers	HepG2	liver
34	chr17:45505200-45550200	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr17:45505400-45508000	Enhancers	Fetal Intestine Small	intestine
36	chr17:45505800-45507800	Enhancers	Fetal Intestine Large	intestine
37	chr17:45506400-45523000	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr17:45507200-45555000	Weak transcription	Fetal Thymus	thymus
39	chr17:45507400-45507600	Enhancers	Left Ventricle	heart
40	chr17:45507400-45507600	Enhancers	Small Intestine	intestine
41	chr17:45507600-45519800	Weak transcription	HepG2	liver
42	chr17:45507600-45554200	Weak transcription	Left Ventricle	heart
43	chr17:45507800-45511800	Weak transcription	Fetal Intestine Large	intestine
44	chr17:45508000-45509200	Weak transcription	Small Intestine	intestine
45	chr17:45508000-45521000	Weak transcription	Fetal Intestine Small	intestine
46	chr17:45509200-45509400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr17:45509400-45527800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr17:45509600-45527800	Weak transcription	Fetal Stomach	stomach
49	chr17:45511800-45512000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr17:45511800-45512000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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