Variant report

Variant	esv33689
Chromosome Location	chr17:45551959-45664575
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1728)
CpG islands
(count:734)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1728 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

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	chr17:45569872-45570174	K562	blood:	n/a	n/a
7	ATF3	chr17:45569908-45570164	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr17:45569636-45570283	A549	lung:	n/a	n/a
9	ATF3	chr17:45569734-45570294	A549	lung:	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	chr17:45569645-45570111	GM12878	blood:	n/a	n/a
13	BATF	chr17:45578032-45578241	GM12878	blood:	n/a	n/a
14	BATF	chr17:45579678-45580209	GM12878	blood:	n/a	chr17:45580000-45580010
15	BCL11A	chr17:45579668-45580125	GM12878	blood:	n/a	chr17:45579999-45580008
16	BCL11A	chr17:45609110-45609438	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
17	BCL11A	chr17:45579757-45579928	GM12878	blood:	n/a	n/a
18	BCLAF1	chr17:45569636-45570116	GM12878	blood:	n/a	chr17:45569672-45569681
19	BCLAF1	chr17:45609125-45609498	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
20	BHLHE40	chr17:45610659-45610881	HepG2	liver:	n/a	n/a
21	BHLHE40	chr17:45605793-45605974	HepG2	liver:	n/a	n/a
22	BHLHE40	chr17:45569770-45570296	HepG2	liver:	n/a	n/a
23	BHLHE40	chr17:45569762-45570255	K562	blood:	n/a	n/a
24	BHLHE40	chr17:45569785-45570156	A549	lung:	n/a	n/a
25	BHLHE40	chr17:45569774-45570248	HepG2	liver:	n/a	n/a
26	BHLHE40	chr17:45569767-45570239	GM12878	blood:	n/a	n/a
27	BRCA1	chr17:45569743-45570065	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr17:45579916-45580110	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr17:45569445-45570802	K562	blood:	n/a	n/a
30	CBX3	chr17:45569612-45570280	K562	blood:	n/a	n/a
31	CBX3	chr17:45609185-45609788	K562	blood:	n/a	n/a
32	CBX3	chr17:45577979-45578350	K562	blood:	n/a	n/a
33	CCNT2	chr17:45569865-45570079	K562	blood:	n/a	n/a
34	CCNT2	chr17:45608329-45608370	K562	blood:	n/a	n/a
35	CEBPB	chr17:45616239-45616426	H1-hESC	embryonic stem cell:	n/a	chr17:45616275-45616286
36	CEBPB	chr17:45593807-45594016	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr17:45569950-45569994	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr17:45569950-45570239	IMR90	lung:	n/a	n/a
39	CEBPB	chr17:45569930-45570084	HepG2	liver:	n/a	n/a
40	CEBPB	chr17:45579926-45580036	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr17:45616208-45616423	IMR90	lung:	n/a	chr17:45616275-45616286
42	CEBPB	chr17:45570633-45571101	K562	blood:	n/a	chr17:45571024-45571035 chr17:45571024-45571035 chr17:45571024-45571037 chr17:45571025-45571036
43	CEBPB	chr17:45569865-45570260	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr17:45569419-45570032	GM12878	blood:	n/a	n/a
45	CEBPB	chr17:45570649-45571036	A549	lung:	n/a	chr17:45571024-45571035 chr17:45571024-45571035 chr17:45571025-45571036
46	CEBPB	chr17:45632282-45632410	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr17:45589395-45589618	K562	blood:	n/a	n/a
48	CEBPB	chr17:45616203-45616429	Hela-S3	cervix:	n/a	chr17:45616275-45616286
49	CEBPB	chr17:45616089-45616461	K562	blood:	n/a	chr17:45616275-45616286
50	CEBPB	chr17:45569940-45570140	HepG2	liver:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45608823-45608873	LNCaP	prostate:	n/a
2	chr17:45608114-45608164	ProgFib	skin:	n/a
3	chr17:45608823-45608873	LNCaP	prostate:	n/a
4	chr17:45608114-45608164	ProgFib	skin:	n/a
5	chr17:45608315-45608365	ECC-1	luminal epithelium:	n/a
6	chr17:45608114-45608164	MCF10A-Er-Src	breast:	n/a
7	chr17:45566670-45566720	AG04449	skin:	fetal
8	chr17:45570048-45570098	HepG2	liver:	n/a
9	chr17:45570168-45570218	GM12892	blood:	n/a
10	chr17:45569959-45570009	AG04450	lung:	fetal
11	chr17:45570048-45570098	Hepatocyte	liver:	n/a
12	chr17:45573695-45573745	HepG2	liver:	n/a
13	chr17:45608315-45608365	PFSK-1	brain:	n/a
14	chr17:45570168-45570218	HCF	heart:	n/a
15	chr17:45608823-45608873	BJ	skin:	n/a
16	chr17:45608315-45608365	PrEC	prostate:	n/a
17	chr17:45608315-45608365	Jurkat	blood:	n/a
18	chr17:45570048-45570098	HRCEpiC	kidney:	n/a
19	chr17:45570133-45570183	SAEC	small airway:	n/a
20	chr17:45612338-45612388	Caco-2	colon:	n/a
21	chr17:45573695-45573745	RPTEC	kidney:	n/a
22	chr17:45570133-45570183	H1-hESC	embryonic stem cell:	embryo
23	chr17:45573695-45573745	HCPEpiC	choroid plexus:	n/a
24	chr17:45608114-45608164	IMR90	lung:	fetal
25	chr17:45570048-45570098	HRPEpiC	eye:	n/a
26	chr17:45573695-45573745	Hela-S3	cervix:	n/a
27	chr17:45570048-45570098	LNCaP	prostate:	n/a
28	chr17:45566670-45566720	U87	brain:	n/a
29	chr17:45604514-45604564	AG09319	gingival:	n/a
30	chr17:45570168-45570218	HCPEpiC	choroid plexus:	n/a
31	chr17:45566670-45566720	NB4	blood:	n/a
32	chr17:45609121-45609171	AG04449	skin:	fetal
33	chr17:45608315-45608365	GM12878	blood:	n/a
34	chr17:45608114-45608164	HRPEpiC	eye:	n/a
35	chr17:45570168-45570218	PFSK-1	brain:	n/a
36	chr17:45570048-45570098	HCPEpiC	choroid plexus:	n/a
37	chr17:45612338-45612388	IMR90	lung:	fetal
38	chr17:45570168-45570218	HMEC	breast:	n/a
39	chr17:45609121-45609171	HepG2	liver:	n/a
40	chr17:45604514-45604564	T-47D	breast:	n/a
41	chr17:45604514-45604564	NB4	blood:	n/a
42	chr17:45608114-45608164	AG09309	skin:	n/a
43	chr17:45570048-45570098	Hela-S3	cervix:	n/a
44	chr17:45566670-45566720	HAEpiC	amniotic membrane:	n/a
45	chr17:45609121-45609171	AG09309	skin:	n/a
46	chr17:45570133-45570183	HNPCEpiC	eye:	n/a
47	chr17:45608823-45608873	HepG2	liver:	n/a
48	chr17:45570133-45570183	AoSMC	blood vessel:	n/a
49	chr17:45573695-45573745	HMEC	breast:	n/a
50	chr17:45608114-45608164	GM12891	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45569553..45571642-chr17:45608535..45610078,2	MCF-7	breast:
2	chr14:38063458..38065003-chr17:45607681..45609442,2	MCF-7	breast:
3	chr17:45568465..45570063-chr17:45725230..45727294,2	K562	blood:
4	chr17:45567844..45569771-chr17:45694216..45696585,2	K562	blood:
5	chr17:45608528..45610827-chr17:45614421..45616919,2	MCF-7	breast:
6	chr17:45569553..45571642-chr17:45608535..45610078,2	MCF-7	breast:
7	chr17:45607951..45610083-chr17:45616920..45619918,2	MCF-7	breast:

No data

Variant related genes	Relation type
NPEPPS	TF binding region
ENSG00000206734	TF binding region
MRPL45P2	TF binding region
NPEPPS	CpG island
ENSG00000206734	CpG island
MRPL45P2	CpG island
ENSG00000108424	chromatin interactions
ENSG00000228782	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000263766	chromatin interactions
ENSG00000141279	chromatin interactions

Extended variants
information (count: 3797 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:3797 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543463889	chr17:45551990-45551991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs527344368	chr17:45552032-45552033	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186020497	chr17:45552108-45552109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs28458768	chr17:45552140-45552141	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs576963039	chr17:45552176-45552177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536150532	chr17:45552182-45552183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549705926	chr17:45552226-45552227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569615048	chr17:45552249-45552250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368105902	chr17:45552258-45552259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144811487	chr17:45552369-45552370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371777400	chr17:45552393-45552394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372022922	chr17:45552473-45552474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535068230	chr17:45552551-45552552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555010025	chr17:45552603-45552604	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574924567	chr17:45552623-45552624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148565936	chr17:45552664-45552665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113088165	chr17:45552665-45552666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577449919	chr17:45552713-45552714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546095478	chr17:45552717-45552718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559867621	chr17:45552780-45552781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112195872	chr17:45552840-45552841	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559668146	chr17:45552875-45552876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs59850765	chr17:45552887-45552888	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs111486506	chr17:45552982-45552983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560640737	chr17:45553060-45553061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529687918	chr17:45553105-45553106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549347034	chr17:45553106-45553107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563636270	chr17:45553107-45553108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538892508	chr17:45553196-45553197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1221387	chr17:45553204-45553205	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111541649	chr17:45553233-45553234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113533556	chr17:45553236-45553237	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12944100	chr17:45553262-45553263	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12944103	chr17:45553267-45553268	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs149785085	chr17:45553291-45553292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs62076537	chr17:45553309-45553310	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs537476332	chr17:45553347-45553348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557357283	chr17:45553530-45553531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577487807	chr17:45553544-45553545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571319553	chr17:45553641-45553642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs57303096	chr17:45553653-45553654	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs59206426	chr17:45553657-45553658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs61229982	chr17:45553659-45553660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200881391	chr17:45553661-45553662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs59411537	chr17:45553663-45553664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373719473	chr17:45553664-45553665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs58507273	chr17:45553665-45553666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs60260859	chr17:45553667-45553668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs61287521	chr17:45553669-45553670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546430848	chr17:45553715-45553716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	21163964	CNVD
Epithelial cancer	20478067	CNVD

Chromatin state (count:1718 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45501400-45554200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr17:45501400-45554400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr17:45501600-45555400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr17:45501600-45556400	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr17:45507200-45555000	Weak transcription	Fetal Thymus	thymus
6	chr17:45507600-45554200	Weak transcription	Left Ventricle	heart
7	chr17:45515600-45554200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr17:45516000-45556400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr17:45516800-45553200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr17:45518000-45568800	Weak transcription	K562	blood
11	chr17:45518200-45554200	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr17:45518600-45569200	Weak transcription	Brain Anterior Caudate	brain
13	chr17:45519400-45569400	Weak transcription	Primary B cells from peripheral blood	blood
14	chr17:45519800-45555000	Weak transcription	Thymus	Thymus
15	chr17:45523200-45556400	Weak transcription	GM12878-XiMat	blood
16	chr17:45526200-45556000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr17:45526400-45568800	Weak transcription	Brain Angular Gyrus	brain
18	chr17:45526600-45568800	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr17:45527000-45568800	Weak transcription	Colon Smooth Muscle	Colon
20	chr17:45527800-45568800	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr17:45529800-45558200	Weak transcription	Brain Hippocampus Middle	brain
22	chr17:45530200-45568800	Weak transcription	A549	lung
23	chr17:45530400-45554400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr17:45531200-45560000	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr17:45531400-45568800	Weak transcription	Duodenum Mucosa	Duodenum
26	chr17:45531600-45555000	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr17:45531600-45569200	Weak transcription	Primary T cells from cord blood	blood
28	chr17:45534800-45569400	Weak transcription	Esophagus	oesophagus
29	chr17:45537800-45569000	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr17:45538200-45569000	Weak transcription	Brain Substantia Nigra	brain
31	chr17:45539800-45569400	Weak transcription	Brain Germinal Matrix	brain
32	chr17:45540400-45569600	Weak transcription	Small Intestine	intestine
33	chr17:45540600-45568800	Weak transcription	Right Ventricle	heart
34	chr17:45541200-45559000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr17:45541400-45554400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr17:45541800-45568800	Weak transcription	NHEK	skin
37	chr17:45542800-45554000	Weak transcription	Fetal Lung	lung
38	chr17:45542800-45558000	Weak transcription	Primary B cells from cord blood	blood
39	chr17:45543600-45568800	Weak transcription	Brain Cingulate Gyrus	brain
40	chr17:45543600-45568800	Weak transcription	Stomach Smooth Muscle	stomach
41	chr17:45543800-45568800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr17:45544000-45556200	Weak transcription	NHDF-Ad	bronchial
43	chr17:45544000-45569600	Weak transcription	Spleen	Spleen
44	chr17:45544400-45559600	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr17:45544400-45568800	Weak transcription	NH-A	brain
46	chr17:45544400-45569000	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr17:45544600-45559400	Strong transcription	Fetal Stomach	stomach
48	chr17:45544800-45554200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr17:45544800-45556800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr17:45545000-45569000	Weak transcription	HSMMtube	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links