Variant report

Variant	esv3352132
Chromosome Location	chr5:177572746-177576144
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:541)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:177575979-177576295	K562	blood:	n/a	n/a
2	ATF2	chr5:177572941-177573400	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr5:177573084-177573623	GM12878	blood:	n/a	n/a
4	ATF2	chr5:177572945-177573449	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:177573843-177573998	K562	blood:	n/a	n/a
6	BACH1	chr5:177574935-177574938	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr5:177573234-177573570	GM12878	blood:	n/a	chr5:177573402-177573413
8	BCL3	chr5:177572873-177573803	A549	lung:	n/a	n/a
9	BCL3	chr5:177574826-177575381	A549	lung:	n/a	n/a
10	BCL3	chr5:177575798-177576474	A549	lung:	n/a	n/a
11	BHLHE40	chr5:177574017-177574133	K562	blood:	n/a	n/a
12	BHLHE40	chr5:177573043-177573343	K562	blood:	n/a	n/a
13	BRCA1	chr5:177573019-177573286	HepG2	liver:	n/a	n/a
14	BRCA1	chr5:177573055-177573417	H1-hESC	embryonic stem cell:	n/a	n/a
15	CCNT2	chr5:177574486-177574686	K562	blood:	n/a	n/a
16	CEBPB	chr5:177575749-177575994	K562	blood:	n/a	n/a
17	CEBPB	chr5:177573128-177573849	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr5:177573446-177573825	A549	lung:	n/a	n/a
19	CEBPB	chr5:177572829-177574632	MCF-7	breast:	n/a	n/a
20	CEBPB	chr5:177573075-177574066	MCF-7	breast:	n/a	n/a
21	CEBPB	chr5:177573020-177573384	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr5:177573579-177573854	K562	blood:	n/a	n/a
23	CHD1	chr5:177572849-177573413	IMR90	lung:	n/a	n/a
24	CHD2	chr5:177572892-177573319	K562	blood:	n/a	n/a
25	CHD2	chr5:177573728-177573914	K562	blood:	n/a	n/a
26	CHD2	chr5:177572962-177573283	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr5:177575605-177576106	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr5:177574970-177575130	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr5:177573100-177573365	HepG2	liver:	n/a	n/a
30	CHD2	chr5:177572986-177573320	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr5:177572982-177573237	A549	lung:	n/a	n/a
32	CTCF	chr5:177573040-177573190	MCF-7	breast:	n/a	n/a
33	CTCF	chr5:177573120-177573270	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr5:177573003-177573380	GM12878	blood:	n/a	n/a
35	CTCF	chr5:177573100-177573250	GM12871	blood:	n/a	n/a
36	CTCF	chr5:177573060-177573210	BE2_C	brain:	n/a	n/a
37	CTCF	chr5:177573140-177573290	GM12873	blood:	n/a	n/a
38	CTCF	chr5:177572973-177573334	A549	lung:	n/a	n/a
39	CTCF	chr5:177573081-177573304	Lung_OC	lung:	n/a	n/a
40	CTCF	chr5:177573381-177573577	GM12878	blood:	n/a	n/a
41	CTCF	chr5:177572989-177573344	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr5:177573080-177573230	AG04450	lung:	n/a	n/a
43	CTCF	chr5:177573520-177573670	GM12868	blood:	n/a	n/a
44	CTCF	chr5:177573038-177573335	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:177573631-177573632	GM12892	blood:	n/a	n/a
46	CTCF	chr5:177575060-177575210	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:177573039-177573330	GM10248	blood:	n/a	n/a
48	CTCF	chr5:177573033-177573335	K562	blood:	n/a	n/a
49	CTCF	chr5:177575060-177575210	GM12878	blood:	n/a	n/a
50	CTCF	chr5:177573080-177573230	HUVEC	blood vessel:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177575216-177575266	SAEC	small airway:	n/a
2	chr5:177573275-177573325	HIPEpiC	eye:	n/a
3	chr5:177575216-177575266	NHBE	bronchial:	n/a
4	chr5:177573275-177573325	SK-N-SH	brain:	n/a
5	chr5:177573275-177573325	AG04449	skin:	fetal
6	chr5:177575216-177575266	CMK	blood:	n/a
7	chr5:177575216-177575266	MCF-7	breast:	n/a
8	chr5:177573275-177573325	SK-N-SH_RA	brain:	n/a
9	chr5:177573275-177573325	HRPEpiC	eye:	n/a
10	chr5:177573275-177573325	GM12878	blood:	n/a
11	chr5:177575216-177575266	AG04449	skin:	fetal
12	chr5:177573275-177573325	K562	blood:	n/a
13	chr5:177573275-177573325	ECC-1	luminal epithelium:	n/a
14	chr5:177575216-177575266	SKMC	muscle:	n/a
15	chr5:177573275-177573325	PrEC	prostate:	n/a
16	chr5:177573275-177573325	IMR90	lung:	fetal
17	chr5:177573275-177573325	AG04450	lung:	fetal
18	chr5:177573275-177573325	HPAEpiC	pulmonary alveolar:	n/a
19	chr5:177573275-177573325	RPTEC	kidney:	n/a
20	chr5:177575216-177575266	ovcar-3	ovarian:	n/a
21	chr5:177573275-177573325	HUVEC	blood vessel:	n/a
22	chr5:177575216-177575266	HCT-116	colon:	n/a
23	chr5:177575216-177575266	AG10803	skin:	n/a
24	chr5:177575216-177575266	Hepatocyte	liver:	n/a
25	chr5:177573275-177573325	A549	lung:	n/a
26	chr5:177573275-177573325	HCPEpiC	choroid plexus:	n/a
27	chr5:177575216-177575266	GM19239	blood:	n/a
28	chr5:177573275-177573325	HCT-116	colon:	n/a
29	chr5:177573275-177573325	GM12891	blood:	n/a
30	chr5:177575216-177575266	HNPCEpiC	eye:	n/a
31	chr5:177575216-177575266	HRE	kidney:	n/a
32	chr5:177573275-177573325	HCF	heart:	n/a
33	chr5:177573275-177573325	GM06990	blood:	n/a
34	chr5:177575216-177575266	IMR90	lung:	fetal
35	chr5:177573275-177573325	NB4	blood:	n/a
36	chr5:177573275-177573325	BJ	skin:	n/a
37	chr5:177575216-177575266	HepG2	liver:	n/a
38	chr5:177575216-177575266	HCF	heart:	n/a
39	chr5:177575216-177575266	U87	brain:	n/a
40	chr5:177573275-177573325	HEEpiC	esophagus:	n/a
41	chr5:177575216-177575266	HIPEpiC	eye:	n/a
42	chr5:177573275-177573325	HepG2	liver:	n/a
43	chr5:177575216-177575266	HEK293	kidney:	embryo
44	chr5:177573275-177573325	NH-A	brain:	n/a
45	chr5:177573275-177573325	H1-hESC	embryonic stem cell:	embryo
46	chr5:177573275-177573325	NHBE	bronchial:	n/a
47	chr5:177573275-177573325	GM19239	blood:	n/a
48	chr5:177573275-177573325	HAEpiC	amniotic membrane:	n/a
49	chr5:177575216-177575266	GM06990	blood:	n/a
50	chr5:177575216-177575266	Jurkat	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:149222391..149224886-chr5:177572662..177574353,2	MCF-7	breast:
2	chr5:177572705..177577722-chr5:177630592..177633512,5	MCF-7	breast:
3	chr5:177573926..177577755-chr5:177626660..177630083,3	MCF-7	breast:
4	chr5:177573566..177575503-chr5:177631642..177633223,2	K562	blood:
5	chr5:177547044..177549748-chr5:177575234..177578369,3	K562	blood:
6	chr5:177556109..177558644-chr5:177574334..177576029,3	K562	blood:
7	chr5:177556214..177559808-chr5:177575521..177582645,10	K562	blood:
8	chr5:177556060..177559089-chr5:177572421..177574313,3	K562	blood:
9	chr5:177556060..177559207-chr5:177571980..177574313,5	K562	blood:
10	chr5:177571121..177572812-chr8:122157856..122160060,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-N4BP3-1	chr5:177574970-177575478	NONHSAT105516

No data

Variant related genes	Relation type
RMND5B	TF binding region
RMND5B	CpG island
ENSG00000206737	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000145916	chromatin interactions

Extended variants
information (count: 188 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:188 , 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	rs112730404	chr5:177572776-177572777	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs545288894	chr5:177572840-177572841	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs6873523	chr5:177572927-177572928	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs113907080	chr5:177572952-177572953	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs116440779	chr5:177572987-177572988	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs571432112	chr5:177573000-177573001	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs548966178	chr5:177573008-177573009	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs113996248	chr5:177573011-177573012	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs557477091	chr5:177573013-177573014	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs372227344	chr5:177573070-177573071	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs375928165	chr5:177573091-177573092	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs200794085	chr5:177573094-177573095	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs4490608	chr5:177573100-177573101	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs146514336	chr5:177573140-177573141	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs141123042	chr5:177573141-177573142	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs199566204	chr5:177573150-177573151	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs144728558	chr5:177573151-177573152	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs552043062	chr5:177573196-177573197	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs570300631	chr5:177573215-177573216	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs370172551	chr5:177573220-177573221	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs36110411	chr5:177573221-177573222	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs537622846	chr5:177573222-177573223	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs138696545	chr5:177573228-177573229	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs573747497	chr5:177573233-177573234	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs73804715	chr5:177573248-177573249	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs574041577	chr5:177573265-177573266	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs139570120	chr5:177573274-177573275	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs148121600	chr5:177573275-177573276	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs373385402	chr5:177573278-177573279	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs375799811	chr5:177573317-177573318	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs149787154	chr5:177573346-177573347	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs544717355	chr5:177573359-177573360	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs563594161	chr5:177573394-177573395	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs575187706	chr5:177573443-177573444	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs543042778	chr5:177573460-177573461	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs76183331	chr5:177573486-177573487	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs560764546	chr5:177573527-177573528	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs529319661	chr5:177573530-177573531	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs373508848	chr5:177573548-177573549	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs553070599	chr5:177573567-177573568	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs547880225	chr5:177573592-177573593	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs559631464	chr5:177573596-177573597	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs533360309	chr5:177573616-177573617	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs573225093	chr5:177573624-177573625	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs118006676	chr5:177573625-177573626	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs534685345	chr5:177573659-177573660	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs570315454	chr5:177573675-177573676	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs531249983	chr5:177573684-177573685	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs549574081	chr5:177573778-177573779	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs79507429	chr5:177573786-177573787	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	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
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:221 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177558800-177576800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr5:177559000-177572800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:177559000-177572800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr5:177559000-177574000	Weak transcription	Small Intestine	intestine
5	chr5:177559000-177580000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr5:177559000-177580000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr5:177559200-177573000	Weak transcription	Psoas Muscle	Psoas
8	chr5:177559200-177573200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr5:177559200-177579800	Weak transcription	Right Atrium	heart
10	chr5:177559800-177577600	Weak transcription	Fetal Brain Male	brain
11	chr5:177560200-177579400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr5:177560200-177579600	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr5:177560200-177579800	Strong transcription	HUES6 Cell Line	embryonic stem cell
14	chr5:177560400-177578400	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr5:177560400-177578400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr5:177560400-177578600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr5:177560600-177579400	Strong transcription	Fetal Intestine Small	intestine
18	chr5:177560800-177579400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr5:177560800-177579600	Strong transcription	HUES48 Cell Line	embryonic stem cell
20	chr5:177561000-177572800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr5:177561000-177578000	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr5:177561000-177578200	Strong transcription	Adipose Nuclei	Adipose
23	chr5:177561000-177578800	Strong transcription	Thymus	Thymus
24	chr5:177561000-177579200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr5:177561000-177579400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr5:177561000-177579800	Strong transcription	H1 Cell Line	embryonic stem cell
27	chr5:177561200-177578800	Strong transcription	Primary T cells from cord blood	blood
28	chr5:177561200-177579400	Strong transcription	Fetal Thymus	thymus
29	chr5:177562200-177577400	Strong transcription	Primary neutrophils fromperipheralblood	blood
30	chr5:177562200-177578800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
31	chr5:177564000-177572800	Weak transcription	Stomach Mucosa	stomach
32	chr5:177566600-177572800	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr5:177566800-177576400	Strong transcription	Dnd41	blood
34	chr5:177566800-177576800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr5:177567000-177578000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr5:177567000-177578200	Strong transcription	Primary T helper cells PMA-I stimulated	--
37	chr5:177567000-177578800	Strong transcription	Rectal Mucosa Donor 29	rectum
38	chr5:177567000-177579000	Strong transcription	Cortex derived primary cultured neurospheres	brain
39	chr5:177567200-177578600	Strong transcription	Sigmoid Colon	Sigmoid Colon
40	chr5:177567400-177572800	Weak transcription	Fetal Kidney	kidney
41	chr5:177567400-177579000	Strong transcription	Fetal Brain Female	brain
42	chr5:177568000-177578600	Strong transcription	HepG2	liver
43	chr5:177568000-177578800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr5:177568200-177579400	Strong transcription	Duodenum Mucosa	Duodenum
45	chr5:177568400-177578600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr5:177568400-177578600	Strong transcription	Colonic Mucosa	Colon
47	chr5:177568600-177576200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr5:177568800-177576400	Strong transcription	Primary T helper cells fromperipheralblood	blood
49	chr5:177568800-177576400	Strong transcription	Brain Hippocampus Middle	brain
50	chr5:177568800-177577000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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