Variant report

Variant	nsv965520
Chromosome Location	chr5:177570961-177577311
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:673)
CpG islands
(count:244)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:177576887-177577045	K562	blood:	n/a	n/a
2	ATF1	chr5:177575979-177576295	K562	blood:	n/a	n/a
3	ATF2	chr5:177572941-177573400	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr5:177576600-177577013	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:177572945-177573449	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr5:177573084-177573623	GM12878	blood:	n/a	n/a
7	BACH1	chr5:177573843-177573998	K562	blood:	n/a	n/a
8	BACH1	chr5:177574935-177574938	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr5:177573234-177573570	GM12878	blood:	n/a	chr5:177573402-177573413
10	BCL3	chr5:177574826-177575381	A549	lung:	n/a	n/a
11	BCL3	chr5:177575798-177576474	A549	lung:	n/a	n/a
12	BCL3	chr5:177572873-177573803	A549	lung:	n/a	n/a
13	BHLHE40	chr5:177573043-177573343	K562	blood:	n/a	n/a
14	BHLHE40	chr5:177574017-177574133	K562	blood:	n/a	n/a
15	BRCA1	chr5:177573019-177573286	HepG2	liver:	n/a	n/a
16	BRCA1	chr5:177573055-177573417	H1-hESC	embryonic stem cell:	n/a	n/a
17	CCNT2	chr5:177574486-177574686	K562	blood:	n/a	n/a
18	CEBPB	chr5:177575749-177575994	K562	blood:	n/a	n/a
19	CEBPB	chr5:177573579-177573854	K562	blood:	n/a	n/a
20	CEBPB	chr5:177573446-177573825	A549	lung:	n/a	n/a
21	CEBPB	chr5:177577004-177577248	K562	blood:	n/a	n/a
22	CEBPB	chr5:177573075-177574066	MCF-7	breast:	n/a	n/a
23	CEBPB	chr5:177572829-177574632	MCF-7	breast:	n/a	n/a
24	CEBPB	chr5:177573020-177573384	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr5:177573128-177573849	Hela-S3	cervix:	n/a	n/a
26	CHD1	chr5:177571237-177571386	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr5:177572849-177573413	IMR90	lung:	n/a	n/a
28	CHD2	chr5:177572986-177573320	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr5:177574970-177575130	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr5:177572962-177573283	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr5:177573100-177573365	HepG2	liver:	n/a	n/a
32	CHD2	chr5:177576871-177577035	K562	blood:	n/a	n/a
33	CHD2	chr5:177572892-177573319	K562	blood:	n/a	n/a
34	CHD2	chr5:177575605-177576106	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr5:177576743-177576959	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr5:177573728-177573914	K562	blood:	n/a	n/a
37	CREB1	chr5:177572982-177573237	A549	lung:	n/a	n/a
38	CTCF	chr5:177573448-177573583	GM19240	blood:	n/a	n/a
39	CTCF	chr5:177573445-177573557	GM19239	blood:	n/a	n/a
40	CTCF	chr5:177576711-177576725	GM19238	blood:	n/a	n/a
41	CTCF	chr5:177573100-177573250	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr5:177573140-177573290	WI-38	lung:	n/a	n/a
43	CTCF	chr5:177573120-177573270	GM12864	blood:	n/a	n/a
44	CTCF	chr5:177573080-177573230	HMF	breast:	n/a	n/a
45	CTCF	chr5:177573120-177573270	HMF	breast:	n/a	n/a
46	CTCF	chr5:177572930-177573400	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr5:177573100-177573250	GM12869	blood:	n/a	n/a
48	CTCF	chr5:177573080-177573230	BJ	skin:	n/a	n/a
49	CTCF	chr5:177572993-177573301	ECC-1	luminal epithelium:	n/a	n/a
50	CTCF	chr5:177573039-177573330	GM10248	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177571022-177571072	NHDF-neo	bronchial:	n/a
2	chr5:177575216-177575266	PFSK-1	brain:	n/a
3	chr5:177573275-177573325	T-47D	breast:	n/a
4	chr5:177571022-177571072	GM12892	blood:	n/a
5	chr5:177575216-177575266	HL-60	blood:	n/a
6	chr5:177571022-177571072	SAEC	small airway:	n/a
7	chr5:177575216-177575266	CMK	blood:	n/a
8	chr5:177575216-177575266	HCT-116	colon:	n/a
9	chr5:177571022-177571072	HCF	heart:	n/a
10	chr5:177571022-177571072	HPAEpiC	pulmonary alveolar:	n/a
11	chr5:177576684-177576734	HCF	heart:	n/a
12	chr5:177575216-177575266	Hela-S3	cervix:	n/a
13	chr5:177576684-177576734	NHBE	bronchial:	n/a
14	chr5:177573275-177573325	SK-N-MC	brain:	n/a
15	chr5:177575216-177575266	A549	lung:	n/a
16	chr5:177576684-177576734	PANC-1	pancreas:	n/a
17	chr5:177576684-177576734	NT2-D1	testis:	n/a
18	chr5:177573275-177573325	U87	brain:	n/a
19	chr5:177576684-177576734	HPAEpiC	pulmonary alveolar:	n/a
20	chr5:177573275-177573325	SKMC	muscle:	n/a
21	chr5:177576684-177576734	HCM	heart:	n/a
22	chr5:177575216-177575266	HCM	heart:	n/a
23	chr5:177576684-177576734	SK-N-SH_RA	brain:	n/a
24	chr5:177571022-177571072	HepG2	liver:	n/a
25	chr5:177571022-177571072	AoSMC	blood vessel:	n/a
26	chr5:177575216-177575266	HNPCEpiC	eye:	n/a
27	chr5:177576684-177576734	NH-A	brain:	n/a
28	chr5:177575216-177575266	HEEpiC	esophagus:	n/a
29	chr5:177571022-177571072	PrEC	prostate:	n/a
30	chr5:177575216-177575266	BJ	skin:	n/a
31	chr5:177576684-177576734	T-47D	breast:	n/a
32	chr5:177575216-177575266	HPAEpiC	pulmonary alveolar:	n/a
33	chr5:177576684-177576734	GM12878	blood:	n/a
34	chr5:177573275-177573325	HCM	heart:	n/a
35	chr5:177575216-177575266	MCF-7	breast:	n/a
36	chr5:177575216-177575266	HUVEC	blood vessel:	n/a
37	chr5:177576684-177576734	PrEC	prostate:	n/a
38	chr5:177576684-177576734	CMK	blood:	n/a
39	chr5:177576684-177576734	U87	brain:	n/a
40	chr5:177573275-177573325	NH-A	brain:	n/a
41	chr5:177576684-177576734	Hela-S3	cervix:	n/a
42	chr5:177575216-177575266	U87	brain:	n/a
43	chr5:177573275-177573325	HUVEC	blood vessel:	n/a
44	chr5:177575216-177575266	H1-hESC	embryonic stem cell:	embryo
45	chr5:177573275-177573325	A549	lung:	n/a
46	chr5:177573275-177573325	HAEpiC	amniotic membrane:	n/a
47	chr5:177573275-177573325	HRE	kidney:	n/a
48	chr5:177575216-177575266	HRE	kidney:	n/a
49	chr5:177576684-177576734	K562	blood:	n/a
50	chr5:177573275-177573325	MCF10A-Er-Src	breast:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:177571121..177572812-chr8:122157856..122160060,2	MCF-7	breast:
2	chr5:177573566..177575503-chr5:177631642..177633223,2	K562	blood:
3	chr5:177502832..177503538-chr5:177571735..177572454,2	MCF-7	breast:
4	chr5:177556060..177559207-chr5:177571980..177574313,5	K562	blood:
5	chr5:177556060..177559089-chr5:177572421..177574313,3	K562	blood:
6	chr1:149222391..149224886-chr5:177572662..177574353,2	MCF-7	breast:
7	chr5:177539043..177545979-chr5:177577141..177584026,12	K562	blood:
8	chr5:177572705..177577722-chr5:177630592..177633512,5	MCF-7	breast:
9	chr5:177573926..177577755-chr5:177626660..177630083,3	MCF-7	breast:
10	chr5:177556214..177559808-chr5:177575521..177582645,10	K562	blood:
11	chr5:177556109..177558644-chr5:177574334..177576029,3	K562	blood:
12	chr5:177547044..177549748-chr5:177575234..177578369,3	K562	blood:

(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
ENSG00000145911	chromatin interactions
ENSG00000145916	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000206737	chromatin interactions

Extended variants
information (count: 328 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142121381	chr5:177570981-177570982	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs535396518	chr5:177571008-177571009	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs376722623	chr5:177571022-177571023	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs369617974	chr5:177571043-177571044	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs151177853	chr5:177571045-177571046	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs140069738	chr5:177571066-177571067	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs150309056	chr5:177571067-177571068	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs373548331	chr5:177571094-177571095	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs374441747	chr5:177571103-177571104	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs368667116	chr5:177571106-177571107	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs371214275	chr5:177571107-177571108	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs35063864	chr5:177571127-177571128	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs375912875	chr5:177571130-177571131	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs368001512	chr5:177571153-177571154	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs56712710	chr5:177571248-177571249	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs572244556	chr5:177571297-177571298	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs534852046	chr5:177571302-177571303	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs531461638	chr5:177571316-177571317	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs116607328	chr5:177571325-177571326	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs561689272	chr5:177571366-177571367	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs149472117	chr5:177571390-177571391	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs143957952	chr5:177571392-177571393	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs59768441	chr5:177571404-177571405	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs74819912	chr5:177571438-177571439	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs6601219	chr5:177571474-177571475	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs551582608	chr5:177571497-177571498	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs574941214	chr5:177571504-177571505	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs35618073	chr5:177571546-177571547	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs6601220	chr5:177571554-177571555	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs370245739	chr5:177571562-177571563	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs541243010	chr5:177571578-177571579	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs370423867	chr5:177571588-177571589	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs543906873	chr5:177571596-177571597	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs535708447	chr5:177571604-177571605	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs13175750	chr5:177571655-177571656	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs572743746	chr5:177571656-177571657	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs189875416	chr5:177571698-177571699	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs6876480	chr5:177571706-177571707	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs543501440	chr5:177571722-177571723	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs558364491	chr5:177571750-177571751	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs576028747	chr5:177571799-177571800	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs118177590	chr5:177571836-177571837	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs368621424	chr5:177571853-177571854	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs75498640	chr5:177571886-177571887	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs34342590	chr5:177571909-177571910	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs181932632	chr5:177571945-177571946	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs559666005	chr5:177571947-177571948	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs73349889	chr5:177571967-177571968	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs533294071	chr5:177572068-177572069	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs551586893	chr5:177572205-177572206	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 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:327 , 50 per page) page: 1 2 3 4 5 6 7

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	chr5:177561000-177571600	Strong transcription	Liver	Liver
21	chr5:177561000-177572800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr5:177561000-177578000	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr5:177561000-177578200	Strong transcription	Adipose Nuclei	Adipose
24	chr5:177561000-177578800	Strong transcription	Thymus	Thymus
25	chr5:177561000-177579200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr5:177561000-177579400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr5:177561000-177579800	Strong transcription	H1 Cell Line	embryonic stem cell
28	chr5:177561200-177578800	Strong transcription	Primary T cells from cord blood	blood
29	chr5:177561200-177579400	Strong transcription	Fetal Thymus	thymus
30	chr5:177562000-177571000	Strong transcription	Duodenum Smooth Muscle	Duodenum
31	chr5:177562200-177571800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr5:177562200-177577400	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr5:177562200-177578800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
34	chr5:177564000-177572800	Weak transcription	Stomach Mucosa	stomach
35	chr5:177566600-177571400	Strong transcription	NHEK	skin
36	chr5:177566600-177572800	Strong transcription	Primary T cells fromperipheralblood	blood
37	chr5:177566800-177571800	Strong transcription	H9 Cell Line	embryonic stem cell
38	chr5:177566800-177576400	Strong transcription	Dnd41	blood
39	chr5:177566800-177576800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr5:177567000-177571000	Strong transcription	A549	lung
41	chr5:177567000-177571400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr5:177567000-177571800	Strong transcription	Brain Anterior Caudate	brain
43	chr5:177567000-177578000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr5:177567000-177578200	Strong transcription	Primary T helper cells PMA-I stimulated	--
45	chr5:177567000-177578800	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr5:177567000-177579000	Strong transcription	Cortex derived primary cultured neurospheres	brain
47	chr5:177567200-177578600	Strong transcription	Sigmoid Colon	Sigmoid Colon
48	chr5:177567400-177572800	Weak transcription	Fetal Kidney	kidney
49	chr5:177567400-177579000	Strong transcription	Fetal Brain Female	brain
50	chr5:177568000-177578600	Strong transcription	HepG2	liver

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