Variant report

Variant	nsv883185
Chromosome Location	chr5:177357964-177401509
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:563)
CpG islands
(count:1466)
Chromatin interactive
region (count:3)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:563 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:177384217-177384416	K562	blood:	n/a	n/a
2	ATF1	chr5:177397729-177397797	K562	blood:	n/a	n/a
3	BACH1	chr5:177385596-177386218	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr5:177388724-177389177	GM12878	blood:	n/a	n/a
5	BATF	chr5:177376161-177376489	GM12878	blood:	n/a	n/a
6	BATF	chr5:177376217-177376466	GM12878	blood:	n/a	n/a
7	BCL11A	chr5:177376116-177376485	GM12878	blood:	n/a	chr5:177376335-177376344
8	BCL11A	chr5:177382431-177382600	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:177388404-177388659	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:177388361-177389261	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:177371451-177371583	GM12878	blood:	n/a	n/a
12	BHLHE40	chr5:177382002-177382214	GM12878	blood:	n/a	n/a
13	CBX3	chr5:177368609-177368827	K562	blood:	n/a	n/a
14	CBX3	chr5:177368192-177368988	K562	blood:	n/a	n/a
15	CEBPB	chr5:177368534-177368609	K562	blood:	n/a	n/a
16	CEBPD	chr5:177368178-177368824	K562	blood:	n/a	n/a
17	CHD2	chr5:177385654-177386621	H1-hESC	embryonic stem cell:	n/a	n/a
18	CREB1	chr5:177372985-177373198	GM12878	blood:	n/a	n/a
19	CREB1	chr5:177372951-177373271	GM12878	blood:	n/a	n/a
20	CTBP2	chr5:177385796-177386503	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr5:177375164-177375355	MCF-7	breast:	n/a	chr5:177375249-177375258
22	CTCF	chr5:177361400-177361550	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr5:177361400-177361550	HMEC	breast:	n/a	n/a
24	CTCF	chr5:177361300-177361450	WI-38	lung:	n/a	n/a
25	CTCF	chr5:177361300-177361450	GM12868	blood:	n/a	n/a
26	CTCF	chr5:177375134-177375373	K562	blood:	n/a	chr5:177375249-177375258
27	CTCF	chr5:177361363-177361476	GM19240	blood:	n/a	n/a
28	CTCF	chr5:177378808-177378864	GM10266	blood:	n/a	n/a
29	CTCF	chr5:177361400-177361690	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr5:177361212-177361519	GM12878	blood:	n/a	n/a
31	CTCF	chr5:177375163-177375358	GM19238	blood:	n/a	chr5:177375249-177375258
32	CTCF	chr5:177375188-177375317	GM13976	blood:	n/a	chr5:177375249-177375258
33	CTCF	chr5:177375209-177375321	GM10266	blood:	n/a	chr5:177375249-177375258
34	CTCF	chr5:177366903-177366978	LNCaP	prostate:	n/a	n/a
35	CTCF	chr5:177361337-177361453	HepG2	liver:	n/a	n/a
36	CTCF	chr5:177361400-177361550	AG10803	skin:	n/a	n/a
37	CTCF	chr5:177361400-177361690	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr5:177368886-177368926	Lung_OC	lung:	n/a	chr5:177368886-177368904 chr5:177368888-177368901
39	CTCF	chr5:177375080-177375230	HMEC	breast:	n/a	n/a
40	CTCF	chr5:177400180-177400330	HVMF	connective:	n/a	n/a
41	CTCF	chr5:177361316-177361605	A549	lung:	n/a	n/a
42	CTCF	chr5:177375231-177375334	GM20000	blood:	n/a	chr5:177375249-177375258
43	CTCF	chr5:177375060-177375210	HAc	cerebellar:	n/a	n/a
44	CTCF	chr5:177361400-177361670	BJ	skin:	n/a	n/a
45	CTCF	chr5:177361400-177361550	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr5:177370512-177370600	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr5:177371400-177371550	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr5:177361320-177361494	GM13976	blood:	n/a	n/a
49	CTCF	chr5:177375181-177375350	GM19239	blood:	n/a	chr5:177375249-177375258
50	CTCF	chr5:177361328-177361511	Medullo	brain:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177387597-177387647	AG04449	skin:	fetal
2	chr5:177376282-177376332	HAEpiC	amniotic membrane:	n/a
3	chr5:177387597-177387647	AG04449	skin:	fetal
4	chr5:177376282-177376332	HAEpiC	amniotic membrane:	n/a
5	chr5:177398429-177398479	U87	brain:	n/a
6	chr5:177364048-177364098	HIPEpiC	eye:	n/a
7	chr5:177385478-177385528	AG10803	skin:	n/a
8	chr5:177374926-177374976	LNCaP	prostate:	n/a
9	chr5:177398433-177398483	SK-N-MC	brain:	n/a
10	chr5:177378100-177378150	HCF	heart:	n/a
11	chr5:177378100-177378150	GM12878	blood:	n/a
12	chr5:177396838-177396888	MCF-7	breast:	n/a
13	chr5:177387597-177387647	HEEpiC	esophagus:	n/a
14	chr5:177395755-177395805	SKMC	muscle:	n/a
15	chr5:177366867-177366917	AoSMC	blood vessel:	n/a
16	chr5:177396838-177396888	SKMC	muscle:	n/a
17	chr5:177376282-177376332	HMEC	breast:	n/a
18	chr5:177385478-177385528	HCT-116	colon:	n/a
19	chr5:177365747-177365797	NHBE	bronchial:	n/a
20	chr5:177371702-177371752	HEK293	kidney:	embryo
21	chr5:177399722-177399772	BE2_C	brain:	n/a
22	chr5:177377361-177377411	HUVEC	blood vessel:	n/a
23	chr5:177399722-177399772	HEEpiC	esophagus:	n/a
24	chr5:177365747-177365797	U87	brain:	n/a
25	chr5:177366867-177366917	Caco-2	colon:	n/a
26	chr5:177366867-177366917	SKMC	muscle:	n/a
27	chr5:177370476-177370526	ProgFib	skin:	n/a
28	chr5:177370977-177371027	H1-hESC	embryonic stem cell:	embryo
29	chr5:177391178-177391228	NH-A	brain:	n/a
30	chr5:177371702-177371752	NH-A	brain:	n/a
31	chr5:177366867-177366917	RPTEC	kidney:	n/a
32	chr5:177367013-177367063	HIPEpiC	eye:	n/a
33	chr5:177395755-177395805	GM19239	blood:	n/a
34	chr5:177395755-177395805	AG10803	skin:	n/a
35	chr5:177370977-177371027	SK-N-MC	brain:	n/a
36	chr5:177376282-177376332	SK-N-SH	brain:	n/a
37	chr5:177364048-177364098	GM12878	blood:	n/a
38	chr5:177378100-177378150	HepG2	liver:	n/a
39	chr5:177378100-177378150	CMK	blood:	n/a
40	chr5:177366867-177366917	NHDF-neo	bronchial:	n/a
41	chr5:177376282-177376332	HL-60	blood:	n/a
42	chr5:177387682-177387732	HIPEpiC	eye:	n/a
43	chr5:177398429-177398479	CMK	blood:	n/a
44	chr5:177378100-177378150	PFSK-1	brain:	n/a
45	chr5:177391178-177391228	ECC-1	luminal epithelium:	n/a
46	chr5:177377361-177377411	HCM	heart:	n/a
47	chr5:177364048-177364098	SAEC	small airway:	n/a
48	chr5:177366442-177366492	PrEC	prostate:	n/a
49	chr5:177395755-177395805	SK-N-MC	brain:	n/a
50	chr5:177378100-177378150	ProgFib	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:177399899..177402240-chr5:177658876..177660987,2	K562	blood:
2	chr5:177389362..177391423-chr5:177551819..177554278,2	MCF-7	breast:
3	chr5:175625956..175628511-chr5:177366543..177368721,3	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM153C-6	chr5:177358798-177359278	ENSG00000250963.1
2	lnc-FAM153C-4	chr5:177378718-177378957	ENSG00000249684.1
3	lnc-FAM153C-4	chr5:177377336-177377566	ENSG00000249684.1
4	lnc-FAM153C-2	chr5:177389519-177390144	XLOC_004670
5	lnc-FAM153C-4	chr5:177378414-177378519	ENSG00000249684.1
6	lnc-FAM153C-4	chr5:177378949-177378957	ENSG00000249684.1
7	lnc-FAM153C-4	chr5:177390828-177390961	ENSG00000249684.1
8	lnc-PROP1-2	chr5:177388755-177388871	XLOC_005099
9	lnc-FAM153C-4	chr5:177386720-177387150	ENSG00000249684.1
10	lnc-FAM153C-4	chr5:177380166-177380293	ENSG00000249684.1
11	lnc-FAM153C-5	chr5:177377183-177377566	NONHSAT105484
12	lnc-FAM153C-4	chr5:177384610-177384751	ENSG00000249684.1
13	lnc-FAM153C-4	chr5:177384610-177384680	ENSG00000249684.1
14	lnc-FAM153C-4	chr5:177384610-177384760	ENSG00000249684.1
15	lnc-FAM153C-4	chr5:177384610-177384680	ENSG00000249684.1
16	lnc-FAM153C-5	chr5:177378718-177378957	NONHSAT105484
17	lnc-FAM153C-4	chr5:177378718-177378957	ENSG00000249684.1
18	lnc-FAM153C-5	chr5:177384610-177384979	NONHSAT105484
19	lnc-PROP1-2	chr5:177388524-177388667	XLOC_005099
20	lnc-FAM153C-2	chr5:177389362-177389432	XLOC_004670

No data

Variant related genes	Relation type
ENSG00000250101	TF binding region
ENSG00000249684	TF binding region
SUDS3P1	TF binding region
ENSG00000250101	CpG island
ENSG00000249684	CpG island
SUDS3P1	CpG island
ENSG00000175309	chromatin interactions
ENSG00000248596	chromatin interactions

Extended variants
information (count: 2193 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2193 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4958980	chr5:177357964-177357965	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571702944	chr5:177357979-177357980	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs577852042	chr5:177357980-177357981	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs539058003	chr5:177358045-177358046	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs557347141	chr5:177358051-177358052	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs543360479	chr5:177358106-177358107	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs182662647	chr5:177358109-177358110	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs555193425	chr5:177358122-177358123	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs573337564	chr5:177358135-177358136	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs540560830	chr5:177358281-177358282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565255720	chr5:177358410-177358411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs62397787	chr5:177358447-177358448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577091398	chr5:177358451-177358452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs187619472	chr5:177358474-177358475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs562302069	chr5:177358481-177358482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529835328	chr5:177358534-177358535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs199661839	chr5:177358547-177358548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547976065	chr5:177358560-177358561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149166344	chr5:177358592-177358593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560322930	chr5:177358633-177358634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527477748	chr5:177358666-177358667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192542561	chr5:177358677-177358678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570763519	chr5:177358684-177358685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372366155	chr5:177358761-177358762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551035715	chr5:177358825-177358826	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs144571841	chr5:177358831-177358832	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs141842845	chr5:177358835-177358836	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs184187308	chr5:177358858-177358859	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs117147870	chr5:177358867-177358868	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs534147399	chr5:177358921-177358922	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs112461958	chr5:177358969-177358970	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs558677673	chr5:177359014-177359015	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs577127909	chr5:177359082-177359083	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs544491807	chr5:177359165-177359166	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs556169106	chr5:177359369-177359370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574328908	chr5:177359379-177359380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559558993	chr5:177359446-177359447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187538251	chr5:177359450-177359451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527334783	chr5:177359463-177359464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546030144	chr5:177359580-177359581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376023227	chr5:177359636-177359637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531686111	chr5:177359652-177359653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549787085	chr5:177359653-177359654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569270001	chr5:177359654-177359655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530059624	chr5:177359655-177359656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548537115	chr5:177359686-177359687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566853086	chr5:177359704-177359705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs137958355	chr5:177359793-177359794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192668195	chr5:177359801-177359802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142505571	chr5:177359830-177359831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Autism	20841430	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
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:572 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177356800-177358000	Enhancers	Pancreas	Pancrea
2	chr5:177356800-177358800	Enhancers	Ovary	ovary
3	chr5:177357000-177358000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr5:177357000-177358000	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr5:177357000-177358000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr5:177357000-177358000	Enhancers	Liver	Liver
7	chr5:177357000-177358000	Enhancers	Fetal Heart	heart
8	chr5:177357000-177358200	Enhancers	Fetal Muscle Trunk	muscle
9	chr5:177357200-177358000	Enhancers	H1 Cell Line	embryonic stem cell
10	chr5:177357200-177358000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr5:177357200-177358000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr5:177357200-177358000	Enhancers	Stomach Mucosa	stomach
13	chr5:177357400-177358000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr5:177357400-177358000	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr5:177357400-177365400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr5:177357800-177358200	Active TSS	Skeletal Muscle Female	skeletal muscle
17	chr5:177357800-177365600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr5:177358000-177358600	Enhancers	HSMMtube	muscle
19	chr5:177358000-177365800	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr5:177358000-177365800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr5:177362000-177365400	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr5:177364600-177365000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr5:177364800-177365600	Weak transcription	Pancreas	Pancrea
24	chr5:177364800-177366200	Enhancers	Primary T cells fromperipheralblood	blood
25	chr5:177365000-177365400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr5:177365200-177366000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr5:177365400-177365600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
28	chr5:177365400-177365800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr5:177365400-177365800	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr5:177365400-177365800	Enhancers	Placenta	Placenta
31	chr5:177365400-177366000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr5:177365400-177366200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr5:177365400-177366200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr5:177365400-177366200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr5:177365400-177366200	Bivalent Enhancer	Fetal Muscle Leg	muscle
36	chr5:177365600-177365800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
37	chr5:177365600-177365800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr5:177365600-177365800	Enhancers	Pancreas	Pancrea
39	chr5:177365600-177366000	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr5:177365600-177366000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr5:177365600-177366000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr5:177365600-177366000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr5:177365600-177366000	Bivalent Enhancer	Fetal Brain Female	brain
44	chr5:177365600-177366000	Bivalent Enhancer	Fetal Intestine Small	intestine
45	chr5:177365600-177366200	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr5:177365600-177366200	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr5:177365600-177366200	Bivalent Enhancer	Fetal Stomach	stomach
48	chr5:177365600-177366400	Enhancers	Primary B cells from peripheral blood	blood
49	chr5:177365600-177366800	Active TSS	iPS-15b Cell Line	embryonic stem cell
50	chr5:177365600-177366800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell

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