Variant report

Variant	nsv531994
Chromosome Location	chr5:151292664-151331097
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:416)
CpG islands
(count:1590)
Chromatin interactive
region (count:16)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:151304249-151304350	K562	blood:	n/a	n/a
2	BCL11A	chr5:151297538-151297897	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr5:151297573-151297787	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr5:151304270-151304436	K562	blood:	n/a	n/a
5	BRCA1	chr5:151292659-151292787	H1-hESC	embryonic stem cell:	n/a	n/a
6	CBX3	chr5:151310819-151311219	HCT-116	colon:	n/a	n/a
7	CBX3	chr5:151304140-151304444	K562	blood:	n/a	n/a
8	CBX3	chr5:151310811-151311238	K562	blood:	n/a	n/a
9	CBX3	chr5:151310840-151311215	K562	blood:	n/a	n/a
10	CBX3	chr5:151304094-151304477	K562	blood:	n/a	n/a
11	CCNT2	chr5:151295968-151296108	K562	blood:	n/a	n/a
12	CEBPB	chr5:151304273-151304368	K562	blood:	n/a	n/a
13	CHD2	chr5:151304290-151304291	K562	blood:	n/a	n/a
14	CREB1	chr5:151304118-151304598	K562	blood:	n/a	n/a
15	CREB1	chr5:151304080-151304503	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr5:151304059-151304452	GM12878	blood:	n/a	n/a
17	CREB1	chr5:151304060-151304447	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr5:151303493-151303771	T-47D	breast:	n/a	chr5:151303602-151303618
19	CTCF	chr5:151304283-151304342	MCF-7	breast:	n/a	n/a
20	CTCF	chr5:151304220-151304370	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr5:151303480-151303630	GM12872	blood:	n/a	chr5:151303602-151303618
22	CTCF	chr5:151303520-151303670	A549	lung:	n/a	chr5:151303602-151303618
23	CTCF	chr5:151303540-151303690	WERI-Rb-1	eye:	n/a	chr5:151303602-151303618
24	CTCF	chr5:151303446-151303768	K562	blood:	n/a	chr5:151303602-151303618
25	CTCF	chr5:151303580-151303730	AG10803	skin:	n/a	chr5:151303602-151303618
26	CTCF	chr5:151303540-151303690	HUVEC	blood vessel:	n/a	chr5:151303602-151303618
27	CTCF	chr5:151303500-151303650	HA-sp	spinal cord:	n/a	chr5:151303602-151303618
28	CTCF	chr5:151303500-151303650	GM12866	blood:	n/a	chr5:151303602-151303618
29	CTCF	chr5:151304220-151304370	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr5:151303429-151303853	K562	blood:	n/a	chr5:151303602-151303618
31	CTCF	chr5:151303507-151303716	NHEK	skin:	n/a	chr5:151303602-151303618
32	CTCF	chr5:151303500-151303650	GM12869	blood:	n/a	chr5:151303602-151303618
33	CTCF	chr5:151303565-151303632	Pancreas_OC	pancreas:	n/a	chr5:151303602-151303618
34	CTCF	chr5:151304289-151304345	ProgFib	skin:	n/a	n/a
35	CTCF	chr5:151304220-151304370	SAEC	small airway:	n/a	n/a
36	CTCF	chr5:151303540-151303690	GM12872	blood:	n/a	chr5:151303602-151303618
37	CTCF	chr5:151303560-151303710	MCF-7	breast:	n/a	chr5:151303602-151303618
38	CTCF	chr5:151303500-151303650	HAc	cerebellar:	n/a	chr5:151303602-151303618
39	CTCF	chr5:151303460-151303610	GM12868	blood:	n/a	n/a
40	CTCF	chr5:151303480-151303630	GM12870	blood:	n/a	chr5:151303602-151303618
41	CTCF	chr5:151303539-151303689	GM12891	blood:	n/a	chr5:151303602-151303618
42	CTCF	chr5:151303530-151303680	HepG2	liver:	n/a	chr5:151303602-151303618
43	CTCF	chr5:151303495-151303731	A549	lung:	n/a	chr5:151303602-151303618
44	CTCF	chr5:151303560-151303710	HPAF	blood vessel:	n/a	chr5:151303602-151303618
45	CTCF	chr5:151303448-151303765	Medullo	brain:	n/a	chr5:151303602-151303618
46	CTCF	chr5:151303560-151303710	GM06990	blood:	n/a	chr5:151303602-151303618
47	CTCF	chr5:151298289-151298329	GM10266	blood:	n/a	n/a
48	CTCF	chr5:151303540-151303690	GM12873	blood:	n/a	chr5:151303602-151303618
49	CTCF	chr5:151304248-151304333	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr5:151303460-151303610	HL-60	blood:	n/a	n/a

(count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:151304488-151304538	NHDF-neo	bronchial:	n/a
2	chr5:151296785-151296835	GM06990	blood:	n/a
3	chr5:151329120-151329170	AoSMC	blood vessel:	n/a
4	chr5:151304817-151304867	HAEpiC	amniotic membrane:	n/a
5	chr5:151304488-151304538	NHDF-neo	bronchial:	n/a
6	chr5:151296785-151296835	GM06990	blood:	n/a
7	chr5:151329120-151329170	AoSMC	blood vessel:	n/a
8	chr5:151304817-151304867	HAEpiC	amniotic membrane:	n/a
9	chr5:151305143-151305193	GM06990	blood:	n/a
10	chr5:151301225-151301275	HCPEpiC	choroid plexus:	n/a
11	chr5:151305143-151305193	NHBE	bronchial:	n/a
12	chr5:151305746-151305796	HEEpiC	esophagus:	n/a
13	chr5:151306404-151306454	A549	lung:	n/a
14	chr5:151304542-151304592	SAEC	small airway:	n/a
15	chr5:151303847-151303897	AoSMC	blood vessel:	n/a
16	chr5:151303982-151304032	IMR90	lung:	fetal
17	chr5:151304422-151304472	RPTEC	kidney:	n/a
18	chr5:151328029-151328079	AG04449	skin:	fetal
19	chr5:151304409-151304459	PrEC	prostate:	n/a
20	chr5:151303982-151304032	PrEC	prostate:	n/a
21	chr5:151308141-151308191	IMR90	lung:	fetal
22	chr5:151304312-151304362	LNCaP	prostate:	n/a
23	chr5:151305143-151305193	AG04449	skin:	fetal
24	chr5:151328029-151328079	T-47D	breast:	n/a
25	chr5:151329120-151329170	GM12878	blood:	n/a
26	chr5:151304312-151304362	HPAEpiC	pulmonary alveolar:	n/a
27	chr5:151304547-151304597	HEK293	kidney:	embryo
28	chr5:151304422-151304472	GM06990	blood:	n/a
29	chr5:151303982-151304032	K562	blood:	n/a
30	chr5:151306404-151306454	HIPEpiC	eye:	n/a
31	chr5:151303520-151303570	MCF-7	breast:	n/a
32	chr5:151328842-151328892	AoSMC	blood vessel:	n/a
33	chr5:151301225-151301275	AG09309	skin:	n/a
34	chr5:151304409-151304459	BE2_C	brain:	n/a
35	chr5:151304312-151304362	HEEpiC	esophagus:	n/a
36	chr5:151328029-151328079	NHBE	bronchial:	n/a
37	chr5:151328842-151328892	MCF-7	breast:	n/a
38	chr5:151308141-151308191	HCPEpiC	choroid plexus:	n/a
39	chr5:151304547-151304597	SKMC	muscle:	n/a
40	chr5:151308141-151308191	H1-hESC	embryonic stem cell:	embryo
41	chr5:151304817-151304867	T-47D	breast:	n/a
42	chr5:151306404-151306454	HRE	kidney:	n/a
43	chr5:151303520-151303570	SK-N-MC	brain:	n/a
44	chr5:151304770-151304820	PrEC	prostate:	n/a
45	chr5:151303847-151303897	HAEpiC	amniotic membrane:	n/a
46	chr5:151329120-151329170	HNPCEpiC	eye:	n/a
47	chr5:151304357-151304407	NHDF-neo	bronchial:	n/a
48	chr5:151305143-151305193	AG04450	lung:	fetal
49	chr5:151304547-151304597	BJ	skin:	n/a
50	chr5:151304409-151304459	Jurkat	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:151291529..151293532-chr5:151299170..151301141,2	K562	blood:
2	chr5:151307767..151309684-chr5:151310725..151312458,2	K562	blood:
3	chr5:151319695..151322648-chr5:151325265..151329434,3	K562	blood:
4	chr5:151319178..151320732-chr5:151324965..151326478,2	MCF-7	breast:
5	chr5:151296962..151300362-chr5:151302778..151304994,3	K562	blood:
6	chr5:151302299..151302849-chr5:151522311..151522997,2	MCF-7	breast:
7	chr5:151296962..151299645-chr5:151302778..151304321,2	K562	blood:
8	chr5:151296962..151299645-chr5:151302778..151304321,2	K562	blood:
9	chr5:151296601..151298259-chr5:151299981..151301720,2	K562	blood:
10	chr5:151303110..151303991-chr5:151522441..151523040,2	MCF-7	breast:
11	chr5:151291529..151293532-chr5:151299170..151301141,2	K562	blood:
12	chr5:151319178..151320732-chr5:151324965..151326478,2	MCF-7	breast:
13	chr5:151303407..151303946-chr5:151522386..151523026,2	MCF-7	breast:
14	chr5:151296601..151298259-chr5:151299981..151301720,2	K562	blood:
15	chr5:151307767..151309684-chr5:151310725..151312458,2	K562	blood:
16	chr5:151281430..151283581-chr5:151299945..151301618,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-G3BP1-5	chr5:151304405-151306147	NONHSAT104645
2	lnc-G3BP1-6	chr5:151310728-151310790	ucscGeneNc_uc003luu_1
3	lnc-G3BP1-6	chr5:151309325-151309417	ucscGeneNc_uc003luu_1
4	lnc-G3BP1-4	chr5:151330535-151330597	XLOC_004607
5	lnc-G3BP1-6	chr5:151311392-151311434	ucscGeneNc_uc003luu_1
6	lnc-G3BP1-4	chr5:151329132-151329224	XLOC_004607

No data

Variant related genes	Relation type
ENSG00000254226	TF binding region
GLRA1	TF binding region
ENSG00000254226	CpG island
GLRA1	CpG island
ENSG00000145888	chromatin interactions
ENSG00000254226	chromatin interactions

Extended variants
information (count: 1029 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1029 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141371974	chr5:151292681-151292682	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs112679075	chr5:151292696-151292697	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs111764233	chr5:151292740-151292741	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs528338605	chr5:151292756-151292757	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs186791260	chr5:151292772-151292773	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs200923661	chr5:151292802-151292803	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs35941948	chr5:151292803-151292804	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs398084562	chr5:151292804-151292805	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs397884098	chr5:151292805-151292806	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs190660377	chr5:151292883-151292884	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs181760896	chr5:151292906-151292907	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs186417062	chr5:151292931-151292932	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs145154944	chr5:151292939-151292940	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs10057786	chr5:151292968-151292969	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs573836751	chr5:151293069-151293070	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs139031960	chr5:151293070-151293071	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115310632	chr5:151293086-151293087	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs55719946	chr5:151293087-151293088	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs577636774	chr5:151293089-151293090	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs141588143	chr5:151293118-151293119	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191178149	chr5:151293143-151293144	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs76027915	chr5:151293147-151293148	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs372585833	chr5:151293157-151293158	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114342418	chr5:151293174-151293175	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147450049	chr5:151293182-151293183	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs150288255	chr5:151293187-151293188	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs111391713	chr5:151293224-151293225	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542229543	chr5:151293233-151293234	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540210223	chr5:151293305-151293306	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs564842822	chr5:151293319-151293320	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550403155	chr5:151293340-151293341	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs137916335	chr5:151293444-151293445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550557544	chr5:151293456-151293457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371665699	chr5:151293524-151293525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115983267	chr5:151293557-151293558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116255766	chr5:151293576-151293577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548399939	chr5:151293613-151293614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs74801789	chr5:151293661-151293662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs77532957	chr5:151293738-151293739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553065821	chr5:151293744-151293745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569214091	chr5:151293746-151293747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs149471562	chr5:151293753-151293754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9324715	chr5:151293776-151293777	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs557364648	chr5:151293783-151293784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575930409	chr5:151293798-151293799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs187671675	chr5:151293857-151293858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76979673	chr5:151293871-151293872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548536896	chr5:151293882-151293883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573494734	chr5:151293889-151293890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191290378	chr5:151293927-151293928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	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
Breast cancer	21858162	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
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Renal cell carcinoma	18592004	CNVD
small cell lung cancer	20016488	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
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Hyperekplexia	16941485	CNVD
Myelofibrosis	22110671	CNVD
Crohn''s disease	20877625	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	17603634	CNVD
Crohn''s disease	20106866	CNVD
Breast cancer	20409316	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:197 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:151291600-151293200	Enhancers	Aorta	Aorta
2	chr5:151291800-151292800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
3	chr5:151291800-151293600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:151292000-151292800	Enhancers	H9 Cell Line	embryonic stem cell
5	chr5:151292000-151293200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
6	chr5:151292000-151294600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr5:151292200-151293200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
8	chr5:151292400-151293000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
9	chr5:151292600-151293200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
10	chr5:151292600-151293400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:151292800-151297200	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr5:151293000-151293400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
13	chr5:151293200-151293400	Weak transcription	Aorta	Aorta
14	chr5:151293200-151293400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr5:151293800-151294400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:151293800-151294400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr5:151294000-151294200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
18	chr5:151294000-151294200	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr5:151294200-151294400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:151294200-151294400	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr5:151294400-151297200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr5:151294400-151297200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr5:151294400-151299200	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr5:151295400-151297400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr5:151295800-151296200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:151296000-151297000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
27	chr5:151296400-151296600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
28	chr5:151296600-151296800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
29	chr5:151296800-151297000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
30	chr5:151297000-151297600	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr5:151297000-151298400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr5:151297200-151297400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
33	chr5:151297200-151297800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr5:151297200-151298000	Enhancers	H9 Cell Line	embryonic stem cell
35	chr5:151297200-151298000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr5:151297200-151298400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr5:151297200-151298600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr5:151297400-151297600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
39	chr5:151297400-151297600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr5:151297400-151297800	Enhancers	Brain Germinal Matrix	brain
41	chr5:151297400-151298000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr5:151297400-151298000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr5:151297400-151298000	Enhancers	Spleen	Spleen
44	chr5:151297400-151298200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
45	chr5:151297400-151298400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
46	chr5:151297600-151297800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
47	chr5:151297600-151297800	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr5:151297600-151298000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
49	chr5:151297600-151298000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
50	chr5:151297600-151298000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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