Variant report

Variant	nsv1027183
Chromosome Location	chr5:79837249-79876229
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:79866469-79866515	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr5:79857696-79858031	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr5:79872184-79872716	GM12878	blood:	n/a	n/a
4	BATF	chr5:79872183-79872702	GM12878	blood:	n/a	n/a
5	BCL11A	chr5:79872234-79872497	GM12878	blood:	n/a	n/a
6	CCNT2	chr5:79862771-79862800	K562	blood:	n/a	n/a
7	CEBPB	chr5:79866426-79866607	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr5:79851967-79852118	K562	blood:	n/a	n/a
9	CEBPB	chr5:79850260-79850263	K562	blood:	n/a	n/a
10	CEBPD	chr5:79857249-79857627	K562	blood:	n/a	n/a
11	CHD2	chr5:79866098-79866539	H1-hESC	embryonic stem cell:	n/a	n/a
12	CREB1	chr5:79865871-79866732	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr5:79865919-79866644	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr5:79865908-79866011	MCF-7	breast:	n/a	n/a
15	CTCF	chr5:79866200-79866350	GM12866	blood:	n/a	n/a
16	CTCF	chr5:79866017-79866144	MCF-7	breast:	n/a	n/a
17	CTCF	chr5:79865904-79865976	MCF-7	breast:	n/a	n/a
18	CTCF	chr5:79865980-79866130	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr5:79865973-79866001	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr5:79874418-79874465	GM13977	blood:	n/a	n/a
21	CTCF	chr5:79865780-79865930	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr5:79865600-79865750	GM12875	blood:	n/a	chr5:79865730-79865743
23	E2F4	chr5:79862943-79863134	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr5:79843286-79843345	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F6	chr5:79865742-79866337	A549	lung:	n/a	n/a
26	E2F6	chr5:79864880-79866596	H1-hESC	embryonic stem cell:	n/a	chr5:79864981-79864990 chr5:79865339-79865348
27	E2F6	chr5:79864756-79866673	H1-hESC	embryonic stem cell:	n/a	chr5:79864981-79864990 chr5:79865339-79865348
28	E2F6	chr5:79865493-79866432	A549	lung:	n/a	n/a
29	ELF1	chr5:79865981-79866443	GM12878	blood:	n/a	chr5:79865993-79866002
30	EP300	chr5:79837271-79837597	SK-N-SH_RA	brain:	n/a	chr5:79837435-79837444 chr5:79837434-79837443
31	FOS	chr5:79837325-79837563	MCF10A-Er-Src	breast:	n/a	chr5:79837435-79837444 chr5:79837435-79837443 chr5:79837435-79837442 chr5:79837433-79837445 chr5:79837434-79837443
32	FOS	chr5:79837276-79837611	MCF10A-Er-Src	breast:	n/a	chr5:79837435-79837444 chr5:79837435-79837443 chr5:79837435-79837442 chr5:79837433-79837445 chr5:79837434-79837443
33	FOS	chr5:79857849-79857935	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr5:79837375-79837562	MCF10A-Er-Src	breast:	n/a	chr5:79837435-79837444 chr5:79837435-79837443 chr5:79837435-79837442 chr5:79837433-79837445 chr5:79837434-79837443
35	FOS	chr5:79837316-79837611	MCF10A-Er-Src	breast:	n/a	chr5:79837435-79837444 chr5:79837435-79837443 chr5:79837435-79837442 chr5:79837433-79837445 chr5:79837434-79837443
36	FOS	chr5:79847315-79847401	MCF10A-Er-Src	breast:	n/a	chr5:79847366-79847376 chr5:79847366-79847376 chr5:79847367-79847375 chr5:79847366-79847376 chr5:79847366-79847376
37	FOSL2	chr5:79837157-79837700	SK-N-SH	brain:	n/a	chr5:79837435-79837444 chr5:79837435-79837443 chr5:79837435-79837442 chr5:79837433-79837445 chr5:79837434-79837443
38	FOXA1	chr5:79850952-79851205	HepG2	liver:	n/a	n/a
39	FOXA2	chr5:79850981-79851189	HepG2	liver:	n/a	n/a
40	GATA2	chr5:79857232-79857611	K562	blood:	n/a	chr5:79857267-79857278 chr5:79857239-79857255 chr5:79857302-79857313 chr5:79857237-79857258
41	GATA2	chr5:79850502-79850872	K562	blood:	n/a	n/a
42	GATA3	chr5:79862663-79863072	MCF-7	breast:	n/a	chr5:79862946-79862957
43	GATA3	chr5:79862630-79863210	MCF-7	breast:	n/a	chr5:79862946-79862957
44	GATA3	chr5:79865738-79866471	MCF-7	breast:	n/a	n/a
45	GATA3	chr5:79837201-79837647	SK-N-SH	brain:	n/a	chr5:79837433-79837442
46	GTF2F1	chr5:79868574-79868601	K562	blood:	n/a	n/a
47	GTF2F1	chr5:79868574-79868589	H1-hESC	embryonic stem cell:	n/a	n/a
48	GTF2F1	chr5:79866110-79866222	H1-hESC	embryonic stem cell:	n/a	n/a
49	HA-E2F1	chr5:79865841-79866445	MCF-7	breast:	n/a	n/a
50	HDAC2	chr5:79865712-79866467	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:79869070-79869120	Hepatocyte	liver:	n/a
2	chr5:79868409-79868459	PANC-1	pancreas:	n/a
3	chr5:79866368-79866418	HRE	kidney:	n/a
4	chr5:79869070-79869120	Hepatocyte	liver:	n/a
5	chr5:79868409-79868459	PANC-1	pancreas:	n/a
6	chr5:79866368-79866418	HRE	kidney:	n/a
7	chr5:79866099-79866149	SK-N-MC	brain:	n/a
8	chr5:79869070-79869120	HL-60	blood:	n/a
9	chr5:79867237-79867287	PrEC	prostate:	n/a
10	chr5:79866379-79866429	BJ	skin:	n/a
11	chr5:79862991-79863041	NHDF-neo	bronchial:	n/a
12	chr5:79866319-79866369	NH-A	brain:	n/a
13	chr5:79868409-79868459	NT2-D1	testis:	n/a
14	chr5:79855768-79855818	GM06990	blood:	n/a
15	chr5:79857871-79857921	HRPEpiC	eye:	n/a
16	chr5:79865808-79865858	HEK293	kidney:	embryo
17	chr5:79869070-79869120	SK-N-SH_RA	brain:	n/a
18	chr5:79855768-79855818	AG09309	skin:	n/a
19	chr5:79866368-79866418	GM06990	blood:	n/a
20	chr5:79857871-79857921	Jurkat	blood:	n/a
21	chr5:79866368-79866418	AG09319	gingival:	n/a
22	chr5:79865276-79865326	HRPEpiC	eye:	n/a
23	chr5:79866431-79866481	CMK	blood:	n/a
24	chr5:79869070-79869120	HCM	heart:	n/a
25	chr5:79866099-79866149	NH-A	brain:	n/a
26	chr5:79863923-79863973	HepG2	liver:	n/a
27	chr5:79855768-79855818	Hela-S3	cervix:	n/a
28	chr5:79865276-79865326	BJ	skin:	n/a
29	chr5:79867237-79867287	HCT-116	colon:	n/a
30	chr5:79865276-79865326	HRE	kidney:	n/a
31	chr5:79866368-79866418	NHDF-neo	bronchial:	n/a
32	chr5:79866368-79866418	GM12892	blood:	n/a
33	chr5:79865808-79865858	PFSK-1	brain:	n/a
34	chr5:79866431-79866481	Hela-S3	cervix:	n/a
35	chr5:79863923-79863973	AG09319	gingival:	n/a
36	chr5:79865402-79865452	HCF	heart:	n/a
37	chr5:79862991-79863041	PrEC	prostate:	n/a
38	chr5:79866379-79866429	HCM	heart:	n/a
39	chr5:79862991-79863041	RPTEC	kidney:	n/a
40	chr5:79867237-79867287	Caco-2	colon:	n/a
41	chr5:79861245-79861295	GM12891	blood:	n/a
42	chr5:79865402-79865452	HAEpiC	amniotic membrane:	n/a
43	chr5:79865995-79866045	HCT-116	colon:	n/a
44	chr5:79867237-79867287	NB4	blood:	n/a
45	chr5:79866869-79866919	AG04449	skin:	fetal
46	chr5:79866368-79866418	HNPCEpiC	eye:	n/a
47	chr5:79868409-79868459	ovcar-3	ovarian:	n/a
48	chr5:79865276-79865326	CMK	blood:	n/a
49	chr5:79857871-79857921	NHBE	bronchial:	n/a
50	chr5:79866099-79866149	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:79858028..79859956-chr5:79864775..79867277,2	K562	blood:
2	chr5:79843211..79844887-chr5:79844924..79846535,2	MCF-7	breast:
3	chr5:79852409..79854606-chr5:79949940..79952429,2	MCF-7	breast:
4	chr5:79859883..79861719-chr5:79862893..79865594,2	MCF-7	breast:
5	chr5:79852918..79855762-chr5:79859511..79861433,3	K562	blood:
6	chr5:79844936..79847062-chr5:79859363..79861060,2	MCF-7	breast:
7	chr5:79843211..79844887-chr5:79844924..79846535,2	MCF-7	breast:
8	chr5:79849090..79851828-chr5:79857137..79859911,2	MCF-7	breast:
9	chr5:79864703..79867842-chr5:79869678..79871678,3	K562	blood:
10	chr5:79859883..79861719-chr5:79862893..79865594,2	MCF-7	breast:
11	chr5:79844936..79847062-chr5:79859363..79861060,2	MCF-7	breast:
12	chr5:79857619..79859560-chr5:79943220..79945542,2	MCF-7	breast:
13	chr5:79852918..79855762-chr5:79859511..79861433,3	K562	blood:
14	chr5:79857137..79859837-chr5:79862629..79864172,2	MCF-7	breast:
15	chr5:79847077..79849265-chr5:79858170..79860779,2	MCF-7	breast:
16	chr5:79858408..79862630-chr5:79863192..79865325,4	MCF-7	breast:
17	chr5:79857137..79859837-chr5:79862629..79864172,2	MCF-7	breast:
18	chr5:79853813..79856525-chr5:79858729..79860329,2	MCF-7	breast:
19	chr5:79847077..79849265-chr5:79858170..79860779,2	MCF-7	breast:
20	chr5:79858408..79862630-chr5:79863192..79865325,4	MCF-7	breast:
21	chr5:79849090..79851828-chr5:79857137..79859911,2	MCF-7	breast:
22	chr5:79853813..79856525-chr5:79858729..79860329,2	MCF-7	breast:

Variant related genes	Relation type
ANKRD34B	TF binding region
ANKRD34B	CpG island
ENSG00000189127	chromatin interactions
ENSG00000228716	chromatin interactions
ENSG00000113318	chromatin interactions

Extended variants
information (count: 1201 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1201 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs42416	chr5:79837249-79837250	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs561367321	chr5:79837264-79837265	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555970830	chr5:79837265-79837266	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569857436	chr5:79837425-79837426	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185811036	chr5:79837427-79837428	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373906305	chr5:79837444-79837445	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368080662	chr5:79837445-79837446	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190610363	chr5:79837454-79837455	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373669675	chr5:79837467-79837468	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs367813400	chr5:79837471-79837472	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372277066	chr5:79837486-79837487	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181339470	chr5:79837488-79837489	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138264758	chr5:79837534-79837535	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543521901	chr5:79837564-79837565	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200855590	chr5:79837569-79837570	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555553887	chr5:79837611-79837612	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142754508	chr5:79837613-79837614	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs542011842	chr5:79837660-79837661	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186380131	chr5:79837748-79837749	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545776704	chr5:79837773-79837774	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527969769	chr5:79837924-79837925	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs139154523	chr5:79837941-79837942	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190846988	chr5:79838002-79838003	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115102419	chr5:79838074-79838075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs115931396	chr5:79838079-79838080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375263325	chr5:79838086-79838087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570009796	chr5:79838129-79838130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145191880	chr5:79838159-79838160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528344560	chr5:79838221-79838222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376291088	chr5:79838222-79838223	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534898108	chr5:79838253-79838254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187748310	chr5:79838260-79838261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576102386	chr5:79838285-79838286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577735486	chr5:79838298-79838299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543408057	chr5:79838321-79838322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115090899	chr5:79838322-79838323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544401292	chr5:79838332-79838333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190959488	chr5:79838340-79838341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542451473	chr5:79838392-79838393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201658903	chr5:79838393-79838394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183496327	chr5:79838407-79838408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374133175	chr5:79838446-79838447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114447579	chr5:79838482-79838483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541349251	chr5:79838485-79838486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564408528	chr5:79838536-79838537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540183551	chr5:79838563-79838564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533167581	chr5:79838570-79838571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34348427	chr5:79838627-79838628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147113680	chr5:79838635-79838636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549858303	chr5:79838639-79838640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:394 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:79834400-79837400	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr5:79835400-79837400	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr5:79835800-79837600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:79837200-79837400	Enhancers	Aorta	Aorta
5	chr5:79837200-79837800	Enhancers	Placenta Amnion	Placenta Amnion
6	chr5:79837200-79838000	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr5:79837200-79838400	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr5:79837400-79838000	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr5:79837400-79838200	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr5:79838000-79839600	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr5:79838200-79842400	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr5:79838400-79840000	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr5:79845000-79845200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr5:79845000-79845600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr5:79845600-79850400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr5:79847400-79850400	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr5:79848000-79848200	Bivalent Enhancer	Esophagus	oesophagus
18	chr5:79849600-79851200	Enhancers	K562	blood
19	chr5:79849800-79851200	Enhancers	H1 Cell Line	embryonic stem cell
20	chr5:79850200-79850800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr5:79850400-79850600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr5:79850400-79850600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr5:79850400-79851200	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr5:79850400-79851200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr5:79850400-79851200	Enhancers	H9 Cell Line	embryonic stem cell
26	chr5:79850400-79851200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr5:79850400-79851200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr5:79850400-79851200	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr5:79850400-79851200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr5:79850400-79851200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr5:79850600-79850800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr5:79850600-79851200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr5:79850600-79851200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
34	chr5:79850800-79851000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
35	chr5:79850800-79851200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr5:79850800-79851400	Enhancers	Liver	Liver
37	chr5:79851000-79851200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
38	chr5:79851200-79854400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr5:79851200-79857200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr5:79851200-79857800	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr5:79851200-79858000	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr5:79854400-79855200	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr5:79855200-79855600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
44	chr5:79855200-79855600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
45	chr5:79855200-79855800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
46	chr5:79855200-79855800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
47	chr5:79855200-79857400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr5:79855400-79855600	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr5:79855400-79855800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
50	chr5:79855800-79856000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell

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