Variant report

Variant	nsv1025796
Chromosome Location	chr5:79844255-79880441
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:137)
CpG islands
(count:1160)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:137 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:79857696-79858031	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr5:79866469-79866515	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	chr5:79865780-79865930	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr5:79865980-79866130	WERI-Rb-1	eye:	n/a	n/a
16	CTCF	chr5:79865973-79866001	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr5:79866200-79866350	GM12866	blood:	n/a	n/a
18	CTCF	chr5:79865904-79865976	MCF-7	breast:	n/a	n/a
19	CTCF	chr5:79865600-79865750	GM12875	blood:	n/a	chr5:79865730-79865743
20	CTCF	chr5:79874418-79874465	GM13977	blood:	n/a	n/a
21	CTCF	chr5:79865908-79866011	MCF-7	breast:	n/a	n/a
22	CTCF	chr5:79866017-79866144	MCF-7	breast:	n/a	n/a
23	E2F4	chr5:79862943-79863134	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F6	chr5:79865493-79866432	A549	lung:	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	ELF1	chr5:79865981-79866443	GM12878	blood:	n/a	chr5:79865993-79866002
29	FOS	chr5:79857849-79857935	MCF10A-Er-Src	breast:	n/a	n/a
30	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
31	FOXA1	chr5:79850952-79851205	HepG2	liver:	n/a	n/a
32	FOXA2	chr5:79850981-79851189	HepG2	liver:	n/a	n/a
33	GATA2	chr5:79850502-79850872	K562	blood:	n/a	n/a
34	GATA2	chr5:79857232-79857611	K562	blood:	n/a	chr5:79857267-79857278 chr5:79857239-79857255 chr5:79857302-79857313 chr5:79857237-79857258
35	GATA3	chr5:79865738-79866471	MCF-7	breast:	n/a	n/a
36	GATA3	chr5:79862663-79863072	MCF-7	breast:	n/a	chr5:79862946-79862957
37	GATA3	chr5:79862630-79863210	MCF-7	breast:	n/a	chr5:79862946-79862957
38	GTF2F1	chr5:79866110-79866222	H1-hESC	embryonic stem cell:	n/a	n/a
39	GTF2F1	chr5:79868574-79868601	K562	blood:	n/a	n/a
40	GTF2F1	chr5:79868574-79868589	H1-hESC	embryonic stem cell:	n/a	n/a
41	HA-E2F1	chr5:79865841-79866445	MCF-7	breast:	n/a	n/a
42	HDAC2	chr5:79865712-79866467	MCF-7	breast:	n/a	n/a
43	HDAC2	chr5:79865889-79866244	HepG2	liver:	n/a	n/a
44	IRF4	chr5:79872142-79872687	GM12878	blood:	n/a	n/a
45	IRF4	chr5:79872159-79872632	GM12878	blood:	n/a	n/a
46	JUND	chr5:79850326-79850805	H1-hESC	embryonic stem cell:	n/a	n/a
47	JUND	chr5:79866007-79866334	H1-hESC	embryonic stem cell:	n/a	n/a
48	JUND	chr5:79865903-79866429	H1-hESC	embryonic stem cell:	n/a	n/a
49	JUND	chr5:79864736-79864936	H1-hESC	embryonic stem cell:	n/a	n/a
50	JUND	chr5:79857844-79857946	K562	blood:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:79869215-79869265	HRCEpiC	kidney:	n/a
2	chr5:79869215-79869265	HRCEpiC	kidney:	n/a
3	chr5:79865995-79866045	NB4	blood:	n/a
4	chr5:79869215-79869265	GM12878	blood:	n/a
5	chr5:79863923-79863973	ECC-1	luminal epithelium:	n/a
6	chr5:79855768-79855818	AG04449	skin:	fetal
7	chr5:79868409-79868459	ECC-1	luminal epithelium:	n/a
8	chr5:79869215-79869265	Jurkat	blood:	n/a
9	chr5:79869070-79869120	HCPEpiC	choroid plexus:	n/a
10	chr5:79862991-79863041	HEEpiC	esophagus:	n/a
11	chr5:79866869-79866919	HNPCEpiC	eye:	n/a
12	chr5:79866368-79866418	GM06990	blood:	n/a
13	chr5:79865808-79865858	HMEC	breast:	n/a
14	chr5:79862991-79863041	HIPEpiC	eye:	n/a
15	chr5:79863923-79863973	AG10803	skin:	n/a
16	chr5:79866869-79866919	PANC-1	pancreas:	n/a
17	chr5:79862991-79863041	LNCaP	prostate:	n/a
18	chr5:79869215-79869265	LNCaP	prostate:	n/a
19	chr5:79865995-79866045	PFSK-1	brain:	n/a
20	chr5:79866368-79866418	RPTEC	kidney:	n/a
21	chr5:79866099-79866149	HNPCEpiC	eye:	n/a
22	chr5:79865808-79865858	Hepatocyte	liver:	n/a
23	chr5:79865995-79866045	HCT-116	colon:	n/a
24	chr5:79866319-79866369	BE2_C	brain:	n/a
25	chr5:79866431-79866481	PrEC	prostate:	n/a
26	chr5:79865995-79866045	HIPEpiC	eye:	n/a
27	chr5:79866319-79866369	ProgFib	skin:	n/a
28	chr5:79865808-79865858	NH-A	brain:	n/a
29	chr5:79866869-79866919	MCF-7	breast:	n/a
30	chr5:79866319-79866369	AG09319	gingival:	n/a
31	chr5:79865995-79866045	IMR90	lung:	fetal
32	chr5:79869215-79869265	PANC-1	pancreas:	n/a
33	chr5:79863923-79863973	BE2_C	brain:	n/a
34	chr5:79861245-79861295	GM12891	blood:	n/a
35	chr5:79866869-79866919	K562	blood:	n/a
36	chr5:79866869-79866919	HEEpiC	esophagus:	n/a
37	chr5:79866319-79866369	GM12892	blood:	n/a
38	chr5:79866368-79866418	HRCEpiC	kidney:	n/a
39	chr5:79869070-79869120	IMR90	lung:	fetal
40	chr5:79865995-79866045	HNPCEpiC	eye:	n/a
41	chr5:79855768-79855818	HCM	heart:	n/a
42	chr5:79857871-79857921	IMR90	lung:	fetal
43	chr5:79866319-79866369	GM12878	blood:	n/a
44	chr5:79867237-79867287	BE2_C	brain:	n/a
45	chr5:79865402-79865452	HRE	kidney:	n/a
46	chr5:79865276-79865326	Jurkat	blood:	n/a
47	chr5:79865808-79865858	Hela-S3	cervix:	n/a
48	chr5:79868409-79868459	Hepatocyte	liver:	n/a
49	chr5:79867237-79867287	SK-N-SH	brain:	n/a
50	chr5:79862991-79863041	PrEC	prostate:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:79858408..79862630-chr5:79863192..79865325,4	MCF-7	breast:
2	chr5:79865080..79867445-chr5:79879119..79880833,2	K562	blood:
3	chr5:79857619..79859560-chr5:79943220..79945542,2	MCF-7	breast:
4	chr5:79857137..79859837-chr5:79862629..79864172,2	MCF-7	breast:
5	chr5:79859883..79861719-chr5:79862893..79865594,2	MCF-7	breast:
6	chr5:79853813..79856525-chr5:79858729..79860329,2	MCF-7	breast:
7	chr5:79852918..79855762-chr5:79859511..79861433,3	K562	blood:
8	chr5:79852918..79855762-chr5:79859511..79861433,3	K562	blood:
9	chr5:79844936..79847062-chr5:79859363..79861060,2	MCF-7	breast:
10	chr5:79844936..79847062-chr5:79859363..79861060,2	MCF-7	breast:
11	chr5:79853813..79856525-chr5:79858729..79860329,2	MCF-7	breast:
12	chr5:79864703..79867842-chr5:79869678..79871678,3	K562	blood:
13	chr5:79858028..79859956-chr5:79864775..79867277,2	K562	blood:
14	chr5:79849090..79851828-chr5:79857137..79859911,2	MCF-7	breast:
15	chr5:79847077..79849265-chr5:79858170..79860779,2	MCF-7	breast:
16	chr5:79843211..79844887-chr5:79844924..79846535,2	MCF-7	breast:
17	chr5:79849090..79851828-chr5:79857137..79859911,2	MCF-7	breast:
18	chr5:79859883..79861719-chr5:79862893..79865594,2	MCF-7	breast:
19	chr5:79858408..79862630-chr5:79863192..79865325,4	MCF-7	breast:
20	chr5:79857137..79859837-chr5:79862629..79864172,2	MCF-7	breast:
21	chr5:79843211..79844887-chr5:79844924..79846535,2	MCF-7	breast:
22	chr5:79847077..79849265-chr5:79858170..79860779,2	MCF-7	breast:
23	chr5:79852409..79854606-chr5:79949940..79952429,2	MCF-7	breast:

No data

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

Extended variants
information (count: 1097 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1097 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190339175	chr5:79845000-79845001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs376095638	chr5:79845006-79845007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555675631	chr5:79845018-79845019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs113262732	chr5:79845037-79845038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534560959	chr5:79845042-79845043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557891801	chr5:79845137-79845138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77907366	chr5:79845221-79845222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566049150	chr5:79845235-79845236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546418491	chr5:79845292-79845293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12521109	chr5:79845298-79845299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535163056	chr5:79845316-79845317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181261995	chr5:79845349-79845350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113252627	chr5:79845364-79845365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542133122	chr5:79845371-79845372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs35522939	chr5:79845377-79845378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112590924	chr5:79845388-79845389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141354573	chr5:79845417-79845418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547382948	chr5:79845424-79845425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185846362	chr5:79845431-79845432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533250372	chr5:79845456-79845457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549973328	chr5:79845462-79845463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188115332	chr5:79845637-79845638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150232597	chr5:79845641-79845642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549309608	chr5:79845701-79845702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35587631	chr5:79845734-79845735	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs534652762	chr5:79845743-79845744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10063848	chr5:79845768-79845769	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs577702340	chr5:79845813-79845814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536726208	chr5:79845894-79845895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34500505	chr5:79845954-79845955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556983801	chr5:79846020-79846021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576570310	chr5:79846022-79846023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371282822	chr5:79846052-79846053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs180901376	chr5:79846122-79846123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562090103	chr5:79846128-79846129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576259196	chr5:79846156-79846157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373551069	chr5:79846167-79846168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572393195	chr5:79846205-79846206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541059078	chr5:79846217-79846218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564298501	chr5:79846234-79846235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533327701	chr5:79846329-79846330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs71636236	chr5:79846337-79846338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112715706	chr5:79846373-79846374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563765144	chr5:79846394-79846395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112082979	chr5:79846397-79846398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549197390	chr5:79846467-79846468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62366863	chr5:79846484-79846485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192021444	chr5:79846505-79846506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566021730	chr5:79846573-79846574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184193067	chr5:79846574-79846575	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:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:79845000-79845200	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr5:79845000-79845600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr5:79845600-79850400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr5:79847400-79850400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr5:79848000-79848200	Bivalent Enhancer	Esophagus	oesophagus
6	chr5:79849600-79851200	Enhancers	K562	blood
7	chr5:79849800-79851200	Enhancers	H1 Cell Line	embryonic stem cell
8	chr5:79850200-79850800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr5:79850400-79850600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr5:79850400-79850600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr5:79850400-79851200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr5:79850400-79851200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr5:79850400-79851200	Enhancers	H9 Cell Line	embryonic stem cell
14	chr5:79850400-79851200	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr5:79850400-79851200	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr5:79850400-79851200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr5:79850400-79851200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr5:79850400-79851200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr5:79850600-79850800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr5:79850600-79851200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr5:79850600-79851200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
22	chr5:79850800-79851000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr5:79850800-79851200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr5:79850800-79851400	Enhancers	Liver	Liver
25	chr5:79851000-79851200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
26	chr5:79851200-79854400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr5:79851200-79857200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:79851200-79857800	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr5:79851200-79858000	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr5:79854400-79855200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr5:79855200-79855600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
32	chr5:79855200-79855600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
33	chr5:79855200-79855800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
34	chr5:79855200-79855800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
35	chr5:79855200-79857400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr5:79855400-79855600	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr5:79855400-79855800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
38	chr5:79855800-79856000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
39	chr5:79857200-79858000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
40	chr5:79857200-79858200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr5:79857200-79858600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr5:79857400-79857600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
43	chr5:79857400-79858000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
44	chr5:79857400-79858000	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr5:79857400-79858400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
46	chr5:79857400-79858400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr5:79857600-79858400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
48	chr5:79857600-79858400	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr5:79857800-79858600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr5:79858000-79858200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell

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