Variant report

Variant	nsv1022154
Chromosome Location	chr5:79855710-79897516
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:168)
CpG islands
(count:1159)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:168 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:79887776-79887935	K562	blood:	n/a	n/a
2	ATF1	chr5:79893361-79893530	K562	blood:	n/a	n/a
3	BACH1	chr5:79857696-79858031	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr5:79866469-79866515	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr5:79872183-79872702	GM12878	blood:	n/a	n/a
6	BATF	chr5:79872184-79872716	GM12878	blood:	n/a	n/a
7	BCL11A	chr5:79872234-79872497	GM12878	blood:	n/a	n/a
8	BRCA1	chr5:79893393-79893621	H1-hESC	embryonic stem cell:	n/a	n/a
9	CCNT2	chr5:79862771-79862800	K562	blood:	n/a	n/a
10	CEBPB	chr5:79866426-79866607	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr5:79890642-79890887	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:79888461-79888649	HepG2	liver:	n/a	chr5:79888507-79888518
13	CEBPD	chr5:79857249-79857627	K562	blood:	n/a	n/a
14	CHD2	chr5:79893366-79893611	HepG2	liver:	n/a	n/a
15	CHD2	chr5:79880729-79880928	HepG2	liver:	n/a	n/a
16	CHD2	chr5:79866098-79866539	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr5:79880578-79880957	K562	blood:	n/a	n/a
18	CHD2	chr5:79893379-79893658	K562	blood:	n/a	n/a
19	CHD2	chr5:79893344-79893682	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr5:79865871-79866732	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr5:79865919-79866644	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr5:79865980-79866130	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr5:79866017-79866144	MCF-7	breast:	n/a	n/a
24	CTCF	chr5:79865973-79866001	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr5:79887400-79887550	RPTEC	kidney:	n/a	n/a
26	CTCF	chr5:79866200-79866350	GM12866	blood:	n/a	n/a
27	CTCF	chr5:79865908-79866011	MCF-7	breast:	n/a	n/a
28	CTCF	chr5:79884755-79884922	HepG2	liver:	n/a	n/a
29	CTCF	chr5:79887458-79887546	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr5:79865600-79865750	GM12875	blood:	n/a	chr5:79865730-79865743
31	CTCF	chr5:79865780-79865930	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr5:79865904-79865976	MCF-7	breast:	n/a	n/a
33	CTCF	chr5:79887500-79887650	HRE	kidney:	n/a	n/a
34	CTCF	chr5:79874418-79874465	GM13977	blood:	n/a	n/a
35	CTCF	chr5:79893513-79893599	Fibrobl	skin:	n/a	n/a
36	E2F4	chr5:79862943-79863134	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F6	chr5:79864880-79866596	H1-hESC	embryonic stem cell:	n/a	chr5:79864981-79864990 chr5:79865339-79865348
38	E2F6	chr5:79864756-79866673	H1-hESC	embryonic stem cell:	n/a	chr5:79864981-79864990 chr5:79865339-79865348
39	E2F6	chr5:79865742-79866337	A549	lung:	n/a	n/a
40	E2F6	chr5:79865493-79866432	A549	lung:	n/a	n/a
41	ELF1	chr5:79865981-79866443	GM12878	blood:	n/a	chr5:79865993-79866002
42	ELF1	chr5:79883414-79883715	K562	blood:	n/a	chr5:79883579-79883592
43	EP300	chr5:79887886-79888291	HepG2	liver:	n/a	chr5:79887949-79887963
44	EP300	chr5:79886999-79887795	ECC-1	luminal epithelium:	n/a	n/a
45	EP300	chr5:79887012-79887656	ECC-1	luminal epithelium:	n/a	n/a
46	ESR1	chr5:79888903-79889127	ECC-1	luminal epithelium:	n/a	n/a
47	FOS	chr5:79890334-79890527	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr5:79857849-79857935	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr5:79887325-79887458	MCF10A-Er-Src	breast:	n/a	n/a
50	FOXA1	chr5:79887887-79888277	HepG2	liver:	n/a	n/a

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:79869070-79869120	PFSK-1	brain:	n/a
2	chr5:79855768-79855818	HCPEpiC	choroid plexus:	n/a
3	chr5:79865276-79865326	BJ	skin:	n/a
4	chr5:79865808-79865858	HCM	heart:	n/a
5	chr5:79866869-79866919	IMR90	lung:	fetal
6	chr5:79869070-79869120	NHDF-neo	bronchial:	n/a
7	chr5:79863923-79863973	LNCaP	prostate:	n/a
8	chr5:79861245-79861295	ECC-1	luminal epithelium:	n/a
9	chr5:79866368-79866418	BJ	skin:	n/a
10	chr5:79863923-79863973	Hepatocyte	liver:	n/a
11	chr5:79866379-79866429	HEK293	kidney:	embryo
12	chr5:79866319-79866369	ProgFib	skin:	n/a
13	chr5:79863923-79863973	ovcar-3	ovarian:	n/a
14	chr5:79866368-79866418	AG04449	skin:	fetal
15	chr5:79868409-79868459	MCF10A-Er-Src	breast:	n/a
16	chr5:79865995-79866045	NB4	blood:	n/a
17	chr5:79865808-79865858	PFSK-1	brain:	n/a
18	chr5:79855768-79855818	K562	blood:	n/a
19	chr5:79857871-79857921	RPTEC	kidney:	n/a
20	chr5:79869070-79869120	HEK293	kidney:	embryo
21	chr5:79866368-79866418	Hela-S3	cervix:	n/a
22	chr5:79865808-79865858	CMK	blood:	n/a
23	chr5:79866869-79866919	HAEpiC	amniotic membrane:	n/a
24	chr5:79869215-79869265	SK-N-SH_RA	brain:	n/a
25	chr5:79866869-79866919	ovcar-3	ovarian:	n/a
26	chr5:79865808-79865858	ovcar-3	ovarian:	n/a
27	chr5:79866869-79866919	MCF-7	breast:	n/a
28	chr5:79855768-79855818	HMEC	breast:	n/a
29	chr5:79866368-79866418	PrEC	prostate:	n/a
30	chr5:79869215-79869265	SK-N-MC	brain:	n/a
31	chr5:79861245-79861295	NT2-D1	testis:	n/a
32	chr5:79865808-79865858	SK-N-SH_RA	brain:	n/a
33	chr5:79866368-79866418	AG04450	lung:	fetal
34	chr5:79855768-79855818	HRCEpiC	kidney:	n/a
35	chr5:79861245-79861295	HAEpiC	amniotic membrane:	n/a
36	chr5:79866099-79866149	HNPCEpiC	eye:	n/a
37	chr5:79865808-79865858	BE2_C	brain:	n/a
38	chr5:79869215-79869265	MCF-7	breast:	n/a
39	chr5:79866319-79866369	SK-N-SH	brain:	n/a
40	chr5:79865995-79866045	PANC-1	pancreas:	n/a
41	chr5:79869070-79869120	AG04449	skin:	fetal
42	chr5:79855768-79855818	PANC-1	pancreas:	n/a
43	chr5:79867237-79867287	GM12892	blood:	n/a
44	chr5:79863923-79863973	NHDF-neo	bronchial:	n/a
45	chr5:79866869-79866919	NB4	blood:	n/a
46	chr5:79863923-79863973	HepG2	liver:	n/a
47	chr5:79869070-79869120	ECC-1	luminal epithelium:	n/a
48	chr5:79866368-79866418	T-47D	breast:	n/a
49	chr5:79865276-79865326	HRE	kidney:	n/a
50	chr5:79865402-79865452	CMK	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:79857137..79859837-chr5:79862629..79864172,2	MCF-7	breast:
2	chr5:79847077..79849265-chr5:79858170..79860779,2	MCF-7	breast:
3	chr5:79853813..79856525-chr5:79858729..79860329,2	MCF-7	breast:
4	chr5:79852918..79855762-chr5:79859511..79861433,3	K562	blood:
5	chr5:79853813..79856525-chr5:79858729..79860329,2	MCF-7	breast:
6	chr5:79882125..79884896-chr5:79892515..79894507,2	K562	blood:
7	chr5:79857619..79859560-chr5:79943220..79945542,2	MCF-7	breast:
8	chr5:79844936..79847062-chr5:79859363..79861060,2	MCF-7	breast:
9	chr5:79849090..79851828-chr5:79857137..79859911,2	MCF-7	breast:
10	chr5:79858408..79862630-chr5:79863192..79865325,4	MCF-7	breast:
11	chr5:79859883..79861719-chr5:79862893..79865594,2	MCF-7	breast:
12	chr5:79859883..79861719-chr5:79862893..79865594,2	MCF-7	breast:
13	chr5:79865080..79867445-chr5:79879119..79880833,2	K562	blood:
14	chr5:79864703..79867842-chr5:79869678..79871678,3	K562	blood:
15	chr5:79857137..79859837-chr5:79862629..79864172,2	MCF-7	breast:
16	chr5:79858408..79862630-chr5:79863192..79865325,4	MCF-7	breast:
17	chr5:79852918..79855762-chr5:79859511..79861433,3	K562	blood:
18	chr5:79858028..79859956-chr5:79864775..79867277,2	K562	blood:
19	chr5:79882125..79884896-chr5:79892515..79894507,2	K562	blood:

No data

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

Extended variants
information (count: 1053 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1053 , 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	rs201143692	chr5:79855715-79855716	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559948107	chr5:79855719-79855720	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369135971	chr5:79855723-79855724	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528734024	chr5:79855726-79855727	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142137939	chr5:79855736-79855737	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551674336	chr5:79855742-79855743	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs367829617	chr5:79855757-79855758	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371220836	chr5:79855758-79855759	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201133010	chr5:79855769-79855770	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200046558	chr5:79855783-79855784	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs151166785	chr5:79855797-79855798	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552814333	chr5:79855798-79855799	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200291996	chr5:79855823-79855824	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs367911402	chr5:79855865-79855866	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185775880	chr5:79855869-79855870	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187262	chr5:79855876-79855877	Bivalent/Poised TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs530095969	chr5:79855992-79855993	Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11949130	chr5:79856076-79856077	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs547060446	chr5:79856077-79856078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558430024	chr5:79856200-79856201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148079271	chr5:79856213-79856214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72765505	chr5:79856323-79856324	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs150433067	chr5:79856335-79856336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538859493	chr5:79856343-79856344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558305945	chr5:79856359-79856360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370779665	chr5:79856378-79856379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111416395	chr5:79856451-79856452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544113438	chr5:79856454-79856455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554404784	chr5:79856546-79856547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574100288	chr5:79856637-79856638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190676007	chr5:79856658-79856659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376625972	chr5:79856659-79856660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528247805	chr5:79856676-79856677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs59652717	chr5:79856693-79856694	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs532093617	chr5:79856727-79856728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11949327	chr5:79856771-79856772	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs138187122	chr5:79856780-79856781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181236820	chr5:79856795-79856796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149086445	chr5:79856827-79856828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551297957	chr5:79856838-79856839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186580415	chr5:79856916-79856917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530148660	chr5:79856920-79856921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560180384	chr5:79856959-79856960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs71636238	chr5:79856982-79856983	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs566981010	chr5:79856998-79856999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs367749473	chr5:79857135-79857136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113048064	chr5:79857141-79857142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144771557	chr5:79857143-79857144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552216792	chr5:79857147-79857148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs173606	chr5:79857165-79857166	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:79851200-79857200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:79851200-79857800	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr5:79851200-79858000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:79855200-79855800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
5	chr5:79855200-79855800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
6	chr5:79855200-79857400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr5:79855400-79855800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
8	chr5:79855800-79856000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
9	chr5:79857200-79858000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
10	chr5:79857200-79858200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr5:79857200-79858600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr5:79857400-79857600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
13	chr5:79857400-79858000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
14	chr5:79857400-79858000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr5:79857400-79858400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
16	chr5:79857400-79858400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr5:79857600-79858400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
18	chr5:79857600-79858400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr5:79857800-79858600	Enhancers	H1 Cell Line	embryonic stem cell
20	chr5:79858000-79858200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
21	chr5:79858000-79858400	Enhancers	H9 Cell Line	embryonic stem cell
22	chr5:79858000-79858400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr5:79858000-79858600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
24	chr5:79858000-79858800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr5:79858200-79858400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr5:79858200-79858400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr5:79858400-79858600	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
28	chr5:79858400-79858600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr5:79858600-79858800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
30	chr5:79859200-79859400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr5:79859400-79859600	Enhancers	Brain Anterior Caudate	brain
32	chr5:79859600-79860200	Weak transcription	Brain Anterior Caudate	brain
33	chr5:79859600-79861400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr5:79860200-79860400	Enhancers	Brain Anterior Caudate	brain
35	chr5:79860400-79863800	Weak transcription	Brain Anterior Caudate	brain
36	chr5:79861200-79861400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:79861200-79861400	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr5:79861400-79861600	Enhancers	A549	lung
39	chr5:79861400-79861800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr5:79862600-79863000	Enhancers	A549	lung
41	chr5:79862800-79863000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr5:79862800-79863000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr5:79862800-79863200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr5:79863800-79866400	Active TSS	Brain Anterior Caudate	brain
45	chr5:79864000-79864400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr5:79864200-79864400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
47	chr5:79864200-79864600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
48	chr5:79864400-79864600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr5:79864400-79864800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr5:79864400-79864800	Bivalent Enhancer	Fetal Heart	heart

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