Variant report

Variant	nsv882222
Chromosome Location	chr5:79321439-79354147
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:122)
CpG islands
(count:732)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:122 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:79324093-79324327	HepG2	liver:	n/a	n/a
2	ATF1	chr5:79337452-79337476	K562	blood:	n/a	n/a
3	ATF1	chr5:79342589-79342693	K562	blood:	n/a	n/a
4	BACH1	chr5:79330830-79331030	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr5:79350530-79350841	GM12878	blood:	n/a	chr5:79350717-79350728
6	BATF	chr5:79329368-79329649	GM12878	blood:	n/a	chr5:79329553-79329563
7	BRCA1	chr5:79335424-79335435	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr5:79324055-79324188	HepG2	liver:	n/a	n/a
9	CTCF	chr5:79342538-79342615	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr5:79339480-79339630	GM12878	blood:	n/a	n/a
11	CTCF	chr5:79342460-79342679	HepG2	liver:	n/a	n/a
12	CTCF	chr5:79342560-79342710	HepG2	liver:	n/a	n/a
13	CTCF	chr5:79342523-79342739	GM12878	blood:	n/a	n/a
14	CTCF	chr5:79342513-79342650	K562	blood:	n/a	n/a
15	CTCF	chr5:79354060-79354210	HRE	kidney:	n/a	n/a
16	CTCF	chr5:79329380-79329530	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr5:79342426-79342728	K562	blood:	n/a	n/a
18	CTCF	chr5:79342520-79342670	AG09309	skin:	n/a	n/a
19	CTCF	chr5:79342520-79342670	BE2_C	brain:	n/a	n/a
20	CTCF	chr5:79339520-79339670	Caco-2	colon:	n/a	chr5:79339640-79339661
21	CTCF	chr5:79339787-79339899	Lung_OC	lung:	n/a	n/a
22	CUX1	chr5:79333620-79333684	GM12878	blood:	n/a	n/a
23	EBF1	chr5:79351519-79351997	GM12878	blood:	n/a	chr5:79351694-79351705 chr5:79351780-79351791
24	EGR1	chr5:79324108-79324367	K562	blood:	n/a	n/a
25	EP300	chr5:79351315-79352243	ECC-1	luminal epithelium:	n/a	chr5:79351934-79351943
26	ESR1	chr5:79351666-79352101	ECC-1	luminal epithelium:	n/a	n/a
27	FOS	chr5:79350511-79350910	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr5:79350546-79350868	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr5:79351627-79351877	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr5:79351751-79351915	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr5:79350548-79350867	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr5:79350516-79350883	MCF10A-Er-Src	breast:	n/a	n/a
33	FOXA1	chr5:79337241-79337478	T-47D	breast:	n/a	n/a
34	FOXA1	chr5:79322712-79322950	T-47D	breast:	n/a	n/a
35	FOXA1	chr5:79324060-79324398	HepG2	liver:	n/a	n/a
36	FOXA1	chr5:79324089-79324399	HepG2	liver:	n/a	n/a
37	FOXA1	chr5:79325742-79326151	HepG2	liver:	n/a	n/a
38	FOXA1	chr5:79324013-79324292	HepG2	liver:	n/a	n/a
39	FOXA2	chr5:79324058-79324350	HepG2	liver:	n/a	n/a
40	GABPA	chr5:79331120-79331398	H1-hESC	embryonic stem cell:	n/a	n/a
41	GTF2F1	chr5:79330455-79330623	H1-hESC	embryonic stem cell:	n/a	n/a
42	HMGN3	chr5:79331220-79331420	K562	blood:	n/a	n/a
43	IKZF1	chr5:79333373-79333672	GM12878	blood:	n/a	n/a
44	JUN	chr5:79330860-79330920	H1-hESC	embryonic stem cell:	n/a	n/a
45	JUN	chr5:79329577-79329659	K562	blood:	n/a	n/a
46	JUND	chr5:79350562-79350828	HCT-116	colon:	n/a	n/a
47	JUND	chr5:79330896-79331034	H1-hESC	embryonic stem cell:	n/a	n/a
48	JUND	chr5:79331314-79331448	H1-hESC	embryonic stem cell:	n/a	n/a
49	JUND	chr5:79324107-79324133	K562	blood:	n/a	n/a
50	JUND	chr5:79331107-79331308	H1-hESC	embryonic stem cell:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:79330096-79330146	NH-A	brain:	n/a
2	chr5:79334767-79334817	HEEpiC	esophagus:	n/a
3	chr5:79331850-79331900	AoSMC	blood vessel:	n/a
4	chr5:79330943-79330993	HMEC	breast:	n/a
5	chr5:79331850-79331900	Hela-S3	cervix:	n/a
6	chr5:79330669-79330719	HRPEpiC	eye:	n/a
7	chr5:79330096-79330146	HEEpiC	esophagus:	n/a
8	chr5:79330929-79330979	HCT-116	colon:	n/a
9	chr5:79330259-79330309	Hepatocyte	liver:	n/a
10	chr5:79330096-79330146	RPTEC	kidney:	n/a
11	chr5:79330929-79330979	AG09319	gingival:	n/a
12	chr5:79330799-79330849	HCPEpiC	choroid plexus:	n/a
13	chr5:79330959-79331009	NH-A	brain:	n/a
14	chr5:79330096-79330146	ProgFib	skin:	n/a
15	chr5:79330259-79330309	HRE	kidney:	n/a
16	chr5:79331477-79331527	AG10803	skin:	n/a
17	chr5:79330799-79330849	GM12891	blood:	n/a
18	chr5:79330669-79330719	CMK	blood:	n/a
19	chr5:79331135-79331185	HAEpiC	amniotic membrane:	n/a
20	chr5:79330669-79330719	HCF	heart:	n/a
21	chr5:79331047-79331097	HRPEpiC	eye:	n/a
22	chr5:79331850-79331900	AG04449	skin:	fetal
23	chr5:79334767-79334817	Caco-2	colon:	n/a
24	chr5:79330943-79330993	MCF-7	breast:	n/a
25	chr5:79334767-79334817	MCF10A-Er-Src	breast:	n/a
26	chr5:79330669-79330719	U87	brain:	n/a
27	chr5:79330096-79330146	AG04450	lung:	fetal
28	chr5:79334767-79334817	SK-N-SH	brain:	n/a
29	chr5:79330669-79330719	HCPEpiC	choroid plexus:	n/a
30	chr5:79334767-79334817	ECC-1	luminal epithelium:	n/a
31	chr5:79330096-79330146	HRE	kidney:	n/a
32	chr5:79330259-79330309	AG09309	skin:	n/a
33	chr5:79331850-79331900	NB4	blood:	n/a
34	chr5:79330096-79330146	HCF	heart:	n/a
35	chr5:79330259-79330309	GM12878	blood:	n/a
36	chr5:79331135-79331185	PANC-1	pancreas:	n/a
37	chr5:79330799-79330849	GM06990	blood:	n/a
38	chr5:79331047-79331097	HMEC	breast:	n/a
39	chr5:79331047-79331097	GM12878	blood:	n/a
40	chr5:79330943-79330993	Hepatocyte	liver:	n/a
41	chr5:79331850-79331900	HCM	heart:	n/a
42	chr5:79330096-79330146	H1-hESC	embryonic stem cell:	embryo
43	chr5:79331135-79331185	HCT-116	colon:	n/a
44	chr5:79330929-79330979	T-47D	breast:	n/a
45	chr5:79330799-79330849	H1-hESC	embryonic stem cell:	embryo
46	chr5:79331135-79331185	BJ	skin:	n/a
47	chr5:79334767-79334817	LNCaP	prostate:	n/a
48	chr5:79330669-79330719	HL-60	blood:	n/a
49	chr5:79334767-79334817	PANC-1	pancreas:	n/a
50	chr5:79331477-79331527	PFSK-1	brain:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:79348642..79351231-chr5:79351742..79353321,2	MCF-7	breast:
2	chr5:79333872..79336859-chr5:79337691..79339554,2	K562	blood:
3	chr5:79342559..79344595-chr5:79353378..79355370,2	MCF-7	breast:
4	chr5:79348642..79351231-chr5:79351742..79353321,2	MCF-7	breast:
5	chr5:79196588..79198348-chr5:79339313..79342153,2	K562	blood:
6	chr5:79333872..79336859-chr5:79337691..79339554,2	K562	blood:
7	chr5:79341846..79342632-chr5:79379301..79379935,2	K562	blood:
8	chr5:79332099..79334519-chr5:79339709..79341668,2	K562	blood:
9	chr5:79313494..79316436-chr5:79324403..79326793,2	K562	blood:
10	chr5:79342559..79344595-chr5:79353378..79355370,2	MCF-7	breast:
11	chr5:79332099..79334519-chr5:79339709..79341668,2	K562	blood:
12	chr5:79335840..79338759-chr5:79340815..79343092,2	K562	blood:
13	chr5:79350174..79351742-chr5:79371407..79373227,2	MCF-7	breast:
14	chr5:79335840..79338759-chr5:79340815..79343092,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SERINC5-1	chr5:79348197-79348724	ENSG00000249825.1

No data

Variant related genes	Relation type
TRMT112P2	TF binding region
THBS4	TF binding region
TRMT112P2	CpG island
THBS4	CpG island
ENSG00000251050	chromatin interactions
ENSG00000249825	chromatin interactions

Extended variants
information (count: 1073 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1073 , 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	rs2434273	chr5:79321439-79321440	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190449703	chr5:79321473-79321474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181630396	chr5:79321482-79321483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2434274	chr5:79321546-79321547	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs2434275	chr5:79321554-79321555	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs186764687	chr5:79321576-79321577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114615948	chr5:79321584-79321585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561943750	chr5:79321607-79321608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143631390	chr5:79321610-79321611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532811098	chr5:79321622-79321623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572347651	chr5:79321656-79321657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs116672470	chr5:79321676-79321677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564804283	chr5:79321709-79321710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533146596	chr5:79321713-79321714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201840506	chr5:79321773-79321774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146774982	chr5:79321776-79321777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190827024	chr5:79321814-79321815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs77797330	chr5:79321823-79321824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555856853	chr5:79321866-79321867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549545630	chr5:79321873-79321874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140613471	chr5:79321884-79321885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143696127	chr5:79321935-79321936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181250515	chr5:79321937-79321938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546519811	chr5:79322001-79322002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs148039078	chr5:79322011-79322012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116444641	chr5:79322255-79322256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556897238	chr5:79322279-79322280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573350268	chr5:79322296-79322297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150134920	chr5:79322357-79322358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552663146	chr5:79322368-79322369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185836349	chr5:79322377-79322378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541633777	chr5:79322387-79322388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373640112	chr5:79322411-79322412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs578186046	chr5:79322415-79322416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6874832	chr5:79322488-79322489	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs531752125	chr5:79322513-79322514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189761629	chr5:79322546-79322547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138675089	chr5:79322553-79322554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551370889	chr5:79322612-79322613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559887108	chr5:79322620-79322621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115395686	chr5:79322723-79322724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568568172	chr5:79322754-79322755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529846048	chr5:79322770-79322771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551566278	chr5:79322790-79322791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571385678	chr5:79322813-79322814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549836247	chr5:79322914-79322915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546813927	chr5:79322928-79322929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530833235	chr5:79323065-79323066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs566339316	chr5:79323115-79323116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550643503	chr5:79323131-79323132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:79319200-79323800	Weak transcription	Primary T cells from cord blood	blood
2	chr5:79323000-79323200	Enhancers	Sigmoid Colon	Sigmoid Colon
3	chr5:79323800-79324400	Enhancers	Primary T cells from cord blood	blood
4	chr5:79323800-79324400	Enhancers	Fetal Thymus	thymus
5	chr5:79324000-79324200	Enhancers	Dnd41	blood
6	chr5:79324000-79324400	Enhancers	HepG2	liver
7	chr5:79324000-79325000	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr5:79324200-79324400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr5:79324400-79326400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr5:79324400-79326600	Weak transcription	Dnd41	blood
11	chr5:79324400-79326800	Weak transcription	Primary T cells from cord blood	blood
12	chr5:79324400-79326800	Weak transcription	Fetal Thymus	thymus
13	chr5:79324800-79325000	Enhancers	Fetal Brain Female	brain
14	chr5:79326400-79327600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr5:79326600-79326800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr5:79326600-79328400	Enhancers	Dnd41	blood
17	chr5:79326800-79327400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr5:79326800-79327600	Enhancers	Fetal Thymus	thymus
19	chr5:79326800-79327800	Enhancers	Primary T cells from cord blood	blood
20	chr5:79327000-79327200	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr5:79327000-79327400	Enhancers	Primary hematopoietic stem cells	blood
22	chr5:79327000-79327600	Enhancers	Thymus	Thymus
23	chr5:79327400-79327600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
24	chr5:79327400-79327600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr5:79327400-79327600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr5:79329200-79329400	Bivalent Enhancer	Primary T cells from cord blood	blood
27	chr5:79330000-79330400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
28	chr5:79330000-79330600	Bivalent Enhancer	Fetal Kidney	kidney
29	chr5:79330200-79330600	Bivalent Enhancer	Fetal Muscle Leg	muscle
30	chr5:79330200-79332200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
31	chr5:79330400-79330600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
32	chr5:79330400-79330600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
33	chr5:79330400-79330600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
34	chr5:79330400-79330600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
35	chr5:79330400-79330600	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
36	chr5:79330400-79330800	Active TSS	Ovary	ovary
37	chr5:79330400-79331400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
38	chr5:79330400-79331600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
39	chr5:79330400-79331600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr5:79330400-79332000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
41	chr5:79330400-79332200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
42	chr5:79330600-79330800	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr5:79330600-79330800	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr5:79330600-79330800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:79330600-79330800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
46	chr5:79330600-79330800	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
47	chr5:79330600-79330800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
48	chr5:79330600-79330800	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
49	chr5:79330600-79330800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr5:79330600-79330800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin

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