Variant report

Variant	nsv462429
Chromosome Location	chr5:120388986-120452856
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	CEBPB	chr5:120388712-120389167	MCF-7	breast:	n/a	n/a
2	CEBPB	chr5:120407480-120407657	HepG2	liver:	n/a	chr5:120407589-120407602
3	CEBPB	chr5:120388756-120389126	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr5:120409404-120409415	K562	blood:	n/a	n/a
5	CTCF	chr5:120396480-120396630	GM12875	blood:	n/a	n/a
6	CTCF	chr5:120443661-120443763	Spleen_OC	spleen:	n/a	n/a
7	CTCF	chr5:120423660-120423810	GM12873	blood:	n/a	n/a
8	CTCF	chr5:120398360-120398510	HVMF	connective:	n/a	n/a
9	CTCF	chr5:120423520-120423670	GM12868	blood:	n/a	n/a
10	CTCF	chr5:120389160-120389310	BE2_C	brain:	n/a	n/a
11	E2F4	chr5:120436254-120436454	MCF10A-Er-Src	breast:	n/a	n/a
12	ELK1	chr5:120390270-120390366	GM12878	blood:	n/a	n/a
13	EP300	chr5:120388676-120389373	SK-N-SH_RA	brain:	n/a	chr5:120389215-120389229
14	EP300	chr5:120388733-120389180	SK-N-SH_RA	brain:	n/a	n/a
15	EP300	chr5:120388067-120389799	SK-N-SH	brain:	n/a	chr5:120389215-120389229
16	FOXA1	chr5:120438247-120438428	T-47D	breast:	n/a	n/a
17	FOXA1	chr5:120436644-120436932	T-47D	breast:	n/a	chr5:120436840-120436855
18	FOXA1	chr5:120438218-120438518	T-47D	breast:	n/a	n/a
19	FOXA1	chr5:120436647-120437070	T-47D	breast:	n/a	chr5:120436840-120436855
20	FOXA2	chr5:120400059-120400750	A549	lung:	n/a	n/a
21	FOXA2	chr5:120400276-120400594	A549	lung:	n/a	n/a
22	GATA2	chr5:120388198-120389497	SH-SY5Y	brain:	n/a	chr5:120388989-120388998
23	GATA2	chr5:120413066-120413595	SH-SY5Y	brain:	n/a	chr5:120413088-120413098 chr5:120413090-120413107 chr5:120413212-120413223
24	GATA3	chr5:120388561-120389390	SK-N-SH	brain:	n/a	chr5:120388989-120388998
25	GATA3	chr5:120436671-120436986	T-47D	breast:	n/a	n/a
26	GATA3	chr5:120388668-120389272	MCF-7	breast:	n/a	chr5:120388989-120388998
27	GATA3	chr5:120388691-120389280	SH-SY5Y	brain:	n/a	chr5:120388989-120388998
28	GATA3	chr5:120436592-120436978	T-47D	breast:	n/a	n/a
29	GATA3	chr5:120409039-120409063	SH-SY5Y	brain:	n/a	n/a
30	GATA3	chr5:120388609-120389313	SK-N-SH	brain:	n/a	chr5:120388989-120388998
31	GATA3	chr5:120413173-120413620	SH-SY5Y	brain:	n/a	chr5:120413575-120413596 chr5:120413212-120413223
32	GATA3	chr5:120388844-120389108	T-47D	breast:	n/a	chr5:120388989-120388998
33	HEY1	chr5:120443181-120443364	K562	blood:	n/a	n/a
34	IRF1	chr5:120435817-120435819	K562	blood:	n/a	n/a
35	IRF3	chr5:120431289-120431347	GM12878	blood:	n/a	n/a
36	JUN	chr5:120437772-120437792	K562	blood:	n/a	n/a
37	JUND	chr5:120426594-120426841	HepG2	liver:	n/a	n/a
38	KAP1	chr5:120411327-120411527	K562	blood:	n/a	n/a
39	MAFF	chr5:120445521-120445900	HepG2	liver:	n/a	chr5:120445707-120445721 chr5:120445708-120445726
40	MAFF	chr5:120426165-120426373	HepG2	liver:	n/a	chr5:120426269-120426287
41	MAFF	chr5:120445514-120445896	K562	blood:	n/a	chr5:120445707-120445721 chr5:120445708-120445726
42	MAFK	chr5:120445544-120445887	K562	blood:	n/a	chr5:120445707-120445721 chr5:120445708-120445717 chr5:120445704-120445724 chr5:120445711-120445720 chr5:120445709-120445724 chr5:120445708-120445718 chr5:120445706-120445722
43	MAFK	chr5:120445531-120445889	HepG2	liver:	n/a	chr5:120445707-120445721 chr5:120445708-120445717 chr5:120445704-120445724 chr5:120445711-120445720 chr5:120445709-120445724 chr5:120445708-120445718 chr5:120445706-120445722
44	MAFK	chr5:120445392-120446005	GM12878	blood:	n/a	chr5:120445707-120445721 chr5:120445956-120445965 chr5:120445708-120445717 chr5:120445704-120445724 chr5:120445711-120445720 chr5:120445709-120445724 chr5:120445708-120445718 chr5:120445706-120445722
45	MAFK	chr5:120445529-120445902	HepG2	liver:	n/a	chr5:120445707-120445721 chr5:120445708-120445717 chr5:120445704-120445724 chr5:120445711-120445720 chr5:120445709-120445724 chr5:120445708-120445718 chr5:120445706-120445722
46	MAFK	chr5:120445528-120445902	IMR90	lung:	n/a	chr5:120445707-120445721 chr5:120445708-120445717 chr5:120445704-120445724 chr5:120445711-120445720 chr5:120445709-120445724 chr5:120445708-120445718 chr5:120445706-120445722
47	MAFK	chr5:120426139-120426378	HepG2	liver:	n/a	chr5:120426271-120426286
48	MAFK	chr5:120437930-120437962	HepG2	liver:	n/a	n/a
49	MAFK	chr5:120437940-120438115	IMR90	lung:	n/a	n/a
50	MAFK	chr5:120426156-120426418	IMR90	lung:	n/a	chr5:120426271-120426286

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:120444080-120444130	AG10803	skin:	n/a
2	chr5:120444080-120444130	AG10803	skin:	n/a
3	chr5:120444080-120444130	GM06990	blood:	n/a
4	chr5:120444080-120444130	AG04449	skin:	fetal
5	chr5:120444080-120444130	NH-A	brain:	n/a
6	chr5:120444080-120444130	RPTEC	kidney:	n/a
7	chr5:120444080-120444130	GM12891	blood:	n/a
8	chr5:120444080-120444130	BE2_C	brain:	n/a
9	chr5:120444080-120444130	NHDF-neo	bronchial:	n/a
10	chr5:120444080-120444130	MCF-7	breast:	n/a
11	chr5:120400115-120400165	HRPEpiC	eye:	n/a
12	chr5:120444080-120444130	ECC-1	luminal epithelium:	n/a
13	chr5:120400115-120400165	NB4	blood:	n/a
14	chr5:120400115-120400165	HPAEpiC	pulmonary alveolar:	n/a
15	chr5:120444080-120444130	HRCEpiC	kidney:	n/a
16	chr5:120444080-120444130	U87	brain:	n/a
17	chr5:120444080-120444130	PFSK-1	brain:	n/a
18	chr5:120400115-120400165	AoSMC	blood vessel:	n/a
19	chr5:120400115-120400165	GM12878	blood:	n/a
20	chr5:120400115-120400165	HCM	heart:	n/a
21	chr5:120400115-120400165	HNPCEpiC	eye:	n/a
22	chr5:120444080-120444130	NB4	blood:	n/a
23	chr5:120400115-120400165	HCT-116	colon:	n/a
24	chr5:120444080-120444130	HepG2	liver:	n/a
25	chr5:120444080-120444130	Hepatocyte	liver:	n/a
26	chr5:120444080-120444130	HL-60	blood:	n/a
27	chr5:120400115-120400165	ProgFib	skin:	n/a
28	chr5:120400115-120400165	ovcar-3	ovarian:	n/a
29	chr5:120444080-120444130	HNPCEpiC	eye:	n/a
30	chr5:120400115-120400165	GM12892	blood:	n/a
31	chr5:120444080-120444130	HIPEpiC	eye:	n/a
32	chr5:120400115-120400165	SK-N-MC	brain:	n/a
33	chr5:120400115-120400165	MCF-7	breast:	n/a
34	chr5:120400115-120400165	Hepatocyte	liver:	n/a
35	chr5:120400115-120400165	IMR90	lung:	fetal
36	chr5:120400115-120400165	RPTEC	kidney:	n/a
37	chr5:120444080-120444130	BJ	skin:	n/a
38	chr5:120444080-120444130	SK-N-MC	brain:	n/a
39	chr5:120444080-120444130	HRE	kidney:	n/a
40	chr5:120400115-120400165	T-47D	breast:	n/a
41	chr5:120400115-120400165	HEEpiC	esophagus:	n/a
42	chr5:120400115-120400165	ECC-1	luminal epithelium:	n/a
43	chr5:120400115-120400165	GM06990	blood:	n/a
44	chr5:120400115-120400165	GM19239	blood:	n/a
45	chr5:120400115-120400165	HepG2	liver:	n/a
46	chr5:120400115-120400165	H1-hESC	embryonic stem cell:	embryo
47	chr5:120444080-120444130	AG04450	lung:	fetal
48	chr5:120444080-120444130	H1-hESC	embryonic stem cell:	embryo
49	chr5:120400115-120400165	HMEC	breast:	n/a
50	chr5:120444080-120444130	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
2	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
3	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
4	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:
5	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
6	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRR16-3	chr5:120394939-120395040	NONHSAT103451
2	lnc-PRR16-3	chr5:120396085-120396648	NONHSAT103451

Variant related genes	Relation type
ENSG00000248853	TF binding region
ENSG00000248853	CpG island

Extended variants
information (count: 903 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:903 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7727775	chr5:120388986-120388987	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182900424	chr5:120388997-120388998	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs558207939	chr5:120389047-120389048	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs572658938	chr5:120389081-120389082	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs17506765	chr5:120389110-120389111	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs564123150	chr5:120389160-120389161	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs17447285	chr5:120389173-120389174	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs562449655	chr5:120389182-120389183	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs529827837	chr5:120389186-120389187	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs549611596	chr5:120389204-120389205	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs10059678	chr5:120389224-120389225	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs560400701	chr5:120389231-120389232	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs186669004	chr5:120389236-120389237	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs191041015	chr5:120389256-120389257	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs570686607	chr5:120389257-120389258	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs115026554	chr5:120389274-120389275	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs549923796	chr5:120389311-120389312	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs568087629	chr5:120389358-120389359	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs535559046	chr5:120389437-120389438	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs144592863	chr5:120389448-120389449	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs137897213	chr5:120389510-120389511	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs142321384	chr5:120389522-120389523	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs372939302	chr5:120389524-120389525	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs145973893	chr5:120389558-120389559	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs571748037	chr5:120389563-120389564	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs533211247	chr5:120389566-120389567	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs10059997	chr5:120389570-120389571	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs183231656	chr5:120389571-120389572	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs566287258	chr5:120389627-120389628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs187652524	chr5:120389639-120389640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139843146	chr5:120389646-120389647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs17147289	chr5:120389697-120389698	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs193132667	chr5:120389738-120389739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142923676	chr5:120389756-120389757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs150678524	chr5:120389779-120389780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564273110	chr5:120389794-120389795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369799013	chr5:120389833-120389834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531530414	chr5:120389840-120389841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs74744350	chr5:120389872-120389873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183116927	chr5:120389908-120389909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561757560	chr5:120389941-120389942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529287293	chr5:120389947-120389948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372599681	chr5:120389949-120389950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs377147935	chr5:120389984-120389985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs115921932	chr5:120390032-120390033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76985687	chr5:120390050-120390051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs188198552	chr5:120390061-120390062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs551695202	chr5:120390062-120390063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570201347	chr5:120390094-120390095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192585082	chr5:120390095-120390096	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
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
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
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	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
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:120388200-120389400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:120388400-120389400	Enhancers	Hela-S3	cervix
3	chr5:120388400-120389600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr5:120388800-120389600	Flanking Active TSS	Dnd41	blood
5	chr5:120389000-120389600	Enhancers	Fetal Kidney	kidney
6	chr5:120389600-120392200	Enhancers	Dnd41	blood
7	chr5:120399800-120400200	Enhancers	H1 Cell Line	embryonic stem cell
8	chr5:120399800-120400400	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr5:120399800-120400400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr5:120399800-120400400	Active TSS	HUES6 Cell Line	embryonic stem cell
11	chr5:120400000-120400200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr5:120400000-120400400	Active TSS	H9 Cell Line	embryonic stem cell
13	chr5:120400000-120400400	Active TSS	HUES64 Cell Line	embryonic stem cell
14	chr5:120400000-120400400	Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr5:120400000-120400400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr5:120400000-120400400	Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr5:120413000-120414200	Enhancers	Dnd41	blood
18	chr5:120423200-120424400	ZNF genes & repeats	Dnd41	blood
19	chr5:120424400-120425400	Weak transcription	Dnd41	blood
20	chr5:120425400-120427000	Enhancers	Dnd41	blood
21	chr5:120440400-120440800	Enhancers	Spleen	Spleen
22	chr5:120442200-120442800	ZNF genes & repeats	Dnd41	blood
23	chr5:120442800-120444000	Weak transcription	Dnd41	blood
24	chr5:120443000-120447600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr5:120443400-120445000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr5:120443800-120444000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr5:120444000-120444400	ZNF genes & repeats	Dnd41	blood
28	chr5:120444000-120444600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
29	chr5:120444000-120444600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr5:120444000-120444800	Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr5:120444200-120444400	Active TSS	iPS-15b Cell Line	embryonic stem cell
32	chr5:120444200-120444600	Enhancers	H1 Cell Line	embryonic stem cell
33	chr5:120444400-120444600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
34	chr5:120444400-120444800	Enhancers	Placenta	Placenta
35	chr5:120444400-120444800	Active TSS	Hela-S3	cervix
36	chr5:120444400-120445600	Enhancers	Dnd41	blood
37	chr5:120444600-120444800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr5:120445000-120449000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:120447600-120447800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
40	chr5:120449000-120449600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:120449600-120450200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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