Variant report

Variant	nsv1027701
Chromosome Location	chr5:116138286-116185586
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:132)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:132 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr5:116179791-116179894	GM12878	blood:	n/a	n/a
2	CEBPB	chr5:116185036-116185175	HepG2	liver:	n/a	n/a
3	CEBPB	chr5:116184726-116185303	HepG2	liver:	n/a	n/a
4	CEBPB	chr5:116178787-116179034	HepG2	liver:	n/a	chr5:116178952-116178965 chr5:116179009-116179026 chr5:116179014-116179025 chr5:116179014-116179025
5	CEBPB	chr5:116178558-116179017	A549	lung:	n/a	chr5:116178952-116178965
6	CEBPB	chr5:116184736-116185309	HepG2	liver:	n/a	n/a
7	CEBPB	chr5:116184800-116184994	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD1	chr5:116156777-116156783	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD1	chr5:116156439-116156449	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr5:116185481-116185558	GM12878	blood:	n/a	n/a
11	CTBP2	chr5:116151713-116152439	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr5:116180867-116180957	MCF-7	breast:	n/a	n/a
13	CTCF	chr5:116180840-116180990	HEK293	kidney:	n/a	n/a
14	CTCF	chr5:116175277-116175331	GM10266	blood:	n/a	n/a
15	CTCF	chr5:116180840-116180990	HepG2	liver:	n/a	n/a
16	CTCF	chr5:116176178-116176248	GM20000	blood:	n/a	n/a
17	CTCF	chr5:116180906-116181000	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr5:116146286-116146319	HepG2	liver:	n/a	n/a
19	CTCF	chr5:116149180-116149330	HepG2	liver:	n/a	n/a
20	CTCF	chr5:116180760-116180910	GM12872	blood:	n/a	n/a
21	E2F4	chr5:116155803-116155935	MCF10A-Er-Src	breast:	n/a	n/a
22	ELK1	chr5:116172659-116172660	GM12878	blood:	n/a	n/a
23	EP300	chr5:116184676-116185290	HepG2	liver:	n/a	chr5:116184892-116184906
24	EP300	chr5:116173816-116174200	SK-N-SH_RA	brain:	n/a	n/a
25	EP300	chr5:116184919-116185199	HepG2	liver:	n/a	n/a
26	EP300	chr5:116173776-116174328	SK-N-SH_RA	brain:	n/a	n/a
27	EP300	chr5:116184790-116185217	GM12878	blood:	n/a	chr5:116184892-116184906
28	EP300	chr5:116179839-116179937	GM12878	blood:	n/a	n/a
29	EP300	chr5:116179786-116180039	GM12878	blood:	n/a	n/a
30	FAM48A	chr5:116173745-116173865	GM12878	blood:	n/a	n/a
31	FOS	chr5:116185116-116185119	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr5:116161480-116161647	MCF10A-Er-Src	breast:	n/a	n/a
33	FOXA1	chr5:116173612-116174015	HepG2	liver:	n/a	chr5:116173782-116173797
34	FOXA1	chr5:116173616-116173884	HepG2	liver:	n/a	chr5:116173782-116173797
35	FOXA1	chr5:116184793-116185248	HepG2	liver:	n/a	n/a
36	FOXA1	chr5:116173628-116173902	HepG2	liver:	n/a	chr5:116173782-116173797
37	FOXA1	chr5:116140260-116140585	HepG2	liver:	n/a	n/a
38	FOXA1	chr5:116173676-116173916	HepG2	liver:	n/a	chr5:116173782-116173797
39	FOXA2	chr5:116156891-116157137	A549	lung:	n/a	n/a
40	FOXA2	chr5:116173612-116173926	HepG2	liver:	n/a	n/a
41	FOXA2	chr5:116184845-116185226	HepG2	liver:	n/a	n/a
42	FOXA2	chr5:116156846-116157313	A549	lung:	n/a	n/a
43	GATA2	chr5:116162580-116163038	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr5:116174031-116174294	SH-SY5Y	brain:	n/a	n/a
45	GTF2F1	chr5:116152064-116152127	H1-hESC	embryonic stem cell:	n/a	n/a
46	GTF2F1	chr5:116158401-116158441	H1-hESC	embryonic stem cell:	n/a	n/a
47	HDAC2	chr5:116151857-116152325	H1-hESC	embryonic stem cell:	n/a	chr5:116152251-116152265
48	HNF4A	chr5:116184863-116185229	HepG2	liver:	n/a	n/a
49	HNF4G	chr5:116184832-116185178	HepG2	liver:	n/a	n/a
50	JUN	chr5:116142655-116142870	HepG2	liver:	n/a	chr5:116142782-116142791 chr5:116142778-116142791

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:116150282-116150332	GM12891	blood:	n/a
2	chr5:116150282-116150332	AoSMC	blood vessel:	n/a
3	chr5:116150282-116150332	MCF-7	breast:	n/a
4	chr5:116150282-116150332	SKMC	muscle:	n/a
5	chr5:116150282-116150332	NB4	blood:	n/a
6	chr5:116150282-116150332	PANC-1	pancreas:	n/a
7	chr5:116150282-116150332	Hela-S3	cervix:	n/a
8	chr5:116150282-116150332	IMR90	lung:	fetal
9	chr5:116150282-116150332	Hepatocyte	liver:	n/a
10	chr5:116150282-116150332	K562	blood:	n/a
11	chr5:116150282-116150332	HPAEpiC	pulmonary alveolar:	n/a
12	chr5:116150282-116150332	PFSK-1	brain:	n/a
13	chr5:116150282-116150332	AG09319	gingival:	n/a
14	chr5:116150282-116150332	ECC-1	luminal epithelium:	n/a
15	chr5:116150282-116150332	GM06990	blood:	n/a
16	chr5:116150282-116150332	SK-N-SH	brain:	n/a
17	chr5:116150282-116150332	HRE	kidney:	n/a
18	chr5:116150282-116150332	BE2_C	brain:	n/a
19	chr5:116150282-116150332	T-47D	breast:	n/a
20	chr5:116150282-116150332	HUVEC	blood vessel:	n/a
21	chr5:116150282-116150332	HCPEpiC	choroid plexus:	n/a
22	chr5:116150282-116150332	ProgFib	skin:	n/a
23	chr5:116150282-116150332	HCF	heart:	n/a
24	chr5:116150282-116150332	AG09309	skin:	n/a
25	chr5:116150282-116150332	HepG2	liver:	n/a
26	chr5:116150282-116150332	BJ	skin:	n/a
27	chr5:116150282-116150332	AG04449	skin:	fetal
28	chr5:116150282-116150332	NHDF-neo	bronchial:	n/a
29	chr5:116150282-116150332	SK-N-MC	brain:	n/a
30	chr5:116150282-116150332	U87	brain:	n/a
31	chr5:116150282-116150332	Jurkat	blood:	n/a
32	chr5:116150282-116150332	HEEpiC	esophagus:	n/a
33	chr5:116150282-116150332	NH-A	brain:	n/a
34	chr5:116150282-116150332	HRPEpiC	eye:	n/a
35	chr5:116150282-116150332	H1-hESC	embryonic stem cell:	embryo
36	chr5:116150282-116150332	HRCEpiC	kidney:	n/a
37	chr5:116150282-116150332	HIPEpiC	eye:	n/a
38	chr5:116150282-116150332	NHBE	bronchial:	n/a
39	chr5:116150282-116150332	GM12878	blood:	n/a
40	chr5:116150282-116150332	PrEC	prostate:	n/a
41	chr5:116150282-116150332	HMEC	breast:	n/a
42	chr5:116150282-116150332	Caco-2	colon:	n/a
43	chr5:116150282-116150332	AG04450	lung:	fetal
44	chr5:116150282-116150332	ovcar-3	ovarian:	n/a
45	chr5:116150282-116150332	NT2-D1	testis:	n/a
46	chr5:116150282-116150332	SAEC	small airway:	n/a
47	chr5:116150282-116150332	HCM	heart:	n/a
48	chr5:116150282-116150332	GM12892	blood:	n/a
49	chr5:116150282-116150332	LNCaP	prostate:	n/a
50	chr5:116150282-116150332	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:116141325..116143664-chr5:116165603..116167947,2	K562	blood:
2	chr5:116159664..116161786-chr5:116162291..116165318,3	MCF-7	breast:
3	chr5:116159664..116161786-chr5:116162291..116165318,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COMMD10-10	chr5:116143614-116143900	NONHSAT103378
2	lnc-COMMD10-10	chr5:116145051-116147613	NONHSAT103378
3	lnc-COMMD10-10	chr5:116147785-116149816	NONHSAT103378

No data

Variant related genes	Relation type
ENSG00000249150	TF binding region
ENSG00000249150	CpG island
ENSG00000249150	chromatin interactions

Extended variants
information (count: 1747 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1747 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2964693	chr5:116138286-116138287	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574622861	chr5:116138320-116138321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535549095	chr5:116138333-116138334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550699266	chr5:116138337-116138338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2913600	chr5:116138341-116138342	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs576890586	chr5:116138357-116138358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373371259	chr5:116138370-116138371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs80281122	chr5:116138385-116138386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200766302	chr5:116138404-116138405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113639952	chr5:116138407-116138408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs111527056	chr5:116138441-116138442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2964692	chr5:116138525-116138526	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs548800928	chr5:116138555-116138556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562397795	chr5:116138592-116138593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141125095	chr5:116138596-116138597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375183121	chr5:116138602-116138603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150762496	chr5:116138608-116138609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2545407	chr5:116138609-116138610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550969003	chr5:116138616-116138617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116783655	chr5:116138628-116138629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113429887	chr5:116138650-116138651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs59059700	chr5:116138651-116138652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150381782	chr5:116138658-116138659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138068291	chr5:116138661-116138662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs397954863	chr5:116138671-116138672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539926071	chr5:116138677-116138678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531253930	chr5:116138714-116138715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546729637	chr5:116138724-116138725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10035548	chr5:116138725-116138726	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs184639857	chr5:116138743-116138744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369576078	chr5:116138748-116138749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs10035520	chr5:116138753-116138754	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs144924066	chr5:116138772-116138773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35842111	chr5:116138780-116138781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536917365	chr5:116138791-116138792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181496223	chr5:116138793-116138794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373979104	chr5:116138804-116138805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576720626	chr5:116138805-116138806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs111473727	chr5:116138840-116138841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573597911	chr5:116138855-116138856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545809565	chr5:116138873-116138874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7725600	chr5:116138896-116138897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370344153	chr5:116138897-116138898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532730361	chr5:116138906-116138907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373090155	chr5:116138934-116138935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114959968	chr5:116138951-116138952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141779690	chr5:116138954-116138955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145437439	chr5:116138984-116138985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376094183	chr5:116139010-116139011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138817971	chr5:116139024-116139025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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	21215367	CNVD

Chromatin state (count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116131800-116142600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr5:116142200-116143000	Enhancers	Fetal Lung	lung
3	chr5:116142400-116143000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:116142400-116143000	Enhancers	HepG2	liver
5	chr5:116142600-116143000	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr5:116142600-116143000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr5:116142600-116143000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr5:116142600-116143000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr5:116142600-116143000	Enhancers	Fetal Muscle Leg	muscle
10	chr5:116142600-116143000	Enhancers	HSMMtube	muscle
11	chr5:116142600-116143200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr5:116143000-116143800	Weak transcription	Fetal Muscle Leg	muscle
13	chr5:116143000-116145600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr5:116143000-116146000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr5:116143000-116146000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr5:116143000-116146000	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr5:116143000-116146200	Weak transcription	HepG2	liver
18	chr5:116143200-116146200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr5:116143800-116144000	Enhancers	Fetal Muscle Leg	muscle
20	chr5:116145000-116148000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr5:116145400-116147200	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr5:116145600-116147400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr5:116145800-116147400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr5:116146000-116146200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:116146000-116146400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:116146000-116146800	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr5:116146000-116147000	Enhancers	H9 Cell Line	embryonic stem cell
28	chr5:116146000-116147200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr5:116146000-116147200	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr5:116146000-116147200	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr5:116146000-116147200	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr5:116146000-116147200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr5:116146000-116147600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr5:116146000-116147600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr5:116146200-116146800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr5:116146200-116147000	Enhancers	H1 Cell Line	embryonic stem cell
37	chr5:116146200-116147000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr5:116146200-116147000	Enhancers	HepG2	liver
39	chr5:116146200-116147200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr5:116146400-116147000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:116146400-116147000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr5:116146400-116148200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr5:116146400-116150400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr5:116146400-116156400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:116146800-116147800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr5:116146800-116150800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr5:116147000-116150200	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr5:116147000-116150200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr5:116147000-116150200	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr5:116147000-116150200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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