Variant report

Variant	nsv537084
Chromosome Location	chr4:47977844-48022511
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:744)
CpG islands
(count:915)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:744 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:48018132-48018188	HepG2	liver:	n/a	n/a
2	ATF2	chr4:48018278-48019455	GM12878	blood:	n/a	chr4:48019284-48019295
3	BACH1	chr4:48018370-48019458	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr4:48005709-48005916	GM12878	blood:	n/a	n/a
5	BCLAF1	chr4:48018183-48019163	GM12878	blood:	n/a	chr4:48018766-48018779 chr4:48018770-48018783
6	BHLHE40	chr4:48018511-48018517	K562	blood:	n/a	n/a
7	BHLHE40	chr4:48018901-48018997	K562	blood:	n/a	n/a
8	BRCA1	chr4:48019219-48019391	H1-hESC	embryonic stem cell:	n/a	n/a
9	CBX3	chr4:48018255-48018700	K562	blood:	n/a	n/a
10	CBX3	chr4:48007812-48008107	K562	blood:	n/a	n/a
11	CBX3	chr4:47992221-47992485	K562	blood:	n/a	n/a
12	CBX3	chr4:47992214-47992563	K562	blood:	n/a	n/a
13	CBX3	chr4:48007825-48008006	K562	blood:	n/a	n/a
14	CCNT2	chr4:48019235-48019428	K562	blood:	n/a	n/a
15	CCNT2	chr4:48018566-48019028	K562	blood:	n/a	chr4:48018739-48018748
16	CEBPB	chr4:48018370-48018651	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr4:48018466-48018510	K562	blood:	n/a	n/a
18	CEBPB	chr4:48000862-48001172	HepG2	liver:	n/a	chr4:48001028-48001039
19	CEBPB	chr4:48019219-48019560	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:48018427-48018849	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:48018547-48018683	A549	lung:	n/a	n/a
22	CEBPB	chr4:48018434-48018807	Hela-S3	cervix:	n/a	n/a
23	CEBPD	chr4:48018376-48018957	HepG2	liver:	n/a	n/a
24	CEBPZ	chr4:48010185-48010320	HepG2	liver:	n/a	n/a
25	CHD2	chr4:48018557-48018567	K562	blood:	n/a	n/a
26	CHD2	chr4:48019228-48019446	K562	blood:	n/a	n/a
27	CHD2	chr4:48019212-48019544	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr4:48018499-48018974	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr4:48019260-48019493	HepG2	liver:	n/a	n/a
30	CHD2	chr4:48018283-48019513	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr4:48018411-48018918	HepG2	liver:	n/a	n/a
32	CREB1	chr4:48018508-48018775	A549	lung:	n/a	n/a
33	CREB1	chr4:48018849-48019510	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTBP2	chr4:48018238-48019635	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr4:48005600-48005750	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr4:48018290-48018614	GM19240	blood:	n/a	n/a
37	CTCF	chr4:48018340-48018490	AG09319	gingival:	n/a	n/a
38	CTCF	chr4:48018400-48018550	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr4:48005636-48005942	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr4:48005700-48005850	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr4:48018300-48018450	MCF-7	breast:	n/a	n/a
42	CTCF	chr4:48005680-48005830	BJ	skin:	n/a	n/a
43	CTCF	chr4:48005700-48005850	HMF	breast:	n/a	n/a
44	CTCF	chr4:48005700-48005850	GM12869	blood:	n/a	n/a
45	CTCF	chr4:48018360-48018510	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr4:48018380-48018530	GM12870	blood:	n/a	n/a
47	CTCF	chr4:48005468-48005958	K562	blood:	n/a	n/a
48	CTCF	chr4:48018300-48018450	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr4:48005570-48005933	K562	blood:	n/a	n/a
50	CTCF	chr4:48005631-48005871	HepG2	liver:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:48018263-48018313	GM12892	blood:	n/a
2	chr4:48018631-48018681	HIPEpiC	eye:	n/a
3	chr4:47982821-47982871	MCF10A-Er-Src	breast:	n/a
4	chr4:48018263-48018313	LNCaP	prostate:	n/a
5	chr4:48019347-48019397	AG10803	skin:	n/a
6	chr4:48015981-48016031	HPAEpiC	pulmonary alveolar:	n/a
7	chr4:48019347-48019397	HEK293	kidney:	embryo
8	chr4:48018755-48018805	GM06990	blood:	n/a
9	chr4:48018582-48018632	GM12892	blood:	n/a
10	chr4:48019555-48019605	HUVEC	blood vessel:	n/a
11	chr4:48019347-48019397	AoSMC	blood vessel:	n/a
12	chr4:48018755-48018805	AoSMC	blood vessel:	n/a
13	chr4:48018954-48019004	SK-N-MC	brain:	n/a
14	chr4:48018695-48018745	ECC-1	luminal epithelium:	n/a
15	chr4:48018695-48018745	NHDF-neo	bronchial:	n/a
16	chr4:48015490-48015540	NB4	blood:	n/a
17	chr4:48022241-48022291	HMEC	breast:	n/a
18	chr4:47982821-47982871	HCM	heart:	n/a
19	chr4:48018631-48018681	HepG2	liver:	n/a
20	chr4:48018582-48018632	SK-N-SH_RA	brain:	n/a
21	chr4:48018582-48018632	PrEC	prostate:	n/a
22	chr4:48019347-48019397	HCF	heart:	n/a
23	chr4:48018631-48018681	AG09309	skin:	n/a
24	chr4:48018631-48018681	SK-N-MC	brain:	n/a
25	chr4:48018695-48018745	BE2_C	brain:	n/a
26	chr4:47982821-47982871	HCPEpiC	choroid plexus:	n/a
27	chr4:48015490-48015540	SAEC	small airway:	n/a
28	chr4:48019347-48019397	NHBE	bronchial:	n/a
29	chr4:48015490-48015540	LNCaP	prostate:	n/a
30	chr4:48018755-48018805	ovcar-3	ovarian:	n/a
31	chr4:48019347-48019397	LNCaP	prostate:	n/a
32	chr4:48022241-48022291	IMR90	lung:	fetal
33	chr4:48019555-48019605	HCM	heart:	n/a
34	chr4:48018631-48018681	GM12891	blood:	n/a
35	chr4:48015981-48016031	AG09309	skin:	n/a
36	chr4:48015981-48016031	H1-hESC	embryonic stem cell:	embryo
37	chr4:48015490-48015540	HepG2	liver:	n/a
38	chr4:48019555-48019605	GM12892	blood:	n/a
39	chr4:48018263-48018313	HCM	heart:	n/a
40	chr4:48019347-48019397	Caco-2	colon:	n/a
41	chr4:48018954-48019004	AG09309	skin:	n/a
42	chr4:48022241-48022291	K562	blood:	n/a
43	chr4:48022241-48022291	GM19239	blood:	n/a
44	chr4:48018263-48018313	T-47D	breast:	n/a
45	chr4:47982821-47982871	HRE	kidney:	n/a
46	chr4:48022241-48022291	AG09319	gingival:	n/a
47	chr4:48022241-48022291	AG09309	skin:	n/a
48	chr4:48018755-48018805	HCPEpiC	choroid plexus:	n/a
49	chr4:48015981-48016031	MCF10A-Er-Src	breast:	n/a
50	chr4:47984394-47984444	ovcar-3	ovarian:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:47915045..47916605-chr4:48017433..48018940,2	MCF-7	breast:
2	chr4:48018226..48018849-chr5:157285675..157286547,2	HCT-116	colon:
3	chr4:48019190..48021605-chr4:48023120..48025588,2	K562	blood:
4	chr4:48015687..48018286-chr4:48032689..48034980,2	K562	blood:
5	chr4:48018009..48020666-chr4:48022242..48023763,2	K562	blood:
6	chr4:48019513..48022096-chr4:48074921..48077158,2	MCF-7	breast:
7	chr4:48021540..48023440-chr4:48027193..48032829,5	MCF-7	breast:
8	chr4:48016518..48018197-chr4:48024501..48026849,2	K562	blood:
9	chr4:47914296..47917191-chr4:48017364..48021197,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NIPAL1-1	chr4:47991683-47992754	NONHSAT096275

No data

Variant related genes	Relation type
ENSG00000221764	TF binding region
NIPAL1	TF binding region
CNGA1	TF binding region
ENSG00000221764	CpG island
NIPAL1	CpG island
CNGA1	CpG island
ENSG00000163293	chromatin interactions
ENSG00000198515	chromatin interactions
ENSG00000170448	chromatin interactions
ENSG00000113282	chromatin interactions

Extended variants
information (count: 1060 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1060 , 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	rs573678844	chr4:47983649-47983650	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs527431345	chr4:47983660-47983661	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs374415412	chr4:47983664-47983665	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs538519475	chr4:47983875-47983876	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs556932709	chr4:47983896-47983897	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs114172621	chr4:47983964-47983965	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs6838837	chr4:47983976-47983977	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs11939754	chr4:47983989-47983990	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs190905187	chr4:47984415-47984416	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs1507922	chr4:47984429-47984430	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs528904513	chr4:47984434-47984435	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs543217822	chr4:47984738-47984739	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs375996263	chr4:47984743-47984744	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs530554534	chr4:47986477-47986478	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs546810354	chr4:47988078-47988079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571409557	chr4:47988094-47988095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538883511	chr4:47988123-47988124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557244924	chr4:47988187-47988188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575618515	chr4:47988199-47988200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573042253	chr4:47988343-47988344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536221718	chr4:47988372-47988373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116557666	chr4:47991701-47991702	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs574808138	chr4:47991716-47991717	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs373908596	chr4:47991739-47991740	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs367840566	chr4:47991758-47991759	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs541946477	chr4:47991763-47991764	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs554853557	chr4:47991779-47991780	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs571860947	chr4:47991795-47991796	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs115268343	chr4:47991802-47991803	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs115991820	chr4:47991803-47991804	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs191370277	chr4:47991810-47991811	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs543340150	chr4:47991843-47991844	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs561512728	chr4:47991846-47991847	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs528924240	chr4:47991864-47991865	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs3113882	chr4:47991882-47991883	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs543717432	chr4:47991885-47991886	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs548451795	chr4:47991886-47991887	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs374120154	chr4:47991890-47991891	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs565771928	chr4:47991916-47991917	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs368707785	chr4:47991935-47991936	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs200907791	chr4:47991983-47991984	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs527848840	chr4:47991998-47991999	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs139640195	chr4:47992001-47992002	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs552821727	chr4:47992020-47992021	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs182417378	chr4:47992060-47992061	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs375530746	chr4:47992069-47992070	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs538519546	chr4:47992122-47992123	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs34145430	chr4:47992182-47992183	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs2581496	chr4:47992183-47992184	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs114441544	chr4:47992211-47992212	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Olfactory neuroblastoma	18408657	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	16616336	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Renal cell carcinoma	18765545	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47988000-47988400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:47995200-47997000	Enhancers	Primary T cells from cord blood	blood
3	chr4:47996200-47998400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:47998000-47998400	ZNF genes & repeats	Liver	Liver
5	chr4:47998000-47998600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:47998000-48000200	ZNF genes & repeats	Fetal Intestine Large	intestine
7	chr4:47998400-48000000	Weak transcription	Liver	Liver
8	chr4:48000000-48001800	ZNF genes & repeats	Liver	Liver
9	chr4:48001400-48001800	ZNF genes & repeats	Fetal Intestine Large	intestine
10	chr4:48001800-48003800	Weak transcription	Liver	Liver
11	chr4:48003800-48005200	Enhancers	Liver	Liver
12	chr4:48005200-48011200	Weak transcription	Liver	Liver
13	chr4:48005400-48017400	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr4:48006200-48006400	ZNF genes & repeats	Fetal Intestine Small	intestine
15	chr4:48006400-48006800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
16	chr4:48006400-48007800	ZNF genes & repeats	Fetal Intestine Large	intestine
17	chr4:48006400-48013000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
18	chr4:48007400-48013200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
19	chr4:48007600-48013000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
20	chr4:48008000-48017600	Weak transcription	Psoas Muscle	Psoas
21	chr4:48008600-48013800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
22	chr4:48009000-48010400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr4:48009200-48012800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
24	chr4:48009400-48009800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:48009400-48010200	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
26	chr4:48010200-48017200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr4:48010200-48017600	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr4:48010400-48011000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr4:48010600-48012600	ZNF genes & repeats	Fetal Intestine Large	intestine
30	chr4:48010600-48014400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:48010800-48011200	Weak transcription	Esophagus	oesophagus
32	chr4:48011000-48017400	Weak transcription	Colonic Mucosa	Colon
33	chr4:48011000-48017600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:48011000-48017600	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr4:48011200-48011400	ZNF genes & repeats	Esophagus	oesophagus
36	chr4:48011200-48013000	ZNF genes & repeats	Fetal Intestine Small	intestine
37	chr4:48011200-48013200	Strong transcription	Liver	Liver
38	chr4:48011200-48017600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:48011400-48017600	Weak transcription	Esophagus	oesophagus
40	chr4:48011600-48011800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr4:48011600-48013000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
42	chr4:48011800-48017800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:48011800-48018200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr4:48012400-48012800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
45	chr4:48012600-48013000	Strong transcription	Fetal Intestine Large	intestine
46	chr4:48012800-48016600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr4:48012800-48017400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr4:48013000-48013400	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr4:48013000-48013400	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr4:48013000-48013600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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