Variant report

Variant	nsv1049203
Chromosome Location	chr14:44842257-44927982
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:263)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr14:44918300-44918537	K562	blood:	n/a	n/a
2	BACH1	chr14:44862483-44862496	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr14:44918875-44919187	HepG2	liver:	n/a	n/a
4	BHLHE40	chr14:44918215-44918640	K562	blood:	n/a	n/a
5	BHLHE40	chr14:44918841-44919166	HepG2	liver:	n/a	n/a
6	BRCA1	chr14:44887139-44887316	Hela-S3	cervix:	n/a	n/a
7	CCNT2	chr14:44870973-44871349	K562	blood:	n/a	n/a
8	CCNT2	chr14:44918261-44918573	K562	blood:	n/a	n/a
9	CEBPB	chr14:44865484-44865848	HepG2	liver:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
10	CEBPB	chr14:44860656-44860866	HepG2	liver:	n/a	chr14:44860752-44860763
11	CEBPB	chr14:44862132-44862411	HepG2	liver:	n/a	chr14:44862299-44862316 chr14:44862302-44862315
12	CEBPB	chr14:44865514-44865808	IMR90	lung:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
13	CEBPB	chr14:44865449-44865776	MCF-7	breast:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
14	CEBPB	chr14:44845840-44846035	A549	lung:	n/a	n/a
15	CEBPB	chr14:44865476-44865832	A549	lung:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
16	CEBPB	chr14:44865547-44865773	H1-hESC	embryonic stem cell:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
17	CEBPB	chr14:44859620-44859752	H1-hESC	embryonic stem cell:	n/a	chr14:44859701-44859712
18	CEBPB	chr14:44892241-44892441	IMR90	lung:	n/a	chr14:44892371-44892382
19	CEBPB	chr14:44865546-44865783	Hela-S3	cervix:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
20	CEBPB	chr14:44865478-44865918	MCF-7	breast:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
21	CEBPB	chr14:44859595-44859755	HepG2	liver:	n/a	chr14:44859701-44859712
22	CEBPB	chr14:44892321-44892509	HepG2	liver:	n/a	chr14:44892371-44892382
23	CEBPD	chr14:44918203-44918635	K562	blood:	n/a	n/a
24	CEBPD	chr14:44918285-44918591	K562	blood:	n/a	n/a
25	CTCF	chr14:44922811-44922942	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr14:44926160-44926203	GM10266	blood:	n/a	n/a
27	CTCF	chr14:44884447-44884520	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr14:44922602-44923043	T-47D	breast:	n/a	n/a
29	CTCF	chr14:44857548-44857591	GM13977	blood:	n/a	n/a
30	CTCF	chr14:44922768-44922939	MCF-7	breast:	n/a	n/a
31	CTCF	chr14:44882613-44882697	Lung_OC	lung:	n/a	n/a
32	CTCF	chr14:44890993-44890999	GM13976	blood:	n/a	n/a
33	CTCF	chr14:44890953-44890989	GM13976	blood:	n/a	n/a
34	CTCF	chr14:44922804-44922869	NHEK	skin:	n/a	n/a
35	CTCF	chr14:44922681-44922975	T-47D	breast:	n/a	n/a
36	CTCF	chr14:44922568-44923005	MCF-7	breast:	n/a	n/a
37	CTCF	chr14:44894642-44894669	GM13976	blood:	n/a	n/a
38	CTCF	chr14:44922798-44922912	Gliobla	brain:	n/a	n/a
39	CTCF	chr14:44922769-44922938	LNCaP	prostate:	n/a	n/a
40	CTCF	chr14:44846025-44846080	GM13976	blood:	n/a	n/a
41	CTCF	chr14:44922840-44922990	NHEK	skin:	n/a	n/a
42	CTCF	chr14:44922829-44922893	K562	blood:	n/a	n/a
43	CTCF	chr14:44922737-44922969	MCF-7	breast:	n/a	n/a
44	CTCF	chr14:44922780-44922930	NHEK	skin:	n/a	n/a
45	CTCF	chr14:44922760-44922910	MCF-7	breast:	n/a	n/a
46	CTCF	chr14:44867820-44867970	HepG2	liver:	n/a	n/a
47	CTCF	chr14:44922763-44922910	LNCaP	prostate:	n/a	n/a
48	CTCF	chr14:44922545-44923128	MCF-7	breast:	n/a	n/a
49	CTCF	chr14:44922746-44922968	GM12878	blood:	n/a	n/a
50	CTCF	chr14:44922840-44922990	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:44853952-44854002	Hela-S3	cervix:	n/a
2	chr14:44853952-44854002	NHBE	bronchial:	n/a
3	chr14:44853952-44854002	RPTEC	kidney:	n/a
4	chr14:44853952-44854002	AoSMC	blood vessel:	n/a
5	chr14:44853952-44854002	HL-60	blood:	n/a
6	chr14:44853952-44854002	AG04449	skin:	fetal
7	chr14:44853952-44854002	MCF-7	breast:	n/a
8	chr14:44853952-44854002	HIPEpiC	eye:	n/a
9	chr14:44853952-44854002	T-47D	breast:	n/a
10	chr14:44853952-44854002	BE2_C	brain:	n/a
11	chr14:44853952-44854002	HEK293	kidney:	embryo
12	chr14:44853952-44854002	Hepatocyte	liver:	n/a
13	chr14:44853952-44854002	ProgFib	skin:	n/a
14	chr14:44853952-44854002	HCF	heart:	n/a
15	chr14:44853952-44854002	SK-N-SH_RA	brain:	n/a
16	chr14:44853952-44854002	HCPEpiC	choroid plexus:	n/a
17	chr14:44853952-44854002	AG04450	lung:	fetal
18	chr14:44853952-44854002	SK-N-SH	brain:	n/a
19	chr14:44853952-44854002	SK-N-MC	brain:	n/a
20	chr14:44853952-44854002	ovcar-3	ovarian:	n/a
21	chr14:44853952-44854002	GM12892	blood:	n/a
22	chr14:44853952-44854002	SAEC	small airway:	n/a
23	chr14:44853952-44854002	HMEC	breast:	n/a
24	chr14:44853952-44854002	LNCaP	prostate:	n/a
25	chr14:44853952-44854002	BJ	skin:	n/a
26	chr14:44853952-44854002	H1-hESC	embryonic stem cell:	embryo
27	chr14:44853952-44854002	AG09319	gingival:	n/a
28	chr14:44853952-44854002	NH-A	brain:	n/a
29	chr14:44853952-44854002	HRCEpiC	kidney:	n/a
30	chr14:44853952-44854002	HAEpiC	amniotic membrane:	n/a
31	chr14:44853952-44854002	GM12878	blood:	n/a
32	chr14:44853952-44854002	IMR90	lung:	fetal
33	chr14:44853952-44854002	CMK	blood:	n/a
34	chr14:44853952-44854002	HUVEC	blood vessel:	n/a
35	chr14:44853952-44854002	HNPCEpiC	eye:	n/a
36	chr14:44853952-44854002	HEEpiC	esophagus:	n/a
37	chr14:44853952-44854002	MCF10A-Er-Src	breast:	n/a
38	chr14:44853952-44854002	PANC-1	pancreas:	n/a
39	chr14:44853952-44854002	PFSK-1	brain:	n/a
40	chr14:44853952-44854002	AG10803	skin:	n/a
41	chr14:44853952-44854002	HepG2	liver:	n/a
42	chr14:44853952-44854002	A549	lung:	n/a
43	chr14:44853952-44854002	Jurkat	blood:	n/a
44	chr14:44853952-44854002	HRE	kidney:	n/a
45	chr14:44853952-44854002	Caco-2	colon:	n/a
46	chr14:44853952-44854002	HPAEpiC	pulmonary alveolar:	n/a
47	chr14:44853952-44854002	SKMC	muscle:	n/a
48	chr14:44853952-44854002	GM06990	blood:	n/a
49	chr14:44853952-44854002	NT2-D1	testis:	n/a
50	chr14:44853952-44854002	GM19239	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:44838166..44839882-chr14:44873785..44875324,2	MCF-7	breast:
2	chr14:44856514..44860245-chr14:44862169..44864602,3	K562	blood:
3	chr14:44857399..44860693-chr14:44862169..44864634,3	K562	blood:
4	chr14:44922572..44923387-chr14:45126451..45127121,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSCB-1	chr14:44862812-44862914	ENSG00000259126
2	lnc-FSCB-1	chr14:44913950-44914025	ENSG00000258487
3	lnc-FSCB-1	chr14:44861734-44861893	ENSG00000259126
4	lnc-FSCB-1	chr14:44913910-44914002	XLOC_011006
5	lnc-FSCB-1	chr14:44862812-44862997	XLOC_011006
6	lnc-FSCB-1	chr14:44915851-44915996	ENSG00000258487
7	lnc-FSCB-1	chr14:44913926-44914025	NONHSAT036608
8	lnc-FSCB-1	chr14:44862821-44862919	ENSG00000259126
9	lnc-FSCB-1	chr14:44862209-44862941	XLOC_011006
10	lnc-FSCB-2	chr14:44853680-44853748	ENSG00000258969
11	lnc-FSCB-1	chr14:44861702-44861893	XLOC_011006
12	lnc-FSCB-1	chr14:44861745-44861893	ENSG00000259126

No data

Variant related genes	Relation type
ENSG00000258969	TF binding region
ENSG00000259126	TF binding region
ENSG00000258969	CpG island
ENSG00000259126	CpG island
ENSG00000259126	chromatin interactions
FAM134B	miRNA target sites
B4GALT1	miRNA target sites

Extended variants
information (count: 1807 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1807 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147141072	chr14:44842275-44842276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs374200739	chr14:44842344-44842345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574103295	chr14:44842345-44842346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541569264	chr14:44842425-44842426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185365299	chr14:44842477-44842478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188115017	chr14:44842564-44842565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567626668	chr14:44842590-44842591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs79391890	chr14:44843418-44843419	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs398077727	chr14:44843423-44843424	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs545595913	chr14:44843453-44843454	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs78798745	chr14:44843454-44843455	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs531431059	chr14:44843461-44843462	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs531109540	chr14:44843468-44843469	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs34594917	chr14:44843492-44843493	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs561615246	chr14:44843498-44843499	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs528122321	chr14:44843500-44843501	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs148554036	chr14:44843517-44843518	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs571019138	chr14:44843567-44843568	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs371377157	chr14:44843573-44843574	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs571326734	chr14:44843590-44843591	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs144436296	chr14:44843662-44843663	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs146574226	chr14:44843722-44843723	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs536433516	chr14:44843730-44843731	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs554610749	chr14:44843750-44843751	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs573175189	chr14:44843783-44843784	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs374900016	chr14:44843791-44843792	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs553366869	chr14:44843812-44843813	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs578157828	chr14:44843831-44843832	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs545198506	chr14:44843913-44843914	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs557411276	chr14:44843920-44843921	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs114603795	chr14:44843983-44843984	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs575275563	chr14:44844007-44844008	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs544500194	chr14:44844022-44844023	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs372726788	chr14:44844028-44844029	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs543203050	chr14:44844039-44844040	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs141322152	chr14:44844157-44844158	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs536678034	chr14:44844162-44844163	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs528719452	chr14:44844175-44844176	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs539858215	chr14:44844205-44844206	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs564513208	chr14:44844232-44844233	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs531961155	chr14:44844278-44844279	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs74046312	chr14:44844298-44844299	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs533552800	chr14:44844336-44844337	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs568927263	chr14:44844354-44844355	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs529896763	chr14:44844356-44844357	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs548321081	chr14:44844402-44844403	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs566785366	chr14:44844452-44844453	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs534049323	chr14:44844469-44844470	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs558867477	chr14:44844500-44844501	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs571701255	chr14:44844511-44844512	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:44838400-44842600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr14:44840800-44842400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr14:44841200-44842400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr14:44841200-44842600	Enhancers	Fetal Intestine Large	intestine
5	chr14:44841800-44842400	Weak transcription	HMEC	breast
6	chr14:44842400-44842600	Enhancers	HMEC	breast
7	chr14:44843400-44850200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr14:44845200-44846600	ZNF genes & repeats	Fetal Intestine Small	intestine
9	chr14:44848000-44849200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr14:44848400-44849200	Enhancers	Adipose Nuclei	Adipose
11	chr14:44849200-44851000	Weak transcription	Adipose Nuclei	Adipose
12	chr14:44849200-44851600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr14:44850200-44851000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr14:44851000-44852800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr14:44851000-44853600	Enhancers	Adipose Nuclei	Adipose
16	chr14:44851600-44853600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr14:44852600-44852800	Enhancers	Ovary	ovary
18	chr14:44852800-44853600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr14:44853000-44853600	Enhancers	Fetal Stomach	stomach
20	chr14:44853400-44853600	Enhancers	Ovary	ovary
21	chr14:44853400-44853800	Enhancers	Fetal Brain Female	brain
22	chr14:44853800-44857400	Weak transcription	Fetal Brain Female	brain
23	chr14:44854200-44854400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr14:44857400-44857600	Enhancers	Fetal Brain Female	brain
25	chr14:44861800-44862400	Enhancers	Fetal Intestine Large	intestine
26	chr14:44862400-44862800	Active TSS	Rectal Mucosa Donor 29	rectum
27	chr14:44872000-44872600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr14:44872000-44874400	Enhancers	Fetal Brain Male	brain
29	chr14:44872400-44874600	Enhancers	Fetal Brain Female	brain
30	chr14:44872600-44874000	Enhancers	Fetal Heart	heart
31	chr14:44873200-44874600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr14:44873400-44874400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr14:44873600-44874600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr14:44873600-44874600	Enhancers	Adipose Nuclei	Adipose
35	chr14:44873600-44875200	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr14:44873800-44874200	Enhancers	Fetal Kidney	kidney
37	chr14:44874200-44874600	Enhancers	Fetal Lung	lung
38	chr14:44881200-44882400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr14:44881600-44882600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr14:44881600-44882600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr14:44882000-44882600	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr14:44882000-44882600	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr14:44882000-44882600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr14:44882000-44882600	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr14:44882000-44882600	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr14:44882000-44882800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr14:44882000-44883000	Enhancers	Fetal Heart	heart
48	chr14:44882000-44883000	Enhancers	Fetal Intestine Large	intestine
49	chr14:44882000-44883400	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr14:44882000-44883400	Enhancers	Fetal Intestine Small	intestine

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