Variant report

Variant	esv1820642
Chromosome Location	chr14:37738197-37846877
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:355)
CpG islands
(count:122)
Chromatin interactive
region (count:28)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:355 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:37739891-37740124	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:37747860-37748994	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:37798163-37799893	HepG2	liver:	n/a	n/a
4	CEBPB	chr14:37792920-37793213	IMR90	lung:	n/a	n/a
5	CEBPB	chr14:37793032-37793130	K562	blood:	n/a	n/a
6	CEBPB	chr14:37759000-37759350	HepG2	liver:	n/a	chr14:37759174-37759185
7	CEBPB	chr14:37762208-37762458	A549	lung:	n/a	n/a
8	CEBPB	chr14:37789298-37789551	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr14:37752037-37752257	HepG2	liver:	n/a	chr14:37752149-37752160
10	CEBPB	chr14:37798396-37799173	HepG2	liver:	n/a	chr14:37799007-37799020
11	CEBPB	chr14:37762282-37762392	K562	blood:	n/a	n/a
12	CEBPB	chr14:37837419-37837687	HepG2	liver:	n/a	chr14:37837498-37837511 chr14:37837569-37837580 chr14:37837568-37837581
13	CEBPB	chr14:37743895-37744121	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:37745230-37745497	HepG2	liver:	n/a	chr14:37745395-37745406
15	CEBPB	chr14:37759006-37759363	IMR90	lung:	n/a	chr14:37759174-37759185
16	CEBPB	chr14:37748824-37749024	HepG2	liver:	n/a	chr14:37748930-37748941
17	CEBPB	chr14:37792980-37793071	A549	lung:	n/a	n/a
18	CEBPB	chr14:37759009-37759340	A549	lung:	n/a	chr14:37759174-37759185
19	CEBPB	chr14:37837475-37837651	A549	lung:	n/a	chr14:37837498-37837511 chr14:37837569-37837580 chr14:37837568-37837581
20	CEBPB	chr14:37792902-37793196	HepG2	liver:	n/a	n/a
21	CEBPB	chr14:37745286-37745472	A549	lung:	n/a	chr14:37745395-37745406
22	CEBPB	chr14:37762134-37762483	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:37798555-37799221	A549	lung:	n/a	chr14:37799007-37799020
24	CEBPB	chr14:37745361-37745435	K562	blood:	n/a	chr14:37745395-37745406
25	CTCF	chr14:37809780-37809930	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr14:37753300-37753450	HMF	breast:	n/a	n/a
27	CTCF	chr14:37809537-37809947	MCF-7	breast:	n/a	n/a
28	CTCF	chr14:37806631-37806677	Fibrobl	skin:	n/a	n/a
29	CTCF	chr14:37809753-37809875	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr14:37783420-37783570	HepG2	liver:	n/a	n/a
31	CTCF	chr14:37809674-37809928	MCF-7	breast:	n/a	n/a
32	CTCF	chr14:37809740-37809890	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr14:37751549-37751592	MCF-7	breast:	n/a	n/a
34	CTCF	chr14:37809720-37809870	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr14:37809661-37809920	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr14:37832920-37833070	HepG2	liver:	n/a	n/a
37	CTCF	chr14:37809720-37809870	HepG2	liver:	n/a	n/a
38	CTCF	chr14:37809760-37809910	HCT-116	colon:	n/a	n/a
39	CTCF	chr14:37809760-37809910	HMF	breast:	n/a	n/a
40	CTCF	chr14:37809800-37809950	A549	lung:	n/a	n/a
41	CTCF	chr14:37809720-37809870	SAEC	small airway:	n/a	n/a
42	CTCF	chr14:37809760-37809910	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr14:37809708-37809903	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr14:37809820-37809970	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr14:37809780-37809930	WI-38	lung:	n/a	n/a
46	CTCF	chr14:37809760-37809910	HEK293	kidney:	n/a	n/a
47	CTCF	chr14:37809760-37809910	GM12872	blood:	n/a	n/a
48	CTCF	chr14:37809760-37809910	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr14:37758557-37758591	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr14:37809780-37809930	HEEpiC	esophagus:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:37773865-37773915	Jurkat	blood:	n/a
2	chr14:37773865-37773915	GM12891	blood:	n/a
3	chr14:37825967-37826017	T-47D	breast:	n/a
4	chr14:37825967-37826017	U87	brain:	n/a
5	chr14:37773865-37773915	SK-N-SH_RA	brain:	n/a
6	chr14:37825967-37826017	H1-hESC	embryonic stem cell:	embryo
7	chr14:37825967-37826017	HAEpiC	amniotic membrane:	n/a
8	chr14:37773865-37773915	BJ	skin:	n/a
9	chr14:37773865-37773915	IMR90	lung:	fetal
10	chr14:37825967-37826017	MCF-7	breast:	n/a
11	chr14:37825967-37826017	BE2_C	brain:	n/a
12	chr14:37773865-37773915	NB4	blood:	n/a
13	chr14:37773865-37773915	HNPCEpiC	eye:	n/a
14	chr14:37773865-37773915	U87	brain:	n/a
15	chr14:37825967-37826017	BJ	skin:	n/a
16	chr14:37825967-37826017	SKMC	muscle:	n/a
17	chr14:37773865-37773915	T-47D	breast:	n/a
18	chr14:37825967-37826017	HRPEpiC	eye:	n/a
19	chr14:37825967-37826017	MCF10A-Er-Src	breast:	n/a
20	chr14:37825967-37826017	AG10803	skin:	n/a
21	chr14:37825967-37826017	AG09319	gingival:	n/a
22	chr14:37773865-37773915	AG10803	skin:	n/a
23	chr14:37773865-37773915	SK-N-SH	brain:	n/a
24	chr14:37773865-37773915	PFSK-1	brain:	n/a
25	chr14:37825967-37826017	Hepatocyte	liver:	n/a
26	chr14:37825967-37826017	HCF	heart:	n/a
27	chr14:37773865-37773915	ovcar-3	ovarian:	n/a
28	chr14:37825967-37826017	AG04449	skin:	fetal
29	chr14:37773865-37773915	H1-hESC	embryonic stem cell:	embryo
30	chr14:37773865-37773915	A549	lung:	n/a
31	chr14:37773865-37773915	AG04449	skin:	fetal
32	chr14:37825967-37826017	HCPEpiC	choroid plexus:	n/a
33	chr14:37825967-37826017	GM12892	blood:	n/a
34	chr14:37825967-37826017	NHBE	bronchial:	n/a
35	chr14:37825967-37826017	GM12878	blood:	n/a
36	chr14:37773865-37773915	HepG2	liver:	n/a
37	chr14:37825967-37826017	PrEC	prostate:	n/a
38	chr14:37825967-37826017	IMR90	lung:	fetal
39	chr14:37773865-37773915	HPAEpiC	pulmonary alveolar:	n/a
40	chr14:37773865-37773915	LNCaP	prostate:	n/a
41	chr14:37825967-37826017	A549	lung:	n/a
42	chr14:37825967-37826017	HepG2	liver:	n/a
43	chr14:37773865-37773915	ECC-1	luminal epithelium:	n/a
44	chr14:37773865-37773915	NHDF-neo	bronchial:	n/a
45	chr14:37773865-37773915	HL-60	blood:	n/a
46	chr14:37825967-37826017	K562	blood:	n/a
47	chr14:37825967-37826017	SAEC	small airway:	n/a
48	chr14:37825967-37826017	AoSMC	blood vessel:	n/a
49	chr14:37773865-37773915	AG04450	lung:	fetal
50	chr14:37825967-37826017	HCM	heart:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:37743207..37745238-chr14:37747689..37750127,2	MCF-7	breast:
2	chr14:37797120..37799536-chr14:37801001..37803434,2	MCF-7	breast:
3	chr14:37776717..37778378-chr14:37785144..37786956,2	MCF-7	breast:
4	chr14:37811526..37813219-chr14:38057927..38059734,2	MCF-7	breast:
5	chr14:37793105..37794977-chr14:37796804..37798845,2	MCF-7	breast:
6	chr14:37743207..37745238-chr14:37747689..37750127,2	MCF-7	breast:
7	chr14:37773087..37774613-chr14:38035112..38036997,2	MCF-7	breast:
8	chr14:37744550..37746871-chr14:38059550..38062065,2	MCF-7	breast:
9	chr14:37789885..37792148-chr14:37882206..37884543,2	MCF-7	breast:
10	chr11:116508203..116508771-chr14:37786310..37786828,2	MCF-7	breast:
11	chr14:37738574..37741001-chr14:37743646..37745651,2	MCF-7	breast:
12	chr14:37814771..37816556-chr14:38063329..38065680,2	MCF-7	breast:
13	chr14:37749616..37751782-chr14:38055400..38058293,2	MCF-7	breast:
14	chr14:37845196..37847206-chr14:37851691..37853679,2	K562	blood:
15	chr14:37747627..37749985-chr14:38051291..38052830,2	MCF-7	breast:
16	chr14:37840146..37842839-chr14:37843811..37846339,2	K562	blood:
17	chr14:37840146..37842839-chr14:37843811..37846339,2	K562	blood:
18	chr14:37781292..37783643-chr14:37787358..37789012,2	MCF-7	breast:
19	chr14:37781292..37783643-chr14:37787358..37789012,2	MCF-7	breast:
20	chr14:37734748..37736405-chr14:37736490..37738328,2	MCF-7	breast:
21	chr14:37793105..37794977-chr14:37796804..37798845,2	MCF-7	breast:
22	chr14:37729939..37731852-chr14:37742042..37744319,2	K562	blood:
23	chr14:37738574..37741001-chr14:37743646..37745651,2	MCF-7	breast:
24	chr14:37802283..37804083-chr14:38062449..38064880,2	MCF-7	breast:
25	chr14:37723949..37726058-chr14:37737860..37739770,2	MCF-7	breast:
26	chr14:37735920..37738317-chr14:37741909..37743974,2	MCF-7	breast:
27	chr14:37730985..37733871-chr14:37737549..37739404,2	MCF-7	breast:
28	chr14:37797120..37799536-chr14:37801001..37803434,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-537P22.1.1-1	chr14:37737668-37742505	l_969_chr14:37729807-37741737_76bGuttman_hES

No data

Variant related genes	Relation type
MIPOL1	TF binding region
MIPOL1	CpG island
ENSG00000129514	chromatin interactions
ENSG00000259087	chromatin interactions
ENSG00000151338	chromatin interactions
ENSG00000139865	chromatin interactions

Extended variants
information (count: 3973 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:3973 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10145536	chr14:37738197-37738198	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs138707837	chr14:37738217-37738218	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs114041257	chr14:37738234-37738235	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs572709718	chr14:37738261-37738262	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs541626681	chr14:37738280-37738281	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs561423401	chr14:37738315-37738316	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs530224376	chr14:37738326-37738327	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs1956517	chr14:37738427-37738428	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs563726296	chr14:37738481-37738482	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs186307616	chr14:37738484-37738485	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs60287404	chr14:37738517-37738518	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs571198559	chr14:37738521-37738522	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs533783355	chr14:37738586-37738587	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs547191885	chr14:37738604-37738605	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs567308856	chr14:37738634-37738635	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs536361889	chr14:37738640-37738641	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs555955646	chr14:37738658-37738659	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs569659441	chr14:37738662-37738663	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs17106530	chr14:37738694-37738695	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs559330910	chr14:37738735-37738736	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs572782780	chr14:37738736-37738737	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs112851412	chr14:37738770-37738771	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs149438360	chr14:37738929-37738930	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs1956518	chr14:37739061-37739062	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs543924681	chr14:37739064-37739065	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs573486957	chr14:37739094-37739095	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs563615262	chr14:37739095-37739096	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs375438887	chr14:37739096-37739097	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs532413217	chr14:37739105-37739106	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs1956519	chr14:37739118-37739119	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs559275458	chr14:37739119-37739120	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs369931348	chr14:37739181-37739182	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs527588565	chr14:37739222-37739223	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs60243444	chr14:37739255-37739256	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs183329210	chr14:37739262-37739263	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs187107652	chr14:37739290-37739291	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs190891705	chr14:37739297-37739298	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs569640092	chr14:37739314-37739315	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs146107480	chr14:37739435-37739436	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs113395275	chr14:37739479-37739480	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs139247255	chr14:37739510-37739511	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs576965382	chr14:37739535-37739536	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs565646882	chr14:37739566-37739567	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs535364046	chr14:37739585-37739586	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs544328009	chr14:37739586-37739587	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs183466649	chr14:37739588-37739589	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs200064903	chr14:37739606-37739607	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs377432855	chr14:37739613-37739614	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs543645223	chr14:37739634-37739635	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs368719428	chr14:37739636-37739637	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Osteosarcoma	21215367	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD

Chromatin state (count:362 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37694800-37756400	Weak transcription	Aorta	Aorta
2	chr14:37716000-37770600	Weak transcription	A549	lung
3	chr14:37717800-37738600	Weak transcription	Fetal Intestine Small	intestine
4	chr14:37726800-37740000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr14:37727000-37740400	Weak transcription	HSMMtube	muscle
6	chr14:37732000-37739600	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr14:37732200-37739800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr14:37733600-37758200	Weak transcription	Fetal Lung	lung
9	chr14:37735000-37742600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr14:37735600-37738600	Weak transcription	Brain Hippocampus Middle	brain
11	chr14:37736400-37744200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr14:37736800-37758400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr14:37737200-37744400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr14:37737400-37738200	Strong transcription	HUVEC	blood vessel
15	chr14:37737800-37738200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr14:37738000-37755000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr14:37738000-37756400	Weak transcription	Ovary	ovary
18	chr14:37738200-37739800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr14:37738200-37739800	Weak transcription	HUVEC	blood vessel
20	chr14:37738400-37757600	Weak transcription	Adipose Nuclei	Adipose
21	chr14:37739600-37739800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr14:37739600-37740600	Enhancers	HepG2	liver
23	chr14:37739800-37740200	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr14:37739800-37740200	Enhancers	HUVEC	blood vessel
25	chr14:37739800-37740400	Genic enhancers	HUES48 Cell Line	embryonic stem cell
26	chr14:37739800-37740600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr14:37740000-37740200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr14:37740000-37762000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr14:37740200-37757800	Weak transcription	HUVEC	blood vessel
30	chr14:37740400-37760200	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr14:37740600-37743600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr14:37743200-37745800	Weak transcription	Psoas Muscle	Psoas
33	chr14:37743600-37744000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr14:37744400-37745400	Enhancers	Liver	Liver
35	chr14:37744400-37745600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr14:37745400-37747400	Weak transcription	Liver	Liver
37	chr14:37747400-37748200	Enhancers	Liver	Liver
38	chr14:37747800-37749200	Enhancers	HepG2	liver
39	chr14:37748200-37749200	Flanking Active TSS	Liver	Liver
40	chr14:37748600-37758400	Weak transcription	Psoas Muscle	Psoas
41	chr14:37748800-37758600	Weak transcription	Fetal Stomach	stomach
42	chr14:37749200-37749400	Enhancers	Liver	Liver
43	chr14:37749200-37749600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr14:37749200-37761000	Weak transcription	Pancreas	Pancrea
45	chr14:37749200-37761800	Weak transcription	HepG2	liver
46	chr14:37749600-37761200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr14:37749800-37758600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr14:37750200-37758200	Weak transcription	Stomach Smooth Muscle	stomach
49	chr14:37750600-37761400	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr14:37750600-37761800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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