Variant report

Variant	esv3368767
Chromosome Location	chr14:64268248-64321769
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:827)
CpG islands
(count:672)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:827 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:64276060-64276100	HepG2	liver:	n/a	n/a
2	BATF	chr14:64283407-64283685	GM12878	blood:	n/a	chr14:64283578-64283589
3	BATF	chr14:64319119-64319461	GM12878	blood:	n/a	n/a
4	BHLHE40	chr14:64320113-64320436	GM12878	blood:	n/a	chr14:64320182-64320198
5	BHLHE40	chr14:64320179-64320341	HepG2	liver:	n/a	chr14:64320182-64320198
6	BHLHE40	chr14:64320654-64320953	GM12878	blood:	n/a	n/a
7	BHLHE40	chr14:64278436-64278680	HepG2	liver:	n/a	n/a
8	BHLHE40	chr14:64299467-64299798	HepG2	liver:	n/a	n/a
9	BHLHE40	chr14:64320253-64320376	K562	blood:	n/a	n/a
10	BRCA1	chr14:64320590-64321133	Hela-S3	cervix:	n/a	chr14:64320623-64320630
11	BRCA1	chr14:64320968-64321079	GM12878	blood:	n/a	n/a
12	CBX3	chr14:64278719-64278999	K562	blood:	n/a	n/a
13	CCNT2	chr14:64320126-64320398	K562	blood:	n/a	n/a
14	CEBPB	chr14:64276036-64276292	HepG2	liver:	n/a	chr14:64276151-64276162
15	CEBPB	chr14:64305289-64305328	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr14:64305163-64305404	HepG2	liver:	n/a	chr14:64305288-64305299
17	CEBPB	chr14:64305231-64305546	A549	lung:	n/a	chr14:64305288-64305299
18	CEBPB	chr14:64305142-64305454	Hela-S3	cervix:	n/a	chr14:64305288-64305299
19	CEBPB	chr14:64272079-64272323	K562	blood:	n/a	chr14:64272160-64272171
20	CEBPB	chr14:64320622-64320926	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr14:64276736-64277026	A549	lung:	n/a	chr14:64276892-64276903
22	CEBPB	chr14:64268139-64268450	MCF-7	breast:	n/a	chr14:64268342-64268353
23	CEBPB	chr14:64272115-64272315	HepG2	liver:	n/a	chr14:64272160-64272171
24	CEBPB	chr14:64319571-64319813	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr14:64276736-64276998	Hela-S3	cervix:	n/a	chr14:64276892-64276903
26	CEBPB	chr14:64305164-64305374	IMR90	lung:	n/a	chr14:64305288-64305299
27	CEBPB	chr14:64272108-64272191	H1-hESC	embryonic stem cell:	n/a	chr14:64272160-64272171
28	CEBPB	chr14:64305176-64305428	A549	lung:	n/a	chr14:64305288-64305299
29	CEBPB	chr14:64305188-64305485	MCF-7	breast:	n/a	chr14:64305288-64305299
30	CEBPB	chr14:64268325-64268362	HepG2	liver:	n/a	chr14:64268342-64268353
31	CEBPB	chr14:64276720-64277041	HepG2	liver:	n/a	chr14:64276892-64276903
32	CEBPB	chr14:64276737-64277013	IMR90	lung:	n/a	chr14:64276892-64276903
33	CEBPB	chr14:64305013-64305540	A549	lung:	n/a	chr14:64305288-64305299
34	CEBPB	chr14:64320750-64320938	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr14:64320146-64320354	GM12878	blood:	n/a	n/a
36	CHD1	chr14:64320555-64321411	GM12878	blood:	n/a	n/a
37	CHD1	chr14:64319631-64319792	H1-hESC	embryonic stem cell:	n/a	chr14:64319776-64319783 chr14:64319670-64319680
38	CHD2	chr14:64320775-64320807	HepG2	liver:	n/a	n/a
39	CHD2	chr14:64320055-64320347	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr14:64320959-64320976	GM12878	blood:	n/a	n/a
41	CHD2	chr14:64319487-64319824	Hela-S3	cervix:	n/a	chr14:64319776-64319783 chr14:64319670-64319680
42	CHD2	chr14:64320641-64320850	Hela-S3	cervix:	n/a	n/a
43	CREB1	chr14:64319984-64320511	A549	lung:	n/a	n/a
44	CREB1	chr14:64320172-64320390	A549	lung:	n/a	n/a
45	CREB1	chr14:64319426-64319954	A549	lung:	n/a	n/a
46	CTBP2	chr14:64319088-64319839	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr14:64319572-64319633	GM20000	blood:	n/a	n/a
48	CTCF	chr14:64319540-64319690	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr14:64307840-64307990	HMEC	breast:	n/a	n/a
50	CTCF	chr14:64319560-64319710	GM12871	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:64320118-64320168	HRE	kidney:	n/a
2	chr14:64320118-64320168	HRE	kidney:	n/a
3	chr14:64319089-64319139	CMK	blood:	n/a
4	chr14:64320521-64320571	Hepatocyte	liver:	n/a
5	chr14:64320521-64320571	HEEpiC	esophagus:	n/a
6	chr14:64319089-64319139	K562	blood:	n/a
7	chr14:64319812-64319862	HCPEpiC	choroid plexus:	n/a
8	chr14:64319245-64319295	ovcar-3	ovarian:	n/a
9	chr14:64320118-64320168	Jurkat	blood:	n/a
10	chr14:64320049-64320099	HCPEpiC	choroid plexus:	n/a
11	chr14:64317161-64317211	GM12891	blood:	n/a
12	chr14:64319812-64319862	LNCaP	prostate:	n/a
13	chr14:64319245-64319295	HRPEpiC	eye:	n/a
14	chr14:64319245-64319295	GM06990	blood:	n/a
15	chr14:64317161-64317211	T-47D	breast:	n/a
16	chr14:64319812-64319862	SK-N-SH	brain:	n/a
17	chr14:64319245-64319295	HCF	heart:	n/a
18	chr14:64319543-64319593	SK-N-MC	brain:	n/a
19	chr14:64320521-64320571	SK-N-SH	brain:	n/a
20	chr14:64319543-64319593	AG09309	skin:	n/a
21	chr14:64270264-64270314	SK-N-SH	brain:	n/a
22	chr14:64320118-64320168	ProgFib	skin:	n/a
23	chr14:64317161-64317211	PrEC	prostate:	n/a
24	chr14:64319089-64319139	Jurkat	blood:	n/a
25	chr14:64319275-64319325	HepG2	liver:	n/a
26	chr14:64319306-64319356	HCF	heart:	n/a
27	chr14:64319245-64319295	HL-60	blood:	n/a
28	chr14:64270264-64270314	PFSK-1	brain:	n/a
29	chr14:64320049-64320099	CMK	blood:	n/a
30	chr14:64320118-64320168	PANC-1	pancreas:	n/a
31	chr14:64319275-64319325	K562	blood:	n/a
32	chr14:64319306-64319356	ECC-1	luminal epithelium:	n/a
33	chr14:64320118-64320168	GM12891	blood:	n/a
34	chr14:64319543-64319593	RPTEC	kidney:	n/a
35	chr14:64319089-64319139	AoSMC	blood vessel:	n/a
36	chr14:64319275-64319325	HL-60	blood:	n/a
37	chr14:64320118-64320168	NB4	blood:	n/a
38	chr14:64270264-64270314	GM06990	blood:	n/a
39	chr14:64317161-64317211	Hela-S3	cervix:	n/a
40	chr14:64319306-64319356	HCPEpiC	choroid plexus:	n/a
41	chr14:64317161-64317211	HRE	kidney:	n/a
42	chr14:64320049-64320099	HL-60	blood:	n/a
43	chr14:64270264-64270314	HCPEpiC	choroid plexus:	n/a
44	chr14:64270264-64270314	ovcar-3	ovarian:	n/a
45	chr14:64319089-64319139	NHDF-neo	bronchial:	n/a
46	chr14:64319306-64319356	HIPEpiC	eye:	n/a
47	chr14:64320521-64320571	MCF-7	breast:	n/a
48	chr14:64319089-64319139	HAEpiC	amniotic membrane:	n/a
49	chr14:64320118-64320168	PrEC	prostate:	n/a
50	chr14:64320118-64320168	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:64319166..64320923-chr14:64328806..64331982,4	MCF-7	breast:
2	chr14:64319297..64319918-chr6:86352603..86353316,2	Hela-S3	cervix:
3	chr12:13044235..13044810-chr14:64320099..64320720,2	Hela-S3	cervix:
4	chr14:64319483..64322302-chr14:64328481..64332813,5	MCF-7	breast:
5	chr14:64318775..64319715-chr6:26156466..26157229,2	Hela-S3	cervix:
6	chr14:64319794..64321904-chr14:64361235..64363695,2	MCF-7	breast:
7	chr14:64289002..64291923-chr14:64318330..64320835,2	MCF-7	breast:
8	chr14:64319297..64320096-chr2:74425675..74426285,2	Hela-S3	cervix:
9	chr14:64319797..64321605-chr14:64466270..64468504,2	MCF-7	breast:

No data

Variant related genes	Relation type
SYNE2	TF binding region
RPS28P1	TF binding region
ENSG00000202182	TF binding region
SYNE2	CpG island
RPS28P1	CpG island
ENSG00000202182	CpG island
ENSG00000135316	chromatin interactions
ENSG00000054654	chromatin interactions
ENSG00000013588	chromatin interactions
ENSG00000065911	chromatin interactions
ENSG00000168298	chromatin interactions

Extended variants
information (count: 1419 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1419 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149237848	chr14:64268265-64268266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs369314928	chr14:64268270-64268271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143434644	chr14:64268315-64268316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575957693	chr14:64268348-64268349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs180917175	chr14:64268353-64268354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186113455	chr14:64268359-64268360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536619151	chr14:64268418-64268419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7154239	chr14:64268468-64268469	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs369844617	chr14:64268482-64268483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570091567	chr14:64268526-64268527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564751313	chr14:64268543-64268544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373454884	chr14:64268584-64268585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192322621	chr14:64268672-64268673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12892514	chr14:64268685-64268686	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs540772286	chr14:64268778-64268779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112352566	chr14:64268893-64268894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112921923	chr14:64268898-64268899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs111299566	chr14:64268910-64268911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535368211	chr14:64268914-64268915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs8016616	chr14:64268918-64268919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs8017063	chr14:64268919-64268920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373993450	chr14:64268949-64268950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377745538	chr14:64268950-64268951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543367647	chr14:64268959-64268960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371162116	chr14:64268970-64268971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375479254	chr14:64268971-64268972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs367826957	chr14:64268972-64268973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370398390	chr14:64268973-64268974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374007481	chr14:64268985-64268986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs367865140	chr14:64268986-64268987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371982128	chr14:64268995-64268996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375086599	chr14:64268998-64268999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372790046	chr14:64268999-64269000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368296195	chr14:64269002-64269003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372381274	chr14:64269012-64269013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376718481	chr14:64269013-64269014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369107434	chr14:64269018-64269019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372962297	chr14:64269024-64269025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376848249	chr14:64269037-64269038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369106222	chr14:64269044-64269045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374192022	chr14:64269045-64269046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563244449	chr14:64269047-64269048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377675981	chr14:64269052-64269053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371102060	chr14:64269054-64269055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373548811	chr14:64269055-64269056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561084900	chr14:64269063-64269064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377428239	chr14:64269070-64269071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370206307	chr14:64269071-64269072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12896216	chr14:64269077-64269078	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs545482023	chr14:64269078-64269079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Leukemia	18688285	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Autism	22543975	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:543 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64254600-64275200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:64255400-64270000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:64256200-64272200	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr14:64266400-64273600	Weak transcription	Placenta	Placenta
5	chr14:64267200-64269200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr14:64267200-64271800	Weak transcription	Right Atrium	heart
7	chr14:64269200-64269400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr14:64269400-64269800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr14:64273600-64273800	Enhancers	Placenta	Placenta
10	chr14:64274800-64275200	Enhancers	Placenta	Placenta
11	chr14:64275200-64275400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr14:64275200-64276200	Weak transcription	Placenta	Placenta
13	chr14:64275600-64276600	Enhancers	HepG2	liver
14	chr14:64276200-64276800	Enhancers	Placenta	Placenta
15	chr14:64276600-64278000	Weak transcription	HepG2	liver
16	chr14:64276800-64278000	Weak transcription	Placenta	Placenta
17	chr14:64278000-64278600	Enhancers	HepG2	liver
18	chr14:64278000-64279200	Enhancers	Placenta	Placenta
19	chr14:64279200-64279400	Weak transcription	Placenta	Placenta
20	chr14:64283600-64284000	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr14:64284000-64284400	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
22	chr14:64284000-64284600	Weak transcription	Placenta	Placenta
23	chr14:64284400-64285600	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr14:64285600-64286000	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
25	chr14:64286000-64286400	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr14:64296600-64305600	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr14:64300000-64300800	Enhancers	Fetal Heart	heart
28	chr14:64302000-64304800	Weak transcription	Placenta	Placenta
29	chr14:64304800-64305400	Enhancers	Placenta	Placenta
30	chr14:64305400-64307600	Weak transcription	Placenta	Placenta
31	chr14:64305600-64306400	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr14:64306400-64307800	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr14:64307800-64308200	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
34	chr14:64312400-64312800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr14:64312400-64313000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr14:64312400-64313000	Enhancers	Dnd41	blood
37	chr14:64312800-64319200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr14:64315200-64315400	Weak transcription	Left Ventricle	heart
39	chr14:64315400-64315600	Enhancers	Left Ventricle	heart
40	chr14:64315400-64316000	Enhancers	HUVEC	blood vessel
41	chr14:64315400-64316600	Enhancers	Fetal Heart	heart
42	chr14:64315400-64316600	Enhancers	Ovary	ovary
43	chr14:64315600-64316000	Enhancers	Adipose Nuclei	Adipose
44	chr14:64315600-64319000	Weak transcription	Left Ventricle	heart
45	chr14:64315800-64316000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr14:64316000-64316200	Enhancers	Stomach Mucosa	stomach
47	chr14:64316000-64316400	Weak transcription	Adipose Nuclei	Adipose
48	chr14:64316000-64318800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr14:64316000-64319000	Weak transcription	HUVEC	blood vessel
50	chr14:64316200-64317200	Enhancers	Right Ventricle	heart

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