Variant report

Variant	nsv983777
Chromosome Location	chr14:45776402-45971817
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr14:45902392-45902559	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr14:45902380-45902544	A549	lung:	n/a	n/a
3	CEBPB	chr14:45831065-45831305	HepG2	liver:	n/a	chr14:45831179-45831190 chr14:45831134-45831145
4	CEBPB	chr14:45781545-45781804	HepG2	liver:	n/a	chr14:45781644-45781655
5	CEBPB	chr14:45893200-45893264	A549	lung:	n/a	n/a
6	CEBPB	chr14:45784842-45784985	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr14:45831020-45831293	A549	lung:	n/a	chr14:45831179-45831190 chr14:45831134-45831145
8	CEBPB	chr14:45810697-45810951	A549	lung:	n/a	n/a
9	CEBPB	chr14:45781555-45781799	A549	lung:	n/a	chr14:45781644-45781655
10	CEBPB	chr14:45902361-45902662	IMR90	lung:	n/a	n/a
11	CTCF	chr14:45896000-45896150	AG09309	skin:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
12	CTCF	chr14:45896000-45896150	AG10803	skin:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
13	CTCF	chr14:45896040-45896190	GM12869	blood:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
14	CTCF	chr14:45895943-45896154	SK-N-SH_RA	brain:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
15	CTCF	chr14:45895965-45896177	Pancreas_OC	pancreas:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
16	CTCF	chr14:45833708-45833895	LNCaP	prostate:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
17	CTCF	chr14:45896020-45896170	HCT-116	colon:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
18	CTCF	chr14:45833774-45833928	A549	lung:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
19	CTCF	chr14:45895980-45896162	HepG2	liver:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
20	CTCF	chr14:45895903-45896208	Medullo	brain:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
21	CTCF	chr14:45896020-45896170	NHEK	skin:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
22	CTCF	chr14:45787420-45787570	GM12865	blood:	n/a	n/a
23	CTCF	chr14:45895999-45896141	GM13976	blood:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
24	CTCF	chr14:45895920-45896070	HFF	foreskin:	n/a	n/a
25	CTCF	chr14:45878980-45879066	LNCaP	prostate:	n/a	n/a
26	CTCF	chr14:45896020-45896170	GM12865	blood:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
27	CTCF	chr14:45895960-45896110	MCF-7	breast:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
28	CTCF	chr14:45896020-45896170	AG04449	skin:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
29	CTCF	chr14:45896020-45896170	SAEC	small airway:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
30	CTCF	chr14:45895980-45896130	HRE	kidney:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
31	CTCF	chr14:45896020-45896170	HUVEC	blood vessel:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
32	CTCF	chr14:45896060-45896210	NB4	blood:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
33	CTCF	chr14:45825420-45825456	Medullo	brain:	n/a	n/a
34	CTCF	chr14:45895980-45896130	BJ	skin:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
35	CTCF	chr14:45895980-45896130	HRPEpiC	eye:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
36	CTCF	chr14:45833780-45833930	Caco-2	colon:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
37	CTCF	chr14:45895878-45896297	GM12878	blood:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
38	CTCF	chr14:45895975-45896191	LNCaP	prostate:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
39	CTCF	chr14:45833680-45833830	HCT-116	colon:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
40	CTCF	chr14:45895980-45896130	HL-60	blood:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
41	CTCF	chr14:45895980-45896159	Lung_OC	lung:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
42	CTCF	chr14:45896000-45896150	HEK293	kidney:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
43	CTCF	chr14:45895811-45896360	MCF-7	breast:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
44	CTCF	chr14:45895940-45896179	MCF-7	breast:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
45	CTCF	chr14:45895828-45896258	HepG2	liver:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
46	CTCF	chr14:45954854-45954876	GM13976	blood:	n/a	n/a
47	CTCF	chr14:45895968-45896221	A549	lung:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
48	CTCF	chr14:45896000-45896150	BJ	skin:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
49	CTCF	chr14:45895960-45896110	Caco-2	colon:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
50	CTCF	chr14:45896060-45896210	HMEC	breast:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:45840127-45840177	CMK	blood:	n/a
2	chr14:45930824-45930874	CMK	blood:	n/a
3	chr14:45840127-45840177	AG09319	gingival:	n/a
4	chr14:45870299-45870349	A549	lung:	n/a
5	chr14:45930824-45930874	HCF	heart:	n/a
6	chr14:45840127-45840177	U87	brain:	n/a
7	chr14:45870299-45870349	PANC-1	pancreas:	n/a
8	chr14:45870299-45870349	RPTEC	kidney:	n/a
9	chr14:45840127-45840177	AoSMC	blood vessel:	n/a
10	chr14:45870299-45870349	GM19239	blood:	n/a
11	chr14:45840127-45840177	HepG2	liver:	n/a
12	chr14:45930824-45930874	NHDF-neo	bronchial:	n/a
13	chr14:45840127-45840177	HL-60	blood:	n/a
14	chr14:45840127-45840177	SAEC	small airway:	n/a
15	chr14:45870299-45870349	HAEpiC	amniotic membrane:	n/a
16	chr14:45840127-45840177	Hela-S3	cervix:	n/a
17	chr14:45930824-45930874	LNCaP	prostate:	n/a
18	chr14:45930824-45930874	HRE	kidney:	n/a
19	chr14:45930824-45930874	SAEC	small airway:	n/a
20	chr14:45870299-45870349	AG10803	skin:	n/a
21	chr14:45870299-45870349	T-47D	breast:	n/a
22	chr14:45840127-45840177	NHDF-neo	bronchial:	n/a
23	chr14:45870299-45870349	HRE	kidney:	n/a
24	chr14:45870299-45870349	HUVEC	blood vessel:	n/a
25	chr14:45840127-45840177	GM12892	blood:	n/a
26	chr14:45840127-45840177	HCM	heart:	n/a
27	chr14:45930824-45930874	HPAEpiC	pulmonary alveolar:	n/a
28	chr14:45870299-45870349	BJ	skin:	n/a
29	chr14:45870299-45870349	GM12891	blood:	n/a
30	chr14:45870299-45870349	HMEC	breast:	n/a
31	chr14:45930824-45930874	RPTEC	kidney:	n/a
32	chr14:45870299-45870349	HNPCEpiC	eye:	n/a
33	chr14:45840127-45840177	NT2-D1	testis:	n/a
34	chr14:45870299-45870349	HRCEpiC	kidney:	n/a
35	chr14:45930824-45930874	GM12892	blood:	n/a
36	chr14:45840127-45840177	HCF	heart:	n/a
37	chr14:45870299-45870349	ECC-1	luminal epithelium:	n/a
38	chr14:45870299-45870349	CMK	blood:	n/a
39	chr14:45870299-45870349	Hepatocyte	liver:	n/a
40	chr14:45930824-45930874	GM06990	blood:	n/a
41	chr14:45930824-45930874	BE2_C	brain:	n/a
42	chr14:45870299-45870349	K562	blood:	n/a
43	chr14:45930824-45930874	Hepatocyte	liver:	n/a
44	chr14:45870299-45870349	NB4	blood:	n/a
45	chr14:45930824-45930874	HL-60	blood:	n/a
46	chr14:45930824-45930874	NH-A	brain:	n/a
47	chr14:45870299-45870349	H1-hESC	embryonic stem cell:	embryo
48	chr14:45870299-45870349	IMR90	lung:	fetal
49	chr14:45930824-45930874	AG04450	lung:	fetal
50	chr14:45840127-45840177	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:45932172..45934812-chr14:45938386..45940699,2	K562	blood:
2	chr14:45895702..45896616-chr14:45996086..45997189,11	MCF-7	breast:
3	chr14:45827598..45829425-chr14:45832240..45834984,2	MCF-7	breast:
4	chr14:45835845..45838000-chr14:45843048..45845340,2	K562	blood:
5	chr14:45932172..45934812-chr14:45938386..45940699,2	K562	blood:
6	chr14:45827598..45829425-chr14:45832240..45834984,2	MCF-7	breast:
7	chr14:45773220..45776127-chr14:45776332..45778274,2	K562	blood:
8	chr14:45774667..45776638-chr14:45777456..45779936,2	MCF-7	breast:
9	chr14:45833828..45835787-chr14:45839702..45842192,2	K562	blood:
10	chr14:45602740..45605100-chr14:45878381..45880365,2	MCF-7	breast:
11	chr14:45895709..45896868-chr14:45996158..45997180,10	MCF-7	breast:
12	chr14:45774667..45776638-chr14:45777456..45779936,2	MCF-7	breast:
13	chr14:45833828..45835787-chr14:45839702..45842192,2	K562	blood:
14	chr14:45833660..45834242-chr14:45996510..45997327,3	MCF-7	breast:
15	chr14:45835845..45838000-chr14:45843048..45845340,2	K562	blood:

Variant related genes	Relation type
ENSG00000260046	TF binding region
ENSG00000257900	TF binding region
ENSG00000260046	CpG island
ENSG00000257900	CpG island
ENSG00000100442	chromatin interactions

Extended variants
information (count: 2755 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2755 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188384334	chr14:45783019-45783020	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs368046509	chr14:45783023-45783024	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs140923596	chr14:45783042-45783043	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs527767829	chr14:45783048-45783049	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs552639855	chr14:45783160-45783161	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs570877228	chr14:45783168-45783169	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs144597073	chr14:45783194-45783195	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs550214722	chr14:45783236-45783237	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs192665313	chr14:45783283-45783284	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs561712049	chr14:45783358-45783359	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs554321309	chr14:45783475-45783476	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs571842837	chr14:45783493-45783494	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs539160782	chr14:45783499-45783500	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs557402382	chr14:45783545-45783546	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs17115982	chr14:45783546-45783547	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs569554717	chr14:45783587-45783588	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs537057623	chr14:45783607-45783608	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs146673274	chr14:45783609-45783610	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs561874218	chr14:45783639-45783640	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs573876960	chr14:45783733-45783734	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs540899050	chr14:45783754-45783755	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs140713911	chr14:45783757-45783758	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs577919134	chr14:45784635-45784636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545212547	chr14:45784637-45784638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs74320145	chr14:45784645-45784646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532923271	chr14:45784663-45784664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543486159	chr14:45784667-45784668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149179052	chr14:45784668-45784669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186650451	chr14:45784694-45784695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376001779	chr14:45784731-45784732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs566597695	chr14:45784750-45784751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565993675	chr14:45784784-45784785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112708504	chr14:45784788-45784789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377237171	chr14:45784837-45784838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535471734	chr14:45784857-45784858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs551556190	chr14:45784920-45784921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs114363512	chr14:45784929-45784930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550582893	chr14:45784949-45784950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs200993124	chr14:45784954-45784955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374927535	chr14:45784964-45784965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs539478239	chr14:45784968-45784969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537137870	chr14:45784981-45784982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369946229	chr14:45784986-45784987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555137802	chr14:45785019-45785020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs17115984	chr14:45785039-45785040	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs534278485	chr14:45785073-45785074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553342833	chr14:45785111-45785112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577995199	chr14:45785152-45785153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs545249201	chr14:45785177-45785178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557175352	chr14:45785184-45785185	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
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
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:153 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:45783000-45783800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr14:45784600-45785000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:45784600-45785000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr14:45784600-45785000	Enhancers	Pancreas	Pancrea
5	chr14:45784600-45785200	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr14:45784600-45785200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr14:45784800-45785200	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr14:45801200-45801800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr14:45801400-45802600	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr14:45801800-45802200	Enhancers	Fetal Heart	heart
11	chr14:45801800-45802600	Enhancers	Left Ventricle	heart
12	chr14:45801800-45802800	Enhancers	Adipose Nuclei	Adipose
13	chr14:45802000-45802600	Enhancers	Psoas Muscle	Psoas
14	chr14:45809600-45810400	Enhancers	Colon Smooth Muscle	Colon
15	chr14:45813400-45813600	Enhancers	Gastric	stomach
16	chr14:45814600-45815200	Active TSS	Right Atrium	heart
17	chr14:45814800-45815400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr14:45815000-45815400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr14:45822400-45822800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr14:45822400-45822800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr14:45822400-45822800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr14:45822400-45823000	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr14:45822600-45823000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr14:45822600-45823400	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr14:45830400-45831600	Enhancers	Fetal Heart	heart
26	chr14:45832200-45832400	Enhancers	Right Atrium	heart
27	chr14:45833200-45834200	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr14:45833800-45834400	Enhancers	Adipose Nuclei	Adipose
29	chr14:45833800-45834600	Enhancers	Right Atrium	heart
30	chr14:45837000-45837200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr14:45837200-45839800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr14:45837400-45841600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr14:45837600-45837800	Enhancers	H9 Cell Line	embryonic stem cell
34	chr14:45837800-45838000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr14:45837800-45838600	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr14:45838000-45839000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr14:45838600-45838800	Enhancers	H9 Cell Line	embryonic stem cell
38	chr14:45839000-45840400	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr14:45839400-45840400	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr14:45839600-45840200	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr14:45839600-45840400	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr14:45839600-45840600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr14:45839800-45840600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr14:45839800-45840800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr14:45840000-45840400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr14:45840000-45840600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr14:45840200-45843200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr14:45840400-45842800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr14:45840400-45843000	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr14:45840400-45843000	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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