Variant report

Variant	nsv916721
Chromosome Location	chr14:45753973-45979614
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	ARID3A	chr14:45756958-45756994	K562	blood:	n/a	n/a
2	CEBPB	chr14:45831020-45831293	A549	lung:	n/a	chr14:45831179-45831190 chr14:45831134-45831145
3	CEBPB	chr14:45784842-45784985	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr14:45831065-45831305	HepG2	liver:	n/a	chr14:45831179-45831190 chr14:45831134-45831145
5	CEBPB	chr14:45902392-45902559	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr14:45810697-45810951	A549	lung:	n/a	n/a
7	CEBPB	chr14:45902361-45902662	IMR90	lung:	n/a	n/a
8	CEBPB	chr14:45757725-45757874	IMR90	lung:	n/a	n/a
9	CEBPB	chr14:45781545-45781804	HepG2	liver:	n/a	chr14:45781644-45781655
10	CEBPB	chr14:45893200-45893264	A549	lung:	n/a	n/a
11	CEBPB	chr14:45902380-45902544	A549	lung:	n/a	n/a
12	CEBPB	chr14:45781555-45781799	A549	lung:	n/a	chr14:45781644-45781655
13	CHD1	chr14:45764004-45764054	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr14:45754340-45754490	NHEK	skin:	n/a	n/a
15	CTCF	chr14:45756879-45757144	GM12878	blood:	n/a	chr14:45757001-45757019 chr14:45757006-45757014 chr14:45757002-45757018 chr14:45757003-45757024
16	CTCF	chr14:45868854-45868856	MCF-7	breast:	n/a	n/a
17	CTCF	chr14:45833737-45833861	HepG2	liver:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
18	CTCF	chr14:45754120-45754270	MCF-7	breast:	n/a	chr14:45754192-45754210 chr14:45754193-45754209 chr14:45754187-45754208
19	CTCF	chr14:45764678-45764780	Spleen_OC	spleen:	n/a	n/a
20	CTCF	chr14:45825280-45825430	HMEC	breast:	n/a	n/a
21	CTCF	chr14:45754120-45754270	HVMF	connective:	n/a	chr14:45754192-45754210 chr14:45754193-45754209 chr14:45754187-45754208
22	CTCF	chr14:45895920-45896070	HCM	heart:	n/a	n/a
23	CTCF	chr14:45833722-45833865	HepG2	liver:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
24	CTCF	chr14:45754260-45754410	HUVEC	blood vessel:	n/a	n/a
25	CTCF	chr14:45825377-45825433	MCF-7	breast:	n/a	n/a
26	CTCF	chr14:45895980-45896130	MCF-7	breast:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
27	CTCF	chr14:45759190-45759262	MCF-7	breast:	n/a	chr14:45759205-45759214
28	CTCF	chr14:45833697-45833927	MCF-7	breast:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
29	CTCF	chr14:45881220-45881271	LNCaP	prostate:	n/a	n/a
30	CTCF	chr14:45798680-45798830	GM12878	blood:	n/a	n/a
31	CTCF	chr14:45895828-45896258	HepG2	liver:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
32	CTCF	chr14:45833708-45833873	Hela-S3	cervix:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
33	CTCF	chr14:45817252-45817270	MCF-7	breast:	n/a	n/a
34	CTCF	chr14:45756826-45757078	H1-hESC	embryonic stem cell:	n/a	chr14:45757001-45757019 chr14:45757006-45757014 chr14:45757002-45757018 chr14:45757003-45757024
35	CTCF	chr14:45754100-45754250	GM12870	blood:	n/a	chr14:45754192-45754210 chr14:45754193-45754209 chr14:45754187-45754208
36	CTCF	chr14:45896000-45896150	HA-sp	spinal cord:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
37	CTCF	chr14:45895980-45896130	Caco-2	colon:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
38	CTCF	chr14:45833670-45833900	HCT-116	colon:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
39	CTCF	chr14:45895939-45896305	H1-hESC	embryonic stem cell:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
40	CTCF	chr14:45896060-45896210	HMEC	breast:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
41	CTCF	chr14:45896000-45896150	AG09319	gingival:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
42	CTCF	chr14:45754120-45754270	HMEC	breast:	n/a	chr14:45754192-45754210 chr14:45754193-45754209 chr14:45754187-45754208
43	CTCF	chr14:45895903-45896208	Medullo	brain:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
44	CTCF	chr14:45756920-45757070	MCF-7	breast:	n/a	chr14:45757001-45757019 chr14:45757006-45757014 chr14:45757002-45757018 chr14:45757003-45757024
45	CTCF	chr14:45896020-45896170	HRE	kidney:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
46	CTCF	chr14:45754100-45754250	HMF	breast:	n/a	chr14:45754192-45754210 chr14:45754193-45754209 chr14:45754187-45754208
47	CTCF	chr14:45896020-45896170	HUVEC	blood vessel:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
48	CTCF	chr14:45895980-45896130	GM12801	blood:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
49	CTCF	chr14:45754100-45754250	GM12871	blood:	n/a	chr14:45754192-45754210 chr14:45754193-45754209 chr14:45754187-45754208
50	CTCF	chr14:45895980-45896130	GM06990	blood:	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	AG10803	skin:	n/a
2	chr14:45840127-45840177	AG10803	skin:	n/a
3	chr14:45840127-45840177	GM19239	blood:	n/a
4	chr14:45840127-45840177	HEEpiC	esophagus:	n/a
5	chr14:45759143-45759193	PANC-1	pancreas:	n/a
6	chr14:45870299-45870349	AG09309	skin:	n/a
7	chr14:45930824-45930874	HepG2	liver:	n/a
8	chr14:45870299-45870349	HUVEC	blood vessel:	n/a
9	chr14:45930824-45930874	PFSK-1	brain:	n/a
10	chr14:45930824-45930874	HAEpiC	amniotic membrane:	n/a
11	chr14:45840127-45840177	MCF10A-Er-Src	breast:	n/a
12	chr14:45930824-45930874	Caco-2	colon:	n/a
13	chr14:45930824-45930874	HRCEpiC	kidney:	n/a
14	chr14:45930824-45930874	SAEC	small airway:	n/a
15	chr14:45840127-45840177	HIPEpiC	eye:	n/a
16	chr14:45759143-45759193	HL-60	blood:	n/a
17	chr14:45759143-45759193	HNPCEpiC	eye:	n/a
18	chr14:45930824-45930874	Hepatocyte	liver:	n/a
19	chr14:45870299-45870349	LNCaP	prostate:	n/a
20	chr14:45930824-45930874	PANC-1	pancreas:	n/a
21	chr14:45840127-45840177	RPTEC	kidney:	n/a
22	chr14:45930824-45930874	HL-60	blood:	n/a
23	chr14:45759143-45759193	T-47D	breast:	n/a
24	chr14:45930824-45930874	AoSMC	blood vessel:	n/a
25	chr14:45840127-45840177	T-47D	breast:	n/a
26	chr14:45840127-45840177	HCT-116	colon:	n/a
27	chr14:45840127-45840177	HCF	heart:	n/a
28	chr14:45840127-45840177	NB4	blood:	n/a
29	chr14:45930824-45930874	HMEC	breast:	n/a
30	chr14:45840127-45840177	Hela-S3	cervix:	n/a
31	chr14:45930824-45930874	GM06990	blood:	n/a
32	chr14:45870299-45870349	GM12892	blood:	n/a
33	chr14:45870299-45870349	H1-hESC	embryonic stem cell:	embryo
34	chr14:45840127-45840177	AoSMC	blood vessel:	n/a
35	chr14:45930824-45930874	A549	lung:	n/a
36	chr14:45759143-45759193	Jurkat	blood:	n/a
37	chr14:45840127-45840177	GM06990	blood:	n/a
38	chr14:45759143-45759193	AG04449	skin:	fetal
39	chr14:45759143-45759193	A549	lung:	n/a
40	chr14:45870299-45870349	ProgFib	skin:	n/a
41	chr14:45759143-45759193	HMEC	breast:	n/a
42	chr14:45840127-45840177	ProgFib	skin:	n/a
43	chr14:45759143-45759193	AG10803	skin:	n/a
44	chr14:45840127-45840177	Jurkat	blood:	n/a
45	chr14:45870299-45870349	T-47D	breast:	n/a
46	chr14:45870299-45870349	SAEC	small airway:	n/a
47	chr14:45759143-45759193	HCPEpiC	choroid plexus:	n/a
48	chr14:45870299-45870349	HRE	kidney:	n/a
49	chr14:45840127-45840177	HEK293	kidney:	embryo
50	chr14:45840127-45840177	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:45602740..45605100-chr14:45878381..45880365,2	MCF-7	breast:
2	chr14:45932172..45934812-chr14:45938386..45940699,2	K562	blood:
3	chr14:45833828..45835787-chr14:45839702..45842192,2	K562	blood:
4	chr14:45827598..45829425-chr14:45832240..45834984,2	MCF-7	breast:
5	chr14:45895702..45896616-chr14:45996086..45997189,11	MCF-7	breast:
6	chr14:45827598..45829425-chr14:45832240..45834984,2	MCF-7	breast:
7	chr14:45833828..45835787-chr14:45839702..45842192,2	K562	blood:
8	chr14:45773220..45776127-chr14:45776332..45778274,2	K562	blood:
9	chr14:45973970..45976424-chr14:45980516..45983044,2	MCF-7	breast:
10	chr14:45932172..45934812-chr14:45938386..45940699,2	K562	blood:
11	chr14:45835845..45838000-chr14:45843048..45845340,2	K562	blood:
12	chr14:45774667..45776638-chr14:45777456..45779936,2	MCF-7	breast:
13	chr14:45835845..45838000-chr14:45843048..45845340,2	K562	blood:
14	chr14:45895709..45896868-chr14:45996158..45997180,10	MCF-7	breast:
15	chr14:45774667..45776638-chr14:45777456..45779936,2	MCF-7	breast:
16	chr14:45773220..45776127-chr14:45776332..45778274,2	K562	blood:
17	chr14:45833660..45834242-chr14:45996510..45997327,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-8	chr14:45759239-45759589	NONHSAT036654
2	lnc-FANCM-8	chr14:45759209-45759392	NONHSAT036653
3	lnc-FANCM-8	chr14:45759448-45759483	NONHSAT036653
4	lnc-FANCM-8	chr14:45759448-45759479	NONHSAT036652
5	lnc-FANCM-8	chr14:45759144-45759367	NONHSAT036652

Variant related genes	Relation type
ENSG00000260046	TF binding region
DNAJC19P9	TF binding region
ENSG00000257900	TF binding region
ENSG00000258746	TF binding region
ENSG00000260046	CpG island
DNAJC19P9	CpG island
ENSG00000257900	CpG island
ENSG00000258746	CpG island
ENSG00000100442	chromatin interactions

Extended variants
information (count: 3117 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3117 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544554447	chr14:45754263-45754264	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs531993956	chr14:45754264-45754265	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs544037895	chr14:45754267-45754268	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs562296972	chr14:45754360-45754361	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs529025538	chr14:45754377-45754378	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs114038673	chr14:45756805-45756806	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs371930919	chr14:45756814-45756815	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs542555284	chr14:45756815-45756816	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs560226995	chr14:45756839-45756840	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs34725908	chr14:45756842-45756843	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs143342646	chr14:45756849-45756850	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs575205443	chr14:45756878-45756879	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs542615423	chr14:45756903-45756904	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs560711341	chr14:45756904-45756905	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs72672942	chr14:45756928-45756929	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs528429706	chr14:45756935-45756936	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs148317426	chr14:45757075-45757076	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs567845053	chr14:45757101-45757102	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs74714396	chr14:45757134-45757135	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs186044327	chr14:45757184-45757185	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs140506177	chr14:45757245-45757246	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs190314677	chr14:45757256-45757257	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs182558301	chr14:45757257-45757258	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs185321101	chr14:45757260-45757261	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs76982759	chr14:45757286-45757287	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs567531671	chr14:45757291-45757292	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs535362976	chr14:45757293-45757294	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs150398464	chr14:45757308-45757309	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs571583318	chr14:45757350-45757351	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs113093455	chr14:45757352-45757353	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs531062340	chr14:45757798-45757799	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs549194362	chr14:45757810-45757811	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs138164123	chr14:45757814-45757815	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs567716277	chr14:45757919-45757920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs35573899	chr14:45759125-45759126	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs397734487	chr14:45759134-45759135	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs62000306	chr14:45759139-45759140	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs148634589	chr14:45759148-45759149	Inactive region	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs77745360	chr14:45759162-45759163	Inactive region	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs574630708	chr14:45759196-45759197	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs372869993	chr14:45759232-45759233	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs541670972	chr14:45759246-45759247	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs560287999	chr14:45759276-45759277	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs386777048	chr14:45759280-45759281	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs114744485	chr14:45759281-45759282	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs115939305	chr14:45759282-45759283	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs372918865	chr14:45759297-45759298	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs182403911	chr14:45759309-45759310	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs150718165	chr14:45759321-45759322	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs563042597	chr14:45759344-45759345	Inactive region	lncRNA	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:188 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:45757800-45758000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:45761600-45762200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr14:45762400-45764000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr14:45762600-45762800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
5	chr14:45762800-45764800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr14:45763000-45764000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
7	chr14:45763000-45764800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
8	chr14:45763000-45764800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
9	chr14:45763400-45763800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
10	chr14:45763600-45763800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
11	chr14:45763600-45764800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
12	chr14:45763800-45764000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr14:45763800-45764000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
14	chr14:45763800-45764000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
15	chr14:45763800-45764800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
16	chr14:45764000-45764400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
17	chr14:45764000-45764600	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr14:45764000-45764600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
19	chr14:45764400-45764600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
20	chr14:45764600-45764800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
21	chr14:45764600-45765600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr14:45765600-45765800	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr14:45766200-45766400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
24	chr14:45766200-45766400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr14:45766200-45766600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr14:45766800-45767000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr14:45767600-45768000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr14:45767600-45768200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr14:45767800-45768000	Enhancers	H9 Cell Line	embryonic stem cell
30	chr14:45767800-45768000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr14:45767800-45768200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr14:45767800-45768400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr14:45774800-45775600	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr14:45783000-45783800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr14:45784600-45785000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr14:45784600-45785000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr14:45784600-45785000	Enhancers	Pancreas	Pancrea
38	chr14:45784600-45785200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr14:45784600-45785200	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr14:45784800-45785200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr14:45801200-45801800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr14:45801400-45802600	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr14:45801800-45802200	Enhancers	Fetal Heart	heart
44	chr14:45801800-45802600	Enhancers	Left Ventricle	heart
45	chr14:45801800-45802800	Enhancers	Adipose Nuclei	Adipose
46	chr14:45802000-45802600	Enhancers	Psoas Muscle	Psoas
47	chr14:45809600-45810400	Enhancers	Colon Smooth Muscle	Colon
48	chr14:45813400-45813600	Enhancers	Gastric	stomach
49	chr14:45814600-45815200	Active TSS	Right Atrium	heart
50	chr14:45814800-45815400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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