Variant report

Variant	nsv1040279
Chromosome Location	chr14:45808006-46015706
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	chr14:46000477-46000804	HepG2	liver:	n/a	chr14:46000620-46000631
2	CEBPB	chr14:45902380-45902544	A549	lung:	n/a	n/a
3	CEBPB	chr14:45893200-45893264	A549	lung:	n/a	n/a
4	CEBPB	chr14:45902392-45902559	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr14:45831020-45831293	A549	lung:	n/a	chr14:45831179-45831190 chr14:45831134-45831145
6	CEBPB	chr14:45902361-45902662	IMR90	lung:	n/a	n/a
7	CEBPB	chr14:45831065-45831305	HepG2	liver:	n/a	chr14:45831179-45831190 chr14:45831134-45831145
8	CEBPB	chr14:45990474-45990674	IMR90	lung:	n/a	chr14:45990587-45990604
9	CEBPB	chr14:45810697-45810951	A549	lung:	n/a	n/a
10	CHD2	chr14:45996268-45996394	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr14:45895960-45896110	A549	lung:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
12	CTCF	chr14:45996580-45996730	HEK293	kidney:	n/a	n/a
13	CTCF	chr14:45833780-45833930	HMEC	breast:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
14	CTCF	chr14:45996489-45996878	GM12878	blood:	n/a	n/a
15	CTCF	chr14:45895975-45896191	LNCaP	prostate:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
16	CTCF	chr14:45895909-45896315	MCF-7	breast:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
17	CTCF	chr14:45896020-45896170	BE2_C	brain:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
18	CTCF	chr14:45896000-45896150	HPAF	blood vessel:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
19	CTCF	chr14:45833700-45833850	MCF-7	breast:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
20	CTCF	chr14:45996541-45996809	ECC-1	luminal epithelium:	n/a	n/a
21	CTCF	chr14:45996546-45996739	GM19238	blood:	n/a	n/a
22	CTCF	chr14:45996529-45996766	NHEK	skin:	n/a	n/a
23	CTCF	chr14:45833780-45833930	Caco-2	colon:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
24	CTCF	chr14:45996560-45996710	GM12865	blood:	n/a	n/a
25	CTCF	chr14:45895960-45896110	WERI-Rb-1	eye:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
26	CTCF	chr14:45996580-45996730	BE2_C	brain:	n/a	n/a
27	CTCF	chr14:45896040-45896190	GM12868	blood:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
28	CTCF	chr14:45825420-45825456	Medullo	brain:	n/a	n/a
29	CTCF	chr14:45996587-45996773	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr14:45996600-45996750	GM12872	blood:	n/a	n/a
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	chr14:45833697-45833927	MCF-7	breast:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
33	CTCF	chr14:45996600-45996750	GM12864	blood:	n/a	n/a
34	CTCF	chr14:45895980-45896162	HepG2	liver:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
35	CTCF	chr14:45996620-45996770	HCT-116	colon:	n/a	n/a
36	CTCF	chr14:45996600-45996750	GM12866	blood:	n/a	n/a
37	CTCF	chr14:45996600-45996750	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr14:45895960-45896110	HEK293	kidney:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
39	CTCF	chr14:45996427-45996815	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr14:45996620-45996770	GM12875	blood:	n/a	n/a
41	CTCF	chr14:45895860-45896263	ECC-1	luminal epithelium:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
42	CTCF	chr14:45996600-45996750	GM12871	blood:	n/a	n/a
43	CTCF	chr14:45896020-45896170	GM12865	blood:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
44	CTCF	chr14:45896000-45896150	WERI-Rb-1	eye:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
45	CTCF	chr14:45996600-45996750	GM12874	blood:	n/a	n/a
46	CTCF	chr14:45833761-45833868	Gliobla	brain:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
47	CTCF	chr14:45895980-45896130	HRE	kidney:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
48	CTCF	chr14:45895999-45896141	GM13976	blood:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
49	CTCF	chr14:45996640-45996790	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr14:45896260-45896410	AoAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:45840127-45840177	T-47D	breast:	n/a
2	chr14:45930824-45930874	HMEC	breast:	n/a
3	chr14:45930824-45930874	GM12878	blood:	n/a
4	chr14:45930824-45930874	AG09309	skin:	n/a
5	chr14:45840127-45840177	AoSMC	blood vessel:	n/a
6	chr14:45840127-45840177	HIPEpiC	eye:	n/a
7	chr14:45840127-45840177	HMEC	breast:	n/a
8	chr14:45870299-45870349	GM19239	blood:	n/a
9	chr14:45870299-45870349	SKMC	muscle:	n/a
10	chr14:45930824-45930874	HEK293	kidney:	embryo
11	chr14:45840127-45840177	HEK293	kidney:	embryo
12	chr14:45840127-45840177	MCF10A-Er-Src	breast:	n/a
13	chr14:45870299-45870349	HepG2	liver:	n/a
14	chr14:45870299-45870349	AG09319	gingival:	n/a
15	chr14:45870299-45870349	GM12891	blood:	n/a
16	chr14:45930824-45930874	K562	blood:	n/a
17	chr14:45870299-45870349	HL-60	blood:	n/a
18	chr14:45930824-45930874	HPAEpiC	pulmonary alveolar:	n/a
19	chr14:45840127-45840177	A549	lung:	n/a
20	chr14:45840127-45840177	SKMC	muscle:	n/a
21	chr14:45840127-45840177	BE2_C	brain:	n/a
22	chr14:45930824-45930874	HNPCEpiC	eye:	n/a
23	chr14:45840127-45840177	HNPCEpiC	eye:	n/a
24	chr14:45930824-45930874	GM19239	blood:	n/a
25	chr14:45840127-45840177	RPTEC	kidney:	n/a
26	chr14:45870299-45870349	HAEpiC	amniotic membrane:	n/a
27	chr14:45930824-45930874	HRCEpiC	kidney:	n/a
28	chr14:45870299-45870349	HEEpiC	esophagus:	n/a
29	chr14:45840127-45840177	CMK	blood:	n/a
30	chr14:45870299-45870349	MCF10A-Er-Src	breast:	n/a
31	chr14:45930824-45930874	GM12892	blood:	n/a
32	chr14:45930824-45930874	HCM	heart:	n/a
33	chr14:45870299-45870349	GM12892	blood:	n/a
34	chr14:45870299-45870349	AG09309	skin:	n/a
35	chr14:45930824-45930874	AG04450	lung:	fetal
36	chr14:45930824-45930874	RPTEC	kidney:	n/a
37	chr14:45930824-45930874	Caco-2	colon:	n/a
38	chr14:45840127-45840177	HRPEpiC	eye:	n/a
39	chr14:45870299-45870349	HCM	heart:	n/a
40	chr14:45870299-45870349	NT2-D1	testis:	n/a
41	chr14:45930824-45930874	HIPEpiC	eye:	n/a
42	chr14:45870299-45870349	HCPEpiC	choroid plexus:	n/a
43	chr14:45840127-45840177	SK-N-MC	brain:	n/a
44	chr14:45870299-45870349	AG04449	skin:	fetal
45	chr14:45930824-45930874	MCF-7	breast:	n/a
46	chr14:45870299-45870349	GM12878	blood:	n/a
47	chr14:45870299-45870349	HPAEpiC	pulmonary alveolar:	n/a
48	chr14:45930824-45930874	NT2-D1	testis:	n/a
49	chr14:45870299-45870349	SK-N-SH	brain:	n/a
50	chr14:45870299-45870349	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:45932172..45934812-chr14:45938386..45940699,2	K562	blood:
2	chr14:45973970..45976424-chr14:45980516..45983044,2	MCF-7	breast:
3	chr14:45833660..45834242-chr14:45996510..45997327,3	MCF-7	breast:
4	chr14:45895702..45896616-chr14:45996086..45997189,11	MCF-7	breast:
5	chr14:45895702..45896616-chr14:45996086..45997189,11	MCF-7	breast:
6	chr14:45833660..45834242-chr14:45996510..45997327,3	MCF-7	breast:
7	chr14:45973970..45976424-chr14:45980516..45983044,2	MCF-7	breast:
8	chr14:45827598..45829425-chr14:45832240..45834984,2	MCF-7	breast:
9	chr14:45980303..45983033-chr14:45994308..45996794,2	MCF-7	breast:
10	chr14:45833828..45835787-chr14:45839702..45842192,2	K562	blood:
11	chr14:45602740..45605100-chr14:45878381..45880365,2	MCF-7	breast:
12	chr14:45980303..45983033-chr14:45994308..45996794,2	MCF-7	breast:
13	chr14:45895709..45896868-chr14:45996158..45997180,10	MCF-7	breast:
14	chr14:45932172..45934812-chr14:45938386..45940699,2	K562	blood:
15	chr14:45895709..45896868-chr14:45996158..45997180,10	MCF-7	breast:
16	chr14:45827598..45829425-chr14:45832240..45834984,2	MCF-7	breast:
17	chr14:45833828..45835787-chr14:45839702..45842192,2	K562	blood:
18	chr14:45835845..45838000-chr14:45843048..45845340,2	K562	blood:
19	chr14:45835845..45838000-chr14:45843048..45845340,2	K562	blood:

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

Extended variants
information (count: 2864 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2864 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189024227	chr14:45809601-45809602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs193183271	chr14:45809602-45809603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552502506	chr14:45809636-45809637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185116202	chr14:45809658-45809659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542942336	chr14:45809666-45809667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs111783828	chr14:45809696-45809697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572741992	chr14:45809702-45809703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190018468	chr14:45809827-45809828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181273279	chr14:45809832-45809833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577438194	chr14:45809952-45809953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533274452	chr14:45809973-45809974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147853338	chr14:45809976-45809977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563738790	chr14:45810004-45810005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530788292	chr14:45810139-45810140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565951806	chr14:45810142-45810143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534831633	chr14:45810178-45810179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185333283	chr14:45810260-45810261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548118297	chr14:45810288-45810289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567948983	chr14:45810289-45810290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79522259	chr14:45810321-45810322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535292535	chr14:45810339-45810340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377729621	chr14:45810343-45810344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556310908	chr14:45810361-45810362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535641804	chr14:45813403-45813404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553969071	chr14:45813422-45813423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576124533	chr14:45813453-45813454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534259560	chr14:45813479-45813480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542031206	chr14:45813504-45813505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558696863	chr14:45813514-45813515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577156349	chr14:45813570-45813571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564205148	chr14:45814696-45814697	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs531248825	chr14:45814718-45814719	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs549754458	chr14:45814736-45814737	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs75321270	chr14:45814751-45814752	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs529220691	chr14:45814786-45814787	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs547699711	chr14:45814845-45814846	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs565912495	chr14:45814864-45814865	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs539643537	chr14:45815003-45815004	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs552434703	chr14:45815022-45815023	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs373037915	chr14:45815203-45815204	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs375496631	chr14:45815278-45815279	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs570936196	chr14:45815282-45815283	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs186980622	chr14:45815289-45815290	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs556539929	chr14:45815360-45815361	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs112568137	chr14:45815365-45815366	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs191447599	chr14:45815370-45815371	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs535778685	chr14:45815373-45815374	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs554020614	chr14:45815374-45815375	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs181268317	chr14:45815396-45815397	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs546367539	chr14:45815397-45815398	Enhancers Active TSS	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:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:45809600-45810400	Enhancers	Colon Smooth Muscle	Colon
2	chr14:45813400-45813600	Enhancers	Gastric	stomach
3	chr14:45814600-45815200	Active TSS	Right Atrium	heart
4	chr14:45814800-45815400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr14:45815000-45815400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr14:45822400-45822800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr14:45822400-45822800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr14:45822400-45822800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr14:45822400-45823000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr14:45822600-45823000	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr14:45822600-45823400	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr14:45830400-45831600	Enhancers	Fetal Heart	heart
13	chr14:45832200-45832400	Enhancers	Right Atrium	heart
14	chr14:45833200-45834200	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr14:45833800-45834400	Enhancers	Adipose Nuclei	Adipose
16	chr14:45833800-45834600	Enhancers	Right Atrium	heart
17	chr14:45837000-45837200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr14:45837200-45839800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr14:45837400-45841600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr14:45837600-45837800	Enhancers	H9 Cell Line	embryonic stem cell
21	chr14:45837800-45838000	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr14:45837800-45838600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr14:45838000-45839000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr14:45838600-45838800	Enhancers	H9 Cell Line	embryonic stem cell
25	chr14:45839000-45840400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr14:45839400-45840400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr14:45839600-45840200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr14:45839600-45840400	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr14:45839600-45840600	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr14:45839800-45840600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr14:45839800-45840800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr14:45840000-45840400	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr14:45840000-45840600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr14:45840200-45843200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr14:45840400-45842800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr14:45840400-45843000	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr14:45840400-45843000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr14:45840400-45843200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr14:45840600-45842800	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr14:45840600-45843000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr14:45840800-45843000	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr14:45841600-45841800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr14:45841800-45843000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:45842800-45843400	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr14:45842800-45843600	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr14:45843000-45843400	Enhancers	H1 Cell Line	embryonic stem cell
47	chr14:45843000-45843400	Enhancers	H9 Cell Line	embryonic stem cell
48	chr14:45843000-45843400	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr14:45843000-45843400	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr14:45843000-45843400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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