Variant report

Variant	nsv442340
Chromosome Location	chr14:45826056-46015718
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	chr14:45893200-45893264	A549	lung:	n/a	n/a
2	CEBPB	chr14:45990474-45990674	IMR90	lung:	n/a	chr14:45990587-45990604
3	CEBPB	chr14:45902392-45902559	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr14:45831020-45831293	A549	lung:	n/a	chr14:45831179-45831190 chr14:45831134-45831145
5	CEBPB	chr14:46000477-46000804	HepG2	liver:	n/a	chr14:46000620-46000631
6	CEBPB	chr14:45831065-45831305	HepG2	liver:	n/a	chr14:45831179-45831190 chr14:45831134-45831145
7	CEBPB	chr14:45902380-45902544	A549	lung:	n/a	n/a
8	CEBPB	chr14:45902361-45902662	IMR90	lung:	n/a	n/a
9	CHD2	chr14:45996268-45996394	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr14:45833559-45834062	MCF-7	breast:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
11	CTCF	chr14:45996660-45996810	HVMF	connective:	n/a	n/a
12	CTCF	chr14:45833708-45833895	LNCaP	prostate:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
13	CTCF	chr14:45896000-45896150	HAc	cerebellar:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
14	CTCF	chr14:45896000-45896150	HCFaa	heart:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
15	CTCF	chr14:45895811-45896360	MCF-7	breast:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
16	CTCF	chr14:45895980-45896159	Lung_OC	lung:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
17	CTCF	chr14:45996543-45996720	GM12891	blood:	n/a	n/a
18	CTCF	chr14:45896020-45896170	HRE	kidney:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
19	CTCF	chr14:45996640-45996790	HCT-116	colon:	n/a	n/a
20	CTCF	chr14:45895980-45896130	HRE	kidney:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
21	CTCF	chr14:45833780-45833930	HMEC	breast:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
22	CTCF	chr14:45896020-45896170	HFF-Myc	foreskin:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
23	CTCF	chr14:45996580-45996730	GM12867	blood:	n/a	n/a
24	CTCF	chr14:45896020-45896170	SK-N-SH_RA	brain:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
25	CTCF	chr14:45996580-45996730	HEEpiC	esophagus:	n/a	n/a
26	CTCF	chr14:45833653-45833901	H1-hESC	embryonic stem cell:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
27	CTCF	chr14:45896780-45896930	HMEC	breast:	n/a	n/a
28	CTCF	chr14:45895940-45896090	HPF	lung:	n/a	chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
29	CTCF	chr14:45881220-45881271	LNCaP	prostate:	n/a	n/a
30	CTCF	chr14:45996541-45996809	ECC-1	luminal epithelium:	n/a	n/a
31	CTCF	chr14:45895980-45896130	GM12867	blood:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
32	CTCF	chr14:45895974-45896192	GM13977	blood:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
33	CTCF	chr14:45833680-45833830	HCT-116	colon:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
34	CTCF	chr14:45996569-45996809	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr14:45896040-45896190	HPF	lung:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
36	CTCF	chr14:45868854-45868856	MCF-7	breast:	n/a	n/a
37	CTCF	chr14:45996600-45996750	GM12872	blood:	n/a	n/a
38	CTCF	chr14:45895980-45896130	Caco-2	colon:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
39	CTCF	chr14:45996600-45996750	GM12874	blood:	n/a	n/a
40	CTCF	chr14:45895975-45896191	LNCaP	prostate:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
41	CTCF	chr14:45996640-45996790	GM12866	blood:	n/a	n/a
42	CTCF	chr14:45895980-45896130	MCF-7	breast:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
43	CTCF	chr14:45996580-45996730	GM12870	blood:	n/a	n/a
44	CTCF	chr14:45895903-45896208	Medullo	brain:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
45	CTCF	chr14:45896020-45896170	NHEK	skin:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
46	CTCF	chr14:45996579-45996787	GM10266	blood:	n/a	n/a
47	CTCF	chr14:45996620-45996770	HMEC	breast:	n/a	n/a
48	CTCF	chr14:45895980-45896130	AoAF	blood vessel:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
49	CTCF	chr14:45895908-45896214	A549	lung:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
50	CTCF	chr14:45896020-45896170	AG04449	skin:	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	AG04450	lung:	fetal
2	chr14:45930824-45930874	GM12891	blood:	n/a
3	chr14:45870299-45870349	RPTEC	kidney:	n/a
4	chr14:45870299-45870349	BE2_C	brain:	n/a
5	chr14:45840127-45840177	GM12892	blood:	n/a
6	chr14:45870299-45870349	HCM	heart:	n/a
7	chr14:45840127-45840177	RPTEC	kidney:	n/a
8	chr14:45840127-45840177	IMR90	lung:	fetal
9	chr14:45930824-45930874	NHBE	bronchial:	n/a
10	chr14:45930824-45930874	LNCaP	prostate:	n/a
11	chr14:45840127-45840177	GM12878	blood:	n/a
12	chr14:45870299-45870349	SKMC	muscle:	n/a
13	chr14:45870299-45870349	HRE	kidney:	n/a
14	chr14:45870299-45870349	HPAEpiC	pulmonary alveolar:	n/a
15	chr14:45840127-45840177	HRCEpiC	kidney:	n/a
16	chr14:45870299-45870349	PrEC	prostate:	n/a
17	chr14:45870299-45870349	GM19239	blood:	n/a
18	chr14:45840127-45840177	AG09309	skin:	n/a
19	chr14:45870299-45870349	HepG2	liver:	n/a
20	chr14:45870299-45870349	K562	blood:	n/a
21	chr14:45930824-45930874	PANC-1	pancreas:	n/a
22	chr14:45840127-45840177	HCM	heart:	n/a
23	chr14:45840127-45840177	SAEC	small airway:	n/a
24	chr14:45930824-45930874	HEEpiC	esophagus:	n/a
25	chr14:45870299-45870349	AG09309	skin:	n/a
26	chr14:45930824-45930874	HL-60	blood:	n/a
27	chr14:45930824-45930874	A549	lung:	n/a
28	chr14:45930824-45930874	HRCEpiC	kidney:	n/a
29	chr14:45870299-45870349	HCPEpiC	choroid plexus:	n/a
30	chr14:45840127-45840177	Caco-2	colon:	n/a
31	chr14:45870299-45870349	AG09319	gingival:	n/a
32	chr14:45840127-45840177	HCPEpiC	choroid plexus:	n/a
33	chr14:45870299-45870349	T-47D	breast:	n/a
34	chr14:45840127-45840177	HCF	heart:	n/a
35	chr14:45870299-45870349	HAEpiC	amniotic membrane:	n/a
36	chr14:45930824-45930874	NHDF-neo	bronchial:	n/a
37	chr14:45870299-45870349	NB4	blood:	n/a
38	chr14:45870299-45870349	SK-N-SH	brain:	n/a
39	chr14:45930824-45930874	AG09319	gingival:	n/a
40	chr14:45930824-45930874	GM12878	blood:	n/a
41	chr14:45930824-45930874	MCF-7	breast:	n/a
42	chr14:45870299-45870349	H1-hESC	embryonic stem cell:	embryo
43	chr14:45840127-45840177	GM06990	blood:	n/a
44	chr14:45840127-45840177	Hepatocyte	liver:	n/a
45	chr14:45870299-45870349	BJ	skin:	n/a
46	chr14:45870299-45870349	HRPEpiC	eye:	n/a
47	chr14:45930824-45930874	HepG2	liver:	n/a
48	chr14:45840127-45840177	HepG2	liver:	n/a
49	chr14:45870299-45870349	ovcar-3	ovarian:	n/a
50	chr14:45930824-45930874	HIPEpiC	eye:	n/a

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

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

Extended variants
information (count: 2775 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2775 , 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	rs74737269	chr14:45830421-45830422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs568514438	chr14:45830497-45830498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145961591	chr14:45830524-45830525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561970541	chr14:45830528-45830529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs17116033	chr14:45830623-45830624	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs139875505	chr14:45830670-45830671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149661881	chr14:45830690-45830691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533637544	chr14:45830714-45830715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557643082	chr14:45830722-45830723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552015610	chr14:45830745-45830746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563855934	chr14:45830867-45830868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185346506	chr14:45830876-45830877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568648097	chr14:45830914-45830915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370167997	chr14:45830938-45830939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540134936	chr14:45830939-45830940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553977836	chr14:45830997-45830998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145474505	chr14:45831020-45831021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs77331805	chr14:45831061-45831062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546233695	chr14:45831099-45831100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571230437	chr14:45831103-45831104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs116120918	chr14:45831109-45831110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148584593	chr14:45831127-45831128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188471498	chr14:45831132-45831133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192727818	chr14:45831192-45831193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117182511	chr14:45831244-45831245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs184742902	chr14:45831246-45831247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541435461	chr14:45831343-45831344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs142995731	chr14:45831344-45831345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs188369738	chr14:45831380-45831381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs151118842	chr14:45831462-45831463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs112163699	chr14:45831464-45831465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531123398	chr14:45831465-45831466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549271766	chr14:45831488-45831489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76043976	chr14:45831500-45831501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528147545	chr14:45831538-45831539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs146817234	chr14:45832218-45832219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553432149	chr14:45832231-45832232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs578066564	chr14:45832245-45832246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116930329	chr14:45832278-45832279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534264950	chr14:45832286-45832287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs367715645	chr14:45832306-45832307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147894265	chr14:45832311-45832312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546284180	chr14:45832326-45832327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7151665	chr14:45832343-45832344	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs539982201	chr14:45833208-45833209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570547368	chr14:45833238-45833239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191707492	chr14:45833246-45833247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181361534	chr14:45833265-45833266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs575417649	chr14:45833344-45833345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543818070	chr14:45833394-45833395	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:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:45830400-45831600	Enhancers	Fetal Heart	heart
2	chr14:45832200-45832400	Enhancers	Right Atrium	heart
3	chr14:45833200-45834200	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr14:45833800-45834400	Enhancers	Adipose Nuclei	Adipose
5	chr14:45833800-45834600	Enhancers	Right Atrium	heart
6	chr14:45837000-45837200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:45837200-45839800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr14:45837400-45841600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr14:45837600-45837800	Enhancers	H9 Cell Line	embryonic stem cell
10	chr14:45837800-45838000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr14:45837800-45838600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr14:45838000-45839000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr14:45838600-45838800	Enhancers	H9 Cell Line	embryonic stem cell
14	chr14:45839000-45840400	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr14:45839400-45840400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr14:45839600-45840200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr14:45839600-45840400	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr14:45839600-45840600	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr14:45839800-45840600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr14:45839800-45840800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr14:45840000-45840400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr14:45840000-45840600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr14:45840200-45843200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr14:45840400-45842800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr14:45840400-45843000	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr14:45840400-45843000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr14:45840400-45843200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr14:45840600-45842800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr14:45840600-45843000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr14:45840800-45843000	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr14:45841600-45841800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr14:45841800-45843000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr14:45842800-45843400	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr14:45842800-45843600	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr14:45843000-45843400	Enhancers	H1 Cell Line	embryonic stem cell
36	chr14:45843000-45843400	Enhancers	H9 Cell Line	embryonic stem cell
37	chr14:45843000-45843400	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr14:45843000-45843400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr14:45843000-45843400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr14:45843000-45843600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr14:45843000-45843800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr14:45843200-45843400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr14:45843200-45843600	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr14:45843200-45843600	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr14:45843600-45847600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr14:45857400-45858200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr14:45858200-45860200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr14:45860200-45863000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr14:45861400-45861600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr14:45861600-45862000	ZNF genes & repeats	Spleen	Spleen

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