Variant report

Variant	nsv542082
Chromosome Location	chr14:45831717-46035912
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	chr14:45990474-45990674	IMR90	lung:	n/a	chr14:45990587-45990604
2	CEBPB	chr14:46000477-46000804	HepG2	liver:	n/a	chr14:46000620-46000631
3	CEBPB	chr14:46031267-46031422	MCF-7	breast:	n/a	chr14:46031347-46031358
4	CEBPB	chr14:45902361-45902662	IMR90	lung:	n/a	n/a
5	CEBPB	chr14:45893200-45893264	A549	lung:	n/a	n/a
6	CEBPB	chr14:46031190-46031458	HepG2	liver:	n/a	chr14:46031347-46031358
7	CEBPB	chr14:45902380-45902544	A549	lung:	n/a	n/a
8	CEBPB	chr14:45902392-45902559	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr14:45996268-45996394	Hela-S3	cervix:	n/a	n/a
10	CHD2	chr14:46020613-46020614	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr14:46020280-46020430	HEEpiC	esophagus:	n/a	n/a
12	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
13	CTCF	chr14:45996600-45996750	SK-N-SH_RA	brain:	n/a	n/a
14	CTCF	chr14:45895949-45896168	Kidney_OC	kidney:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
15	CTCF	chr14:45996640-45996790	HMF	breast:	n/a	n/a
16	CTCF	chr14:45996379-45996916	A549	lung:	n/a	n/a
17	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
18	CTCF	chr14:45868777-45868853	MCF-7	breast:	n/a	n/a
19	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
20	CTCF	chr14:45895960-45896110	GM12864	blood:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
21	CTCF	chr14:45833739-45833901	MCF-7	breast:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
22	CTCF	chr14:45996560-45996800	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr14:45996600-45996750	Caco-2	colon:	n/a	n/a
24	CTCF	chr14:45896000-45896150	AG09309	skin:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
25	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
26	CTCF	chr14:45996559-45996742	Fibrobl	skin:	n/a	n/a
27	CTCF	chr14:45895980-45896130	RPTEC	kidney:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
28	CTCF	chr14:45895960-45896110	NHDF-neo	bronchial:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
29	CTCF	chr14:45833722-45833865	HepG2	liver:	n/a	chr14:45833787-45833800 chr14:45833786-45833807 chr14:45833784-45833802
30	CTCF	chr14:45996590-45996792	GM10248	blood:	n/a	n/a
31	CTCF	chr14:45996600-45996750	NHEK	skin:	n/a	n/a
32	CTCF	chr14:45996600-45996750	GM12869	blood:	n/a	n/a
33	CTCF	chr14:45996580-45996730	GM12870	blood:	n/a	n/a
34	CTCF	chr14:45896020-45896170	GM12865	blood:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
35	CTCF	chr14:45996600-45996750	A549	lung:	n/a	n/a
36	CTCF	chr14:45917530-45917578	GM10248	blood:	n/a	n/a
37	CTCF	chr14:45896020-45896170	HMF	breast:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
38	CTCF	chr14:45996555-45996844	Medullo	brain:	n/a	n/a
39	CTCF	chr14:45996620-45996770	MCF-7	breast:	n/a	n/a
40	CTCF	chr14:45996580-45996730	GM12864	blood:	n/a	n/a
41	CTCF	chr14:46028980-46029073	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr14:45996517-45996803	Gliobla	brain:	n/a	n/a
43	CTCF	chr14:45996660-45996810	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr14:45996584-45996773	K562	blood:	n/a	n/a
45	CTCF	chr14:45895909-45896315	MCF-7	breast:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
46	CTCF	chr14:45895980-45896159	Lung_OC	lung:	n/a	chr14:45896070-45896091 chr14:45896071-45896084 chr14:45896072-45896079 chr14:45896068-45896086 chr14:45896069-45896085
47	CTCF	chr14:45996541-45996809	ECC-1	luminal epithelium:	n/a	n/a
48	CTCF	chr14:46029000-46029150	GM12866	blood:	n/a	n/a
49	CTCF	chr14:46028960-46029110	HepG2	liver:	n/a	n/a
50	CTCF	chr14:45996580-45996730	GM12865	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:45870299-45870349	SKMC	muscle:	n/a
2	chr14:45870299-45870349	PrEC	prostate:	n/a
3	chr14:45930824-45930874	A549	lung:	n/a
4	chr14:45930824-45930874	LNCaP	prostate:	n/a
5	chr14:45930824-45930874	HUVEC	blood vessel:	n/a
6	chr14:45930824-45930874	MCF-7	breast:	n/a
7	chr14:45930824-45930874	BE2_C	brain:	n/a
8	chr14:45870299-45870349	AG04450	lung:	fetal
9	chr14:45870299-45870349	SK-N-SH	brain:	n/a
10	chr14:45840127-45840177	ovcar-3	ovarian:	n/a
11	chr14:45840127-45840177	IMR90	lung:	fetal
12	chr14:45870299-45870349	HL-60	blood:	n/a
13	chr14:45840127-45840177	NHBE	bronchial:	n/a
14	chr14:45840127-45840177	U87	brain:	n/a
15	chr14:45930824-45930874	ECC-1	luminal epithelium:	n/a
16	chr14:45870299-45870349	HepG2	liver:	n/a
17	chr14:45840127-45840177	Hepatocyte	liver:	n/a
18	chr14:45930824-45930874	U87	brain:	n/a
19	chr14:45870299-45870349	Caco-2	colon:	n/a
20	chr14:45840127-45840177	HEK293	kidney:	embryo
21	chr14:45840127-45840177	BJ	skin:	n/a
22	chr14:45840127-45840177	AG10803	skin:	n/a
23	chr14:45870299-45870349	H1-hESC	embryonic stem cell:	embryo
24	chr14:45930824-45930874	Hepatocyte	liver:	n/a
25	chr14:45840127-45840177	AoSMC	blood vessel:	n/a
26	chr14:45870299-45870349	GM12878	blood:	n/a
27	chr14:45870299-45870349	GM12891	blood:	n/a
28	chr14:45870299-45870349	PFSK-1	brain:	n/a
29	chr14:45930824-45930874	BJ	skin:	n/a
30	chr14:45840127-45840177	ProgFib	skin:	n/a
31	chr14:45870299-45870349	NH-A	brain:	n/a
32	chr14:45930824-45930874	GM12878	blood:	n/a
33	chr14:45870299-45870349	IMR90	lung:	fetal
34	chr14:45840127-45840177	GM06990	blood:	n/a
35	chr14:45930824-45930874	AG04450	lung:	fetal
36	chr14:45840127-45840177	AG09309	skin:	n/a
37	chr14:45840127-45840177	NT2-D1	testis:	n/a
38	chr14:45870299-45870349	PANC-1	pancreas:	n/a
39	chr14:45930824-45930874	Caco-2	colon:	n/a
40	chr14:45840127-45840177	SAEC	small airway:	n/a
41	chr14:45930824-45930874	RPTEC	kidney:	n/a
42	chr14:45870299-45870349	AG10803	skin:	n/a
43	chr14:45930824-45930874	ovcar-3	ovarian:	n/a
44	chr14:45930824-45930874	GM12892	blood:	n/a
45	chr14:45870299-45870349	GM06990	blood:	n/a
46	chr14:45930824-45930874	CMK	blood:	n/a
47	chr14:45930824-45930874	MCF10A-Er-Src	breast:	n/a
48	chr14:45930824-45930874	ProgFib	skin:	n/a
49	chr14:45840127-45840177	GM12891	blood:	n/a
50	chr14:45870299-45870349	NHDF-neo	bronchial:	n/a

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

Variant related genes	Relation type
ENSG00000260046	TF binding region
ENSG00000258746	TF binding region
ENSG00000258845	TF binding region
ENSG00000257900	TF binding region
ENSG00000260046	CpG island
ENSG00000258746	CpG island
ENSG00000258845	CpG island
ENSG00000257900	CpG island
ENSG00000100442	chromatin interactions

Extended variants
information (count: 3014 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3014 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146817234	chr14:45832218-45832219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553432149	chr14:45832231-45832232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs578066564	chr14:45832245-45832246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116930329	chr14:45832278-45832279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534264950	chr14:45832286-45832287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs367715645	chr14:45832306-45832307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs147894265	chr14:45832311-45832312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs546284180	chr14:45832326-45832327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7151665	chr14:45832343-45832344	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs539982201	chr14:45833208-45833209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570547368	chr14:45833238-45833239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191707492	chr14:45833246-45833247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181361534	chr14:45833265-45833266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575417649	chr14:45833344-45833345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543818070	chr14:45833394-45833395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562326384	chr14:45833410-45833411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs72672963	chr14:45833483-45833484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs8019911	chr14:45833490-45833491	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs539466677	chr14:45833506-45833507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs202017788	chr14:45833542-45833543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200388132	chr14:45833543-45833544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs397736135	chr14:45833551-45833552	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs556356519	chr14:45833606-45833607	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs566698588	chr14:45833641-45833642	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs576485113	chr14:45833654-45833655	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs552356059	chr14:45833724-45833725	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs571792054	chr14:45833757-45833758	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs376704856	chr14:45833817-45833818	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs185573743	chr14:45833830-45833831	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs557359888	chr14:45833847-45833848	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs569138507	chr14:45833854-45833855	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs374501581	chr14:45833934-45833935	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs548689563	chr14:45833963-45833964	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs537002501	chr14:45833993-45833994	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs190035080	chr14:45834000-45834001	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs12880670	chr14:45834003-45834004	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs573161648	chr14:45834067-45834068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs112620571	chr14:45834071-45834072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558690886	chr14:45834099-45834100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576561363	chr14:45834102-45834103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs537529563	chr14:45834128-45834129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs149565579	chr14:45834136-45834137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143579532	chr14:45834138-45834139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs557358943	chr14:45834140-45834141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs17116036	chr14:45834141-45834142	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs541767803	chr14:45834188-45834189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182330447	chr14:45834267-45834268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77041371	chr14:45834269-45834270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs138148557	chr14:45834290-45834291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564258051	chr14:45834326-45834327	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:241 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:45832200-45832400	Enhancers	Right Atrium	heart
2	chr14:45833200-45834200	Enhancers	Skeletal Muscle Male	skeletal muscle
3	chr14:45833800-45834400	Enhancers	Adipose Nuclei	Adipose
4	chr14:45833800-45834600	Enhancers	Right Atrium	heart
5	chr14:45837000-45837200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr14:45837200-45839800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:45837400-45841600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr14:45837600-45837800	Enhancers	H9 Cell Line	embryonic stem cell
9	chr14:45837800-45838000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr14:45837800-45838600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr14:45838000-45839000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr14:45838600-45838800	Enhancers	H9 Cell Line	embryonic stem cell
13	chr14:45839000-45840400	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr14:45839400-45840400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr14:45839600-45840200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr14:45839600-45840400	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr14:45839600-45840600	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr14:45839800-45840600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr14:45839800-45840800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr14:45840000-45840400	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr14:45840000-45840600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr14:45840200-45843200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr14:45840400-45842800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr14:45840400-45843000	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr14:45840400-45843000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr14:45840400-45843200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr14:45840600-45842800	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr14:45840600-45843000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr14:45840800-45843000	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr14:45841600-45841800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr14:45841800-45843000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr14:45842800-45843400	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr14:45842800-45843600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr14:45843000-45843400	Enhancers	H1 Cell Line	embryonic stem cell
35	chr14:45843000-45843400	Enhancers	H9 Cell Line	embryonic stem cell
36	chr14:45843000-45843400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr14:45843000-45843400	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr14:45843000-45843400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr14:45843000-45843600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr14:45843000-45843800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr14:45843200-45843400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr14:45843200-45843600	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr14:45843200-45843600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr14:45843600-45847600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr14:45857400-45858200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr14:45858200-45860200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr14:45860200-45863000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr14:45861400-45861600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr14:45861600-45862000	ZNF genes & repeats	Spleen	Spleen
50	chr14:45862200-45870600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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