Variant report

Variant	nsv510642
Chromosome Location	chr14:69983293-70030335
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:776)
CpG islands
(count:610)
Chromatin interactive
region (count:23)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:776 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr14:70019989-70020328	K562	blood:	n/a	n/a
2	ATF2	chr14:70007363-70007761	GM12878	blood:	n/a	n/a
3	ATF2	chr14:70007419-70007748	GM12878	blood:	n/a	n/a
4	ATF3	chr14:70010276-70010782	HCT-116	colon:	n/a	n/a
5	ATF3	chr14:70010362-70010635	K562	blood:	n/a	n/a
6	ATF3	chr14:70020038-70020258	K562	blood:	n/a	n/a
7	ATF3	chr14:70010254-70010775	HCT-116	colon:	n/a	n/a
8	BACH1	chr14:70014404-70015035	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr14:70007397-70007706	GM12878	blood:	n/a	chr14:70007577-70007588
10	BATF	chr14:70007437-70007694	GM12878	blood:	n/a	chr14:70007577-70007588
11	BATF	chr14:70010442-70010629	GM12878	blood:	n/a	n/a
12	BCL11A	chr14:70007356-70007657	GM12878	blood:	n/a	n/a
13	BHLHE40	chr14:70014924-70015018	K562	blood:	n/a	n/a
14	BRCA1	chr14:70010411-70010773	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr14:70014866-70015132	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr14:69996347-69996513	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:70019968-70020260	K562	blood:	n/a	n/a
18	CEBPB	chr14:70006704-70007094	IMR90	lung:	n/a	n/a
19	CEBPB	chr14:70010232-70010796	MCF-7	breast:	n/a	chr14:70010531-70010542
20	CEBPB	chr14:69997428-69997514	A549	lung:	n/a	n/a
21	CEBPB	chr14:70006857-70006894	K562	blood:	n/a	n/a
22	CEBPB	chr14:70019884-70020266	A549	lung:	n/a	n/a
23	CEBPB	chr14:70019934-70020271	A549	lung:	n/a	n/a
24	CEBPB	chr14:69997339-69997516	IMR90	lung:	n/a	n/a
25	CEBPB	chr14:70010318-70010770	Hela-S3	cervix:	n/a	chr14:70010531-70010542
26	CEBPB	chr14:70019969-70020301	K562	blood:	n/a	n/a
27	CEBPB	chr14:70006766-70007167	A549	lung:	n/a	n/a
28	CEBPB	chr14:70006778-70006958	A549	lung:	n/a	n/a
29	CEBPB	chr14:70010294-70010728	A549	lung:	n/a	chr14:70010531-70010542
30	CEBPB	chr14:70010205-70010895	HCT-116	colon:	n/a	chr14:70010531-70010542
31	CEBPB	chr14:70010361-70010711	K562	blood:	n/a	chr14:70010531-70010542
32	CEBPB	chr14:70019956-70020295	IMR90	lung:	n/a	n/a
33	CEBPB	chr14:70010332-70010697	ECC-1	luminal epithelium:	n/a	chr14:70010531-70010542
34	CEBPB	chr14:70010283-70010765	A549	lung:	n/a	chr14:70010531-70010542
35	CEBPB	chr14:70019942-70020321	A549	lung:	n/a	n/a
36	CEBPB	chr14:70010380-70010708	H1-hESC	embryonic stem cell:	n/a	chr14:70010531-70010542
37	CEBPB	chr14:70010276-70010882	HCT-116	colon:	n/a	chr14:70010531-70010542
38	CEBPB	chr14:70010356-70010720	HepG2	liver:	n/a	chr14:70010531-70010542
39	CEBPB	chr14:69996257-69996629	HepG2	liver:	n/a	n/a
40	CEBPB	chr14:70006708-70007044	A549	lung:	n/a	n/a
41	CEBPB	chr14:70006795-70007053	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr14:70010283-70010764	A549	lung:	n/a	chr14:70010531-70010542
43	CEBPB	chr14:70006902-70006908	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr14:70010374-70010710	K562	blood:	n/a	chr14:70010531-70010542
45	CEBPB	chr14:70019916-70020363	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr14:70006798-70006921	HepG2	liver:	n/a	n/a
47	CEBPB	chr14:70019927-70020361	MCF-7	breast:	n/a	n/a
48	CEBPB	chr14:70006691-70007160	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr14:70010369-70010761	ECC-1	luminal epithelium:	n/a	chr14:70010531-70010542
50	CEBPB	chr14:70006659-70007159	MCF-7	breast:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:70015473-70015523	A549	lung:	n/a
2	chr14:69995178-69995228	MCF-7	breast:	n/a
3	chr14:70014548-70014598	HCF	heart:	n/a
4	chr14:70010567-70010617	GM19239	blood:	n/a
5	chr14:70014873-70014923	NB4	blood:	n/a
6	chr14:70014548-70014598	HUVEC	blood vessel:	n/a
7	chr14:70014974-70015024	AG10803	skin:	n/a
8	chr14:70013519-70013569	HAEpiC	amniotic membrane:	n/a
9	chr14:70014974-70015024	BE2_C	brain:	n/a
10	chr14:70013519-70013569	Hela-S3	cervix:	n/a
11	chr14:69986021-69986071	ECC-1	luminal epithelium:	n/a
12	chr14:70014715-70014765	GM06990	blood:	n/a
13	chr14:70010567-70010617	HAEpiC	amniotic membrane:	n/a
14	chr14:70010567-70010617	SKMC	muscle:	n/a
15	chr14:70017574-70017624	BJ	skin:	n/a
16	chr14:69995178-69995228	NH-A	brain:	n/a
17	chr14:70010567-70010617	AG10803	skin:	n/a
18	chr14:70014873-70014923	GM12892	blood:	n/a
19	chr14:70013519-70013569	BE2_C	brain:	n/a
20	chr14:70014873-70014923	AG04450	lung:	fetal
21	chr14:70014974-70015024	LNCaP	prostate:	n/a
22	chr14:70017574-70017624	K562	blood:	n/a
23	chr14:70017574-70017624	A549	lung:	n/a
24	chr14:69995178-69995228	AG10803	skin:	n/a
25	chr14:70013519-70013569	A549	lung:	n/a
26	chr14:70013519-70013569	HCF	heart:	n/a
27	chr14:70010567-70010617	H1-hESC	embryonic stem cell:	embryo
28	chr14:70014715-70014765	GM12878	blood:	n/a
29	chr14:70017574-70017624	U87	brain:	n/a
30	chr14:70010567-70010617	PFSK-1	brain:	n/a
31	chr14:70014974-70015024	MCF10A-Er-Src	breast:	n/a
32	chr14:70017574-70017624	HIPEpiC	eye:	n/a
33	chr14:70015473-70015523	NB4	blood:	n/a
34	chr14:69986021-69986071	Jurkat	blood:	n/a
35	chr14:69986021-69986071	HUVEC	blood vessel:	n/a
36	chr14:70010567-70010617	HCF	heart:	n/a
37	chr14:70015473-70015523	NT2-D1	testis:	n/a
38	chr14:70014974-70015024	ProgFib	skin:	n/a
39	chr14:69986021-69986071	H1-hESC	embryonic stem cell:	embryo
40	chr14:70015473-70015523	HAEpiC	amniotic membrane:	n/a
41	chr14:70010567-70010617	T-47D	breast:	n/a
42	chr14:70014548-70014598	SAEC	small airway:	n/a
43	chr14:70017574-70017624	NHBE	bronchial:	n/a
44	chr14:70017574-70017624	GM06990	blood:	n/a
45	chr14:70014548-70014598	PANC-1	pancreas:	n/a
46	chr14:70015473-70015523	PrEC	prostate:	n/a
47	chr14:69995178-69995228	NHDF-neo	bronchial:	n/a
48	chr14:70015473-70015523	K562	blood:	n/a
49	chr14:70010567-70010617	BE2_C	brain:	n/a
50	chr14:70014548-70014598	K562	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:69979995..69982443-chr14:69986701..69988588,2	MCF-7	breast:
2	chr14:69989183..69991893-chr14:70006349..70008257,2	MCF-7	breast:
3	chr14:69987420..69989705-chr14:69990371..69993160,2	MCF-7	breast:
4	chr14:70001699..70002644-chr14:70040741..70042019,6	MCF-7	breast:
5	chr14:70019966..70021611-chr14:70026583..70029344,2	K562	blood:
6	chr14:69987420..69989705-chr14:69990371..69993160,2	MCF-7	breast:
7	chr14:70002103..70002603-chr14:70041525..70042102,2	K562	blood:
8	chr14:70009624..70012138-chr14:70013181..70015316,2	K562	blood:
9	chr14:69989183..69991893-chr14:70006349..70008257,2	MCF-7	breast:
10	chr14:70009624..70012138-chr14:70013181..70015316,2	K562	blood:
11	chr14:70001746..70002559-chr14:70051373..70051892,2	MCF-7	breast:
12	chr14:70017252..70019408-chr14:70020667..70022465,2	MCF-7	breast:
13	chr14:70013357..70015397-chr14:70020516..70022458,2	K562	blood:
14	chr14:70014454..70015116-chr14:70193405..70194292,6	K562	blood:
15	chr14:70000714..70002427-chr14:70038896..70041033,2	MCF-7	breast:
16	chr14:69970253..69971296-chr14:70001641..70002581,3	MCF-7	breast:
17	chr14:70017252..70019408-chr14:70020667..70022465,2	MCF-7	breast:
18	chr14:70001853..70002635-chr14:70034399..70035068,2	MCF-7	breast:
19	chr14:69993102..69995388-chr14:70040159..70042492,2	K562	blood:
20	chr14:70001801..70002678-chr14:70039788..70040731,3	MCF-7	breast:
21	chr14:70001892..70002546-chr14:70046761..70047295,2	MCF-7	breast:
22	chr14:70001682..70002652-chr14:70041139..70042080,9	MCF-7	breast:
23	chr14:70013357..70015397-chr14:70020516..70022458,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf162-4	chr14:70014555-70014755	NONHSAT037529
2	lnc-C14orf162-4	chr14:70007326-70007396	NONHSAT037529
3	lnc-C14orf162-2	chr14:70027736-70028187	NONHSAT037530

No data

Variant related genes	Relation type
ENSG00000244237	TF binding region
ENSG00000244237	CpG island
ENSG00000244237	chromatin interactions
ENSG00000100650	chromatin interactions
ENSG00000267909	chromatin interactions

Extended variants
information (count: 1614 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1614 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565885501	chr14:69983299-69983300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs539502365	chr14:69983300-69983301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184892806	chr14:69983342-69983343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs73281438	chr14:69983357-69983358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189873920	chr14:69983384-69983385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555100798	chr14:69983387-69983388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs61982437	chr14:69983403-69983404	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs541346273	chr14:69983433-69983434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564353307	chr14:69983464-69983465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559471804	chr14:69983465-69983466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557781556	chr14:69983466-69983467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182473930	chr14:69983471-69983472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112674279	chr14:69983483-69983484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563800084	chr14:69983514-69983515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187107812	chr14:69983529-69983530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549325396	chr14:69983603-69983604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561148791	chr14:69983625-69983626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529156697	chr14:69983630-69983631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138672140	chr14:69983631-69983632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75010449	chr14:69983701-69983702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539643456	chr14:69983721-69983722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374463773	chr14:69983734-69983735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551632810	chr14:69983781-69983782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559956470	chr14:69983862-69983863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569720387	chr14:69983870-69983871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191765331	chr14:69983909-69983910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529005498	chr14:69983913-69983914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs4902725	chr14:69983990-69983991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
29	rs561986032	chr14:69984015-69984016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs142986548	chr14:69984132-69984133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147449322	chr14:69984142-69984143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35784195	chr14:69984198-69984199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139885565	chr14:69984218-69984219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370286604	chr14:69984227-69984228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78769787	chr14:69984247-69984248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374624861	chr14:69984248-69984249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545175106	chr14:69984307-69984308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368726182	chr14:69984342-69984343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145404423	chr14:69984425-69984426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368487659	chr14:69984439-69984440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs35668583	chr14:69984471-69984472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147272870	chr14:69984493-69984494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs116936985	chr14:69984548-69984549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs148769429	chr14:69984559-69984560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs2756966	chr14:69984560-69984561	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs528487352	chr14:69984564-69984565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs527439017	chr14:69984599-69984600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs547064764	chr14:69984631-69984632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552127201	chr14:69984635-69984636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs183293968	chr14:69984653-69984654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
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
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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:447 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69982800-69985200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:69983800-69984400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr14:69984000-69984200	Enhancers	H1 Cell Line	embryonic stem cell
4	chr14:69984000-69984200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr14:69984000-69984400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr14:69984000-69984400	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr14:69984000-69984400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr14:69984200-69984400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr14:69984200-69984600	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr14:69984200-69985200	Enhancers	Fetal Thymus	thymus
11	chr14:69984200-69985600	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr14:69984400-69984600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr14:69984400-69985200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr14:69984400-69985400	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr14:69984400-69985600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr14:69984400-69985600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr14:69984400-69986000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr14:69984600-69985400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr14:69985000-69986400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr14:69985000-69986800	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr14:69985200-69985600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr14:69985200-69986400	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr14:69985400-69985800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
24	chr14:69985400-69985800	Bivalent Enhancer	Fetal Thymus	thymus
25	chr14:69985400-69986000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr14:69985400-69986200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr14:69985400-69986400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr14:69985400-69986400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr14:69985400-69986400	Enhancers	Fetal Muscle Leg	muscle
30	chr14:69985400-69986600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr14:69985400-69986600	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr14:69985400-69986800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr14:69985600-69986000	Enhancers	H1 Cell Line	embryonic stem cell
34	chr14:69985600-69986200	Enhancers	Esophagus	oesophagus
35	chr14:69985600-69986400	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr14:69985600-69986600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr14:69985600-69986800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr14:69986000-69986200	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr14:69986000-69986200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr14:69986000-69986800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr14:69986000-69986800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr14:69986200-69986400	Bivalent Enhancer	HSMM	muscle
43	chr14:69986200-69986600	Enhancers	H1 Cell Line	embryonic stem cell
44	chr14:69986800-69987600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr14:69986800-69988000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr14:69987400-69987800	Enhancers	Lung	lung
47	chr14:69987600-69987800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr14:69988200-69988400	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr14:69990600-69991600	Enhancers	Fetal Thymus	thymus
50	chr14:69991200-69991800	Enhancers	Stomach Mucosa	stomach

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