Variant report

Variant	nsv1334
Chromosome Location	chr14:70002365-70032641
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:535)
CpG islands
(count:488)
Chromatin interactive
region (count:21)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:535 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	chr14:70007419-70007748	GM12878	blood:	n/a	n/a
3	ATF2	chr14:70007363-70007761	GM12878	blood:	n/a	n/a
4	ATF3	chr14:70020038-70020258	K562	blood:	n/a	n/a
5	ATF3	chr14:70010276-70010782	HCT-116	colon:	n/a	n/a
6	ATF3	chr14:70010362-70010635	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	chr14:70010442-70010629	GM12878	blood:	n/a	n/a
10	BATF	chr14:70007397-70007706	GM12878	blood:	n/a	chr14:70007577-70007588
11	BATF	chr14:70007437-70007694	GM12878	blood:	n/a	chr14:70007577-70007588
12	BCL11A	chr14:70007356-70007657	GM12878	blood:	n/a	n/a
13	BHLHE40	chr14:70014924-70015018	K562	blood:	n/a	n/a
14	BRCA1	chr14:70014866-70015132	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr14:70010411-70010773	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr14:70010457-70010623	HepG2	liver:	n/a	chr14:70010531-70010542
17	CEBPB	chr14:70006798-70006921	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:70010361-70010711	K562	blood:	n/a	chr14:70010531-70010542
19	CEBPB	chr14:70006857-70006894	K562	blood:	n/a	n/a
20	CEBPB	chr14:70019916-70020363	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr14:70019968-70020260	K562	blood:	n/a	n/a
22	CEBPB	chr14:70006704-70007094	IMR90	lung:	n/a	n/a
23	CEBPB	chr14:70010283-70010765	A549	lung:	n/a	chr14:70010531-70010542
24	CEBPB	chr14:70010294-70010728	A549	lung:	n/a	chr14:70010531-70010542
25	CEBPB	chr14:70006778-70006958	A549	lung:	n/a	n/a
26	CEBPB	chr14:70010205-70010895	HCT-116	colon:	n/a	chr14:70010531-70010542
27	CEBPB	chr14:70010232-70010796	MCF-7	breast:	n/a	chr14:70010531-70010542
28	CEBPB	chr14:70010318-70010770	Hela-S3	cervix:	n/a	chr14:70010531-70010542
29	CEBPB	chr14:70019942-70020321	A549	lung:	n/a	n/a
30	CEBPB	chr14:70010380-70010708	H1-hESC	embryonic stem cell:	n/a	chr14:70010531-70010542
31	CEBPB	chr14:70019884-70020266	A549	lung:	n/a	n/a
32	CEBPB	chr14:70019956-70020295	IMR90	lung:	n/a	n/a
33	CEBPB	chr14:70010283-70010764	A549	lung:	n/a	chr14:70010531-70010542
34	CEBPB	chr14:70006766-70007167	A549	lung:	n/a	n/a
35	CEBPB	chr14:70006659-70007159	MCF-7	breast:	n/a	n/a
36	CEBPB	chr14:70010374-70010710	K562	blood:	n/a	chr14:70010531-70010542
37	CEBPB	chr14:70006691-70007160	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr14:70006795-70007053	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr14:70010332-70010697	ECC-1	luminal epithelium:	n/a	chr14:70010531-70010542
40	CEBPB	chr14:70019969-70020301	K562	blood:	n/a	n/a
41	CEBPB	chr14:70019934-70020271	A549	lung:	n/a	n/a
42	CEBPB	chr14:70010343-70010737	IMR90	lung:	n/a	chr14:70010531-70010542
43	CEBPB	chr14:70010448-70010632	K562	blood:	n/a	chr14:70010531-70010542
44	CEBPB	chr14:70010276-70010882	HCT-116	colon:	n/a	chr14:70010531-70010542
45	CEBPB	chr14:70019927-70020361	MCF-7	breast:	n/a	n/a
46	CEBPB	chr14:70010366-70010713	HepG2	liver:	n/a	chr14:70010531-70010542
47	CEBPB	chr14:70010369-70010761	ECC-1	luminal epithelium:	n/a	chr14:70010531-70010542
48	CEBPB	chr14:70010356-70010720	HepG2	liver:	n/a	chr14:70010531-70010542
49	CEBPB	chr14:70006902-70006908	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr14:70010304-70010760	MCF-7	breast:	n/a	chr14:70010531-70010542

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:70017574-70017624	SAEC	small airway:	n/a
2	chr14:70010567-70010617	K562	blood:	n/a
3	chr14:70014715-70014765	AG04449	skin:	fetal
4	chr14:70014974-70015024	GM19239	blood:	n/a
5	chr14:70010567-70010617	HEEpiC	esophagus:	n/a
6	chr14:70017574-70017624	NB4	blood:	n/a
7	chr14:70017574-70017624	U87	brain:	n/a
8	chr14:70010567-70010617	ProgFib	skin:	n/a
9	chr14:70014548-70014598	U87	brain:	n/a
10	chr14:70015473-70015523	AG04450	lung:	fetal
11	chr14:70013519-70013569	HPAEpiC	pulmonary alveolar:	n/a
12	chr14:70014873-70014923	ProgFib	skin:	n/a
13	chr14:70015473-70015523	K562	blood:	n/a
14	chr14:70013519-70013569	H1-hESC	embryonic stem cell:	embryo
15	chr14:70013519-70013569	K562	blood:	n/a
16	chr14:70014548-70014598	NHDF-neo	bronchial:	n/a
17	chr14:70014548-70014598	HRCEpiC	kidney:	n/a
18	chr14:70013519-70013569	Jurkat	blood:	n/a
19	chr14:70014974-70015024	BJ	skin:	n/a
20	chr14:70014974-70015024	AG04450	lung:	fetal
21	chr14:70013519-70013569	NB4	blood:	n/a
22	chr14:70013519-70013569	GM12892	blood:	n/a
23	chr14:70013519-70013569	ECC-1	luminal epithelium:	n/a
24	chr14:70010567-70010617	ECC-1	luminal epithelium:	n/a
25	chr14:70010567-70010617	NHBE	bronchial:	n/a
26	chr14:70010567-70010617	HAEpiC	amniotic membrane:	n/a
27	chr14:70010567-70010617	BJ	skin:	n/a
28	chr14:70014715-70014765	HIPEpiC	eye:	n/a
29	chr14:70015473-70015523	AG04449	skin:	fetal
30	chr14:70014974-70015024	HCM	heart:	n/a
31	chr14:70013519-70013569	MCF-7	breast:	n/a
32	chr14:70014715-70014765	NH-A	brain:	n/a
33	chr14:70015473-70015523	GM12891	blood:	n/a
34	chr14:70014715-70014765	K562	blood:	n/a
35	chr14:70017574-70017624	SK-N-MC	brain:	n/a
36	chr14:70014974-70015024	HIPEpiC	eye:	n/a
37	chr14:70014974-70015024	K562	blood:	n/a
38	chr14:70014548-70014598	LNCaP	prostate:	n/a
39	chr14:70017574-70017624	BE2_C	brain:	n/a
40	chr14:70014548-70014598	ovcar-3	ovarian:	n/a
41	chr14:70014974-70015024	HCPEpiC	choroid plexus:	n/a
42	chr14:70014715-70014765	SKMC	muscle:	n/a
43	chr14:70014715-70014765	AG09309	skin:	n/a
44	chr14:70013519-70013569	PrEC	prostate:	n/a
45	chr14:70015473-70015523	HRE	kidney:	n/a
46	chr14:70017574-70017624	HUVEC	blood vessel:	n/a
47	chr14:70014974-70015024	SKMC	muscle:	n/a
48	chr14:70014873-70014923	HPAEpiC	pulmonary alveolar:	n/a
49	chr14:70014873-70014923	ECC-1	luminal epithelium:	n/a
50	chr14:70014974-70015024	HUVEC	blood vessel:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:69970253..69971296-chr14:70001641..70002581,3	MCF-7	breast:
2	chr14:70001699..70002644-chr14:70040741..70042019,6	MCF-7	breast:
3	chr14:70002103..70002603-chr14:70041525..70042102,2	K562	blood:
4	chr14:70009624..70012138-chr14:70013181..70015316,2	K562	blood:
5	chr14:70030912..70032771-chr14:70037845..70040313,2	K562	blood:
6	chr14:70017252..70019408-chr14:70020667..70022465,2	MCF-7	breast:
7	chr14:70009624..70012138-chr14:70013181..70015316,2	K562	blood:
8	chr14:70013357..70015397-chr14:70020516..70022458,2	K562	blood:
9	chr14:70001801..70002678-chr14:70039788..70040731,3	MCF-7	breast:
10	chr14:70013357..70015397-chr14:70020516..70022458,2	K562	blood:
11	chr14:70001853..70002635-chr14:70034399..70035068,2	MCF-7	breast:
12	chr14:69989183..69991893-chr14:70006349..70008257,2	MCF-7	breast:
13	chr14:70001746..70002559-chr14:70051373..70051892,2	MCF-7	breast:
14	chr14:70001682..70002652-chr14:70041139..70042080,9	MCF-7	breast:
15	chr14:70014454..70015116-chr14:70193405..70194292,6	K562	blood:
16	chr14:70017252..70019408-chr14:70020667..70022465,2	MCF-7	breast:
17	chr14:70030422..70032723-chr14:70038343..70040590,3	MCF-7	breast:
18	chr14:70001892..70002546-chr14:70046761..70047295,2	MCF-7	breast:
19	chr14:70031632..70033934-chr14:70036224..70037978,2	MCF-7	breast:
20	chr14:70000714..70002427-chr14:70038896..70041033,2	MCF-7	breast:
21	chr14:70019966..70021611-chr14:70026583..70029344,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLEKHD1-2	chr14:70031849-70032228	NONHSAT037531
2	lnc-C14orf162-4	chr14:70014555-70014755	NONHSAT037529
3	lnc-C14orf162-4	chr14:70007326-70007396	NONHSAT037529
4	lnc-C14orf162-2	chr14:70027736-70028187	NONHSAT037530

No data

Variant related genes	Relation type
ENSG00000244237	TF binding region
ENSG00000244237	CpG island
ENSG00000255994	chromatin interactions
ENSG00000267909	chromatin interactions
ENSG00000244237	chromatin interactions
ENSG00000100650	chromatin interactions

Extended variants
information (count: 1107 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1107 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539235344	chr14:70002390-70002391	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs545957496	chr14:70002425-70002426	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs557929926	chr14:70002443-70002444	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs146538048	chr14:70002474-70002475	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs189192245	chr14:70002485-70002486	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs538627067	chr14:70002521-70002522	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs554397797	chr14:70002532-70002533	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs562256687	chr14:70002627-70002628	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs567906274	chr14:70002700-70002701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529249030	chr14:70002748-70002749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370999342	chr14:70002801-70002802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541448103	chr14:70002842-70002843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374139235	chr14:70002894-70002895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527607241	chr14:70002952-70002953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141218594	chr14:70002955-70002956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570669940	chr14:70002969-70002970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145051664	chr14:70002984-70002985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575595792	chr14:70002992-70002993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556861188	chr14:70003046-70003047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568177912	chr14:70003053-70003054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535091577	chr14:70003071-70003072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553747559	chr14:70003112-70003113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116689719	chr14:70003144-70003145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114436408	chr14:70003185-70003186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558068504	chr14:70003225-70003226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11623783	chr14:70003265-70003266	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs181271331	chr14:70003391-70003392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370595136	chr14:70003472-70003473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77970607	chr14:70003480-70003481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549983392	chr14:70003501-70003502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541040146	chr14:70003513-70003514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372030609	chr14:70003550-70003551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374957978	chr14:70003552-70003553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572947658	chr14:70003559-70003560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185860808	chr14:70003566-70003567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188984386	chr14:70003648-70003649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs36059242	chr14:70003678-70003679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540064824	chr14:70003704-70003705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs531515085	chr14:70003706-70003707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181512551	chr14:70003793-70003794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565368653	chr14:70003808-70003809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561596047	chr14:70003828-70003829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs8017561	chr14:70003884-70003885	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs186810256	chr14:70003926-70003927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs375560581	chr14:70003986-70003987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs565658647	chr14:70004023-70004024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs192119495	chr14:70004083-70004084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs371739023	chr14:70004093-70004094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551637024	chr14:70004241-70004242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs183878949	chr14:70004252-70004253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Breast cancer	22522925	CNVD

Chromatin state (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70000400-70003200	Weak transcription	Esophagus	oesophagus
2	chr14:70001800-70002400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr14:70001800-70002600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr14:70002000-70002400	Enhancers	Stomach Mucosa	stomach
5	chr14:70002200-70002400	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr14:70002200-70002400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr14:70002200-70002400	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
8	chr14:70002200-70002400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr14:70002200-70002400	Enhancers	Brain Anterior Caudate	brain
10	chr14:70002200-70002400	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr14:70002200-70002400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
12	chr14:70002200-70002400	Bivalent Enhancer	HUVEC	blood vessel
13	chr14:70002200-70002400	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr14:70002200-70002400	Bivalent Enhancer	Osteobl	bone
15	chr14:70002200-70002600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr14:70002200-70002600	Enhancers	Hela-S3	cervix
17	chr14:70002400-70003600	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr14:70002400-70004200	Weak transcription	Stomach Mucosa	stomach
19	chr14:70002400-70007000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr14:70002400-70014600	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr14:70002600-70003800	Weak transcription	Hela-S3	cervix
22	chr14:70002600-70006200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr14:70003600-70003800	Enhancers	Placenta	Placenta
24	chr14:70003600-70004600	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr14:70003600-70005400	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr14:70003800-70005600	Enhancers	Hela-S3	cervix
27	chr14:70004200-70004400	Enhancers	Stomach Mucosa	stomach
28	chr14:70004400-70004600	Enhancers	Esophagus	oesophagus
29	chr14:70004400-70004800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr14:70004400-70004800	Weak transcription	Stomach Mucosa	stomach
31	chr14:70004600-70005200	Weak transcription	Placenta	Placenta
32	chr14:70004600-70006200	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr14:70004800-70005200	Enhancers	Stomach Mucosa	stomach
34	chr14:70004800-70010000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr14:70005600-70007000	Weak transcription	Hela-S3	cervix
36	chr14:70006200-70006800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr14:70006200-70006800	ZNF genes & repeats	Placenta	Placenta
38	chr14:70006200-70008200	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr14:70006800-70007000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr14:70006800-70007000	Weak transcription	Placenta	Placenta
41	chr14:70007000-70007200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr14:70007000-70007200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr14:70007000-70007200	Enhancers	NHEK	skin
44	chr14:70007000-70007600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr14:70007000-70007600	Enhancers	Brain Anterior Caudate	brain
46	chr14:70007000-70007600	Enhancers	Placenta	Placenta
47	chr14:70007000-70008000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr14:70007000-70008000	Enhancers	Hela-S3	cervix
49	chr14:70007000-70008200	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr14:70007000-70008200	Enhancers	Adipose Nuclei	Adipose

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