Variant report

Variant	nsv1041991
Chromosome Location	chr14:79394408-79644886
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1496)
CpG islands
(count:305)
Chromatin interactive
region (count:16)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1496 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:79451990-79452540	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr14:79451910-79452532	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr14:79557750-79558236	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr14:79557693-79558133	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr14:79560132-79560350	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr14:79452014-79452364	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr14:79557757-79558076	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr14:79452127-79452356	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr14:79557773-79558093	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr14:79435526-79435885	HepG2	liver:	n/a	n/a
11	BHLHE40	chr14:79435560-79435846	K562	blood:	n/a	n/a
12	BHLHE40	chr14:79435570-79435841	A549	lung:	n/a	n/a
13	BHLHE40	chr14:79435497-79435887	GM12878	blood:	n/a	n/a
14	CEBPB	chr14:79601619-79601724	IMR90	lung:	n/a	chr14:79601695-79601708
15	CEBPB	chr14:79404087-79404147	HepG2	liver:	n/a	chr14:79404123-79404136 chr14:79404123-79404134
16	CEBPB	chr14:79434764-79434893	H1-hESC	embryonic stem cell:	n/a	chr14:79434812-79434823
17	CEBPB	chr14:79435562-79436171	IMR90	lung:	n/a	n/a
18	CEBPB	chr14:79557714-79558287	H1-hESC	embryonic stem cell:	n/a	chr14:79558092-79558105 chr14:79558092-79558103
19	CEBPB	chr14:79435698-79435974	K562	blood:	n/a	n/a
20	CEBPB	chr14:79441011-79441431	IMR90	lung:	n/a	n/a
21	CEBPB	chr14:79559878-79560134	HepG2	liver:	n/a	chr14:79560020-79560031 chr14:79560018-79560031
22	CEBPB	chr14:79428090-79428296	HepG2	liver:	n/a	chr14:79428125-79428136
23	CEBPB	chr14:79497978-79498031	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr14:79481452-79481758	HepG2	liver:	n/a	chr14:79481587-79481598
25	CEBPB	chr14:79434652-79434982	HepG2	liver:	n/a	chr14:79434812-79434823
26	CEBPB	chr14:79523178-79523744	IMR90	lung:	n/a	n/a
27	CEBPB	chr14:79435637-79435998	A549	lung:	n/a	n/a
28	CEBPB	chr14:79634306-79634625	IMR90	lung:	n/a	n/a
29	CEBPB	chr14:79435656-79435995	HepG2	liver:	n/a	n/a
30	CEBPB	chr14:79605965-79606029	HepG2	liver:	n/a	n/a
31	CEBPB	chr14:79411769-79412090	IMR90	lung:	n/a	chr14:79411936-79411947
32	CEBPB	chr14:79477855-79478432	IMR90	lung:	n/a	n/a
33	CEBPB	chr14:79434675-79434960	A549	lung:	n/a	chr14:79434812-79434823
34	CEBPB	chr14:79640876-79641125	IMR90	lung:	n/a	chr14:79640950-79640963 chr14:79640950-79640963
35	CEBPB	chr14:79411791-79412066	A549	lung:	n/a	chr14:79411936-79411947
36	CEBPB	chr14:79481495-79481747	H1-hESC	embryonic stem cell:	n/a	chr14:79481587-79481598
37	CEBPB	chr14:79481418-79481781	IMR90	lung:	n/a	chr14:79481587-79481598
38	CEBPB	chr14:79434631-79435000	IMR90	lung:	n/a	chr14:79434812-79434823
39	CEBPB	chr14:79510018-79510268	A549	lung:	n/a	chr14:79510123-79510136
40	CEBPB	chr14:79452055-79452452	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr14:79411783-79412109	HepG2	liver:	n/a	chr14:79411936-79411947
42	CREB1	chr14:79511642-79511933	A549	lung:	n/a	n/a
43	CREB1	chr14:79451957-79452577	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr14:79511763-79511975	A549	lung:	n/a	n/a
45	CTBP2	chr14:79452078-79452398	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr14:79477309-79477442	GM19238	blood:	n/a	n/a
47	CTCF	chr14:79435580-79435730	WERI-Rb-1	eye:	n/a	chr14:79435653-79435666 chr14:79435650-79435668 chr14:79435652-79435673
48	CTCF	chr14:79426140-79426290	AoAF	blood vessel:	n/a	chr14:79426220-79426241 chr14:79426218-79426236 chr14:79426219-79426235 chr14:79426223-79426231
49	CTCF	chr14:79477240-79477390	GM12878	blood:	n/a	n/a
50	CTCF	chr14:79477140-79477290	AG04450	lung:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:79452439-79452489	MCF-7	breast:	n/a
2	chr14:79529179-79529229	HMEC	breast:	n/a
3	chr14:79529179-79529229	NH-A	brain:	n/a
4	chr14:79558823-79558873	HIPEpiC	eye:	n/a
5	chr14:79452439-79452489	SKMC	muscle:	n/a
6	chr14:79558823-79558873	GM12892	blood:	n/a
7	chr14:79511907-79511957	PANC-1	pancreas:	n/a
8	chr14:79511907-79511957	MCF10A-Er-Src	breast:	n/a
9	chr14:79511907-79511957	Hela-S3	cervix:	n/a
10	chr14:79483171-79483221	NH-A	brain:	n/a
11	chr14:79558823-79558873	HEK293	kidney:	embryo
12	chr14:79452439-79452489	H1-hESC	embryonic stem cell:	embryo
13	chr14:79558823-79558873	SKMC	muscle:	n/a
14	chr14:79529179-79529229	BJ	skin:	n/a
15	chr14:79529179-79529229	AG04449	skin:	fetal
16	chr14:79483171-79483221	HCPEpiC	choroid plexus:	n/a
17	chr14:79452439-79452489	AoSMC	blood vessel:	n/a
18	chr14:79483171-79483221	Hepatocyte	liver:	n/a
19	chr14:79529179-79529229	HL-60	blood:	n/a
20	chr14:79483171-79483221	BJ	skin:	n/a
21	chr14:79452439-79452489	HNPCEpiC	eye:	n/a
22	chr14:79529179-79529229	Jurkat	blood:	n/a
23	chr14:79558823-79558873	BJ	skin:	n/a
24	chr14:79483171-79483221	SK-N-SH_RA	brain:	n/a
25	chr14:79452439-79452489	LNCaP	prostate:	n/a
26	chr14:79558823-79558873	AG04450	lung:	fetal
27	chr14:79483171-79483221	H1-hESC	embryonic stem cell:	embryo
28	chr14:79529179-79529229	SK-N-MC	brain:	n/a
29	chr14:79483171-79483221	HRE	kidney:	n/a
30	chr14:79511907-79511957	LNCaP	prostate:	n/a
31	chr14:79483171-79483221	AG10803	skin:	n/a
32	chr14:79452439-79452489	A549	lung:	n/a
33	chr14:79452439-79452489	PFSK-1	brain:	n/a
34	chr14:79529179-79529229	K562	blood:	n/a
35	chr14:79529179-79529229	HEK293	kidney:	embryo
36	chr14:79529179-79529229	GM12892	blood:	n/a
37	chr14:79452439-79452489	AG10803	skin:	n/a
38	chr14:79483171-79483221	HepG2	liver:	n/a
39	chr14:79483171-79483221	HIPEpiC	eye:	n/a
40	chr14:79483171-79483221	ovcar-3	ovarian:	n/a
41	chr14:79558823-79558873	Caco-2	colon:	n/a
42	chr14:79511907-79511957	GM06990	blood:	n/a
43	chr14:79452439-79452489	HUVEC	blood vessel:	n/a
44	chr14:79558823-79558873	ovcar-3	ovarian:	n/a
45	chr14:79558823-79558873	HL-60	blood:	n/a
46	chr14:79558823-79558873	HPAEpiC	pulmonary alveolar:	n/a
47	chr14:79483171-79483221	AG04450	lung:	fetal
48	chr14:79452439-79452489	HRE	kidney:	n/a
49	chr14:79483171-79483221	SAEC	small airway:	n/a
50	chr14:79452439-79452489	ECC-1	luminal epithelium:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:79477327..79478026-chr14:80503480..80504367,2	MCF-7	breast:
2	chr14:79400770..79402966-chr14:79404628..79406999,2	K562	blood:
3	chr14:79633552..79635611-chr14:79637121..79639941,2	MCF-7	breast:
4	chr14:79573779..79574636-chr15:68722745..68723313,2	MCF-7	breast:
5	chr14:79477398..79478037-chr14:79822214..79823031,2	MCF-7	breast:
6	chr14:79554622..79556371-chr14:79563139..79566085,2	K562	blood:
7	chr14:79400140..79400929-chr14:79435226..79435737,2	MCF-7	breast:
8	chr14:79557622..79558152-chr15:97180235..97181024,2	MCF-7	breast:
9	chr14:79431792..79432292-chr2:1115047..1115998,2	MCF-7	breast:
10	chr14:79378742..79380336-chr14:79395070..79396642,2	MCF-7	breast:
11	chr14:79400140..79400929-chr14:79435226..79435737,2	MCF-7	breast:
12	chr14:79400770..79402966-chr14:79404628..79406999,2	K562	blood:
13	chr14:79477488..79478336-chr14:80679721..80680478,2	MCF-7	breast:
14	chr14:79633552..79635611-chr14:79637121..79639941,2	MCF-7	breast:
15	chr14:79425453..79426658-chr14:81316149..81316920,3	MCF-7	breast:
16	chr14:79554622..79556371-chr14:79563139..79566085,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DIO2-5	chr14:79540891-79541105	ENSG00000258829.1
2	lnc-DIO2-5	chr14:79538510-79538846	ENSG00000258829.1
3	lnc-DIO2-5	chr14:79538475-79538818	ENSG00000258829.1
4	lnc-DIO2-5	chr14:79540891-79541110	ENSG00000258829.1
5	lnc-ADCK1-4	chr14:79479847-79480188	l_1017_chr14:79479846-79482353_testes
6	lnc-ADCK1-4	chr14:79482052-79482353	l_1017_chr14:79479846-79482353_testes

No data

Variant related genes	Relation type
ENSG00000258829	TF binding region
ENSG00000258829	CpG island

Extended variants
information (count: 6701 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:6701 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576243652	chr14:79396605-79396606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs79912991	chr14:79396680-79396681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373346557	chr14:79396752-79396753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78200915	chr14:79396766-79396767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561421112	chr14:79396787-79396788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530252456	chr14:79396854-79396855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550548976	chr14:79396888-79396889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560653649	chr14:79396889-79396890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147390455	chr14:79396925-79396926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552198137	chr14:79396972-79396973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568922758	chr14:79396983-79396984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576967471	chr14:79397008-79397009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs117213931	chr14:79397012-79397013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574662717	chr14:79397064-79397065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567702342	chr14:79397096-79397097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568214258	chr14:79397200-79397201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs75726643	chr14:79397215-79397216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs154339	chr14:79397299-79397300	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs570704722	chr14:79397309-79397310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113810306	chr14:79397328-79397329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556153569	chr14:79397331-79397332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs56786334	chr14:79397357-79397358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144372270	chr14:79397414-79397415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541919318	chr14:79397415-79397416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555516752	chr14:79397430-79397431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186584266	chr14:79397431-79397432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs202036530	chr14:79397477-79397478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs118044156	chr14:79397478-79397479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560834750	chr14:79397505-79397506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532732369	chr14:79397523-79397524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191974980	chr14:79397550-79397551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113404492	chr14:79397578-79397579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562517749	chr14:79397622-79397623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531616115	chr14:79397641-79397642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548263730	chr14:79397673-79397674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372493205	chr14:79397712-79397713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546128852	chr14:79397779-79397780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562069917	chr14:79397811-79397812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs73323373	chr14:79397816-79397817	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs113158607	chr14:79397828-79397829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547316848	chr14:79397898-79397899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142472983	chr14:79397949-79397950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539697135	chr14:79397969-79397970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550120285	chr14:79397998-79397999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528554058	chr14:79398010-79398011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569636484	chr14:79398019-79398020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73323374	chr14:79398068-79398069	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs182226261	chr14:79398143-79398144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73323375	chr14:79398155-79398156	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs547119889	chr14:79398180-79398181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	22209245	CNVD
Prostate cancer	22553170	CNVD
Cancer	20164919	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:742 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79396600-79397200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:79396600-79397200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr14:79396600-79397400	Enhancers	HUVEC	blood vessel
4	chr14:79397400-79399600	Weak transcription	HUVEC	blood vessel
5	chr14:79399000-79400400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr14:79399000-79400800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr14:79399600-79399800	Enhancers	HUVEC	blood vessel
8	chr14:79404000-79404800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr14:79404400-79404800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr14:79404400-79405000	Enhancers	H9 Cell Line	embryonic stem cell
11	chr14:79404400-79405000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr14:79404400-79405200	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr14:79404600-79404800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr14:79404600-79405000	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr14:79405000-79405400	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr14:79405400-79405800	Enhancers	H9 Cell Line	embryonic stem cell
17	chr14:79412200-79412400	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr14:79412800-79413000	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr14:79413000-79413200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr14:79413000-79414400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr14:79413200-79414600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr14:79414600-79414800	Enhancers	Fetal Intestine Large	intestine
23	chr14:79414600-79415800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr14:79414800-79416200	Weak transcription	Fetal Intestine Large	intestine
25	chr14:79415200-79415400	Enhancers	Fetal Intestine Small	intestine
26	chr14:79415400-79416600	Weak transcription	Fetal Intestine Small	intestine
27	chr14:79415800-79416600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr14:79416200-79417800	Enhancers	Fetal Intestine Large	intestine
29	chr14:79416400-79417800	Enhancers	HUVEC	blood vessel
30	chr14:79416600-79416800	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr14:79416600-79416800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr14:79416600-79417000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr14:79416600-79417400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr14:79416600-79417400	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr14:79416600-79417600	Enhancers	NH-A	brain
36	chr14:79416600-79418000	Enhancers	Fetal Intestine Small	intestine
37	chr14:79416600-79418400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr14:79416800-79417000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr14:79416800-79417200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr14:79416800-79417400	Enhancers	Osteobl	bone
41	chr14:79416800-79418800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr14:79416800-79426200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr14:79416800-79436000	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr14:79417000-79417200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr14:79417000-79417400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr14:79417000-79417400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr14:79417000-79417400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr14:79417000-79417400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr14:79417200-79417400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr14:79417400-79417800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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