Variant report

Variant	nsv1053520
Chromosome Location	chr14:72485195-72537202
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	BATF	chr14:72516106-72516584	GM12878	blood:	n/a	chr14:72516493-72516503
2	BATF	chr14:72489896-72490135	GM12878	blood:	n/a	chr14:72490041-72490052
3	BATF	chr14:72489882-72490206	GM12878	blood:	n/a	chr14:72490041-72490052
4	BATF	chr14:72516190-72516541	GM12878	blood:	n/a	chr14:72516493-72516503
5	BCL11A	chr14:72516167-72516573	GM12878	blood:	n/a	n/a
6	BCL11A	chr14:72516212-72516510	GM12878	blood:	n/a	n/a
7	BCL3	chr14:72521697-72521965	GM12878	blood:	n/a	n/a
8	BCL3	chr14:72516008-72516581	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:72521664-72521989	GM12878	blood:	n/a	n/a
10	CEBPB	chr14:72516053-72516789	GM12878	blood:	n/a	n/a
11	CEBPB	chr14:72497234-72497526	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr14:72489676-72491241	GM12878	blood:	n/a	chr14:72490500-72490512
13	CEBPB	chr14:72512483-72512608	H1-hESC	embryonic stem cell:	n/a	chr14:72512575-72512586
14	CEBPB	chr14:72527724-72528001	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr14:72490726-72490946	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr14:72512466-72512768	HepG2	liver:	n/a	chr14:72512575-72512586
17	CEBPB	chr14:72520058-72520329	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr14:72512435-72512767	IMR90	lung:	n/a	chr14:72512575-72512586
19	CEBPB	chr14:72535645-72535809	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr14:72512422-72512724	A549	lung:	n/a	chr14:72512575-72512586
21	CHD1	chr14:72485362-72485364	GM12878	blood:	n/a	n/a
22	CTCF	chr14:72490840-72490990	A549	lung:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
23	CTCF	chr14:72490560-72490710	HVMF	connective:	n/a	n/a
24	CTCF	chr14:72490840-72490990	GM12864	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
25	CTCF	chr14:72516274-72516347	Fibrobl	skin:	n/a	n/a
26	CTCF	chr14:72491220-72491370	GM12867	blood:	n/a	n/a
27	CTCF	chr14:72490820-72490970	AoAF	blood vessel:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
28	CTCF	chr14:72490767-72491033	GM10266	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
29	CTCF	chr14:72490820-72490970	GM12869	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
30	CTCF	chr14:72490780-72490930	GM12869	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
31	CTCF	chr14:72490880-72491030	HCPEpiC	choroid plexus:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
32	CTCF	chr14:72490459-72491316	SK-N-SH	brain:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
33	CTCF	chr14:72491202-72491241	GM10266	blood:	n/a	n/a
34	CTCF	chr14:72490746-72491029	LNCaP	prostate:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
35	CTCF	chr14:72490709-72491023	Spleen_OC	spleen:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
36	CTCF	chr14:72490742-72491031	SK-N-SH_RA	brain:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
37	CTCF	chr14:72490616-72491124	GM12878	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
38	CTCF	chr14:72490860-72491010	HFF-Myc	foreskin:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
39	CTCF	chr14:72490600-72490750	K562	blood:	n/a	n/a
40	CTCF	chr14:72490820-72490970	HPF	lung:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
41	CTCF	chr14:72490900-72491050	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr14:72490800-72490950	AG04450	lung:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
43	CTCF	chr14:72490840-72490990	HMF	breast:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
44	CTCF	chr14:72490860-72491010	WI-38	lung:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
45	CTCF	chr14:72490800-72490950	GM12878	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
46	CTCF	chr14:72490551-72491274	MCF-7	breast:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
47	CTCF	chr14:72490840-72490990	NB4	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
48	CTCF	chr14:72490740-72490890	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr14:72490860-72491010	HMEC	breast:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
50	CTCF	chr14:72490743-72491029	A549	lung:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:72490712-72490762	AG04450	lung:	fetal
2	chr14:72490712-72490762	HRE	kidney:	n/a
3	chr14:72490712-72490762	SK-N-SH	brain:	n/a
4	chr14:72490712-72490762	HIPEpiC	eye:	n/a
5	chr14:72490712-72490762	RPTEC	kidney:	n/a
6	chr14:72490712-72490762	HMEC	breast:	n/a
7	chr14:72490712-72490762	AoSMC	blood vessel:	n/a
8	chr14:72490712-72490762	U87	brain:	n/a
9	chr14:72490712-72490762	GM06990	blood:	n/a
10	chr14:72490712-72490762	Hepatocyte	liver:	n/a
11	chr14:72490712-72490762	HCT-116	colon:	n/a
12	chr14:72490712-72490762	K562	blood:	n/a
13	chr14:72490712-72490762	LNCaP	prostate:	n/a
14	chr14:72490712-72490762	PANC-1	pancreas:	n/a
15	chr14:72490712-72490762	SKMC	muscle:	n/a
16	chr14:72490712-72490762	HepG2	liver:	n/a
17	chr14:72490712-72490762	H1-hESC	embryonic stem cell:	embryo
18	chr14:72490712-72490762	NHDF-neo	bronchial:	n/a
19	chr14:72490712-72490762	GM12891	blood:	n/a
20	chr14:72490712-72490762	NHBE	bronchial:	n/a
21	chr14:72490712-72490762	MCF-7	breast:	n/a
22	chr14:72490712-72490762	Caco-2	colon:	n/a
23	chr14:72490712-72490762	SK-N-MC	brain:	n/a
24	chr14:72490712-72490762	HCPEpiC	choroid plexus:	n/a
25	chr14:72490712-72490762	HPAEpiC	pulmonary alveolar:	n/a
26	chr14:72490712-72490762	ECC-1	luminal epithelium:	n/a
27	chr14:72490712-72490762	HUVEC	blood vessel:	n/a
28	chr14:72490712-72490762	AG09309	skin:	n/a
29	chr14:72490712-72490762	SK-N-SH_RA	brain:	n/a
30	chr14:72490712-72490762	BE2_C	brain:	n/a
31	chr14:72490712-72490762	AG04449	skin:	fetal
32	chr14:72490712-72490762	HNPCEpiC	eye:	n/a
33	chr14:72490712-72490762	Jurkat	blood:	n/a
34	chr14:72490712-72490762	AG10803	skin:	n/a
35	chr14:72490712-72490762	NH-A	brain:	n/a
36	chr14:72490712-72490762	HAEpiC	amniotic membrane:	n/a
37	chr14:72490712-72490762	HRCEpiC	kidney:	n/a
38	chr14:72490712-72490762	CMK	blood:	n/a
39	chr14:72490712-72490762	A549	lung:	n/a
40	chr14:72490712-72490762	AG09319	gingival:	n/a
41	chr14:72490712-72490762	HEEpiC	esophagus:	n/a
42	chr14:72490712-72490762	GM19239	blood:	n/a
43	chr14:72490712-72490762	HL-60	blood:	n/a
44	chr14:72490712-72490762	HCF	heart:	n/a
45	chr14:72490712-72490762	MCF10A-Er-Src	breast:	n/a
46	chr14:72490712-72490762	ProgFib	skin:	n/a
47	chr14:72490712-72490762	BJ	skin:	n/a
48	chr14:72490712-72490762	HCM	heart:	n/a
49	chr14:72490712-72490762	IMR90	lung:	fetal
50	chr14:72490712-72490762	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:72515091..72516687-chr14:72530226..72533191,2	MCF-7	breast:
2	chr14:72490402..72491111-chr14:72887191..72887990,2	MCF-7	breast:
3	chr14:72398692..72399639-chr14:72490586..72491393,3	MCF-7	breast:
4	chr14:72485047..72487639-chr14:72493810..72496038,2	MCF-7	breast:
5	chr14:72485047..72487639-chr14:72493810..72496038,2	MCF-7	breast:
6	chr14:72490629..72491408-chr14:72758856..72759783,5	MCF-7	breast:
7	chr14:72482931..72485550-chr14:72489530..72491362,2	MCF-7	breast:
8	chr14:72482931..72485550-chr14:72489530..72491362,2	MCF-7	breast:
9	chr14:72489255..72491408-chr14:72757396..72759777,2	MCF-7	breast:
10	chr14:72515091..72516687-chr14:72530226..72533191,2	MCF-7	breast:
11	chr14:72505358..72507874-chr14:72509427..72511553,2	MCF-7	breast:
12	chr14:72505358..72507874-chr14:72509427..72511553,2	MCF-7	breast:
13	chr14:72536154..72538445-chr14:72539011..72540844,2	MCF-7	breast:
14	chr14:72490617..72491401-chr14:72887032..72887742,2	K562	blood:

Variant related genes	Relation type
ENSG00000200298	TF binding region
ENSG00000200298	CpG island
ENSG00000182732	chromatin interactions

Extended variants
information (count: 2223 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2223 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11628574	chr14:72485195-72485196	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561865903	chr14:72485204-72485205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530305604	chr14:72485214-72485215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188753672	chr14:72485223-72485224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560747798	chr14:72485225-72485226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528016239	chr14:72485239-72485240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7494103	chr14:72485244-72485245	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs570766222	chr14:72485296-72485297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191864831	chr14:72485343-72485344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531784086	chr14:72485420-72485421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115331574	chr14:72485467-72485468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558344585	chr14:72485520-72485521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533467076	chr14:72485558-72485559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535248832	chr14:72485559-72485560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372450319	chr14:72485577-72485578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565603081	chr14:72485629-72485630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184679088	chr14:72485667-72485668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs59707038	chr14:72485681-72485682	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs557686744	chr14:72485697-72485698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575941526	chr14:72485698-72485699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138177958	chr14:72485721-72485722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545040448	chr14:72485733-72485734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11158929	chr14:72485748-72485749	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs542415823	chr14:72485749-72485750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560686420	chr14:72485752-72485753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113135002	chr14:72485768-72485769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148910199	chr14:72485774-72485775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145052747	chr14:72485807-72485808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117561872	chr14:72485840-72485841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148357388	chr14:72485892-72485893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550184950	chr14:72485960-72485961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568186741	chr14:72486042-72486043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373415631	chr14:72486047-72486048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190407344	chr14:72486094-72486095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181720391	chr14:72486100-72486101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187415756	chr14:72486121-72486122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189180787	chr14:72486132-72486133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539666515	chr14:72486160-72486161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551376176	chr14:72486175-72486176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571430284	chr14:72486204-72486205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111901613	chr14:72486245-72486246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533863425	chr14:72486255-72486256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76422714	chr14:72486283-72486284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs11333232	chr14:72486337-72486338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs398025588	chr14:72486338-72486339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs60340667	chr14:72486341-72486342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558252619	chr14:72486393-72486394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111282877	chr14:72486433-72486434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139420969	chr14:72486531-72486532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572675770	chr14:72486550-72486551	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
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	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	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	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 ductal adenocarcinoma	19077451	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
lymphocytic leukemia	21291569	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:138 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72481000-72489200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr14:72482400-72489400	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr14:72487600-72487800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr14:72487800-72489200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr14:72489200-72489400	Enhancers	NHEK	skin
6	chr14:72489200-72489600	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr14:72489200-72490200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr14:72489200-72491000	Enhancers	HMEC	breast
9	chr14:72489400-72489800	Genic enhancers	Cortex derived primary cultured neurospheres	brain
10	chr14:72489400-72490000	Flanking Active TSS	NHEK	skin
11	chr14:72489600-72489800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr14:72489600-72489800	Enhancers	Brain Anterior Caudate	brain
13	chr14:72489600-72490400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr14:72489600-72490600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr14:72489600-72490600	Enhancers	Hela-S3	cervix
16	chr14:72489600-72491200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr14:72489600-72491200	Enhancers	Adipose Nuclei	Adipose
18	chr14:72489600-72491200	Enhancers	GM12878-XiMat	blood
19	chr14:72489800-72490000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr14:72489800-72491600	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr14:72490000-72490200	Enhancers	NHEK	skin
22	chr14:72490000-72494800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr14:72490200-72490400	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr14:72490200-72490600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr14:72490200-72490800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr14:72490200-72490800	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr14:72490200-72490800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr14:72490200-72490800	Enhancers	Fetal Muscle Leg	muscle
29	chr14:72490200-72490800	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr14:72490200-72490800	Flanking Active TSS	NHEK	skin
31	chr14:72490200-72491200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr14:72490200-72491200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr14:72490200-72491600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr14:72490400-72490600	Enhancers	Brain Anterior Caudate	brain
35	chr14:72490400-72490800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
36	chr14:72490400-72490800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr14:72490400-72491200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr14:72490400-72491200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr14:72490400-72491200	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr14:72490400-72491200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr14:72490400-72491200	Enhancers	Left Ventricle	heart
42	chr14:72490600-72491200	Enhancers	H9 Cell Line	embryonic stem cell
43	chr14:72490800-72491200	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr14:72490800-72491200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr14:72490800-72491400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr14:72490800-72491600	Enhancers	NHEK	skin
47	chr14:72491000-72491400	Enhancers	Right Atrium	heart
48	chr14:72491000-72491800	Enhancers	Fetal Heart	heart
49	chr14:72491200-72493200	Weak transcription	Left Ventricle	heart
50	chr14:72491600-72493600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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