Variant report

Variant	nsv902124
Chromosome Location	chr14:83165520-83282163
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	CBX3	chr14:83176601-83176841	K562	blood:	n/a	n/a
2	CEBPB	chr14:83224220-83224593	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr14:83170636-83170898	A549	lung:	n/a	n/a
4	CEBPB	chr14:83176602-83176850	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr14:83237586-83237698	HepG2	liver:	n/a	chr14:83237654-83237665
6	CHD1	chr14:83272941-83273118	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr14:83176720-83176870	HFF	foreskin:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
8	CTCF	chr14:83176700-83176850	HEEpiC	esophagus:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
9	CTCF	chr14:83176720-83176870	AG04449	skin:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
10	CTCF	chr14:83176636-83176924	Medullo	brain:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
11	CTCF	chr14:83176720-83176870	AG04450	lung:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
12	CTCF	chr14:83176640-83176790	HMEC	breast:	n/a	chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
13	CTCF	chr14:83176280-83176430	AG09319	gingival:	n/a	n/a
14	CTCF	chr14:83176663-83176905	HepG2	liver:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
15	CTCF	chr14:83176660-83176810	GM12868	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
16	CTCF	chr14:83226888-83226931	GM20000	blood:	n/a	n/a
17	CTCF	chr14:83176660-83176810	HFF-Myc	foreskin:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
18	CTCF	chr14:83176660-83176810	HCT-116	colon:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
19	CTCF	chr14:83176660-83176852	HepG2	liver:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
20	CTCF	chr14:83176671-83176910	GM12891	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
21	CTCF	chr14:83176340-83176490	HPF	lung:	n/a	n/a
22	CTCF	chr14:83176663-83176906	MCF-7	breast:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
23	CTCF	chr14:83176740-83176890	BJ	skin:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
24	CTCF	chr14:83176557-83177075	MCF-7	breast:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
25	CTCF	chr14:83176680-83176830	GM12872	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
26	CTCF	chr14:83176700-83176850	NB4	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
27	CTCF	chr14:83176632-83176948	H1-hESC	embryonic stem cell:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
28	CTCF	chr14:83176663-83176904	A549	lung:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
29	CTCF	chr14:83176700-83176850	NHLF	lung:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
30	CTCF	chr14:83176638-83176886	K562	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
31	CTCF	chr14:83176700-83176850	HepG2	liver:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
32	CTCF	chr14:83176604-83176994	K562	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
33	CTCF	chr14:83176667-83176905	MCF-7	breast:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
34	CTCF	chr14:83176653-83176898	K562	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
35	CTCF	chr14:83176700-83176850	A549	lung:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
36	CTCF	chr14:83176720-83176870	AG10803	skin:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
37	CTCF	chr14:83176644-83176927	NHEK	skin:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
38	CTCF	chr14:83176680-83176830	AG09309	skin:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
39	CTCF	chr14:83176633-83176933	GM12878	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
40	CTCF	chr14:83176720-83176870	GM12874	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
41	CTCF	chr14:83176720-83176870	Hela-S3	cervix:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
42	CTCF	chr14:83176700-83176850	RPTEC	kidney:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
43	CTCF	chr14:83176700-83176850	AG04449	skin:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
44	CTCF	chr14:83176720-83176870	NHDF-neo	bronchial:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
45	CTCF	chr14:83176430-83177101	SK-N-SH	brain:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
46	CTCF	chr14:83176700-83176850	HFF-Myc	foreskin:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
47	CTCF	chr14:83176720-83176870	HPAF	blood vessel:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
48	CTCF	chr14:83176720-83176870	HRPEpiC	eye:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
49	CTCF	chr14:83176683-83176869	GM13976	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788
50	CTCF	chr14:83176700-83176850	GM12865	blood:	n/a	chr14:83176773-83176794 chr14:83176771-83176789 chr14:83176774-83176787 chr14:83176772-83176788

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:83226240-83226290	LNCaP	prostate:	n/a
2	chr14:83272320-83272370	GM06990	blood:	n/a
3	chr14:83272320-83272370	HRPEpiC	eye:	n/a
4	chr14:83281040-83281090	Caco-2	colon:	n/a
5	chr14:83272320-83272370	HRE	kidney:	n/a
6	chr14:83281040-83281090	HCPEpiC	choroid plexus:	n/a
7	chr14:83226240-83226290	HCT-116	colon:	n/a
8	chr14:83281040-83281090	HL-60	blood:	n/a
9	chr14:83272320-83272370	AG04450	lung:	fetal
10	chr14:83272320-83272370	HIPEpiC	eye:	n/a
11	chr14:83226240-83226290	HCPEpiC	choroid plexus:	n/a
12	chr14:83281040-83281090	SAEC	small airway:	n/a
13	chr14:83272320-83272370	HL-60	blood:	n/a
14	chr14:83281040-83281090	U87	brain:	n/a
15	chr14:83272320-83272370	U87	brain:	n/a
16	chr14:83281040-83281090	GM12891	blood:	n/a
17	chr14:83281040-83281090	A549	lung:	n/a
18	chr14:83272320-83272370	PANC-1	pancreas:	n/a
19	chr14:83281040-83281090	SK-N-MC	brain:	n/a
20	chr14:83226240-83226290	HMEC	breast:	n/a
21	chr14:83226240-83226290	ProgFib	skin:	n/a
22	chr14:83272320-83272370	A549	lung:	n/a
23	chr14:83281040-83281090	PFSK-1	brain:	n/a
24	chr14:83226240-83226290	SAEC	small airway:	n/a
25	chr14:83272320-83272370	PrEC	prostate:	n/a
26	chr14:83272320-83272370	HepG2	liver:	n/a
27	chr14:83272320-83272370	HCPEpiC	choroid plexus:	n/a
28	chr14:83281040-83281090	AG10803	skin:	n/a
29	chr14:83281040-83281090	HMEC	breast:	n/a
30	chr14:83272320-83272370	NB4	blood:	n/a
31	chr14:83226240-83226290	HIPEpiC	eye:	n/a
32	chr14:83272320-83272370	NHBE	bronchial:	n/a
33	chr14:83281040-83281090	SKMC	muscle:	n/a
34	chr14:83281040-83281090	BJ	skin:	n/a
35	chr14:83226240-83226290	HRPEpiC	eye:	n/a
36	chr14:83226240-83226290	T-47D	breast:	n/a
37	chr14:83226240-83226290	PFSK-1	brain:	n/a
38	chr14:83272320-83272370	MCF-7	breast:	n/a
39	chr14:83272320-83272370	AG04449	skin:	fetal
40	chr14:83272320-83272370	ECC-1	luminal epithelium:	n/a
41	chr14:83226240-83226290	MCF10A-Er-Src	breast:	n/a
42	chr14:83226240-83226290	HepG2	liver:	n/a
43	chr14:83281040-83281090	NHDF-neo	bronchial:	n/a
44	chr14:83281040-83281090	NT2-D1	testis:	n/a
45	chr14:83281040-83281090	K562	blood:	n/a
46	chr14:83281040-83281090	MCF10A-Er-Src	breast:	n/a
47	chr14:83226240-83226290	A549	lung:	n/a
48	chr14:83272320-83272370	GM12892	blood:	n/a
49	chr14:83226240-83226290	HL-60	blood:	n/a
50	chr14:83226240-83226290	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:83176690..83177254-chr14:86521578..86522506,2	MCF-7	breast:
2	chr14:83176444..83177428-chr14:86521944..86522598,2	MCF-7	breast:
3	chr14:83176300..83176864-chr14:83537974..83538513,2	MCF-7	breast:
4	chr14:83161282..83164222-chr14:83165028..83167917,2	K562	blood:
5	chr14:83176665..83177254-chr14:86523440..86523991,2	MCF-7	breast:
6	chr14:83192387..83194148-chr14:83198757..83201171,2	K562	blood:
7	chr14:83176409..83177253-chr14:83537916..83538885,7	MCF-7	breast:
8	chr14:83192387..83194148-chr14:83198757..83201171,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSHR-5	chr14:83173045-83173169	ENSG00000258743
2	lnc-SEL1L-4	chr14:83262417-83262565	ENSG00000258683
3	lnc-SEL1L-4	chr14:83254822-83255211	ENSG00000258683

Variant related genes	Relation type
ENSG00000258683	TF binding region
ENSG00000258683	CpG island

Extended variants
information (count: 2432 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2432 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78205312	chr14:83170205-83170206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs567939387	chr14:83170272-83170273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs12891298	chr14:83170305-83170306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147666691	chr14:83170409-83170410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs140664881	chr14:83170422-83170423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568929848	chr14:83170453-83170454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs115042450	chr14:83170467-83170468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558351684	chr14:83170477-83170478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567190466	chr14:83170478-83170479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550167956	chr14:83170518-83170519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113996251	chr14:83170545-83170546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534206119	chr14:83170564-83170565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114930406	chr14:83170567-83170568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144731666	chr14:83170588-83170589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563608274	chr14:83170626-83170627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544160277	chr14:83170629-83170630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562182934	chr14:83170639-83170640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192279199	chr14:83170640-83170641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1952829	chr14:83170657-83170658	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs563922315	chr14:83170680-83170681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs75424421	chr14:83170700-83170701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140842539	chr14:83170706-83170707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs2150333	chr14:83170722-83170723	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs12433540	chr14:83170751-83170752	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs566637144	chr14:83170793-83170794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs67925139	chr14:83173048-83173049	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs542703333	chr14:83173067-83173068	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs566627179	chr14:83173098-83173099	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs561186252	chr14:83173153-83173154	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs531926275	chr14:83181011-83181012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544082553	chr14:83181045-83181046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs144162728	chr14:83181047-83181048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565396477	chr14:83181093-83181094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532539934	chr14:83181152-83181153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111655637	chr14:83181170-83181171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547441868	chr14:83181206-83181207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371302590	chr14:83181230-83181231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559834186	chr14:83181255-83181256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370785581	chr14:83181267-83181268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77779752	chr14:83181277-83181278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs368387279	chr14:83181283-83181284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs567459391	chr14:83181289-83181290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs146477115	chr14:83181324-83181325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550054044	chr14:83181325-83181326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs75193507	chr14:83181358-83181359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556291613	chr14:83181383-83181384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553471901	chr14:83181388-83181389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569484182	chr14:83185603-83185604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540124280	chr14:83185673-83185674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs17117208	chr14:83185699-83185700	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:64)

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
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
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	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
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:198 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:83170200-83170800	Enhancers	Liver	Liver
2	chr14:83181000-83181400	Enhancers	Ovary	ovary
3	chr14:83185600-83186200	Enhancers	Aorta	Aorta
4	chr14:83186000-83187400	Enhancers	Stomach Smooth Muscle	stomach
5	chr14:83186200-83186600	Weak transcription	Aorta	Aorta
6	chr14:83186600-83187800	Enhancers	Aorta	Aorta
7	chr14:83186800-83187000	Enhancers	Fetal Lung	lung
8	chr14:83186800-83187200	Enhancers	Gastric	stomach
9	chr14:83186800-83187200	Enhancers	Lung	lung
10	chr14:83186800-83187200	Enhancers	NHDF-Ad	bronchial
11	chr14:83186800-83187600	Enhancers	Colon Smooth Muscle	Colon
12	chr14:83186800-83187600	Enhancers	Esophagus	oesophagus
13	chr14:83186800-83187600	Enhancers	Fetal Muscle Leg	muscle
14	chr14:83186800-83187600	Enhancers	Rectal Smooth Muscle	rectum
15	chr14:83186800-83187800	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr14:83187000-83187200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr14:83187000-83187800	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr14:83187000-83187800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr14:83187200-83187600	Enhancers	Brain Anterior Caudate	brain
20	chr14:83187200-83191000	Weak transcription	Lung	lung
21	chr14:83187200-83191000	Weak transcription	NHDF-Ad	bronchial
22	chr14:83187400-83187600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr14:83187400-83187600	Flanking Active TSS	Stomach Smooth Muscle	stomach
24	chr14:83187400-83191200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr14:83187600-83187800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr14:83187600-83187800	Active TSS	Stomach Smooth Muscle	stomach
27	chr14:83187600-83191200	Weak transcription	Esophagus	oesophagus
28	chr14:83187600-83191200	Weak transcription	Ovary	ovary
29	chr14:83187800-83191200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr14:83190600-83192000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr14:83191000-83191400	Enhancers	Brain Germinal Matrix	brain
32	chr14:83191000-83191400	Enhancers	Right Atrium	heart
33	chr14:83191000-83191400	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr14:83191000-83191600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr14:83191000-83191600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr14:83191000-83191600	Enhancers	Fetal Brain Male	brain
37	chr14:83191000-83191600	Active TSS	Fetal Kidney	kidney
38	chr14:83191000-83191600	Enhancers	Gastric	stomach
39	chr14:83191000-83191600	Enhancers	Left Ventricle	heart
40	chr14:83191000-83191600	ZNF genes & repeats	Lung	lung
41	chr14:83191000-83191600	Enhancers	Pancreas	Pancrea
42	chr14:83191000-83191600	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
43	chr14:83191000-83191600	Enhancers	Hela-S3	cervix
44	chr14:83191000-83191600	Enhancers	NHDF-Ad	bronchial
45	chr14:83191000-83191800	Enhancers	Right Ventricle	heart
46	chr14:83191200-83191600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr14:83191200-83191600	Enhancers	Esophagus	oesophagus
48	chr14:83191200-83191600	Enhancers	Ovary	ovary
49	chr14:83191200-83191600	Enhancers	NH-A	brain
50	chr14:83191200-83191800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell

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