Variant report

Variant	nsv469855
Chromosome Location	chr14:20371140-20505020
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	ARID3A	chr14:20387153-20387455	HepG2	liver:	n/a	n/a
2	ATF1	chr14:20388271-20388560	K562	blood:	n/a	n/a
3	ATF1	chr14:20374096-20374405	K562	blood:	n/a	n/a
4	CBX3	chr14:20450329-20450560	K562	blood:	n/a	n/a
5	CEBPB	chr14:20386850-20387355	A549	lung:	n/a	n/a
6	CEBPB	chr14:20374865-20375205	K562	blood:	n/a	chr14:20375036-20375045 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375045 chr14:20375036-20375045 chr14:20375034-20375047 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375047
7	CEBPB	chr14:20439827-20439886	Hela-S3	cervix:	n/a	chr14:20439867-20439880 chr14:20439867-20439878 chr14:20439867-20439880 chr14:20439868-20439879
8	CEBPB	chr14:20420501-20420787	A549	lung:	n/a	chr14:20420660-20420671
9	CEBPB	chr14:20387024-20387360	HepG2	liver:	n/a	n/a
10	CEBPB	chr14:20388060-20388537	A549	lung:	n/a	chr14:20388129-20388140
11	CEBPB	chr14:20374900-20375169	HepG2	liver:	n/a	chr14:20375036-20375045 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375045 chr14:20375036-20375045 chr14:20375034-20375047 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375047
12	CEBPB	chr14:20394073-20394339	HepG2	liver:	n/a	chr14:20394191-20394202
13	CEBPB	chr14:20439826-20440010	IMR90	lung:	n/a	chr14:20439990-20440001 chr14:20439867-20439880 chr14:20439867-20439878 chr14:20439867-20439880 chr14:20439868-20439879
14	CEBPB	chr14:20374862-20375189	A549	lung:	n/a	chr14:20375036-20375045 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375045 chr14:20375036-20375045 chr14:20375034-20375047 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375047
15	CEBPB	chr14:20470476-20470862	A549	lung:	n/a	chr14:20470615-20470626
16	CEBPB	chr14:20470519-20470853	K562	blood:	n/a	chr14:20470615-20470626
17	CEBPB	chr14:20386989-20387500	A549	lung:	n/a	n/a
18	CEBPB	chr14:20439841-20439948	K562	blood:	n/a	chr14:20439867-20439880 chr14:20439867-20439878 chr14:20439867-20439880 chr14:20439868-20439879
19	CEBPB	chr14:20413462-20413846	A549	lung:	n/a	n/a
20	CEBPB	chr14:20434694-20434707	K562	blood:	n/a	n/a
21	CEBPB	chr14:20470509-20470786	IMR90	lung:	n/a	chr14:20470615-20470626
22	CEBPB	chr14:20470478-20470832	HepG2	liver:	n/a	chr14:20470615-20470626
23	CEBPB	chr14:20387030-20387353	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr14:20374855-20375196	IMR90	lung:	n/a	chr14:20375036-20375045 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375045 chr14:20375036-20375045 chr14:20375034-20375047 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375047
25	CEBPB	chr14:20388043-20388243	HepG2	liver:	n/a	chr14:20388129-20388140
26	CEBPB	chr14:20387999-20388479	K562	blood:	n/a	chr14:20388129-20388140
27	CEBPB	chr14:20415039-20415202	HepG2	liver:	n/a	chr14:20415154-20415165
28	CEBPB	chr14:20420582-20420802	HepG2	liver:	n/a	chr14:20420660-20420671
29	CEBPB	chr14:20386088-20387344	MCF-7	breast:	n/a	n/a
30	CEBPB	chr14:20439816-20439966	A549	lung:	n/a	chr14:20439867-20439880 chr14:20439867-20439878 chr14:20439867-20439880 chr14:20439868-20439879
31	CEBPB	chr14:20390412-20390477	HepG2	liver:	n/a	n/a
32	CEBPB	chr14:20386146-20386742	MCF-7	breast:	n/a	n/a
33	CEBPB	chr14:20434386-20434443	K562	blood:	n/a	n/a
34	CEBPB	chr14:20386291-20386625	HepG2	liver:	n/a	n/a
35	CEBPB	chr14:20439856-20439879	HepG2	liver:	n/a	chr14:20439867-20439878 chr14:20439868-20439879
36	CEBPZ	chr14:20471063-20471214	HepG2	liver:	n/a	n/a
37	CTCF	chr14:20415940-20416090	GM12864	blood:	n/a	n/a
38	CTCF	chr14:20470706-20470783	MCF-7	breast:	n/a	n/a
39	CTCF	chr14:20415960-20416110	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr14:20462863-20462913	LNCaP	prostate:	n/a	n/a
41	CTCF	chr14:20415900-20416050	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr14:20415880-20416158	K562	blood:	n/a	n/a
43	CTCF	chr14:20415920-20416070	HL-60	blood:	n/a	n/a
44	CTCF	chr14:20386320-20386470	MCF-7	breast:	n/a	n/a
45	CTCF	chr14:20381945-20382009	GM20000	blood:	n/a	n/a
46	CTCF	chr14:20415938-20416075	K562	blood:	n/a	n/a
47	CTCF	chr14:20416120-20416270	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr14:20410458-20410482	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr14:20379876-20379909	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr14:20415980-20416130	BE2_C	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20403845-20403895	HIPEpiC	eye:	n/a
2	chr14:20502658-20502708	HepG2	liver:	n/a
3	chr14:20403845-20403895	HIPEpiC	eye:	n/a
4	chr14:20502658-20502708	HepG2	liver:	n/a
5	chr14:20502658-20502708	T-47D	breast:	n/a
6	chr14:20389177-20389227	ovcar-3	ovarian:	n/a
7	chr14:20389177-20389227	RPTEC	kidney:	n/a
8	chr14:20403239-20403289	A549	lung:	n/a
9	chr14:20502658-20502708	SK-N-MC	brain:	n/a
10	chr14:20387292-20387342	MCF10A-Er-Src	breast:	n/a
11	chr14:20502658-20502708	BE2_C	brain:	n/a
12	chr14:20403845-20403895	AG04449	skin:	fetal
13	chr14:20404281-20404331	K562	blood:	n/a
14	chr14:20403239-20403289	HCM	heart:	n/a
15	chr14:20482899-20482949	AG10803	skin:	n/a
16	chr14:20403239-20403289	SK-N-MC	brain:	n/a
17	chr14:20387292-20387342	HepG2	liver:	n/a
18	chr14:20403845-20403895	MCF-7	breast:	n/a
19	chr14:20444164-20444214	HL-60	blood:	n/a
20	chr14:20502658-20502708	HCT-116	colon:	n/a
21	chr14:20403239-20403289	SK-N-SH	brain:	n/a
22	chr14:20387292-20387342	NT2-D1	testis:	n/a
23	chr14:20482899-20482949	HMEC	breast:	n/a
24	chr14:20482899-20482949	HNPCEpiC	eye:	n/a
25	chr14:20389177-20389227	IMR90	lung:	fetal
26	chr14:20444164-20444214	AG10803	skin:	n/a
27	chr14:20444164-20444214	MCF-7	breast:	n/a
28	chr14:20444164-20444214	Hela-S3	cervix:	n/a
29	chr14:20404281-20404331	AG04449	skin:	fetal
30	chr14:20403239-20403289	GM06990	blood:	n/a
31	chr14:20404281-20404331	AG09309	skin:	n/a
32	chr14:20403239-20403289	RPTEC	kidney:	n/a
33	chr14:20389177-20389227	AG04449	skin:	fetal
34	chr14:20403239-20403289	IMR90	lung:	fetal
35	chr14:20482899-20482949	RPTEC	kidney:	n/a
36	chr14:20387292-20387342	PrEC	prostate:	n/a
37	chr14:20403845-20403895	HepG2	liver:	n/a
38	chr14:20444164-20444214	AG04450	lung:	fetal
39	chr14:20502658-20502708	AG04449	skin:	fetal
40	chr14:20403845-20403895	Hepatocyte	liver:	n/a
41	chr14:20403239-20403289	ProgFib	skin:	n/a
42	chr14:20403239-20403289	NHBE	bronchial:	n/a
43	chr14:20404281-20404331	RPTEC	kidney:	n/a
44	chr14:20502658-20502708	GM19239	blood:	n/a
45	chr14:20403239-20403289	HRPEpiC	eye:	n/a
46	chr14:20403239-20403289	HEK293	kidney:	embryo
47	chr14:20389177-20389227	A549	lung:	n/a
48	chr14:20389177-20389227	PANC-1	pancreas:	n/a
49	chr14:20387292-20387342	PANC-1	pancreas:	n/a
50	chr14:20403239-20403289	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:20378405..20379102-chr22:33621834..33622612,2	MCF-7	breast:
2	chr14:20453392..20455779-chr14:20560575..20562246,2	K562	blood:
3	chr14:20382435..20385861-chr14:20389212..20390807,3	K562	blood:
4	chr14:20479309..20481272-chr14:20484820..20486760,2	K562	blood:
5	chr14:20421291..20423829-chr14:20424473..20427279,2	MCF-7	breast:
6	chr14:20382435..20385861-chr14:20389212..20390807,3	K562	blood:
7	chr14:20479309..20481272-chr14:20484820..20486760,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4K14-1	chr14:20376255-20376808	NONHSAT035546

Variant related genes	Relation type
ENSG00000265199	TF binding region
ENSG00000259016	TF binding region
OR4K5	TF binding region
OR4K15	TF binding region
OR4Q2	TF binding region
OR4K13	TF binding region
OR4K4P	TF binding region
OR4K16P	TF binding region
OR4K14	TF binding region
OR4K1	TF binding region
ENSG00000265199	CpG island
ENSG00000259016	CpG island
OR4K5	CpG island
OR4K15	CpG island
OR4Q2	CpG island
OR4K13	CpG island
OR4K4P	CpG island
OR4K16P	CpG island
OR4K14	CpG island
OR4K1	CpG island
ENSG00000258641	chromatin interactions
ENSG00000258822	chromatin interactions

Extended variants
information (count: 2269 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2269 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535476639	chr14:20371163-20371164	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs553780815	chr14:20371173-20371174	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs368734469	chr14:20371187-20371188	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs572218758	chr14:20371200-20371201	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs545873857	chr14:20371257-20371258	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs544626408	chr14:20371295-20371296	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs113239623	chr14:20371310-20371311	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs75748167	chr14:20371318-20371319	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs140239010	chr14:20371344-20371345	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs546876993	chr14:20371375-20371376	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs2318499	chr14:20371394-20371395	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs187875194	chr14:20371457-20371458	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs144571203	chr14:20371468-20371469	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs200551655	chr14:20371469-20371470	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs574779115	chr14:20371471-20371472	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs566764923	chr14:20371476-20371477	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs191266119	chr14:20371478-20371479	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs112766068	chr14:20371481-20371482	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs527789769	chr14:20371485-20371486	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs200499592	chr14:20371531-20371532	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs377756209	chr14:20371571-20371572	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs182676981	chr14:20371572-20371573	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs140708691	chr14:20371602-20371603	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs11844744	chr14:20371615-20371616	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs138190021	chr14:20371632-20371633	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs35808173	chr14:20371650-20371651	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs186948722	chr14:20371662-20371663	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs535745035	chr14:20371673-20371674	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs541770845	chr14:20371744-20371745	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs76463931	chr14:20371746-20371747	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs35497393	chr14:20371758-20371759	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs530748936	chr14:20371774-20371775	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs192218220	chr14:20371844-20371845	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs557807024	chr14:20371859-20371860	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs577383589	chr14:20371884-20371885	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs538468257	chr14:20371899-20371900	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs79480741	chr14:20371946-20371947	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs112023765	chr14:20371997-20371998	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs371966974	chr14:20372003-20372004	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs374026692	chr14:20372012-20372013	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs1686579	chr14:20372048-20372049	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs560115103	chr14:20372084-20372085	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs572375583	chr14:20372113-20372114	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs117779265	chr14:20372121-20372122	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs564637947	chr14:20372227-20372228	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs531688016	chr14:20372280-20372281	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs12886653	chr14:20372319-20372320	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs12886659	chr14:20372326-20372327	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs61976735	chr14:20372334-20372335	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs143258123	chr14:20372356-20372357	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:20369000-20379600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr14:20370200-20372000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
3	chr14:20373800-20374600	ZNF genes & repeats	Fetal Brain Male	brain
4	chr14:20374200-20374600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:20378200-20379400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr14:20383200-20385000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
7	chr14:20386400-20386800	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr14:20386800-20389000	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr14:20388200-20391000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr14:20389000-20389200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
11	chr14:20389000-20389600	Active TSS	Brain Substantia Nigra	brain
12	chr14:20389200-20390000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
13	chr14:20392000-20392400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr14:20393800-20394200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
15	chr14:20404400-20404800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
16	chr14:20406200-20406800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
17	chr14:20410000-20410400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr14:20411600-20412200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr14:20412800-20413000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr14:20415600-20416000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr14:20415600-20416000	Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr14:20415600-20416000	Active TSS	HepG2	liver
23	chr14:20415600-20416200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr14:20415600-20416200	Active TSS	A549	lung
25	chr14:20416200-20417200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr14:20416400-20417000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
27	chr14:20417200-20417800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr14:20420200-20420600	Enhancers	Adipose Nuclei	Adipose
29	chr14:20437800-20438200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr14:20437800-20438200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr14:20438000-20438800	Enhancers	Dnd41	blood
32	chr14:20438200-20438600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr14:20438200-20441400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr14:20438600-20438800	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr14:20438600-20438800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr14:20438800-20441400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr14:20438800-20441400	Weak transcription	Dnd41	blood
38	chr14:20440000-20440800	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr14:20440200-20440400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr14:20440200-20440400	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr14:20440200-20444000	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr14:20440400-20441400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr14:20440600-20441600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr14:20440800-20441200	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr14:20441200-20444200	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr14:20441400-20441600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr14:20441400-20442200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr14:20441400-20443800	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr14:20441400-20444200	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr14:20441400-20444400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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