Variant report

Variant	nsv870207
Chromosome Location	chr14:20330619-20470454
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	chr14:20346241-20346527	K562	blood:	n/a	n/a
2	ARID3A	chr14:20387153-20387455	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:20346227-20346537	HepG2	liver:	n/a	n/a
4	ATF1	chr14:20374096-20374405	K562	blood:	n/a	n/a
5	ATF1	chr14:20388271-20388560	K562	blood:	n/a	n/a
6	BACH1	chr14:20348120-20348235	K562	blood:	n/a	n/a
7	CBX3	chr14:20450329-20450560	K562	blood:	n/a	n/a
8	CEBPB	chr14:20353081-20353403	A549	lung:	n/a	n/a
9	CEBPB	chr14:20386146-20386742	MCF-7	breast:	n/a	n/a
10	CEBPB	chr14:20439856-20439879	HepG2	liver:	n/a	chr14:20439867-20439878 chr14:20439868-20439879
11	CEBPB	chr14:20386291-20386625	HepG2	liver:	n/a	n/a
12	CEBPB	chr14:20420582-20420802	HepG2	liver:	n/a	chr14:20420660-20420671
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	chr14:20388060-20388537	A549	lung:	n/a	chr14:20388129-20388140
15	CEBPB	chr14:20370608-20370903	IMR90	lung:	n/a	chr14:20370744-20370755 chr14:20370732-20370743
16	CEBPB	chr14:20388043-20388243	HepG2	liver:	n/a	chr14:20388129-20388140
17	CEBPB	chr14:20390412-20390477	HepG2	liver:	n/a	n/a
18	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
19	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
20	CEBPB	chr14:20386088-20387344	MCF-7	breast:	n/a	n/a
21	CEBPB	chr14:20370643-20370895	Hela-S3	cervix:	n/a	chr14:20370744-20370755 chr14:20370732-20370743
22	CEBPB	chr14:20386850-20387355	A549	lung:	n/a	n/a
23	CEBPB	chr14:20346421-20346658	HepG2	liver:	n/a	chr14:20346574-20346585
24	CEBPB	chr14:20439841-20439948	K562	blood:	n/a	chr14:20439867-20439880 chr14:20439867-20439878 chr14:20439867-20439880 chr14:20439868-20439879
25	CEBPB	chr14:20387999-20388479	K562	blood:	n/a	chr14:20388129-20388140
26	CEBPB	chr14:20415039-20415202	HepG2	liver:	n/a	chr14:20415154-20415165
27	CEBPB	chr14:20439816-20439966	A549	lung:	n/a	chr14:20439867-20439880 chr14:20439867-20439878 chr14:20439867-20439880 chr14:20439868-20439879
28	CEBPB	chr14:20386989-20387500	A549	lung:	n/a	n/a
29	CEBPB	chr14:20387024-20387360	HepG2	liver:	n/a	n/a
30	CEBPB	chr14:20370568-20370914	HepG2	liver:	n/a	chr14:20370744-20370755 chr14:20370732-20370743
31	CEBPB	chr14:20434694-20434707	K562	blood:	n/a	n/a
32	CEBPB	chr14:20353121-20353345	HepG2	liver:	n/a	n/a
33	CEBPB	chr14:20434386-20434443	K562	blood:	n/a	n/a
34	CEBPB	chr14:20370645-20370888	K562	blood:	n/a	chr14:20370744-20370755 chr14:20370732-20370743
35	CEBPB	chr14:20420501-20420787	A549	lung:	n/a	chr14:20420660-20420671
36	CEBPB	chr14:20370579-20370921	A549	lung:	n/a	chr14:20370744-20370755 chr14:20370732-20370743
37	CEBPB	chr14:20365988-20366164	HepG2	liver:	n/a	n/a
38	CEBPB	chr14:20353091-20353443	IMR90	lung:	n/a	n/a
39	CEBPB	chr14:20347421-20347704	K562	blood:	n/a	n/a
40	CEBPB	chr14:20394073-20394339	HepG2	liver:	n/a	chr14:20394191-20394202
41	CEBPB	chr14:20439827-20439886	Hela-S3	cervix:	n/a	chr14:20439867-20439880 chr14:20439867-20439878 chr14:20439867-20439880 chr14:20439868-20439879
42	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
43	CEBPB	chr14:20387030-20387353	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr14:20413462-20413846	A549	lung:	n/a	n/a
45	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
46	CEBPB	chr14:20337012-20337281	K562	blood:	n/a	n/a
47	CTCF	chr14:20376680-20376830	GM12864	blood:	n/a	n/a
48	CTCF	chr14:20404080-20404230	GM12868	blood:	n/a	n/a
49	CTCF	chr14:20346220-20346370	AG09309	skin:	n/a	n/a
50	CTCF	chr14:20346320-20346470	GM12871	blood:	n/a	chr14:20346379-20346397 chr14:20346374-20346395 chr14:20346386-20346394

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20389177-20389227	PFSK-1	brain:	n/a
2	chr14:20403845-20403895	SK-N-SH_RA	brain:	n/a
3	chr14:20389177-20389227	PFSK-1	brain:	n/a
4	chr14:20403845-20403895	SK-N-SH_RA	brain:	n/a
5	chr14:20444164-20444214	SK-N-SH_RA	brain:	n/a
6	chr14:20344083-20344133	HRE	kidney:	n/a
7	chr14:20444164-20444214	HMEC	breast:	n/a
8	chr14:20444164-20444214	BE2_C	brain:	n/a
9	chr14:20387292-20387342	BE2_C	brain:	n/a
10	chr14:20344920-20344970	Caco-2	colon:	n/a
11	chr14:20444164-20444214	SKMC	muscle:	n/a
12	chr14:20403239-20403289	NHDF-neo	bronchial:	n/a
13	chr14:20344394-20344444	LNCaP	prostate:	n/a
14	chr14:20344394-20344444	AG04450	lung:	fetal
15	chr14:20404281-20404331	PANC-1	pancreas:	n/a
16	chr14:20344083-20344133	HRCEpiC	kidney:	n/a
17	chr14:20344394-20344444	U87	brain:	n/a
18	chr14:20344083-20344133	H1-hESC	embryonic stem cell:	embryo
19	chr14:20344394-20344444	HRE	kidney:	n/a
20	chr14:20403845-20403895	RPTEC	kidney:	n/a
21	chr14:20344394-20344444	T-47D	breast:	n/a
22	chr14:20403845-20403895	HUVEC	blood vessel:	n/a
23	chr14:20444164-20444214	HEK293	kidney:	embryo
24	chr14:20389177-20389227	Hepatocyte	liver:	n/a
25	chr14:20389177-20389227	RPTEC	kidney:	n/a
26	chr14:20389177-20389227	MCF-7	breast:	n/a
27	chr14:20404281-20404331	HepG2	liver:	n/a
28	chr14:20403845-20403895	A549	lung:	n/a
29	chr14:20344394-20344444	HPAEpiC	pulmonary alveolar:	n/a
30	chr14:20344920-20344970	T-47D	breast:	n/a
31	chr14:20389177-20389227	Hela-S3	cervix:	n/a
32	chr14:20403239-20403289	AG04449	skin:	fetal
33	chr14:20344083-20344133	T-47D	breast:	n/a
34	chr14:20404281-20404331	HMEC	breast:	n/a
35	chr14:20444164-20444214	A549	lung:	n/a
36	chr14:20403845-20403895	NH-A	brain:	n/a
37	chr14:20403239-20403289	MCF10A-Er-Src	breast:	n/a
38	chr14:20403239-20403289	SK-N-SH	brain:	n/a
39	chr14:20344083-20344133	HCPEpiC	choroid plexus:	n/a
40	chr14:20444164-20444214	GM06990	blood:	n/a
41	chr14:20387292-20387342	GM19239	blood:	n/a
42	chr14:20344394-20344444	HCPEpiC	choroid plexus:	n/a
43	chr14:20403239-20403289	AG09309	skin:	n/a
44	chr14:20344083-20344133	BJ	skin:	n/a
45	chr14:20344920-20344970	MCF-7	breast:	n/a
46	chr14:20404281-20404331	AoSMC	blood vessel:	n/a
47	chr14:20403845-20403895	AG04449	skin:	fetal
48	chr14:20344083-20344133	Hela-S3	cervix:	n/a
49	chr14:20387292-20387342	NHDF-neo	bronchial:	n/a
50	chr14:20403845-20403895	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:20378405..20379102-chr22:33621834..33622612,2	MCF-7	breast:
2	chr14:20382435..20385861-chr14:20389212..20390807,3	K562	blood:
3	chr14:20421291..20423829-chr14:20424473..20427279,2	MCF-7	breast:
4	chr14:20453392..20455779-chr14:20560575..20562246,2	K562	blood:
5	chr14:20382435..20385861-chr14:20389212..20390807,3	K562	blood:
6	chr14:20330082..20332945-chr14:20336237..20338891,2	K562	blood:

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

Variant related genes	Relation type
ENSG00000259016	TF binding region
OR4K5	TF binding region
OR4K4P	TF binding region
OR4K3	TF binding region
OR4K16P	TF binding region
OR4K1	TF binding region
OR4K15	TF binding region
OR4Q2	TF binding region
OR4K2	TF binding region
ENSG00000259016	CpG island
OR4K5	CpG island
OR4K4P	CpG island
OR4K3	CpG island
OR4K16P	CpG island
OR4K1	CpG island
OR4K15	CpG island
OR4Q2	CpG island
OR4K2	CpG island
ENSG00000258822	chromatin interactions
ENSG00000176290	chromatin interactions
ENSG00000258641	chromatin interactions

Extended variants
information (count: 3215 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:3215 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144101492	chr14:20330674-20330675	ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs148688503	chr14:20330691-20330692	ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs558785537	chr14:20330697-20330698	ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs186411190	chr14:20330707-20330708	ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs377605456	chr14:20330712-20330713	ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs190811352	chr14:20330836-20330837	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs546619801	chr14:20330841-20330842	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs577205477	chr14:20330848-20330849	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538626570	chr14:20330850-20330851	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs113333405	chr14:20330892-20330893	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs568837061	chr14:20330904-20330905	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141387526	chr14:20330925-20330926	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs555645987	chr14:20330929-20330930	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs574015744	chr14:20330931-20330932	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs534941711	chr14:20330950-20330951	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs181793887	chr14:20330969-20330970	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs186019657	chr14:20330970-20330971	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs563875333	chr14:20330976-20330977	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs545071233	chr14:20330992-20330993	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs10138389	chr14:20330999-20331000	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs562772282	chr14:20331020-20331021	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542825930	chr14:20331094-20331095	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs190884579	chr14:20331105-20331106	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs373169936	chr14:20331106-20331107	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs1686582	chr14:20331117-20331118	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs565173080	chr14:20331138-20331139	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs116068434	chr14:20331163-20331164	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs550291534	chr14:20331166-20331167	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs568947985	chr14:20331213-20331214	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs529724949	chr14:20331219-20331220	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs549558537	chr14:20331262-20331263	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs567481601	chr14:20331328-20331329	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs534879972	chr14:20331354-20331355	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553299009	chr14:20331409-20331410	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs183024468	chr14:20331433-20331434	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs1686581	chr14:20331451-20331452	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs557041365	chr14:20331483-20331484	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs111661526	chr14:20331518-20331519	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs529524851	chr14:20331524-20331525	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs542712285	chr14:20331525-20331526	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs542825524	chr14:20331552-20331553	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs201655129	chr14:20331603-20331604	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs540404103	chr14:20331638-20331639	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs376135193	chr14:20331662-20331663	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs565211979	chr14:20331666-20331667	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs532271590	chr14:20331667-20331668	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs544215927	chr14:20331692-20331693	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs562296929	chr14:20331693-20331694	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs529806778	chr14:20331701-20331702	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs548021137	chr14:20331746-20331747	Inactive region	Chromatin interactive region	1 gene(s)	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
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	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

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:20329200-20330800	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr14:20330600-20331400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
3	chr14:20341000-20341600	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr14:20341000-20341600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
5	chr14:20341200-20341400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr14:20341200-20341400	Active TSS	Adipose Nuclei	Adipose
7	chr14:20341200-20341400	Bivalent/Poised TSS	Brain Angular Gyrus	brain
8	chr14:20341200-20341400	Flanking Active TSS	A549	lung
9	chr14:20341200-20341600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr14:20341200-20341600	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
11	chr14:20341200-20341600	Active TSS	K562	blood
12	chr14:20341400-20341600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr14:20341400-20341600	Flanking Active TSS	Adipose Nuclei	Adipose
14	chr14:20341400-20341600	Bivalent Enhancer	Brain Angular Gyrus	brain
15	chr14:20341400-20341800	Active TSS	A549	lung
16	chr14:20341600-20341800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr14:20341600-20341800	Enhancers	Adipose Nuclei	Adipose
18	chr14:20341600-20341800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
19	chr14:20342800-20343400	Enhancers	HepG2	liver
20	chr14:20343200-20352400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
21	chr14:20350200-20350400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
22	chr14:20351200-20351600	ZNF genes & repeats	Fetal Brain Male	brain
23	chr14:20351200-20352200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
24	chr14:20351200-20354200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr14:20355400-20356200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
26	chr14:20355800-20358400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
27	chr14:20359000-20366000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr14:20360400-20363800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
29	chr14:20360600-20364000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
30	chr14:20361800-20364200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr14:20362000-20363200	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
32	chr14:20362400-20364800	ZNF genes & repeats	Adipose Nuclei	Adipose
33	chr14:20368800-20370800	Enhancers	Adipose Nuclei	Adipose
34	chr14:20369000-20379600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
35	chr14:20370200-20372000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
36	chr14:20373800-20374600	ZNF genes & repeats	Fetal Brain Male	brain
37	chr14:20374200-20374600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr14:20378200-20379400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
39	chr14:20383200-20385000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
40	chr14:20386400-20386800	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr14:20386800-20389000	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr14:20388200-20391000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr14:20389000-20389200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
44	chr14:20389000-20389600	Active TSS	Brain Substantia Nigra	brain
45	chr14:20389200-20390000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
46	chr14:20392000-20392400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr14:20393800-20394200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
48	chr14:20404400-20404800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
49	chr14:20406200-20406800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
50	chr14:20410000-20410400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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