Variant report

Variant	nsv585542
Chromosome Location	chr20:14867228-15073680
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1820)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1820 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14965101-14967567	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:14986003-14986310	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:14971646-14973208	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:15041045-15042049	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:14959886-14961038	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:14936639-14937073	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:15042539-15043096	HepG2	liver:	n/a	n/a
8	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
9	ATF3	chr20:14965454-14966225	A549	lung:	n/a	n/a
10	ATF3	chr20:14966529-14967363	A549	lung:	n/a	n/a
11	ATF3	chr20:14966508-14967301	A549	lung:	n/a	n/a
12	BACH1	chr20:14952997-14953174	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
14	BATF	chr20:15040971-15041310	GM12878	blood:	n/a	n/a
15	BATF	chr20:15041087-15041347	GM12878	blood:	n/a	n/a
16	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
17	BATF	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
18	BCL11A	chr20:14883093-14883400	GM12878	blood:	n/a	chr20:14883229-14883238
19	BCL11A	chr20:14883096-14883392	GM12878	blood:	n/a	chr20:14883229-14883238
20	BCL3	chr20:14966427-14967324	A549	lung:	n/a	n/a
21	BCL3	chr20:14965529-14966338	A549	lung:	n/a	chr20:14966177-14966184
22	BCL3	chr20:14966411-14967352	A549	lung:	n/a	n/a
23	BHLHE40	chr20:14977538-14977786	HepG2	liver:	n/a	n/a
24	BHLHE40	chr20:14960125-14960599	HepG2	liver:	n/a	n/a
25	BHLHE40	chr20:15041038-15041678	HepG2	liver:	n/a	n/a
26	BHLHE40	chr20:14965455-14966238	HepG2	liver:	n/a	n/a
27	BHLHE40	chr20:15042548-15042950	HepG2	liver:	n/a	n/a
28	BRCA1	chr20:15042587-15042806	HepG2	liver:	n/a	n/a
29	BRCA1	chr20:14966739-14967191	HepG2	liver:	n/a	n/a
30	BRCA1	chr20:14936483-14937509	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr20:14960587-14960671	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr20:15054620-15054671	HepG2	liver:	n/a	n/a
33	BRCA1	chr20:14965501-14966238	HepG2	liver:	n/a	n/a
34	BRCA1	chr20:14943807-14944695	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr20:15041931-15042029	HepG2	liver:	n/a	n/a
36	BRCA1	chr20:15043714-15043822	HepG2	liver:	n/a	n/a
37	CEBPB	chr20:14965601-14966250	HepG2	liver:	n/a	n/a
38	CEBPB	chr20:15041207-15041504	HepG2	liver:	n/a	chr20:15041402-15041419 chr20:15041403-15041414 chr20:15041404-15041415 chr20:15041403-15041416 chr20:15041403-15041416
39	CEBPB	chr20:14932597-14932787	HepG2	liver:	n/a	n/a
40	CEBPB	chr20:14989586-14989920	HepG2	liver:	n/a	chr20:14989740-14989751 chr20:14989742-14989753 chr20:14989740-14989753 chr20:14989742-14989751
41	CEBPB	chr20:14966892-14967224	HepG2	liver:	n/a	chr20:14967070-14967081
42	CEBPB	chr20:14966705-14967614	HepG2	liver:	n/a	chr20:14967070-14967081
43	CEBPB	chr20:14978534-14978808	A549	lung:	n/a	n/a
44	CEBPB	chr20:14971734-14971993	HepG2	liver:	n/a	chr20:14971798-14971811
45	CEBPB	chr20:15019716-15020261	MCF-7	breast:	n/a	n/a
46	CEBPB	chr20:14940158-14940544	HepG2	liver:	n/a	n/a
47	CEBPB	chr20:14900166-14900714	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr20:14971590-14972027	A549	lung:	n/a	chr20:14971798-14971811
49	CEBPB	chr20:14965680-14966111	HepG2	liver:	n/a	n/a
50	CEBPB	chr20:14966662-14967594	A549	lung:	n/a	chr20:14967070-14967081

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:14904432-14904482	NB4	blood:	n/a
2	chr20:14904432-14904482	HCT-116	colon:	n/a
3	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
4	chr20:14904432-14904482	Caco-2	colon:	n/a
5	chr20:14904432-14904482	HRPEpiC	eye:	n/a
6	chr20:14904432-14904482	GM06990	blood:	n/a
7	chr20:14904432-14904482	SK-N-MC	brain:	n/a
8	chr20:14904432-14904482	HCF	heart:	n/a
9	chr20:14904432-14904482	NHDF-neo	bronchial:	n/a
10	chr20:14904432-14904482	AG09309	skin:	n/a
11	chr20:14904432-14904482	H1-hESC	embryonic stem cell:	embryo
12	chr20:14904432-14904482	SKMC	muscle:	n/a
13	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
14	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
15	chr20:14904432-14904482	SK-N-SH	brain:	n/a
16	chr20:14904432-14904482	SAEC	small airway:	n/a
17	chr20:14904432-14904482	PFSK-1	brain:	n/a
18	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
19	chr20:14904432-14904482	HMEC	breast:	n/a
20	chr20:14904432-14904482	LNCaP	prostate:	n/a
21	chr20:14904432-14904482	GM12891	blood:	n/a
22	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
23	chr20:14904432-14904482	HRE	kidney:	n/a
24	chr20:14904432-14904482	HL-60	blood:	n/a
25	chr20:14904432-14904482	AG10803	skin:	n/a
26	chr20:14904432-14904482	ProgFib	skin:	n/a
27	chr20:14904432-14904482	HEK293	kidney:	embryo
28	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
29	chr20:14904432-14904482	AG04449	skin:	fetal
30	chr20:14904432-14904482	IMR90	lung:	fetal
31	chr20:14904432-14904482	U87	brain:	n/a
32	chr20:14904432-14904482	T-47D	breast:	n/a
33	chr20:14904432-14904482	BJ	skin:	n/a
34	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
35	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
36	chr20:14904432-14904482	GM12878	blood:	n/a
37	chr20:14904432-14904482	HCM	heart:	n/a
38	chr20:14904432-14904482	Hela-S3	cervix:	n/a
39	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
40	chr20:14904432-14904482	K562	blood:	n/a
41	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
42	chr20:14904432-14904482	NT2-D1	testis:	n/a
43	chr20:14904432-14904482	Hepatocyte	liver:	n/a
44	chr20:14904432-14904482	GM19239	blood:	n/a
45	chr20:14904432-14904482	BE2_C	brain:	n/a
46	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
47	chr20:14904432-14904482	AG04450	lung:	fetal
48	chr20:14904432-14904482	CMK	blood:	n/a
49	chr20:14904432-14904482	RPTEC	kidney:	n/a
50	chr20:14904432-14904482	PrEC	prostate:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
2	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
3	chr20:14983136..14983867-chr7:139874694..139875444,2	MCF-7	breast:
4	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
5	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
6	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
7	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
8	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
9	chr20:14913183..14915031-chr20:14915260..14917096,2	MCF-7	breast:
10	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
11	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
12	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
13	chr20:14593902..14596386-chr20:15052997..15054796,2	K562	blood:
14	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
15	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
16	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
17	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
18	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
19	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
20	chr20:14905161..14907169-chr20:14915982..14918854,2	MCF-7	breast:
21	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
22	chr20:14050662..14052329-chr20:14946506..14948938,2	MCF-7	breast:
23	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FLRT3-1	chr20:14885587-14886675	ENSG00000235914.1
2	lnc-FLRT3-1	chr20:14910021-14910164	NR_072988
3	lnc-FLRT3-1	chr20:14868742-14868950	ENSG00000235914.1
4	lnc-FLRT3-1	chr20:14910021-14910154	NONHSAT078722
5	lnc-FLRT3-1	chr20:14910021-14910142	NONHSAT078721
6	lnc-C20orf7-3	chr20:14868789-14869314	NONHSAT078714
7	lnc-FLRT3-2	chr20:14915576-14915720	ENSG00000237832.1
8	lnc-FLRT3-1	chr20:14868742-14868950	NONHSAT078721
9	lnc-FLRT3-2	chr20:14914489-14914588	ENSG00000237832.1
10	lnc-FLRT3-2	chr20:14915884-14916009	ENSG00000237832.1
11	lnc-FLRT3-1	chr20:14910021-14910161	ENSG00000235914.1
12	lnc-FLRT3-1	chr20:14910021-14910164	NR_037841
13	lnc-FLRT3-1	chr20:14868742-14868950	NR_037841
14	lnc-FLRT3-1	chr20:14885587-14886675	NR_072988
15	lnc-FLRT3-1	chr20:14910021-14910164	NR_110318
16	lnc-FLRT3-1	chr20:14910021-14910132	ENSG00000235914.1

No data

Variant related genes	Relation type
ENSG00000237832	TF binding region
RNU6-1159P	TF binding region
RNU6-115P	TF binding region
MACROD2-AS1	TF binding region
ENSG00000237832	CpG island
RNU6-1159P	CpG island
RNU6-115P	CpG island
MACROD2-AS1	CpG island
ENSG00000237832	chromatin interactions

Extended variants
information (count: 6774 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:6774 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs984261	chr20:14867228-14867229	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs539545603	chr20:14867241-14867242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141158653	chr20:14867341-14867342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571051846	chr20:14867355-14867356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150727736	chr20:14867377-14867378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187164434	chr20:14867378-14867379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573225825	chr20:14867381-14867382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1475531	chr20:14867422-14867423	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs554692395	chr20:14867425-14867426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573017157	chr20:14867432-14867433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs16995139	chr20:14867456-14867457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565042453	chr20:14867508-14867509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs77599353	chr20:14867518-14867519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs6034054	chr20:14867530-14867531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs6135291	chr20:14867581-14867582	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs149916850	chr20:14867593-14867594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530014455	chr20:14867595-14867596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147155992	chr20:14867630-14867631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560203133	chr20:14867638-14867639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191547693	chr20:14867652-14867653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538869150	chr20:14867720-14867721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146707688	chr20:14867726-14867727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140087361	chr20:14867740-14867741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559073748	chr20:14867778-14867779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182800552	chr20:14867872-14867873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35270375	chr20:14867877-14867878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533342150	chr20:14867986-14867987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550427396	chr20:14867991-14867992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201729977	chr20:14868046-14868047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529926593	chr20:14868056-14868057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs75094506	chr20:14868058-14868059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34045128	chr20:14868060-14868061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145524401	chr20:14868083-14868084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6042964	chr20:14868088-14868089	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs554653895	chr20:14868090-14868091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs61392935	chr20:14868105-14868106	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs533843179	chr20:14868116-14868117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558383289	chr20:14868120-14868121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34850340	chr20:14868145-14868146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576939182	chr20:14868155-14868156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs6079597	chr20:14868186-14868187	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs556407031	chr20:14868201-14868202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187086368	chr20:14868223-14868224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2210045	chr20:14868225-14868226	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs540582523	chr20:14868247-14868248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560066923	chr20:14868291-14868292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs6074812	chr20:14868300-14868301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373021315	chr20:14868331-14868332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377357064	chr20:14868334-14868335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2225302	chr20:14868353-14868354	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:71)

Disease	PMID	Source
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Glaucoma	21310917	CNVD
Alagille syndrome	22470819	CNVD
Lung cancer	16773561	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Myelofibrosis	22110671	CNVD
Kabuki syndrome	21720541	CNVD
Glioblastoma multiforme	22286061	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Neurocytoma	17123091	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164919	CNVD
Multiple sclerosis	20663923	CNVD
Schizophrenia	20663923	CNVD
brain infarct	20663923	CNVD
Breast cancer	22522925	CNVD
Breast cancer	17142309	CNVD
Cancer	20164920	CNVD
Schizophrenia	23813976	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20531469	CNVD
Melanoma	17363583	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	20967226	CNVD
Cancer	21272361	CNVD
Schizophrenia	19805367	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:1050 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14865400-14869000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr20:14867000-14871000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr20:14867200-14868800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr20:14868200-14869200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr20:14868200-14869400	Enhancers	Dnd41	blood
6	chr20:14868400-14869400	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr20:14868600-14869000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr20:14868600-14869000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr20:14868600-14869200	Enhancers	Fetal Lung	lung
10	chr20:14868800-14869000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr20:14868800-14869200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr20:14868800-14869400	Enhancers	Ovary	ovary
13	chr20:14869000-14869200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr20:14869000-14869200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr20:14869000-14869400	Enhancers	Colon Smooth Muscle	Colon
16	chr20:14869000-14869400	Enhancers	Fetal Heart	heart
17	chr20:14869200-14870200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr20:14870200-14870400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr20:14870200-14871000	Enhancers	NHDF-Ad	bronchial
20	chr20:14872000-14872200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr20:14873400-14874000	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr20:14882200-14882400	Enhancers	GM12878-XiMat	blood
23	chr20:14882400-14882600	Flanking Active TSS	GM12878-XiMat	blood
24	chr20:14882600-14882800	Enhancers	GM12878-XiMat	blood
25	chr20:14882800-14883600	Flanking Active TSS	GM12878-XiMat	blood
26	chr20:14887400-14888200	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr20:14887600-14888000	Enhancers	H9 Cell Line	embryonic stem cell
28	chr20:14887600-14888000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr20:14887600-14888200	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr20:14887600-14888200	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr20:14887600-14888200	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr20:14887600-14888200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr20:14887600-14888400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr20:14887600-14888400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr20:14887600-14888400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr20:14887600-14888400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr20:14887600-14888400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr20:14887800-14888200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr20:14887800-14888200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr20:14887800-14888200	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr20:14888400-14889200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr20:14888400-14894600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr20:14889200-14889400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr20:14889400-14896000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr20:14890600-14891200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr20:14890800-14891400	Enhancers	Fetal Kidney	kidney
47	chr20:14891200-14891400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr20:14891200-14894600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr20:14891400-14899600	Weak transcription	Fetal Kidney	kidney
50	chr20:14894400-14894600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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