Variant report

Variant	nsv1059656
Chromosome Location	chr20:14890631-15045412
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1687)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1687 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14959886-14961038	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:15041045-15042049	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:14971646-14973208	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:14986003-14986310	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:14965101-14967567	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	ATF3	chr20:14965454-14966225	A549	lung:	n/a	n/a
9	ATF3	chr20:14966529-14967363	A549	lung:	n/a	n/a
10	ATF3	chr20:14966508-14967301	A549	lung:	n/a	n/a
11	BACH1	chr20:14952997-14953174	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr20:15041087-15041347	GM12878	blood:	n/a	n/a
13	BATF	chr20:15040971-15041310	GM12878	blood:	n/a	n/a
14	BATF	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
15	BCL3	chr20:14966427-14967324	A549	lung:	n/a	n/a
16	BCL3	chr20:14966411-14967352	A549	lung:	n/a	n/a
17	BCL3	chr20:14965529-14966338	A549	lung:	n/a	chr20:14966177-14966184
18	BHLHE40	chr20:15042548-15042950	HepG2	liver:	n/a	n/a
19	BHLHE40	chr20:15041038-15041678	HepG2	liver:	n/a	n/a
20	BHLHE40	chr20:14960125-14960599	HepG2	liver:	n/a	n/a
21	BHLHE40	chr20:14965455-14966238	HepG2	liver:	n/a	n/a
22	BHLHE40	chr20:14977538-14977786	HepG2	liver:	n/a	n/a
23	BRCA1	chr20:15041931-15042029	HepG2	liver:	n/a	n/a
24	BRCA1	chr20:15042587-15042806	HepG2	liver:	n/a	n/a
25	BRCA1	chr20:14960587-14960671	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr20:14965501-14966238	HepG2	liver:	n/a	n/a
27	BRCA1	chr20:14936483-14937509	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr20:15043714-15043822	HepG2	liver:	n/a	n/a
29	BRCA1	chr20:14943807-14944695	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr20:14966739-14967191	HepG2	liver:	n/a	n/a
31	CEBPB	chr20:14966662-14967594	A549	lung:	n/a	chr20:14967070-14967081
32	CEBPB	chr20:14943854-14944487	A549	lung:	n/a	n/a
33	CEBPB	chr20:14940164-14940465	HepG2	liver:	n/a	n/a
34	CEBPB	chr20:15041173-15041651	HepG2	liver:	n/a	chr20:15041402-15041419 chr20:15041403-15041414 chr20:15041404-15041415 chr20:15041403-15041416 chr20:15041403-15041416
35	CEBPB	chr20:14971530-14972227	A549	lung:	n/a	chr20:14971798-14971811
36	CEBPB	chr20:15041282-15041553	A549	lung:	n/a	chr20:15041402-15041419 chr20:15041403-15041414 chr20:15041404-15041415 chr20:15041403-15041416 chr20:15041403-15041416
37	CEBPB	chr20:15027696-15027949	HepG2	liver:	n/a	n/a
38	CEBPB	chr20:14949044-14949348	HepG2	liver:	n/a	chr20:14949185-14949196 chr20:14949184-14949197 chr20:14949186-14949195 chr20:14949184-14949195
39	CEBPB	chr20:14940149-14940548	HepG2	liver:	n/a	n/a
40	CEBPB	chr20:15026013-15026308	HepG2	liver:	n/a	n/a
41	CEBPB	chr20:14965680-14966111	HepG2	liver:	n/a	n/a
42	CEBPB	chr20:14972560-14973255	A549	lung:	n/a	chr20:14972825-14972837
43	CEBPB	chr20:14944001-14944439	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr20:14989586-14989920	HepG2	liver:	n/a	chr20:14989740-14989751 chr20:14989742-14989753 chr20:14989740-14989753 chr20:14989742-14989751
45	CEBPB	chr20:14971698-14972061	HepG2	liver:	n/a	chr20:14971798-14971811
46	CEBPB	chr20:14965655-14966093	A549	lung:	n/a	n/a
47	CEBPB	chr20:15042642-15043001	HepG2	liver:	n/a	chr20:15042893-15042904
48	CEBPB	chr20:14902325-14902664	Hela-S3	cervix:	n/a	chr20:14902374-14902386
49	CEBPB	chr20:14965531-14966128	HepG2	liver:	n/a	n/a
50	CEBPB	chr20:15042724-15042972	HepG2	liver:	n/a	chr20:15042893-15042904

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:14904432-14904482	AG10803	skin:	n/a
2	chr20:14904432-14904482	SAEC	small airway:	n/a
3	chr20:14904432-14904482	SK-N-SH	brain:	n/a
4	chr20:14904432-14904482	GM12878	blood:	n/a
5	chr20:14904432-14904482	NHDF-neo	bronchial:	n/a
6	chr20:14904432-14904482	Hepatocyte	liver:	n/a
7	chr20:14904432-14904482	SKMC	muscle:	n/a
8	chr20:14904432-14904482	HRE	kidney:	n/a
9	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
10	chr20:14904432-14904482	ProgFib	skin:	n/a
11	chr20:14904432-14904482	HepG2	liver:	n/a
12	chr20:14904432-14904482	NB4	blood:	n/a
13	chr20:14904432-14904482	Jurkat	blood:	n/a
14	chr20:14904432-14904482	AG09319	gingival:	n/a
15	chr20:14904432-14904482	Hela-S3	cervix:	n/a
16	chr20:14904432-14904482	HL-60	blood:	n/a
17	chr20:14904432-14904482	PFSK-1	brain:	n/a
18	chr20:14904432-14904482	GM12891	blood:	n/a
19	chr20:14904432-14904482	BE2_C	brain:	n/a
20	chr20:14904432-14904482	MCF-7	breast:	n/a
21	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
22	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
23	chr20:14904432-14904482	HIPEpiC	eye:	n/a
24	chr20:14904432-14904482	GM12892	blood:	n/a
25	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
26	chr20:14904432-14904482	HMEC	breast:	n/a
27	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
28	chr20:14904432-14904482	LNCaP	prostate:	n/a
29	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
30	chr20:14904432-14904482	HCF	heart:	n/a
31	chr20:14904432-14904482	IMR90	lung:	fetal
32	chr20:14904432-14904482	NH-A	brain:	n/a
33	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
34	chr20:14904432-14904482	AG04449	skin:	fetal
35	chr20:14904432-14904482	U87	brain:	n/a
36	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
37	chr20:14904432-14904482	RPTEC	kidney:	n/a
38	chr20:14904432-14904482	GM06990	blood:	n/a
39	chr20:14904432-14904482	NHBE	bronchial:	n/a
40	chr20:14904432-14904482	T-47D	breast:	n/a
41	chr20:14904432-14904482	PANC-1	pancreas:	n/a
42	chr20:14904432-14904482	AG09309	skin:	n/a
43	chr20:14904432-14904482	GM19239	blood:	n/a
44	chr20:14904432-14904482	HCM	heart:	n/a
45	chr20:14904432-14904482	PrEC	prostate:	n/a
46	chr20:14904432-14904482	HRPEpiC	eye:	n/a
47	chr20:14904432-14904482	K562	blood:	n/a
48	chr20:14904432-14904482	SK-N-MC	brain:	n/a
49	chr20:14904432-14904482	A549	lung:	n/a
50	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a

(count:19 , 50 per page) page: 1

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

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FLRT3-1	chr20:14910021-14910132	ENSG00000235914.1
2	lnc-FLRT3-2	chr20:14914489-14914588	ENSG00000237832.1
3	lnc-FLRT3-1	chr20:14910021-14910142	NONHSAT078721
4	lnc-FLRT3-1	chr20:14910021-14910164	NR_037841
5	lnc-FLRT3-1	chr20:14910021-14910161	ENSG00000235914.1
6	lnc-FLRT3-1	chr20:14910021-14910164	NR_072988
7	lnc-FLRT3-1	chr20:14910021-14910164	NR_110318
8	lnc-FLRT3-2	chr20:14915884-14916009	ENSG00000237832.1
9	lnc-FLRT3-2	chr20:14915576-14915720	ENSG00000237832.1
10	lnc-FLRT3-1	chr20:14910021-14910154	NONHSAT078722

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: 5479 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:5479 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139086493	chr20:14890636-14890637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs201170662	chr20:14890647-14890648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534959519	chr20:14890649-14890650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182667743	chr20:14890670-14890671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559607600	chr20:14890733-14890734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185468460	chr20:14890774-14890775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528555523	chr20:14890782-14890783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs144048088	chr20:14890804-14890805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs114749037	chr20:14890810-14890811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115142199	chr20:14890846-14890847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs578241071	chr20:14890891-14890892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs146440615	chr20:14890901-14890902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573907104	chr20:14890921-14890922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531497441	chr20:14890932-14890933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559723167	chr20:14890955-14890956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545428981	chr20:14890989-14890990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140563855	chr20:14891001-14891002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369056241	chr20:14891008-14891009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545029668	chr20:14891047-14891048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190969374	chr20:14891104-14891105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184007425	chr20:14891152-14891153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs551513254	chr20:14891226-14891227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549087527	chr20:14891356-14891357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561125037	chr20:14891363-14891364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571292405	chr20:14891372-14891373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs77335400	chr20:14891391-14891392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550859488	chr20:14891406-14891407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546884560	chr20:14891409-14891410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567576246	chr20:14891499-14891500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189146638	chr20:14891500-14891501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539326926	chr20:14891509-14891510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553499023	chr20:14891515-14891516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150027647	chr20:14891535-14891536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs193033549	chr20:14891542-14891543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1536899	chr20:14891588-14891589	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs116407468	chr20:14891595-14891596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182918475	chr20:14891596-14891597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553209980	chr20:14891611-14891612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373883006	chr20:14891628-14891629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538710301	chr20:14891667-14891668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577823205	chr20:14891732-14891733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78145211	chr20:14891762-14891763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563507035	chr20:14891772-14891773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1571518	chr20:14891787-14891788	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs187217109	chr20:14891800-14891801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542696986	chr20:14891809-14891810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369848952	chr20:14891852-14891853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115177610	chr20:14891858-14891859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191874662	chr20:14891866-14891867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546749439	chr20:14891918-14891919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

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:957 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14888400-14894600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr20:14889400-14896000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr20:14890600-14891200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr20:14890800-14891400	Enhancers	Fetal Kidney	kidney
5	chr20:14891200-14891400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr20:14891200-14894600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr20:14891400-14899600	Weak transcription	Fetal Kidney	kidney
8	chr20:14894400-14894600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr20:14894400-14895200	Enhancers	HUVEC	blood vessel
10	chr20:14894400-14897400	Enhancers	Fetal Brain Male	brain
11	chr20:14894600-14894800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr20:14894600-14894800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr20:14894600-14895000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr20:14894600-14895000	Enhancers	Fetal Muscle Leg	muscle
15	chr20:14894600-14895200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr20:14894600-14895200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr20:14894600-14895600	Enhancers	Fetal Brain Female	brain
18	chr20:14894800-14895000	Enhancers	Fetal Lung	lung
19	chr20:14894800-14895000	Enhancers	Ovary	ovary
20	chr20:14894800-14896200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr20:14894800-14897800	Enhancers	Fetal Heart	heart
22	chr20:14894800-14898000	Enhancers	Fetal Stomach	stomach
23	chr20:14895000-14896000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr20:14895000-14896200	Weak transcription	Fetal Muscle Leg	muscle
25	chr20:14895200-14896200	Weak transcription	Fetal Lung	lung
26	chr20:14895200-14900000	Weak transcription	HUVEC	blood vessel
27	chr20:14895200-14900200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr20:14895200-14900200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr20:14895600-14896000	Enhancers	Colon Smooth Muscle	Colon
30	chr20:14895600-14896200	Flanking Active TSS	Fetal Brain Female	brain
31	chr20:14895800-14896000	Enhancers	Brain Hippocampus Middle	brain
32	chr20:14895800-14896000	Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr20:14895800-14896200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr20:14895800-14896200	Active TSS	Ovary	ovary
35	chr20:14895800-14896200	Active TSS	Stomach Smooth Muscle	stomach
36	chr20:14895800-14896600	Enhancers	H9 Cell Line	embryonic stem cell
37	chr20:14895800-14896800	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr20:14896000-14896400	Enhancers	H1 Cell Line	embryonic stem cell
39	chr20:14896000-14896400	Enhancers	Brain Angular Gyrus	brain
40	chr20:14896000-14896400	Active TSS	Brain Hippocampus Middle	brain
41	chr20:14896000-14896400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
42	chr20:14896000-14896400	Active TSS	Psoas Muscle	Psoas
43	chr20:14896000-14896400	Active TSS	Rectal Smooth Muscle	rectum
44	chr20:14896000-14896400	Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr20:14896000-14896400	Active TSS	Skeletal Muscle Female	skeletal muscle
46	chr20:14896000-14896600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr20:14896000-14896800	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr20:14896000-14896800	Flanking Active TSS	Colon Smooth Muscle	Colon
49	chr20:14896200-14896400	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr20:14896200-14896400	Flanking Active TSS	Ovary	ovary

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