Variant report

Variant	nsv912769
Chromosome Location	chr20:14872313-15126507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1923)
CpG islands
(count:61)
Chromatin interactive
region (count:21)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1923 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:15042539-15043096	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:14959886-14961038	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:14936639-14937073	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:14986003-14986310	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:14971646-14973208	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:14965101-14967567	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:15041045-15042049	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	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
14	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
15	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
16	BATF	chr20:15041087-15041347	GM12878	blood:	n/a	n/a
17	BATF	chr20:15040971-15041310	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	chr20:14966411-14967352	A549	lung:	n/a	n/a
21	BCL3	chr20:14965529-14966338	A549	lung:	n/a	chr20:14966177-14966184
22	BCL3	chr20:14966427-14967324	A549	lung:	n/a	n/a
23	BHLHE40	chr20:15042548-15042950	HepG2	liver:	n/a	n/a
24	BHLHE40	chr20:14965455-14966238	HepG2	liver:	n/a	n/a
25	BHLHE40	chr20:14960125-14960599	HepG2	liver:	n/a	n/a
26	BHLHE40	chr20:14977538-14977786	HepG2	liver:	n/a	n/a
27	BHLHE40	chr20:15041038-15041678	HepG2	liver:	n/a	n/a
28	BRCA1	chr20:14943807-14944695	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr20:14966739-14967191	HepG2	liver:	n/a	n/a
30	BRCA1	chr20:14965501-14966238	HepG2	liver:	n/a	n/a
31	BRCA1	chr20:15042587-15042806	HepG2	liver:	n/a	n/a
32	BRCA1	chr20:15043714-15043822	HepG2	liver:	n/a	n/a
33	BRCA1	chr20:14960587-14960671	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr20:15041931-15042029	HepG2	liver:	n/a	n/a
35	BRCA1	chr20:15054620-15054671	HepG2	liver:	n/a	n/a
36	BRCA1	chr20:14936483-14937509	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr20:14972648-14973239	A549	lung:	n/a	chr20:14972825-14972837
38	CEBPB	chr20:14873115-14873441	HepG2	liver:	n/a	chr20:14873258-14873269
39	CEBPB	chr20:14936709-14937068	HepG2	liver:	n/a	n/a
40	CEBPB	chr20:14971698-14972061	HepG2	liver:	n/a	chr20:14971798-14971811
41	CEBPB	chr20:14940158-14940544	HepG2	liver:	n/a	n/a
42	CEBPB	chr20:15102391-15102522	A549	lung:	n/a	n/a
43	CEBPB	chr20:14940171-14940542	IMR90	lung:	n/a	n/a
44	CEBPB	chr20:14940187-14940533	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr20:14966581-14967363	A549	lung:	n/a	chr20:14967070-14967081
46	CEBPB	chr20:14966473-14967444	A549	lung:	n/a	chr20:14967070-14967081
47	CEBPB	chr20:14989638-14989863	A549	lung:	n/a	chr20:14989740-14989751 chr20:14989742-14989753 chr20:14989740-14989753 chr20:14989742-14989751
48	CEBPB	chr20:14965655-14966093	A549	lung:	n/a	n/a
49	CEBPB	chr20:14966677-14967240	HepG2	liver:	n/a	chr20:14967070-14967081
50	CEBPB	chr20:14940149-14940548	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:14904432-14904482	SKMC	muscle:	n/a
2	chr20:14904432-14904482	MCF-7	breast:	n/a
3	chr20:14904432-14904482	A549	lung:	n/a
4	chr20:14904432-14904482	AG04449	skin:	fetal
5	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
6	chr20:14904432-14904482	AG09319	gingival:	n/a
7	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
8	chr20:14904432-14904482	RPTEC	kidney:	n/a
9	chr20:14904432-14904482	BJ	skin:	n/a
10	chr20:14904432-14904482	Jurkat	blood:	n/a
11	chr20:14904432-14904482	NB4	blood:	n/a
12	chr20:14904432-14904482	IMR90	lung:	fetal
13	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
14	chr20:14904432-14904482	H1-hESC	embryonic stem cell:	embryo
15	chr20:14904432-14904482	PFSK-1	brain:	n/a
16	chr20:14904432-14904482	HRPEpiC	eye:	n/a
17	chr20:14904432-14904482	BE2_C	brain:	n/a
18	chr20:14904432-14904482	Hela-S3	cervix:	n/a
19	chr20:14904432-14904482	AG09309	skin:	n/a
20	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
21	chr20:14904432-14904482	Hepatocyte	liver:	n/a
22	chr20:14904432-14904482	LNCaP	prostate:	n/a
23	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
24	chr20:14904432-14904482	HRE	kidney:	n/a
25	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
26	chr20:14904432-14904482	HCM	heart:	n/a
27	chr20:14904432-14904482	ProgFib	skin:	n/a
28	chr20:14904432-14904482	HCT-116	colon:	n/a
29	chr20:14904432-14904482	AG04450	lung:	fetal
30	chr20:14904432-14904482	GM12891	blood:	n/a
31	chr20:14904432-14904482	GM06990	blood:	n/a
32	chr20:14904432-14904482	T-47D	breast:	n/a
33	chr20:14904432-14904482	GM12892	blood:	n/a
34	chr20:14904432-14904482	Caco-2	colon:	n/a
35	chr20:14904432-14904482	PANC-1	pancreas:	n/a
36	chr20:14904432-14904482	GM19239	blood:	n/a
37	chr20:14904432-14904482	NHBE	bronchial:	n/a
38	chr20:14904432-14904482	GM12878	blood:	n/a
39	chr20:14904432-14904482	HEK293	kidney:	embryo
40	chr20:14904432-14904482	SAEC	small airway:	n/a
41	chr20:14904432-14904482	SK-N-MC	brain:	n/a
42	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
43	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
44	chr20:14904432-14904482	AG10803	skin:	n/a
45	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
46	chr20:14904432-14904482	NH-A	brain:	n/a
47	chr20:14904432-14904482	U87	brain:	n/a
48	chr20:14904432-14904482	HL-60	blood:	n/a
49	chr20:14904432-14904482	K562	blood:	n/a
50	chr20:14904432-14904482	NHDF-neo	bronchial:	n/a

(count:21 , 50 per page) page: 1

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

(count:12 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 7788 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:7788 , 50 per page) page: 1 2 3 4 5 6 7 ... 156

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6042971	chr20:14873478-14873479	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs138638302	chr20:14873481-14873482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs142778176	chr20:14873486-14873487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147376948	chr20:14873513-14873514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185968021	chr20:14873527-14873528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548419431	chr20:14873556-14873557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566953369	chr20:14873559-14873560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6135293	chr20:14873574-14873575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs66577403	chr20:14873617-14873618	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs114438955	chr20:14873627-14873628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190292474	chr20:14873628-14873629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538284073	chr20:14873716-14873717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557083638	chr20:14873741-14873742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575458065	chr20:14873750-14873751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113943036	chr20:14873769-14873770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374874027	chr20:14873778-14873779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115178721	chr20:14873807-14873808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs6079599	chr20:14873820-14873821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561026162	chr20:14873880-14873881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575797889	chr20:14873907-14873908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531946457	chr20:14873915-14873916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182513916	chr20:14873930-14873931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565063859	chr20:14873943-14873944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs67508130	chr20:14873955-14873956	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs186285348	chr20:14873963-14873964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111817069	chr20:14882220-14882221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs140790928	chr20:14882233-14882234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs6079600	chr20:14882266-14882267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560663578	chr20:14882279-14882280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572538254	chr20:14882407-14882408	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs150113250	chr20:14882417-14882418	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs113658419	chr20:14882465-14882466	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs183499715	chr20:14882479-14882480	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs570040548	chr20:14882536-14882537	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs188509554	chr20:14882570-14882571	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs6042986	chr20:14882621-14882622	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs562990718	chr20:14882630-14882631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs529718821	chr20:14882658-14882659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547958581	chr20:14882740-14882741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77283238	chr20:14882771-14882772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191208651	chr20:14882824-14882825	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs6034058	chr20:14882842-14882843	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs142914181	chr20:14882868-14882869	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs537714200	chr20:14882890-14882891	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs565982424	chr20:14882900-14882901	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs146154282	chr20:14882903-14882904	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs568342281	chr20:14882991-14882992	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs369066676	chr20:14883009-14883010	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs535877461	chr20:14883011-14883012	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs183271807	chr20:14883073-14883074	Flanking Active TSS	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:1119 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14873400-14874000	Enhancers	Rectal Mucosa Donor 31	rectum
2	chr20:14882200-14882400	Enhancers	GM12878-XiMat	blood
3	chr20:14882400-14882600	Flanking Active TSS	GM12878-XiMat	blood
4	chr20:14882600-14882800	Enhancers	GM12878-XiMat	blood
5	chr20:14882800-14883600	Flanking Active TSS	GM12878-XiMat	blood
6	chr20:14887400-14888200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr20:14887600-14888000	Enhancers	H9 Cell Line	embryonic stem cell
8	chr20:14887600-14888000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr20:14887600-14888200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr20:14887600-14888200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr20:14887600-14888200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr20:14887600-14888200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr20:14887600-14888400	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr20:14887600-14888400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr20:14887600-14888400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr20:14887600-14888400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr20:14887600-14888400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr20:14887800-14888200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr20:14887800-14888200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr20:14887800-14888200	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr20:14888400-14889200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr20:14888400-14894600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr20:14889200-14889400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr20:14889400-14896000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr20:14890600-14891200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr20:14890800-14891400	Enhancers	Fetal Kidney	kidney
27	chr20:14891200-14891400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr20:14891200-14894600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr20:14891400-14899600	Weak transcription	Fetal Kidney	kidney
30	chr20:14894400-14894600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr20:14894400-14895200	Enhancers	HUVEC	blood vessel
32	chr20:14894400-14897400	Enhancers	Fetal Brain Male	brain
33	chr20:14894600-14894800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr20:14894600-14894800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr20:14894600-14895000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr20:14894600-14895000	Enhancers	Fetal Muscle Leg	muscle
37	chr20:14894600-14895200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr20:14894600-14895200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr20:14894600-14895600	Enhancers	Fetal Brain Female	brain
40	chr20:14894800-14895000	Enhancers	Fetal Lung	lung
41	chr20:14894800-14895000	Enhancers	Ovary	ovary
42	chr20:14894800-14896200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr20:14894800-14897800	Enhancers	Fetal Heart	heart
44	chr20:14894800-14898000	Enhancers	Fetal Stomach	stomach
45	chr20:14895000-14896000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr20:14895000-14896200	Weak transcription	Fetal Muscle Leg	muscle
47	chr20:14895200-14896200	Weak transcription	Fetal Lung	lung
48	chr20:14895200-14900000	Weak transcription	HUVEC	blood vessel
49	chr20:14895200-14900200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr20:14895200-14900200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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