Variant report

Variant	nsv1055606
Chromosome Location	chr20:14883338-15045817
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1715)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1715 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

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	chr20:14936639-14937073	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:15042539-15043096	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:14971646-14973208	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:14959886-14961038	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	chr20:14966508-14967301	A549	lung:	n/a	n/a
11	ATF3	chr20:14966529-14967363	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	chr20:15040971-15041310	GM12878	blood:	n/a	n/a
17	BATF	chr20:15041087-15041347	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	chr20:14965529-14966338	A549	lung:	n/a	chr20:14966177-14966184
21	BCL3	chr20:14966427-14967324	A549	lung:	n/a	n/a
22	BCL3	chr20:14966411-14967352	A549	lung:	n/a	n/a
23	BHLHE40	chr20:14960125-14960599	HepG2	liver:	n/a	n/a
24	BHLHE40	chr20:15042548-15042950	HepG2	liver:	n/a	n/a
25	BHLHE40	chr20:14965455-14966238	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	chr20:14965501-14966238	HepG2	liver:	n/a	n/a
29	BRCA1	chr20:14960587-14960671	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr20:15043714-15043822	HepG2	liver:	n/a	n/a
31	BRCA1	chr20:14943807-14944695	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr20:15042587-15042806	HepG2	liver:	n/a	n/a
33	BRCA1	chr20:14966739-14967191	HepG2	liver:	n/a	n/a
34	BRCA1	chr20:14936483-14937509	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr20:15041931-15042029	HepG2	liver:	n/a	n/a
36	CEBPB	chr20:14943854-14944487	A549	lung:	n/a	n/a
37	CEBPB	chr20:14971613-14972080	HepG2	liver:	n/a	chr20:14971798-14971811
38	CEBPB	chr20:14902325-14902664	Hela-S3	cervix:	n/a	chr20:14902374-14902386
39	CEBPB	chr20:14937314-14937645	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr20:14940149-14940548	HepG2	liver:	n/a	n/a
41	CEBPB	chr20:14971698-14972061	HepG2	liver:	n/a	chr20:14971798-14971811
42	CEBPB	chr20:14978443-14978984	A549	lung:	n/a	n/a
43	CEBPB	chr20:15019746-15020183	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr20:15041173-15041651	HepG2	liver:	n/a	chr20:15041402-15041419 chr20:15041403-15041414 chr20:15041404-15041415 chr20:15041403-15041416 chr20:15041403-15041416
45	CEBPB	chr20:14943969-14944439	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr20:14965680-14966111	HepG2	liver:	n/a	n/a
47	CEBPB	chr20:14900166-14900714	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr20:14936709-14937068	HepG2	liver:	n/a	n/a
49	CEBPB	chr20:14972681-14973140	A549	lung:	n/a	chr20:14972825-14972837
50	CEBPB	chr20:14999859-15000028	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	HEK293	kidney:	embryo
2	chr20:14904432-14904482	HCF	heart:	n/a
3	chr20:14904432-14904482	HMEC	breast:	n/a
4	chr20:14904432-14904482	HepG2	liver:	n/a
5	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
6	chr20:14904432-14904482	T-47D	breast:	n/a
7	chr20:14904432-14904482	CMK	blood:	n/a
8	chr20:14904432-14904482	A549	lung:	n/a
9	chr20:14904432-14904482	BE2_C	brain:	n/a
10	chr20:14904432-14904482	SAEC	small airway:	n/a
11	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
12	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
13	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
14	chr20:14904432-14904482	PFSK-1	brain:	n/a
15	chr20:14904432-14904482	ProgFib	skin:	n/a
16	chr20:14904432-14904482	AG09319	gingival:	n/a
17	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
18	chr20:14904432-14904482	AG04449	skin:	fetal
19	chr20:14904432-14904482	AG09309	skin:	n/a
20	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
21	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
22	chr20:14904432-14904482	NB4	blood:	n/a
23	chr20:14904432-14904482	SKMC	muscle:	n/a
24	chr20:14904432-14904482	GM12878	blood:	n/a
25	chr20:14904432-14904482	NHBE	bronchial:	n/a
26	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
27	chr20:14904432-14904482	HRE	kidney:	n/a
28	chr20:14904432-14904482	MCF-7	breast:	n/a
29	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
30	chr20:14904432-14904482	NH-A	brain:	n/a
31	chr20:14904432-14904482	PrEC	prostate:	n/a
32	chr20:14904432-14904482	Hela-S3	cervix:	n/a
33	chr20:14904432-14904482	RPTEC	kidney:	n/a
34	chr20:14904432-14904482	K562	blood:	n/a
35	chr20:14904432-14904482	LNCaP	prostate:	n/a
36	chr20:14904432-14904482	HRPEpiC	eye:	n/a
37	chr20:14904432-14904482	Jurkat	blood:	n/a
38	chr20:14904432-14904482	BJ	skin:	n/a
39	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
40	chr20:14904432-14904482	AG04450	lung:	fetal
41	chr20:14904432-14904482	GM12892	blood:	n/a
42	chr20:14904432-14904482	Hepatocyte	liver:	n/a
43	chr20:14904432-14904482	HL-60	blood:	n/a
44	chr20:14904432-14904482	H1-hESC	embryonic stem cell:	embryo
45	chr20:14904432-14904482	GM19239	blood:	n/a
46	chr20:14904432-14904482	HCM	heart:	n/a
47	chr20:14904432-14904482	PANC-1	pancreas:	n/a
48	chr20:14904432-14904482	Caco-2	colon:	n/a
49	chr20:14904432-14904482	NHDF-neo	bronchial:	n/a
50	chr20:14904432-14904482	AG10803	skin:	n/a

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FLRT3-1	chr20:14910021-14910164	NR_037841
2	lnc-FLRT3-2	chr20:14914489-14914588	ENSG00000237832.1
3	lnc-FLRT3-1	chr20:14885587-14886675	ENSG00000235914.1
4	lnc-FLRT3-1	chr20:14910021-14910164	NR_110318
5	lnc-FLRT3-1	chr20:14910021-14910142	NONHSAT078721
6	lnc-FLRT3-1	chr20:14910021-14910161	ENSG00000235914.1
7	lnc-FLRT3-1	chr20:14910021-14910154	NONHSAT078722
8	lnc-FLRT3-1	chr20:14885587-14886675	NR_072988
9	lnc-FLRT3-1	chr20:14910021-14910164	NR_072988
10	lnc-FLRT3-1	chr20:14910021-14910132	ENSG00000235914.1
11	lnc-FLRT3-2	chr20:14915884-14916009	ENSG00000237832.1
12	lnc-FLRT3-2	chr20:14915576-14915720	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: 5681 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:5681 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149426851	chr20:14883345-14883346	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs527347274	chr20:14883376-14883377	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs551871342	chr20:14883378-14883379	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs570283872	chr20:14883391-14883392	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs531430793	chr20:14883425-14883426	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs549792848	chr20:14883455-14883456	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs112621611	chr20:14883463-14883464	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs74179752	chr20:14883479-14883480	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs377632167	chr20:14883509-14883510	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs144694445	chr20:14883547-14883548	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs7352597	chr20:14883583-14883584	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs541139342	chr20:14885651-14885652	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs34417663	chr20:14885686-14885687	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs553173121	chr20:14885721-14885722	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs41275416	chr20:14885722-14885723	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs545304360	chr20:14885756-14885757	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs141601465	chr20:14885757-14885758	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs150481049	chr20:14885778-14885779	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs542702097	chr20:14885786-14885787	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs561338520	chr20:14885789-14885790	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs180929978	chr20:14885817-14885818	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs2210047	chr20:14885818-14885819	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs138154945	chr20:14885820-14885821	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs532599952	chr20:14885846-14885847	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs2210048	chr20:14885854-14885855	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs368703969	chr20:14885896-14885897	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs569494409	chr20:14885927-14885928	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs547480299	chr20:14885931-14885932	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs149551060	chr20:14885934-14885935	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs184946177	chr20:14885941-14885942	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs2225304	chr20:14885996-14885997	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs534681068	chr20:14886018-14886019	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs535929122	chr20:14886020-14886021	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs41275418	chr20:14886032-14886033	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs147279110	chr20:14886039-14886040	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs577898313	chr20:14886048-14886049	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs538877932	chr20:14886067-14886068	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs191996172	chr20:14886076-14886077	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs575403366	chr20:14886096-14886097	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs542922317	chr20:14886126-14886127	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs182215799	chr20:14886142-14886143	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs6042991	chr20:14886156-14886157	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs570144983	chr20:14886244-14886245	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs186981308	chr20:14886272-14886273	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs143090043	chr20:14886303-14886304	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs534527040	chr20:14886330-14886331	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs147411762	chr20:14886340-14886341	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs550846750	chr20:14886370-14886371	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs549912275	chr20:14886382-14886383	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs568273290	chr20:14886383-14886384	Inactive region	lncRNA	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:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14882800-14883600	Flanking Active TSS	GM12878-XiMat	blood
2	chr20:14887400-14888200	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr20:14887600-14888000	Enhancers	H9 Cell Line	embryonic stem cell
4	chr20:14887600-14888000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr20:14887600-14888200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr20:14887600-14888200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr20:14887600-14888200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr20:14887600-14888200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr20:14887600-14888400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr20:14887600-14888400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr20:14887600-14888400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr20:14887600-14888400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr20:14887600-14888400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr20:14887800-14888200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr20:14887800-14888200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr20:14887800-14888200	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr20:14888400-14889200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr20:14888400-14894600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr20:14889200-14889400	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr20:14889400-14896000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr20:14890600-14891200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr20:14890800-14891400	Enhancers	Fetal Kidney	kidney
23	chr20:14891200-14891400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr20:14891200-14894600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr20:14891400-14899600	Weak transcription	Fetal Kidney	kidney
26	chr20:14894400-14894600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr20:14894400-14895200	Enhancers	HUVEC	blood vessel
28	chr20:14894400-14897400	Enhancers	Fetal Brain Male	brain
29	chr20:14894600-14894800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr20:14894600-14894800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr20:14894600-14895000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr20:14894600-14895000	Enhancers	Fetal Muscle Leg	muscle
33	chr20:14894600-14895200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr20:14894600-14895200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr20:14894600-14895600	Enhancers	Fetal Brain Female	brain
36	chr20:14894800-14895000	Enhancers	Fetal Lung	lung
37	chr20:14894800-14895000	Enhancers	Ovary	ovary
38	chr20:14894800-14896200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr20:14894800-14897800	Enhancers	Fetal Heart	heart
40	chr20:14894800-14898000	Enhancers	Fetal Stomach	stomach
41	chr20:14895000-14896000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr20:14895000-14896200	Weak transcription	Fetal Muscle Leg	muscle
43	chr20:14895200-14896200	Weak transcription	Fetal Lung	lung
44	chr20:14895200-14900000	Weak transcription	HUVEC	blood vessel
45	chr20:14895200-14900200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr20:14895200-14900200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr20:14895600-14896000	Enhancers	Colon Smooth Muscle	Colon
48	chr20:14895600-14896200	Flanking Active TSS	Fetal Brain Female	brain
49	chr20:14895800-14896000	Enhancers	Brain Hippocampus Middle	brain
50	chr20:14895800-14896000	Active TSS	Duodenum Smooth Muscle	Duodenum

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