Variant report

Variant	nsv1066049
Chromosome Location	chr20:14875878-15104578
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1858)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1858 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:15041045-15042049	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:14959886-14961038	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:14971646-14973208	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:15042539-15043096	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	chr20:14986003-14986310	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	chr20:15040971-15041310	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	chr20:14931782-14932075	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	chr20:14966411-14967352	A549	lung:	n/a	n/a
21	BCL3	chr20:14966427-14967324	A549	lung:	n/a	n/a
22	BCL3	chr20:14965529-14966338	A549	lung:	n/a	chr20:14966177-14966184
23	BHLHE40	chr20:14960125-14960599	HepG2	liver:	n/a	n/a
24	BHLHE40	chr20:14977538-14977786	HepG2	liver:	n/a	n/a
25	BHLHE40	chr20:15042548-15042950	HepG2	liver:	n/a	n/a
26	BHLHE40	chr20:15041038-15041678	HepG2	liver:	n/a	n/a
27	BHLHE40	chr20:14965455-14966238	HepG2	liver:	n/a	n/a
28	BRCA1	chr20:15042587-15042806	HepG2	liver:	n/a	n/a
29	BRCA1	chr20:15043714-15043822	HepG2	liver:	n/a	n/a
30	BRCA1	chr20:14966739-14967191	HepG2	liver:	n/a	n/a
31	BRCA1	chr20:14965501-14966238	HepG2	liver:	n/a	n/a
32	BRCA1	chr20:15054620-15054671	HepG2	liver:	n/a	n/a
33	BRCA1	chr20:14943807-14944695	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr20:14936483-14937509	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr20:14960587-14960671	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr20:15041931-15042029	HepG2	liver:	n/a	n/a
37	CEBPB	chr20:15042545-15043095	MCF-7	breast:	n/a	chr20:15042893-15042904
38	CEBPB	chr20:14971616-14972081	Hela-S3	cervix:	n/a	chr20:14971798-14971811
39	CEBPB	chr20:14971698-14972061	HepG2	liver:	n/a	chr20:14971798-14971811
40	CEBPB	chr20:14943912-14944387	A549	lung:	n/a	n/a
41	CEBPB	chr20:14978469-14978869	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr20:14943969-14944439	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr20:14932469-14932778	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr20:14973654-14974048	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr20:14971734-14971993	HepG2	liver:	n/a	chr20:14971798-14971811
46	CEBPB	chr20:14944001-14944439	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr20:14942108-14942314	A549	lung:	n/a	chr20:14942229-14942240
48	CEBPB	chr20:15041173-15041651	HepG2	liver:	n/a	chr20:15041402-15041419 chr20:15041403-15041414 chr20:15041404-15041415 chr20:15041403-15041416 chr20:15041403-15041416
49	CEBPB	chr20:15041135-15041621	HepG2	liver:	n/a	chr20:15041402-15041419 chr20:15041403-15041414 chr20:15041404-15041415 chr20:15041403-15041416 chr20:15041403-15041416
50	CEBPB	chr20:14965531-14966128	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	SK-N-SH_RA	brain:	n/a
2	chr20:14904432-14904482	CMK	blood:	n/a
3	chr20:14904432-14904482	HCF	heart:	n/a
4	chr20:14904432-14904482	AG04449	skin:	fetal
5	chr20:14904432-14904482	BJ	skin:	n/a
6	chr20:14904432-14904482	U87	brain:	n/a
7	chr20:14904432-14904482	HepG2	liver:	n/a
8	chr20:14904432-14904482	HL-60	blood:	n/a
9	chr20:14904432-14904482	HIPEpiC	eye:	n/a
10	chr20:14904432-14904482	H1-hESC	embryonic stem cell:	embryo
11	chr20:14904432-14904482	Hepatocyte	liver:	n/a
12	chr20:14904432-14904482	A549	lung:	n/a
13	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
14	chr20:14904432-14904482	IMR90	lung:	fetal
15	chr20:14904432-14904482	GM19239	blood:	n/a
16	chr20:14904432-14904482	Jurkat	blood:	n/a
17	chr20:14904432-14904482	T-47D	breast:	n/a
18	chr20:14904432-14904482	LNCaP	prostate:	n/a
19	chr20:14904432-14904482	GM12892	blood:	n/a
20	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
21	chr20:14904432-14904482	NT2-D1	testis:	n/a
22	chr20:14904432-14904482	SKMC	muscle:	n/a
23	chr20:14904432-14904482	BE2_C	brain:	n/a
24	chr20:14904432-14904482	HEK293	kidney:	embryo
25	chr20:14904432-14904482	AG09309	skin:	n/a
26	chr20:14904432-14904482	HRPEpiC	eye:	n/a
27	chr20:14904432-14904482	AG09319	gingival:	n/a
28	chr20:14904432-14904482	K562	blood:	n/a
29	chr20:14904432-14904482	HCT-116	colon:	n/a
30	chr20:14904432-14904482	SK-N-MC	brain:	n/a
31	chr20:14904432-14904482	NH-A	brain:	n/a
32	chr20:14904432-14904482	AG10803	skin:	n/a
33	chr20:14904432-14904482	Hela-S3	cervix:	n/a
34	chr20:14904432-14904482	ProgFib	skin:	n/a
35	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
36	chr20:14904432-14904482	MCF-7	breast:	n/a
37	chr20:14904432-14904482	MCF10A-Er-Src	breast:	n/a
38	chr20:14904432-14904482	RPTEC	kidney:	n/a
39	chr20:14904432-14904482	NB4	blood:	n/a
40	chr20:14904432-14904482	SK-N-SH	brain:	n/a
41	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
42	chr20:14904432-14904482	SAEC	small airway:	n/a
43	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
44	chr20:14904432-14904482	NHBE	bronchial:	n/a
45	chr20:14904432-14904482	GM12878	blood:	n/a
46	chr20:14904432-14904482	PrEC	prostate:	n/a
47	chr20:14904432-14904482	Caco-2	colon:	n/a
48	chr20:14904432-14904482	PFSK-1	brain:	n/a
49	chr20:14904432-14904482	AG04450	lung:	fetal
50	chr20:14904432-14904482	HMEC	breast:	n/a

(count:20 , 50 per page) page: 1

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

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

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

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: 7402 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:7402 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111817069	chr20:14882220-14882221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs140790928	chr20:14882233-14882234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs6079600	chr20:14882266-14882267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560663578	chr20:14882279-14882280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572538254	chr20:14882407-14882408	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs150113250	chr20:14882417-14882418	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs113658419	chr20:14882465-14882466	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs183499715	chr20:14882479-14882480	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs570040548	chr20:14882536-14882537	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs188509554	chr20:14882570-14882571	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs6042986	chr20:14882621-14882622	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs562990718	chr20:14882630-14882631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529718821	chr20:14882658-14882659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547958581	chr20:14882740-14882741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77283238	chr20:14882771-14882772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191208651	chr20:14882824-14882825	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs6034058	chr20:14882842-14882843	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs142914181	chr20:14882868-14882869	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs537714200	chr20:14882890-14882891	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs565982424	chr20:14882900-14882901	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs146154282	chr20:14882903-14882904	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs568342281	chr20:14882991-14882992	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs369066676	chr20:14883009-14883010	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs535877461	chr20:14883011-14883012	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs183271807	chr20:14883073-14883074	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs6135303	chr20:14883127-14883128	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs573903273	chr20:14883137-14883138	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs558347505	chr20:14883153-14883154	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs576729490	chr20:14883158-14883159	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs138998132	chr20:14883245-14883246	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs562436271	chr20:14883307-14883308	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs529650590	chr20:14883308-14883309	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs541859549	chr20:14883324-14883325	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs149426851	chr20:14883345-14883346	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs527347274	chr20:14883376-14883377	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs551871342	chr20:14883378-14883379	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs570283872	chr20:14883391-14883392	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs531430793	chr20:14883425-14883426	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs549792848	chr20:14883455-14883456	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs112621611	chr20:14883463-14883464	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs74179752	chr20:14883479-14883480	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs377632167	chr20:14883509-14883510	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs144694445	chr20:14883547-14883548	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs7352597	chr20:14883583-14883584	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs541139342	chr20:14885651-14885652	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs34417663	chr20:14885686-14885687	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs553173121	chr20:14885721-14885722	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs41275416	chr20:14885722-14885723	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs545304360	chr20:14885756-14885757	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs141601465	chr20:14885757-14885758	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:1079 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

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

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