Variant report

Variant	nsv916795
Chromosome Location	chr20:15041479-15345528
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1447)
CpG islands
(count:183)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1447 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:15144336-15144711	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:15041045-15042049	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:15139111-15139485	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:15042539-15043096	HepG2	liver:	n/a	n/a
5	ATF2	chr20:15299899-15300572	GM12878	blood:	n/a	n/a
6	ATF2	chr20:15142556-15143423	GM12878	blood:	n/a	n/a
7	ATF2	chr20:15298201-15298708	GM12878	blood:	n/a	n/a
8	ATF2	chr20:15299283-15299738	GM12878	blood:	n/a	n/a
9	ATF2	chr20:15297929-15299020	GM12878	blood:	n/a	n/a
10	ATF2	chr20:15299152-15299756	GM12878	blood:	n/a	n/a
11	ATF2	chr20:15313045-15313880	GM12878	blood:	n/a	chr20:15313332-15313343
12	ATF2	chr20:15180324-15181228	GM12878	blood:	n/a	n/a
13	ATF2	chr20:15180601-15181187	GM12878	blood:	n/a	n/a
14	ATF2	chr20:15142645-15143351	GM12878	blood:	n/a	n/a
15	BACH1	chr20:15144468-15144534	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr20:15143005-15143338	GM12878	blood:	n/a	n/a
17	BATF	chr20:15298206-15298537	GM12878	blood:	n/a	n/a
18	BATF	chr20:15298652-15298919	GM12878	blood:	n/a	n/a
19	BATF	chr20:15142669-15143382	GM12878	blood:	n/a	n/a
20	BATF	chr20:15229264-15229547	GM12878	blood:	n/a	n/a
21	BATF	chr20:15313268-15313752	GM12878	blood:	n/a	n/a
22	BATF	chr20:15299346-15299710	GM12878	blood:	n/a	n/a
23	BATF	chr20:15142631-15143004	GM12878	blood:	n/a	n/a
24	BATF	chr20:15298174-15298614	GM12878	blood:	n/a	n/a
25	BATF	chr20:15217496-15217756	GM12878	blood:	n/a	n/a
26	BATF	chr20:15299357-15299730	GM12878	blood:	n/a	n/a
27	BATF	chr20:15180351-15181277	GM12878	blood:	n/a	chr20:15180905-15180913
28	BATF	chr20:15180677-15181088	GM12878	blood:	n/a	chr20:15180905-15180913
29	BCL11A	chr20:15180758-15180983	GM12878	blood:	n/a	n/a
30	BCL11A	chr20:15180658-15181150	GM12878	blood:	n/a	n/a
31	BCL3	chr20:15180753-15181061	GM12878	blood:	n/a	n/a
32	BCLAF1	chr20:15298185-15298626	GM12878	blood:	n/a	n/a
33	BCLAF1	chr20:15313142-15313783	GM12878	blood:	n/a	n/a
34	BCLAF1	chr20:15298111-15298900	GM12878	blood:	n/a	n/a
35	BCLAF1	chr20:15142637-15143439	GM12878	blood:	n/a	n/a
36	BHLHE40	chr20:15307828-15307979	K562	blood:	n/a	n/a
37	BHLHE40	chr20:15041038-15041678	HepG2	liver:	n/a	n/a
38	BHLHE40	chr20:15313971-15314073	GM12878	blood:	n/a	n/a
39	BHLHE40	chr20:15180594-15181323	GM12878	blood:	n/a	n/a
40	BHLHE40	chr20:15042548-15042950	HepG2	liver:	n/a	n/a
41	BHLHE40	chr20:15298187-15298590	GM12878	blood:	n/a	n/a
42	BHLHE40	chr20:15313573-15313619	GM12878	blood:	n/a	n/a
43	BRCA1	chr20:15041931-15042029	HepG2	liver:	n/a	n/a
44	BRCA1	chr20:15042587-15042806	HepG2	liver:	n/a	n/a
45	BRCA1	chr20:15043714-15043822	HepG2	liver:	n/a	n/a
46	BRCA1	chr20:15217541-15217700	HepG2	liver:	n/a	n/a
47	BRCA1	chr20:15054620-15054671	HepG2	liver:	n/a	n/a
48	CBX3	chr20:15217421-15217751	HCT-116	colon:	n/a	n/a
49	CEBPB	chr20:15169095-15169451	IMR90	lung:	n/a	chr20:15169267-15169284
50	CEBPB	chr20:15150774-15151075	HepG2	liver:	n/a	chr20:15150914-15150925

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:15176557-15176607	HRE	kidney:	n/a
2	chr20:15177509-15177559	ECC-1	luminal epithelium:	n/a
3	chr20:15177509-15177559	HCF	heart:	n/a
4	chr20:15176830-15176880	AG10803	skin:	n/a
5	chr20:15177509-15177559	AG10803	skin:	n/a
6	chr20:15176557-15176607	HepG2	liver:	n/a
7	chr20:15176557-15176607	ECC-1	luminal epithelium:	n/a
8	chr20:15177509-15177559	GM19239	blood:	n/a
9	chr20:15176830-15176880	HCF	heart:	n/a
10	chr20:15176557-15176607	HMEC	breast:	n/a
11	chr20:15176830-15176880	Hela-S3	cervix:	n/a
12	chr20:15176557-15176607	HRCEpiC	kidney:	n/a
13	chr20:15176830-15176880	PANC-1	pancreas:	n/a
14	chr20:15177509-15177559	AoSMC	blood vessel:	n/a
15	chr20:15176830-15176880	SAEC	small airway:	n/a
16	chr20:15176557-15176607	HRPEpiC	eye:	n/a
17	chr20:15176830-15176880	PrEC	prostate:	n/a
18	chr20:15176557-15176607	GM12878	blood:	n/a
19	chr20:15176830-15176880	GM19239	blood:	n/a
20	chr20:15177509-15177559	HCT-116	colon:	n/a
21	chr20:15176830-15176880	U87	brain:	n/a
22	chr20:15176830-15176880	ovcar-3	ovarian:	n/a
23	chr20:15176830-15176880	LNCaP	prostate:	n/a
24	chr20:15176830-15176880	SK-N-SH_RA	brain:	n/a
25	chr20:15177509-15177559	NHDF-neo	bronchial:	n/a
26	chr20:15176830-15176880	AG09319	gingival:	n/a
27	chr20:15177509-15177559	PrEC	prostate:	n/a
28	chr20:15176557-15176607	AoSMC	blood vessel:	n/a
29	chr20:15176557-15176607	A549	lung:	n/a
30	chr20:15176557-15176607	Caco-2	colon:	n/a
31	chr20:15177509-15177559	BE2_C	brain:	n/a
32	chr20:15177509-15177559	AG09319	gingival:	n/a
33	chr20:15176557-15176607	NB4	blood:	n/a
34	chr20:15177509-15177559	Hela-S3	cervix:	n/a
35	chr20:15176830-15176880	GM12891	blood:	n/a
36	chr20:15176830-15176880	CMK	blood:	n/a
37	chr20:15177509-15177559	AG04449	skin:	fetal
38	chr20:15176557-15176607	ovcar-3	ovarian:	n/a
39	chr20:15176830-15176880	SK-N-MC	brain:	n/a
40	chr20:15176557-15176607	HEEpiC	esophagus:	n/a
41	chr20:15177509-15177559	HepG2	liver:	n/a
42	chr20:15177509-15177559	MCF-7	breast:	n/a
43	chr20:15176830-15176880	AG04450	lung:	fetal
44	chr20:15176557-15176607	MCF10A-Er-Src	breast:	n/a
45	chr20:15177509-15177559	NT2-D1	testis:	n/a
46	chr20:15176830-15176880	ProgFib	skin:	n/a
47	chr20:15176830-15176880	ECC-1	luminal epithelium:	n/a
48	chr20:15177509-15177559	LNCaP	prostate:	n/a
49	chr20:15177509-15177559	HRE	kidney:	n/a
50	chr20:15176557-15176607	HCPEpiC	choroid plexus:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:15293454..15295061-chr20:15304426..15306908,2	MCF-7	breast:
2	chr20:15213744..15214594-chr5:107680986..107681674,2	MCF-7	breast:
3	chr20:14335576..14337791-chr20:15315333..15317078,2	MCF-7	breast:
4	chr20:15293454..15295061-chr20:15304426..15306908,2	MCF-7	breast:
5	chr20:15280200..15282422-chr20:15286811..15288380,2	MCF-7	breast:
6	chr20:14593902..14596386-chr20:15052997..15054796,2	K562	blood:
7	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
8	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
9	chr20:14316387..14318274-chr20:15215878..15217670,2	MCF-7	breast:
10	chr20:15222565..15225391-chr20:15228675..15231649,2	MCF-7	breast:
11	chr20:15279663..15281630-chr20:15285386..15287786,2	MCF-7	breast:
12	chr20:15280200..15282422-chr20:15286811..15288380,2	MCF-7	breast:
13	chr20:15222565..15225391-chr20:15228675..15231649,2	MCF-7	breast:
14	chr20:15279663..15281630-chr20:15285386..15287786,2	MCF-7	breast:

No data

Variant related genes	Relation type
MACROD2	TF binding region
RNA5SP475	TF binding region
MACROD2	CpG island
RNA5SP475	CpG island
ENSG00000125848	chromatin interactions

Extended variants
information (count: 9044 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:9044 , 50 per page) page: 1 2 3 4 5 6 7 ... 181

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73897242	chr20:15041481-15041482	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs73897243	chr20:15041494-15041495	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs113927109	chr20:15041499-15041500	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs191290046	chr20:15041512-15041513	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs183484647	chr20:15041553-15041554	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs2235608	chr20:15041561-15041562	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs453626	chr20:15041578-15041579	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs544919427	chr20:15041587-15041588	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs554034456	chr20:15041592-15041593	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs189478129	chr20:15041622-15041623	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs539759657	chr20:15041662-15041663	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs557725684	chr20:15041678-15041679	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs576390032	chr20:15041757-15041758	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs140428428	chr20:15041788-15041789	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs555459240	chr20:15041809-15041810	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs565179562	chr20:15041811-15041812	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs568820126	chr20:15041870-15041871	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs150398906	chr20:15041887-15041888	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs138419647	chr20:15041958-15041959	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs559943148	chr20:15041981-15041982	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs8116193	chr20:15042044-15042045	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs528169742	chr20:15042047-15042048	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs545685715	chr20:15042063-15042064	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs56330183	chr20:15042101-15042102	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs531348208	chr20:15042118-15042119	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs143913220	chr20:15042119-15042120	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs568036928	chr20:15042127-15042128	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs529043161	chr20:15042176-15042177	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs79208591	chr20:15042221-15042222	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs547164181	chr20:15042244-15042245	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs544175193	chr20:15042253-15042254	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs8116462	chr20:15042378-15042379	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs565873904	chr20:15042387-15042388	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs539213711	chr20:15042415-15042416	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs117872427	chr20:15042429-15042430	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs369530598	chr20:15042472-15042473	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs573119247	chr20:15042487-15042488	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs569582216	chr20:15042495-15042496	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs374775589	chr20:15042550-15042551	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs146037519	chr20:15042594-15042595	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs421941	chr20:15042599-15042600	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs573694214	chr20:15042692-15042693	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs6043079	chr20:15042693-15042694	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs6043080	chr20:15042712-15042713	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs541169406	chr20:15042717-15042718	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs553152445	chr20:15042771-15042772	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs138787911	chr20:15042772-15042773	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs545235583	chr20:15042787-15042788	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs75128527	chr20:15042788-15042789	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs6043081	chr20:15042789-15042790	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Cancer	20164920	CNVD
Schizophrenia	23813976	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21272361	CNVD
Schizophrenia	19805367	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:658 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:15040600-15042800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr20:15040800-15042800	Enhancers	Placenta	Placenta
3	chr20:15041000-15042800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr20:15041000-15042800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr20:15041000-15042800	Flanking Active TSS	HepG2	liver
6	chr20:15041000-15045800	Enhancers	Fetal Kidney	kidney
7	chr20:15041200-15041600	Enhancers	GM12878-XiMat	blood
8	chr20:15041400-15042800	Enhancers	HMEC	breast
9	chr20:15041600-15043000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr20:15041600-15043000	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr20:15041800-15042400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr20:15041800-15042600	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr20:15041800-15042800	Enhancers	Ovary	ovary
14	chr20:15042000-15042800	Enhancers	Esophagus	oesophagus
15	chr20:15042000-15042800	Enhancers	NHEK	skin
16	chr20:15042400-15044000	Enhancers	A549	lung
17	chr20:15042600-15042800	Enhancers	Fetal Heart	heart
18	chr20:15042800-15044200	Enhancers	HepG2	liver
19	chr20:15042800-15045400	Weak transcription	Fetal Heart	heart
20	chr20:15043400-15044400	Enhancers	Dnd41	blood
21	chr20:15043400-15045000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr20:15043600-15044400	Enhancers	HUVEC	blood vessel
23	chr20:15045000-15045600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr20:15045200-15046000	Enhancers	Fetal Brain Male	brain
25	chr20:15045400-15045800	Enhancers	Fetal Heart	heart
26	chr20:15045400-15046000	Enhancers	Fetal Lung	lung
27	chr20:15045600-15045800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr20:15046000-15046600	Weak transcription	Fetal Lung	lung
29	chr20:15046200-15055800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr20:15046600-15046800	Enhancers	Fetal Lung	lung
31	chr20:15049200-15049400	Enhancers	Lung	lung
32	chr20:15049200-15049600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr20:15049200-15049800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr20:15049200-15050600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr20:15049600-15050000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr20:15049600-15050000	Weak transcription	Lung	lung
37	chr20:15050000-15050600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr20:15050000-15050800	Enhancers	Lung	lung
39	chr20:15050400-15050800	Enhancers	HepG2	liver
40	chr20:15050600-15058200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr20:15051200-15052200	Enhancers	Fetal Muscle Leg	muscle
42	chr20:15056000-15056600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr20:15056600-15058000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr20:15057200-15059200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr20:15057400-15057600	Enhancers	Brain Germinal Matrix	brain
46	chr20:15058000-15058600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr20:15058000-15059200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr20:15058200-15059000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr20:15058200-15059000	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr20:15058200-15059200	Enhancers	HUES6 Cell Line	embryonic stem cell

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