Variant report

Variant	esv1832768
Chromosome Location	chr3:20507621-20624780
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:517)
CpG islands
(count:245)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:517 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:20553373-20553610	HepG2	liver:	n/a	n/a
2	ATF1	chr3:20521702-20521870	K562	blood:	n/a	n/a
3	BACH1	chr3:20616608-20616882	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:20536253-20536368	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:20535546-20535645	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:20578833-20579051	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr3:20613961-20614099	HepG2	liver:	n/a	chr3:20614031-20614042
8	CEBPB	chr3:20551895-20552228	HepG2	liver:	n/a	n/a
9	CEBPB	chr3:20568523-20568549	K562	blood:	n/a	n/a
10	CHD1	chr3:20617939-20617947	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr3:20595241-20595316	HepG2	liver:	n/a	n/a
12	CTCF	chr3:20553400-20553550	NHEK	skin:	n/a	n/a
13	CTCF	chr3:20619460-20619610	AG04449	skin:	n/a	n/a
14	CTCF	chr3:20553400-20553550	GM12864	blood:	n/a	n/a
15	CTCF	chr3:20553347-20553574	MCF-7	breast:	n/a	n/a
16	CTCF	chr3:20553400-20553550	GM12872	blood:	n/a	n/a
17	CTCF	chr3:20553400-20553550	NHDF-neo	bronchial:	n/a	n/a
18	CTCF	chr3:20553380-20553530	HCFaa	heart:	n/a	n/a
19	CTCF	chr3:20553318-20553597	LNCaP	prostate:	n/a	n/a
20	CTCF	chr3:20553360-20553510	K562	blood:	n/a	n/a
21	CTCF	chr3:20553380-20553530	HMF	breast:	n/a	n/a
22	CTCF	chr3:20553380-20553530	SAEC	small airway:	n/a	n/a
23	CTCF	chr3:20553320-20553470	GM12875	blood:	n/a	n/a
24	CTCF	chr3:20553343-20553566	GM13976	blood:	n/a	n/a
25	CTCF	chr3:20553420-20553570	HepG2	liver:	n/a	n/a
26	CTCF	chr3:20553420-20553570	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr3:20553360-20553510	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr3:20553400-20553550	Caco-2	colon:	n/a	n/a
29	CTCF	chr3:20553400-20553550	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr3:20553360-20553510	GM12871	blood:	n/a	n/a
31	CTCF	chr3:20553381-20553574	NHEK	skin:	n/a	n/a
32	CTCF	chr3:20553738-20553767	GM19238	blood:	n/a	n/a
33	CTCF	chr3:20553360-20553510	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr3:20553380-20553530	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr3:20594480-20594630	MCF-7	breast:	n/a	n/a
36	CTCF	chr3:20553180-20553330	A549	lung:	n/a	n/a
37	CTCF	chr3:20553342-20553573	GM10248	blood:	n/a	n/a
38	CTCF	chr3:20553360-20553510	GM12872	blood:	n/a	n/a
39	CTCF	chr3:20578540-20578690	GM12864	blood:	n/a	n/a
40	CTCF	chr3:20553440-20553590	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr3:20553122-20553828	A549	lung:	n/a	n/a
42	CTCF	chr3:20553440-20553590	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:20553316-20553697	MCF-7	breast:	n/a	n/a
44	CTCF	chr3:20553360-20553510	GM12868	blood:	n/a	n/a
45	CTCF	chr3:20553354-20553584	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr3:20553299-20553624	Medullo	brain:	n/a	n/a
47	CTCF	chr3:20553400-20553550	HepG2	liver:	n/a	n/a
48	CTCF	chr3:20553380-20553530	HCM	heart:	n/a	n/a
49	CTCF	chr3:20553400-20553550	SAEC	small airway:	n/a	n/a
50	CTCF	chr3:20553319-20553622	Gliobla	brain:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:20522301-20522351	GM12892	blood:	n/a
2	chr3:20522301-20522351	GM12892	blood:	n/a
3	chr3:20522301-20522351	AG04450	lung:	fetal
4	chr3:20589671-20589721	NT2-D1	testis:	n/a
5	chr3:20522301-20522351	PrEC	prostate:	n/a
6	chr3:20589760-20589810	GM06990	blood:	n/a
7	chr3:20589671-20589721	T-47D	breast:	n/a
8	chr3:20589760-20589810	AG09309	skin:	n/a
9	chr3:20589671-20589721	MCF10A-Er-Src	breast:	n/a
10	chr3:20575513-20575563	HepG2	liver:	n/a
11	chr3:20589671-20589721	AG04450	lung:	fetal
12	chr3:20522301-20522351	PANC-1	pancreas:	n/a
13	chr3:20589760-20589810	HRPEpiC	eye:	n/a
14	chr3:20589760-20589810	SAEC	small airway:	n/a
15	chr3:20589760-20589810	LNCaP	prostate:	n/a
16	chr3:20589671-20589721	HRE	kidney:	n/a
17	chr3:20589671-20589721	U87	brain:	n/a
18	chr3:20522301-20522351	AG10803	skin:	n/a
19	chr3:20589671-20589721	SKMC	muscle:	n/a
20	chr3:20575513-20575563	GM12878	blood:	n/a
21	chr3:20522301-20522351	IMR90	lung:	fetal
22	chr3:20575513-20575563	NHBE	bronchial:	n/a
23	chr3:20589760-20589810	PrEC	prostate:	n/a
24	chr3:20589671-20589721	GM12878	blood:	n/a
25	chr3:20589671-20589721	SK-N-SH	brain:	n/a
26	chr3:20522301-20522351	NHDF-neo	bronchial:	n/a
27	chr3:20589671-20589721	NB4	blood:	n/a
28	chr3:20575513-20575563	NHDF-neo	bronchial:	n/a
29	chr3:20575513-20575563	NT2-D1	testis:	n/a
30	chr3:20522301-20522351	SAEC	small airway:	n/a
31	chr3:20522301-20522351	NB4	blood:	n/a
32	chr3:20589671-20589721	HIPEpiC	eye:	n/a
33	chr3:20575513-20575563	GM12891	blood:	n/a
34	chr3:20589671-20589721	AoSMC	blood vessel:	n/a
35	chr3:20522301-20522351	MCF-7	breast:	n/a
36	chr3:20522301-20522351	GM12891	blood:	n/a
37	chr3:20589671-20589721	HCT-116	colon:	n/a
38	chr3:20589760-20589810	H1-hESC	embryonic stem cell:	embryo
39	chr3:20589671-20589721	RPTEC	kidney:	n/a
40	chr3:20589671-20589721	NHBE	bronchial:	n/a
41	chr3:20522301-20522351	U87	brain:	n/a
42	chr3:20589760-20589810	HL-60	blood:	n/a
43	chr3:20575513-20575563	AG09309	skin:	n/a
44	chr3:20575513-20575563	Hela-S3	cervix:	n/a
45	chr3:20575513-20575563	HCT-116	colon:	n/a
46	chr3:20522301-20522351	SK-N-MC	brain:	n/a
47	chr3:20575513-20575563	HAEpiC	amniotic membrane:	n/a
48	chr3:20575513-20575563	Hepatocyte	liver:	n/a
49	chr3:20589671-20589721	PrEC	prostate:	n/a
50	chr3:20589760-20589810	RPTEC	kidney:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:20576686..20578791-chr3:20582822..20585429,2	MCF-7	breast:
2	chr3:20618172..20620795-chr3:20622169..20624863,2	MCF-7	breast:
3	chr3:20577616..20580422-chr3:20581225..20583967,3	K562	blood:
4	chr3:20558136..20559640-chr3:20560230..20563085,2	K562	blood:
5	chr3:20618172..20620795-chr3:20622169..20624863,2	MCF-7	breast:
6	chr3:20558136..20559640-chr3:20560230..20563085,2	K562	blood:
7	chr3:20460438..20462411-chr3:20516734..20518648,2	MCF-7	breast:
8	chr3:20514130..20516158-chr3:20517415..20519398,2	K562	blood:
9	chr3:20552973..20553911-chr3:20970672..20972125,8	MCF-7	breast:
10	chr3:20577616..20580422-chr3:20581225..20583967,3	K562	blood:
11	chr3:20553254..20553852-chr3:21257816..21258713,2	MCF-7	breast:
12	chr3:20553366..20553898-chr3:21257700..21258348,2	MCF-7	breast:
13	chr3:20545213..20547317-chr3:20547570..20549760,2	K562	blood:
14	chr1:121485224..121485931-chr3:20620646..20621369,2	MCF-7	breast:
15	chr3:20576686..20578791-chr3:20582822..20585429,2	MCF-7	breast:
16	chr17:57920861..57923845-chr3:20581102..20583235,2	MCF-7	breast:
17	chr3:20553071..20554107-chr3:20781207..20782086,3	MCF-7	breast:
18	chr3:20514130..20516158-chr3:20517415..20519398,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-815P	TF binding region
RNU6-815P	CpG island
ENSG00000206807	chromatin interactions

Extended variants
information (count: 2689 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2689 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191208495	chr3:20508009-20508010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs140046464	chr3:20508012-20508013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535468500	chr3:20508013-20508014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs6804217	chr3:20508031-20508032	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs73187199	chr3:20508047-20508048	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs6768144	chr3:20508064-20508065	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs143590914	chr3:20508069-20508070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572976466	chr3:20508089-20508090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114625284	chr3:20508131-20508132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73819567	chr3:20508133-20508134	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs529313561	chr3:20508189-20508190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545406290	chr3:20508667-20508668	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs560863488	chr3:20508686-20508687	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs75980101	chr3:20508717-20508718	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs398091337	chr3:20508718-20508719	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs77145484	chr3:20508742-20508743	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs139424705	chr3:20508753-20508754	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs529037158	chr3:20508796-20508797	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs565470376	chr3:20508798-20508799	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs6550535	chr3:20512413-20512414	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs546564149	chr3:20512424-20512425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146782477	chr3:20512439-20512440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs58969202	chr3:20512440-20512441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6775230	chr3:20512533-20512534	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs529505393	chr3:20512559-20512560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550934786	chr3:20512563-20512564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs6550536	chr3:20512564-20512565	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs142004409	chr3:20512619-20512620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs6775324	chr3:20512623-20512624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146309063	chr3:20512627-20512628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534622992	chr3:20512663-20512664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556286449	chr3:20512711-20512712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1523347	chr3:20512768-20512769	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
34	rs562209318	chr3:20512782-20512783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575652407	chr3:20512816-20512817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181645639	chr3:20512826-20512827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6550537	chr3:20512867-20512868	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs6769567	chr3:20512961-20512962	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs117280106	chr3:20513002-20513003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs80027138	chr3:20513013-20513014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs60487127	chr3:20513022-20513023	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs186338144	chr3:20513031-20513032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528521948	chr3:20513070-20513071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191972184	chr3:20513092-20513093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115878439	chr3:20513108-20513109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77695842	chr3:20513114-20513115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551235508	chr3:20513145-20513146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376857351	chr3:20513172-20513173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569386239	chr3:20513183-20513184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533589309	chr3:20513212-20513213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:155 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20508000-20508200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr3:20508600-20508800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
3	chr3:20512400-20523200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr3:20516400-20522600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr3:20519800-20520200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr3:20519800-20520400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr3:20519800-20523400	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr3:20520000-20520200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr3:20520000-20520800	Enhancers	Fetal Intestine Large	intestine
10	chr3:20520000-20521000	Enhancers	Fetal Lung	lung
11	chr3:20520200-20521200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr3:20520400-20521400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:20520400-20521400	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr3:20520400-20521400	Enhancers	HUVEC	blood vessel
15	chr3:20520600-20522200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr3:20521000-20522400	Weak transcription	Fetal Lung	lung
17	chr3:20521200-20522800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr3:20521200-20523000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr3:20521400-20521600	Flanking Active TSS	HUVEC	blood vessel
20	chr3:20521400-20522200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:20521400-20522200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr3:20521400-20522800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr3:20521400-20523000	Enhancers	NH-A	brain
24	chr3:20521600-20522000	Enhancers	HUVEC	blood vessel
25	chr3:20522000-20522600	Flanking Active TSS	HUVEC	blood vessel
26	chr3:20522000-20522800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr3:20522200-20522400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr3:20522200-20522600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr3:20522200-20522800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr3:20522200-20523000	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr3:20522200-20523400	Enhancers	H1 Cell Line	embryonic stem cell
32	chr3:20522400-20522600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:20522400-20522600	Enhancers	Fetal Lung	lung
34	chr3:20522600-20523000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr3:20522600-20523000	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr3:20522600-20523800	Enhancers	HUVEC	blood vessel
37	chr3:20522800-20523200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr3:20523200-20523400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr3:20523400-20524000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr3:20524000-20524200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr3:20524000-20524200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr3:20524200-20524600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr3:20524200-20525400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr3:20528800-20536200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr3:20529200-20529800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr3:20529800-20531000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr3:20531000-20532600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:20531400-20532600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr3:20531600-20533200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr3:20532400-20533000	Enhancers	HUVEC	blood vessel

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