Variant report

Variant	nsv589865
Chromosome Location	chr3:20480253-20605302
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:481)
CpG islands
(count:246)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:481 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	chr3:20492146-20492486	K562	blood:	n/a	n/a
4	BACH1	chr3:20536253-20536368	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:20578833-20579051	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:20492139-20492474	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr3:20535546-20535645	H1-hESC	embryonic stem cell:	n/a	n/a
8	CCNT2	chr3:20500973-20501023	K562	blood:	n/a	n/a
9	CEBPB	chr3:20568523-20568549	K562	blood:	n/a	n/a
10	CEBPB	chr3:20551895-20552228	HepG2	liver:	n/a	n/a
11	CHD2	chr3:20595241-20595316	HepG2	liver:	n/a	n/a
12	CTCF	chr3:20553268-20553663	K562	blood:	n/a	n/a
13	CTCF	chr3:20553480-20553630	HFF	foreskin:	n/a	n/a
14	CTCF	chr3:20519920-20520070	RPTEC	kidney:	n/a	n/a
15	CTCF	chr3:20553340-20553490	K562	blood:	n/a	n/a
16	CTCF	chr3:20553400-20553550	MCF-7	breast:	n/a	n/a
17	CTCF	chr3:20553380-20553530	GM12873	blood:	n/a	n/a
18	CTCF	chr3:20553420-20553570	HepG2	liver:	n/a	n/a
19	CTCF	chr3:20553300-20553450	HAc	cerebellar:	n/a	n/a
20	CTCF	chr3:20553400-20553550	SAEC	small airway:	n/a	n/a
21	CTCF	chr3:20553327-20553597	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr3:20553305-20553599	Lung_OC	lung:	n/a	n/a
23	CTCF	chr3:20553380-20553530	AG09319	gingival:	n/a	n/a
24	CTCF	chr3:20553360-20553510	GM12864	blood:	n/a	n/a
25	CTCF	chr3:20553380-20553530	HCFaa	heart:	n/a	n/a
26	CTCF	chr3:20594460-20594610	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr3:20553420-20553570	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr3:20553300-20553450	GM12868	blood:	n/a	n/a
29	CTCF	chr3:20553400-20553550	GM12872	blood:	n/a	n/a
30	CTCF	chr3:20553360-20553510	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr3:20553380-20553530	AG04450	lung:	n/a	n/a
32	CTCF	chr3:20553356-20553590	A549	lung:	n/a	n/a
33	CTCF	chr3:20553340-20553490	BE2_C	brain:	n/a	n/a
34	CTCF	chr3:20553380-20553530	NB4	blood:	n/a	n/a
35	CTCF	chr3:20594521-20594640	A549	lung:	n/a	n/a
36	CTCF	chr3:20553420-20553570	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr3:20522480-20522630	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr3:20553560-20553710	HAc	cerebellar:	n/a	n/a
39	CTCF	chr3:20553359-20553609	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr3:20553400-20553550	Caco-2	colon:	n/a	n/a
41	CTCF	chr3:20553400-20553550	HRE	kidney:	n/a	n/a
42	CTCF	chr3:20553400-20553550	GM12866	blood:	n/a	n/a
43	CTCF	chr3:20553320-20553470	HL-60	blood:	n/a	n/a
44	CTCF	chr3:20594565-20594621	MCF-7	breast:	n/a	n/a
45	CTCF	chr3:20553354-20553584	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr3:20553539-20553557	GM19240	blood:	n/a	n/a
47	CTCF	chr3:20553400-20553550	NHEK	skin:	n/a	n/a
48	CTCF	chr3:20553380-20553530	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr3:20553316-20553697	MCF-7	breast:	n/a	n/a
50	CTCF	chr3:20519940-20520090	HFF	foreskin:	n/a	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:20522301-20522351	HRE	kidney:	n/a
2	chr3:20575513-20575563	ovcar-3	ovarian:	n/a
3	chr3:20522301-20522351	HRE	kidney:	n/a
4	chr3:20575513-20575563	ovcar-3	ovarian:	n/a
5	chr3:20522301-20522351	HL-60	blood:	n/a
6	chr3:20575513-20575563	SK-N-SH	brain:	n/a
7	chr3:20589671-20589721	GM06990	blood:	n/a
8	chr3:20589760-20589810	T-47D	breast:	n/a
9	chr3:20589760-20589810	HCT-116	colon:	n/a
10	chr3:20589760-20589810	LNCaP	prostate:	n/a
11	chr3:20589760-20589810	AG04449	skin:	fetal
12	chr3:20589760-20589810	SK-N-MC	brain:	n/a
13	chr3:20589760-20589810	AG09309	skin:	n/a
14	chr3:20522301-20522351	NT2-D1	testis:	n/a
15	chr3:20589760-20589810	HCM	heart:	n/a
16	chr3:20589671-20589721	T-47D	breast:	n/a
17	chr3:20589671-20589721	IMR90	lung:	fetal
18	chr3:20575513-20575563	HRCEpiC	kidney:	n/a
19	chr3:20575513-20575563	PFSK-1	brain:	n/a
20	chr3:20589671-20589721	MCF10A-Er-Src	breast:	n/a
21	chr3:20589760-20589810	AoSMC	blood vessel:	n/a
22	chr3:20589760-20589810	Jurkat	blood:	n/a
23	chr3:20589671-20589721	ECC-1	luminal epithelium:	n/a
24	chr3:20575513-20575563	BJ	skin:	n/a
25	chr3:20589760-20589810	H1-hESC	embryonic stem cell:	embryo
26	chr3:20589760-20589810	MCF10A-Er-Src	breast:	n/a
27	chr3:20522301-20522351	GM12892	blood:	n/a
28	chr3:20575513-20575563	AG09309	skin:	n/a
29	chr3:20522301-20522351	Caco-2	colon:	n/a
30	chr3:20575513-20575563	ECC-1	luminal epithelium:	n/a
31	chr3:20522301-20522351	PFSK-1	brain:	n/a
32	chr3:20589760-20589810	SKMC	muscle:	n/a
33	chr3:20522301-20522351	IMR90	lung:	fetal
34	chr3:20589760-20589810	IMR90	lung:	fetal
35	chr3:20589671-20589721	GM12892	blood:	n/a
36	chr3:20589760-20589810	AG04450	lung:	fetal
37	chr3:20589760-20589810	ProgFib	skin:	n/a
38	chr3:20589671-20589721	A549	lung:	n/a
39	chr3:20522301-20522351	NHDF-neo	bronchial:	n/a
40	chr3:20575513-20575563	HNPCEpiC	eye:	n/a
41	chr3:20575513-20575563	HCM	heart:	n/a
42	chr3:20522301-20522351	SK-N-MC	brain:	n/a
43	chr3:20522301-20522351	SK-N-SH	brain:	n/a
44	chr3:20575513-20575563	HUVEC	blood vessel:	n/a
45	chr3:20522301-20522351	GM06990	blood:	n/a
46	chr3:20522301-20522351	HEEpiC	esophagus:	n/a
47	chr3:20575513-20575563	AG04450	lung:	fetal
48	chr3:20575513-20575563	AG09319	gingival:	n/a
49	chr3:20589760-20589810	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:20522301-20522351	HPAEpiC	pulmonary alveolar:	n/a

(count:15 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 2499 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2499 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561956043	chr3:20492605-20492606	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs539883483	chr3:20492614-20492615	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs28845172	chr3:20492620-20492621	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs541607883	chr3:20492632-20492633	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs563388146	chr3:20492664-20492665	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs530458677	chr3:20492688-20492689	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs552172236	chr3:20492709-20492710	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs190657909	chr3:20492715-20492716	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs182945649	chr3:20492741-20492742	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs148133204	chr3:20492766-20492767	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs372293450	chr3:20492791-20492792	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs546868480	chr3:20492795-20492796	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs76169037	chr3:20492836-20492837	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs78788982	chr3:20492854-20492855	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs377365461	chr3:20492873-20492874	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs569310464	chr3:20492987-20492988	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs539523406	chr3:20492994-20492995	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs558151222	chr3:20492999-20493000	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs572863155	chr3:20493043-20493044	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs534226880	chr3:20493046-20493047	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs555639289	chr3:20493053-20493054	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs187803579	chr3:20493059-20493060	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs192927338	chr3:20493079-20493080	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs544777463	chr3:20493087-20493088	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs184295747	chr3:20493102-20493103	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs575313036	chr3:20493108-20493109	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs545539096	chr3:20493114-20493115	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs369186222	chr3:20493115-20493116	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs74877867	chr3:20493116-20493117	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs386659104	chr3:20493118-20493119	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs201208988	chr3:20493119-20493120	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs201568507	chr3:20493120-20493121	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs534184441	chr3:20493121-20493122	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs386659105	chr3:20493128-20493129	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs1581466	chr3:20493129-20493130	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs376819221	chr3:20493180-20493181	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs2139525	chr3:20493187-20493188	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs529102531	chr3:20493227-20493228	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs552054016	chr3:20493231-20493232	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs550770242	chr3:20493233-20493234	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs141424101	chr3:20493245-20493246	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs533478548	chr3:20493256-20493257	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs551539756	chr3:20493265-20493266	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs566575132	chr3:20493270-20493271	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs112071821	chr3:20493277-20493278	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs187521246	chr3:20493284-20493285	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs533096276	chr3:20493291-20493292	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs141371560	chr3:20493292-20493293	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs192398533	chr3:20493298-20493299	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs538121365	chr3:20493357-20493358	ZNF genes & repeats	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:128 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20492600-20494000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:20497400-20497600	Enhancers	Fetal Lung	lung
3	chr3:20497600-20499000	Enhancers	Fetal Kidney	kidney
4	chr3:20498400-20498600	Enhancers	Fetal Lung	lung
5	chr3:20498800-20499000	Enhancers	Fetal Stomach	stomach
6	chr3:20499000-20500800	Weak transcription	Fetal Kidney	kidney
7	chr3:20499600-20501400	Enhancers	Fetal Stomach	stomach
8	chr3:20500000-20501600	Enhancers	Fetal Lung	lung
9	chr3:20500800-20501400	Enhancers	Fetal Kidney	kidney
10	chr3:20501000-20501400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr3:20501000-20501600	Enhancers	Ovary	ovary
12	chr3:20503200-20503600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr3:20503200-20504000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr3:20503200-20504200	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr3:20503200-20504400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr3:20503600-20504000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr3:20503600-20504000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr3:20503600-20504200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr3:20503600-20504600	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr3:20503600-20505200	Enhancers	HUVEC	blood vessel
21	chr3:20504000-20504600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr3:20508000-20508200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr3:20508600-20508800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
24	chr3:20512400-20523200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr3:20516400-20522600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr3:20519800-20520200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr3:20519800-20520400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr3:20519800-20523400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr3:20520000-20520200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr3:20520000-20520800	Enhancers	Fetal Intestine Large	intestine
31	chr3:20520000-20521000	Enhancers	Fetal Lung	lung
32	chr3:20520200-20521200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr3:20520400-20521400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:20520400-20521400	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr3:20520400-20521400	Enhancers	HUVEC	blood vessel
36	chr3:20520600-20522200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr3:20521000-20522400	Weak transcription	Fetal Lung	lung
38	chr3:20521200-20522800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr3:20521200-20523000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr3:20521400-20521600	Flanking Active TSS	HUVEC	blood vessel
41	chr3:20521400-20522200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr3:20521400-20522200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr3:20521400-20522800	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr3:20521400-20523000	Enhancers	NH-A	brain
45	chr3:20521600-20522000	Enhancers	HUVEC	blood vessel
46	chr3:20522000-20522600	Flanking Active TSS	HUVEC	blood vessel
47	chr3:20522000-20522800	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr3:20522200-20522400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:20522200-20522600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr3:20522200-20522800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell

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