Variant report

Variant	esv1824644
Chromosome Location	chr3:75604469-75794567
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5343)
CpG islands
(count:3482)
Chromatin interactive
region (count:9)
LncRNA
region (count:25)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:5343 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75739156-75739286	K562	blood:	n/a	n/a
2	ARID3A	chr3:75693043-75693065	K562	blood:	n/a	n/a
3	ARID3A	chr3:75717896-75719229	K562	blood:	n/a	n/a
4	ARID3A	chr3:75770122-75770154	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:75754843-75755270	K562	blood:	n/a	n/a
6	ARID3A	chr3:75719697-75719867	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:75710659-75710674	K562	blood:	n/a	n/a
8	ARID3A	chr3:75736701-75737480	K562	blood:	n/a	n/a
9	ARID3A	chr3:75693851-75694060	K562	blood:	n/a	n/a
10	ARID3A	chr3:75710663-75710916	HepG2	liver:	n/a	n/a
11	ARID3A	chr3:75718141-75718928	HepG2	liver:	n/a	n/a
12	ARID3A	chr3:75691908-75692517	K562	blood:	n/a	n/a
13	ATF1	chr3:75745544-75745744	K562	blood:	n/a	n/a
14	ATF1	chr3:75763746-75764601	K562	blood:	n/a	n/a
15	ATF1	chr3:75765400-75768808	K562	blood:	n/a	n/a
16	ATF1	chr3:75703512-75703565	K562	blood:	n/a	n/a
17	ATF1	chr3:75693870-75694088	K562	blood:	n/a	n/a
18	ATF1	chr3:75787686-75789584	K562	blood:	n/a	n/a
19	ATF1	chr3:75771441-75772260	K562	blood:	n/a	n/a
20	ATF1	chr3:75759504-75760427	K562	blood:	n/a	n/a
21	ATF1	chr3:75783726-75784839	K562	blood:	n/a	n/a
22	ATF1	chr3:75736867-75738707	K562	blood:	n/a	n/a
23	ATF1	chr3:75743644-75744222	K562	blood:	n/a	n/a
24	ATF1	chr3:75730688-75730845	K562	blood:	n/a	n/a
25	ATF1	chr3:75735948-75736287	K562	blood:	n/a	n/a
26	ATF1	chr3:75679956-75680482	K562	blood:	n/a	n/a
27	ATF1	chr3:75735197-75735394	K562	blood:	n/a	n/a
28	ATF1	chr3:75762715-75762961	K562	blood:	n/a	n/a
29	ATF1	chr3:75746545-75746765	K562	blood:	n/a	n/a
30	ATF1	chr3:75685926-75686418	K562	blood:	n/a	n/a
31	ATF1	chr3:75726782-75726783	K562	blood:	n/a	n/a
32	ATF1	chr3:75690145-75690820	K562	blood:	n/a	n/a
33	ATF1	chr3:75755512-75756182	K562	blood:	n/a	n/a
34	ATF1	chr3:75779002-75782622	K562	blood:	n/a	n/a
35	ATF1	chr3:75777037-75777776	K562	blood:	n/a	n/a
36	ATF1	chr3:75754856-75755222	K562	blood:	n/a	n/a
37	ATF1	chr3:75750030-75750205	K562	blood:	n/a	n/a
38	ATF1	chr3:75747229-75747380	K562	blood:	n/a	n/a
39	ATF1	chr3:75769325-75769986	K562	blood:	n/a	n/a
40	ATF1	chr3:75789795-75794952	K562	blood:	n/a	n/a
41	ATF1	chr3:75710744-75710785	K562	blood:	n/a	n/a
42	ATF1	chr3:75733400-75734148	K562	blood:	n/a	n/a
43	ATF1	chr3:75691118-75692520	K562	blood:	n/a	n/a
44	ATF1	chr3:75778219-75778585	K562	blood:	n/a	n/a
45	ATF1	chr3:75773435-75776229	K562	blood:	n/a	n/a
46	ATF1	chr3:75734703-75734852	K562	blood:	n/a	n/a
47	ATF1	chr3:75761625-75762259	K562	blood:	n/a	n/a
48	ATF1	chr3:75695108-75700001	K562	blood:	n/a	n/a
49	ATF1	chr3:75728521-75728535	K562	blood:	n/a	n/a
50	ATF1	chr3:75740338-75740804	K562	blood:	n/a	n/a

(count:3482 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75704824-75704874	PrEC	prostate:	n/a
2	chr3:75708104-75708154	HEEpiC	esophagus:	n/a
3	chr3:75668035-75668085	HCPEpiC	choroid plexus:	n/a
4	chr3:75628819-75628869	RPTEC	kidney:	n/a
5	chr3:75668035-75668085	CMK	blood:	n/a
6	chr3:75704824-75704874	PrEC	prostate:	n/a
7	chr3:75708104-75708154	HEEpiC	esophagus:	n/a
8	chr3:75668035-75668085	HCPEpiC	choroid plexus:	n/a
9	chr3:75628819-75628869	RPTEC	kidney:	n/a
10	chr3:75668035-75668085	CMK	blood:	n/a
11	chr3:75628932-75628982	ovcar-3	ovarian:	n/a
12	chr3:75708104-75708154	T-47D	breast:	n/a
13	chr3:75661799-75661849	NH-A	brain:	n/a
14	chr3:75701993-75702043	U87	brain:	n/a
15	chr3:75717248-75717298	HNPCEpiC	eye:	n/a
16	chr3:75704498-75704548	HAEpiC	amniotic membrane:	n/a
17	chr3:75717453-75717503	GM06990	blood:	n/a
18	chr3:75679454-75679504	HPAEpiC	pulmonary alveolar:	n/a
19	chr3:75704498-75704548	AG04450	lung:	fetal
20	chr3:75707990-75708040	Hepatocyte	liver:	n/a
21	chr3:75720199-75720249	BJ	skin:	n/a
22	chr3:75631426-75631476	GM12891	blood:	n/a
23	chr3:75666392-75666442	NHDF-neo	bronchial:	n/a
24	chr3:75669109-75669159	NH-A	brain:	n/a
25	chr3:75668035-75668085	AG04449	skin:	fetal
26	chr3:75658490-75658540	AG04449	skin:	fetal
27	chr3:75631426-75631476	CMK	blood:	n/a
28	chr3:75720876-75720926	GM19239	blood:	n/a
29	chr3:75721888-75721938	H1-hESC	embryonic stem cell:	embryo
30	chr3:75629039-75629089	A549	lung:	n/a
31	chr3:75658490-75658540	Jurkat	blood:	n/a
32	chr3:75707990-75708040	RPTEC	kidney:	n/a
33	chr3:75668924-75668974	GM12891	blood:	n/a
34	chr3:75712404-75712454	Caco-2	colon:	n/a
35	chr3:75712695-75712745	NHBE	bronchial:	n/a
36	chr3:75704951-75705001	HL-60	blood:	n/a
37	chr3:75701993-75702043	CMK	blood:	n/a
38	chr3:75690456-75690506	GM19239	blood:	n/a
39	chr3:75657183-75657233	SK-N-SH	brain:	n/a
40	chr3:75666381-75666431	SK-N-SH_RA	brain:	n/a
41	chr3:75667994-75668044	HCT-116	colon:	n/a
42	chr3:75671115-75671165	HepG2	liver:	n/a
43	chr3:75708104-75708154	HCT-116	colon:	n/a
44	chr3:75690456-75690506	Hepatocyte	liver:	n/a
45	chr3:75668627-75668677	AG04450	lung:	fetal
46	chr3:75721577-75721627	HEK293	kidney:	embryo
47	chr3:75704498-75704548	HNPCEpiC	eye:	n/a
48	chr3:75715783-75715833	HIPEpiC	eye:	n/a
49	chr3:75628932-75628982	ProgFib	skin:	n/a
50	chr3:75704824-75704874	HEK293	kidney:	embryo

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:75718137..75719895-chr9:68411990..68414461,3	MCF-7	breast:
2	chr16:436504..437180-chr3:75674246..75674764,2	MCF-7	breast:
3	chr3:75790783..75791412-chr6:15280318..15280818,2	MCF-7	breast:
4	chr3:75692090..75692596-chr7:138578273..138578773,2	K562	blood:
5	chr3:75717548..75719836-chr9:68411784..68414340,4	MCF-7	breast:
6	chr19:22025273..22026773-chr3:75695462..75697658,2	MCF-7	breast:
7	chr3:75693392..75694000-chr5:103852101..103852601,2	MCF-7	breast:
8	chr16:33943186..33943816-chr3:75719164..75719883,2	MCF-7	breast:
9	chr17:56709052..56711813-chr3:75770362..75772517,2	MCF-7	breast:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-2	chr3:75608026-75608433	XLOC_002712
2	lnc-ZNF717-1	chr3:75719171-75721122	ENSG00000234317
3	lnc-FRG2C-2	chr3:75606117-75606146	XLOC_002712
4	lnc-FRG2C-7	chr3:75713481-75713708	NR_037925
5	lnc-ZNF717-3	chr3:75629129-75629150	ENSG00000272710.1
6	lnc-FRG2C-7	chr3:75714678-75716368	NR_037925
7	lnc-ZNF717-1	chr3:75719171-75719204	NONHSAT090540
8	lnc-FRG2C-2	chr3:75606223-75606260	XLOC_002712
9	lnc-ZNF717-1	chr3:75716700-75717742	NONHSAT090545
10	lnc-ZNF717-2	chr3:75691158-75691575	XLOC_003164
11	lnc-ZNF717-2	chr3:75695572-75695597	XLOC_003164
12	lnc-FRG2C-10	chr3:75691156-75691895	NONHSAT090542
13	lnc-FRG2C-1	chr3:75723564-75725031	ENSG00000242516
14	lnc-FRG2C-2	chr3:75608026-75608398	XLOC_002712
15	lnc-CNTN3-1	chr3:75762167-75762465	NONHSAT090550
16	lnc-FRG2C-7	chr3:75713970-75714047	NR_037925
17	lnc-FRG2C-1	chr3:75725119-75725776	ENSG00000242516
18	lnc-ZNF717-1	chr3:75719171-75721030	NONHSAT090545
19	lnc-FRG2C-7	chr3:75714277-75714354	NR_037925
20	lnc-ZNF717-1	chr3:75674122-75674304	NONHSAT090540
21	lnc-ZNF717-1	chr3:75679231-75679352	NONHSAT090540
22	lnc-FRG2C-10	chr3:75694930-75696049	NONHSAT090542
23	lnc-ZNF717-1	chr3:75716700-75717742	ENSG00000234317
24	lnc-ZNF717-1	chr3:75721121-75721241	NONHSAT090545
25	lnc-FRG2C-10	chr3:75687750-75688507	NONHSAT090542

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4273	chr3:75787441-75787458	MIMAT0016903
hsa-miR-1324	chr3:75679974-75679997	MIMAT0005956

No data

Variant related genes	Relation type
UNC93B3	TF binding region
FRG2C	TF binding region
ENSG00000243422	TF binding region
ENSG00000239383	TF binding region
MIR4273	TF binding region
AGGF1P3	TF binding region
LINC00960	TF binding region
OR7E121P	TF binding region
RN7SL92P	TF binding region
RARRES2P1	TF binding region
ENSG00000236138	TF binding region
ENSG00000272710	TF binding region
MIR1324	TF binding region
UNC93B3	CpG island
FRG2C	CpG island
ENSG00000243422	CpG island
ENSG00000239383	CpG island
MIR4273	CpG island
AGGF1P3	CpG island
LINC00960	CpG island
OR7E121P	CpG island
RN7SL92P	CpG island
RARRES2P1	CpG island
ENSG00000236138	CpG island
ENSG00000272710	CpG island
MIR1324	CpG island
ENSG00000232815	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000236829	chromatin interactions
ENSG00000129925	chromatin interactions

Extended variants
information (count: 12812 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:12812 , 50 per page) page: 1 2 3 4 5 6 7 ... 257

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35334330	chr3:75606130-75606131	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34074158	chr3:75606136-75606137	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs527838558	chr3:75606144-75606145	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs143070119	chr3:75606236-75606237	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs182084436	chr3:75608006-75608007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557352150	chr3:75608015-75608016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575869753	chr3:75608026-75608027	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs550015741	chr3:75608050-75608051	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs56316115	chr3:75608060-75608061	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs557690169	chr3:75608068-75608069	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs572906091	chr3:75608073-75608074	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs34668777	chr3:75608078-75608079	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs540328616	chr3:75608086-75608087	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs561879362	chr3:75608087-75608088	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs185495505	chr3:75608089-75608090	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs544366364	chr3:75608092-75608093	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs561767385	chr3:75608122-75608123	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs367837075	chr3:75608124-75608125	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs547141019	chr3:75608152-75608153	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs562557275	chr3:75608155-75608156	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs144394594	chr3:75608160-75608161	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs529269723	chr3:75608170-75608171	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs189911556	chr3:75608177-75608178	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs560185299	chr3:75608181-75608182	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs57508935	chr3:75608252-75608253	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs183846908	chr3:75608263-75608264	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs114977374	chr3:75608271-75608272	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs537567595	chr3:75608277-75608278	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs551122258	chr3:75608282-75608283	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs12491376	chr3:75608283-75608284	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs540078558	chr3:75608285-75608286	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs558078717	chr3:75608312-75608313	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs113163849	chr3:75608324-75608325	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs113758790	chr3:75608345-75608346	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs188338141	chr3:75608353-75608354	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs72892734	chr3:75608370-75608371	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs368441203	chr3:75608375-75608376	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs544389493	chr3:75608390-75608391	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs62258798	chr3:75608396-75608397	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs62258799	chr3:75608406-75608407	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs372087600	chr3:75608431-75608432	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs146561229	chr3:75608432-75608433	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs146543553	chr3:75608435-75608436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140388245	chr3:75608457-75608458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545311969	chr3:75608466-75608467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs199627346	chr3:75608479-75608480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs376386823	chr3:75608483-75608484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs4677549	chr3:75608488-75608489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs193286587	chr3:75608491-75608492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs200104722	chr3:75608524-75608525	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	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
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:2685 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75608000-75608600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr3:75625600-75626000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr3:75625600-75628000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:75625800-75626800	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr3:75626000-75627400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr3:75626800-75628200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr3:75627400-75628200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr3:75628000-75629000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr3:75628200-75628400	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr3:75628200-75628400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr3:75628200-75628400	Bivalent Enhancer	Fetal Kidney	kidney
12	chr3:75628200-75629400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:75628400-75628600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
14	chr3:75628400-75628600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
15	chr3:75628400-75628600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr3:75628400-75628600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
17	chr3:75628400-75628600	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
18	chr3:75628400-75628600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr3:75628400-75629400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
20	chr3:75628400-75629400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
21	chr3:75628400-75629400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
22	chr3:75628400-75629400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
23	chr3:75628400-75629600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
24	chr3:75628400-75629600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
25	chr3:75628400-75629600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
26	chr3:75628400-75629600	Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr3:75628400-75629600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr3:75628400-75629800	Active TSS	Brain Cingulate Gyrus	brain
29	chr3:75628600-75628800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr3:75628600-75628800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr3:75628600-75628800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
32	chr3:75628600-75628800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr3:75628600-75628800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr3:75628600-75628800	Enhancers	Brain Hippocampus Middle	brain
35	chr3:75628600-75628800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr3:75628600-75629000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr3:75628600-75629000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr3:75628600-75629000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr3:75628600-75629000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
40	chr3:75628600-75629200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
41	chr3:75628600-75629200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
42	chr3:75628600-75629200	Bivalent/Poised TSS	Fetal Intestine Large	intestine
43	chr3:75628600-75629400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr3:75628600-75629600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
45	chr3:75628600-75629600	Active TSS	H9 Cell Line	embryonic stem cell
46	chr3:75628600-75629600	Active TSS	Cortex derived primary cultured neurospheres	brain
47	chr3:75628600-75629600	Active TSS	Fetal Brain Female	brain
48	chr3:75628600-75629800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr3:75628600-75629800	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr3:75628600-75629800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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