Variant report

Variant	esv1831988
Chromosome Location	chr3:75568433-75803471
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5799)
CpG islands
(count:3484)
Chromatin interactive
region (count:10)
LncRNA
region (count:27)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:5799 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75710663-75710916	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:75736701-75737480	K562	blood:	n/a	n/a
3	ARID3A	chr3:75739156-75739286	K562	blood:	n/a	n/a
4	ARID3A	chr3:75754843-75755270	K562	blood:	n/a	n/a
5	ARID3A	chr3:75719697-75719867	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:75710659-75710674	K562	blood:	n/a	n/a
7	ARID3A	chr3:75693043-75693065	K562	blood:	n/a	n/a
8	ARID3A	chr3:75770122-75770154	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:75717896-75719229	K562	blood:	n/a	n/a
10	ARID3A	chr3:75691908-75692517	K562	blood:	n/a	n/a
11	ARID3A	chr3:75693851-75694060	K562	blood:	n/a	n/a
12	ARID3A	chr3:75601426-75601483	K562	blood:	n/a	n/a
13	ARID3A	chr3:75718141-75718928	HepG2	liver:	n/a	n/a
14	ATF1	chr3:75759504-75760427	K562	blood:	n/a	n/a
15	ATF1	chr3:75695108-75700001	K562	blood:	n/a	n/a
16	ATF1	chr3:75689319-75689814	K562	blood:	n/a	n/a
17	ATF1	chr3:75743644-75744222	K562	blood:	n/a	n/a
18	ATF1	chr3:75762715-75762961	K562	blood:	n/a	n/a
19	ATF1	chr3:75787686-75789584	K562	blood:	n/a	n/a
20	ATF1	chr3:75685926-75686418	K562	blood:	n/a	n/a
21	ATF1	chr3:75771441-75772260	K562	blood:	n/a	n/a
22	ATF1	chr3:75778219-75778585	K562	blood:	n/a	n/a
23	ATF1	chr3:75779002-75782622	K562	blood:	n/a	n/a
24	ATF1	chr3:75735948-75736287	K562	blood:	n/a	n/a
25	ATF1	chr3:75710744-75710785	K562	blood:	n/a	n/a
26	ATF1	chr3:75789795-75794952	K562	blood:	n/a	n/a
27	ATF1	chr3:75736867-75738707	K562	blood:	n/a	n/a
28	ATF1	chr3:75746545-75746765	K562	blood:	n/a	n/a
29	ATF1	chr3:75783726-75784839	K562	blood:	n/a	n/a
30	ATF1	chr3:75693870-75694088	K562	blood:	n/a	n/a
31	ATF1	chr3:75728521-75728535	K562	blood:	n/a	n/a
32	ATF1	chr3:75733400-75734148	K562	blood:	n/a	n/a
33	ATF1	chr3:75754856-75755222	K562	blood:	n/a	n/a
34	ATF1	chr3:75773435-75776229	K562	blood:	n/a	n/a
35	ATF1	chr3:75728107-75728162	K562	blood:	n/a	n/a
36	ATF1	chr3:75690145-75690820	K562	blood:	n/a	n/a
37	ATF1	chr3:75785062-75787392	K562	blood:	n/a	n/a
38	ATF1	chr3:75769325-75769986	K562	blood:	n/a	n/a
39	ATF1	chr3:75760657-75761408	K562	blood:	n/a	n/a
40	ATF1	chr3:75691118-75692520	K562	blood:	n/a	n/a
41	ATF1	chr3:75745544-75745744	K562	blood:	n/a	n/a
42	ATF1	chr3:75765400-75768808	K562	blood:	n/a	n/a
43	ATF1	chr3:75703512-75703565	K562	blood:	n/a	n/a
44	ATF1	chr3:75763746-75764601	K562	blood:	n/a	n/a
45	ATF1	chr3:75750030-75750205	K562	blood:	n/a	n/a
46	ATF1	chr3:75679956-75680482	K562	blood:	n/a	n/a
47	ATF1	chr3:75747229-75747380	K562	blood:	n/a	n/a
48	ATF1	chr3:75755512-75756182	K562	blood:	n/a	n/a
49	ATF1	chr3:75730688-75730845	K562	blood:	n/a	n/a
50	ATF1	chr3:75726782-75726783	K562	blood:	n/a	n/a

(count:3484 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75707560-75707610	SKMC	muscle:	n/a
2	chr3:75712695-75712745	A549	lung:	n/a
3	chr3:75668369-75668419	HL-60	blood:	n/a
4	chr3:75658552-75658602	CMK	blood:	n/a
5	chr3:75720199-75720249	GM19239	blood:	n/a
6	chr3:75669109-75669159	AG09309	skin:	n/a
7	chr3:75679024-75679074	HRPEpiC	eye:	n/a
8	chr3:75707560-75707610	SKMC	muscle:	n/a
9	chr3:75712695-75712745	A549	lung:	n/a
10	chr3:75668369-75668419	HL-60	blood:	n/a
11	chr3:75658552-75658602	CMK	blood:	n/a
12	chr3:75720199-75720249	GM19239	blood:	n/a
13	chr3:75669109-75669159	AG09309	skin:	n/a
14	chr3:75679024-75679074	HRPEpiC	eye:	n/a
15	chr3:75690456-75690506	Caco-2	colon:	n/a
16	chr3:75671115-75671165	H1-hESC	embryonic stem cell:	embryo
17	chr3:75658735-75658785	SK-N-SH_RA	brain:	n/a
18	chr3:75707990-75708040	GM06990	blood:	n/a
19	chr3:75704951-75705001	ECC-1	luminal epithelium:	n/a
20	chr3:75668758-75668808	HRPEpiC	eye:	n/a
21	chr3:75720199-75720249	HRE	kidney:	n/a
22	chr3:75629039-75629089	HL-60	blood:	n/a
23	chr3:75657183-75657233	BE2_C	brain:	n/a
24	chr3:75690456-75690506	U87	brain:	n/a
25	chr3:75632533-75632583	HPAEpiC	pulmonary alveolar:	n/a
26	chr3:75664059-75664109	AG04449	skin:	fetal
27	chr3:75631426-75631476	ECC-1	luminal epithelium:	n/a
28	chr3:75668035-75668085	PFSK-1	brain:	n/a
29	chr3:75628932-75628982	Jurkat	blood:	n/a
30	chr3:75717248-75717298	BE2_C	brain:	n/a
31	chr3:75712695-75712745	U87	brain:	n/a
32	chr3:75658490-75658540	PFSK-1	brain:	n/a
33	chr3:75629433-75629483	HPAEpiC	pulmonary alveolar:	n/a
34	chr3:75715783-75715833	AoSMC	blood vessel:	n/a
35	chr3:75653319-75653369	SAEC	small airway:	n/a
36	chr3:75658490-75658540	Hela-S3	cervix:	n/a
37	chr3:75659629-75659679	HCPEpiC	choroid plexus:	n/a
38	chr3:75719158-75719208	PrEC	prostate:	n/a
39	chr3:75658490-75658540	HCPEpiC	choroid plexus:	n/a
40	chr3:75628819-75628869	GM06990	blood:	n/a
41	chr3:75712695-75712745	MCF-7	breast:	n/a
42	chr3:75661799-75661849	HCF	heart:	n/a
43	chr3:75668627-75668677	Jurkat	blood:	n/a
44	chr3:75657758-75657808	BE2_C	brain:	n/a
45	chr3:75704498-75704548	NB4	blood:	n/a
46	chr3:75658410-75658460	MCF-7	breast:	n/a
47	chr3:75707990-75708040	PFSK-1	brain:	n/a
48	chr3:75658410-75658460	AoSMC	blood vessel:	n/a
49	chr3:75628932-75628982	MCF-7	breast:	n/a
50	chr3:75628819-75628869	U87	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:22025273..22026773-chr3:75695462..75697658,2	MCF-7	breast:
2	chr3:75693392..75694000-chr5:103852101..103852601,2	MCF-7	breast:
3	chr3:75692090..75692596-chr7:138578273..138578773,2	K562	blood:
4	chr3:75717548..75719836-chr9:68411784..68414340,4	MCF-7	breast:
5	chr3:75343397..75343923-chr3:75600934..75601577,2	MCF-7	breast:
6	chr3:75790783..75791412-chr6:15280318..15280818,2	MCF-7	breast:
7	chr17:56709052..56711813-chr3:75770362..75772517,2	MCF-7	breast:
8	chr3:75718137..75719895-chr9:68411990..68414461,3	MCF-7	breast:
9	chr16:436504..437180-chr3:75674246..75674764,2	MCF-7	breast:
10	chr16:33943186..33943816-chr3:75719164..75719883,2	MCF-7	breast:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-2	chr3:75606117-75606146	XLOC_002712
2	lnc-ZNF717-1	chr3:75719171-75721030	NONHSAT090545
3	lnc-ZNF717-1	chr3:75716700-75717742	ENSG00000234317
4	lnc-FRG2C-2	chr3:75608026-75608398	XLOC_002712
5	lnc-ZNF717-1	chr3:75719171-75721122	ENSG00000234317
6	lnc-FRG2C-10	chr3:75691156-75691895	NONHSAT090542
7	lnc-FRG2C-7	chr3:75713481-75713708	NR_037925
8	lnc-FRG2C-11	chr3:75570954-75571163	NONHSAT090534
9	lnc-FRG2C-2	chr3:75606223-75606260	XLOC_002712
10	lnc-ZNF717-1	chr3:75721121-75721241	NONHSAT090545
11	lnc-FRG2C-1	chr3:75725119-75725776	ENSG00000242516
12	lnc-FRG2C-10	chr3:75687750-75688507	NONHSAT090542
13	lnc-FRG2C-7	chr3:75714678-75716368	NR_037925
14	lnc-ZNF717-2	chr3:75695572-75695597	XLOC_003164
15	lnc-FRG2C-7	chr3:75714277-75714354	NR_037925
16	lnc-ZNF717-3	chr3:75589200-75589378	ENSG00000272710.1
17	lnc-ZNF717-1	chr3:75716700-75717742	NONHSAT090545
18	lnc-FRG2C-2	chr3:75608026-75608433	XLOC_002712
19	lnc-ZNF717-1	chr3:75674122-75674304	NONHSAT090540
20	lnc-FRG2C-10	chr3:75694930-75696049	NONHSAT090542
21	lnc-ZNF717-2	chr3:75691158-75691575	XLOC_003164
22	lnc-ZNF717-3	chr3:75629129-75629150	ENSG00000272710.1
23	lnc-ZNF717-1	chr3:75679231-75679352	NONHSAT090540
24	lnc-FRG2C-1	chr3:75723564-75725031	ENSG00000242516
25	lnc-ZNF717-1	chr3:75719171-75719204	NONHSAT090540
26	lnc-FRG2C-7	chr3:75713970-75714047	NR_037925
27	lnc-CNTN3-1	chr3:75762167-75762465	NONHSAT090550

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
ENSG00000221602	TF binding region
MIR4273	TF binding region
AGGF1P3	TF binding region
LINC00960	TF binding region
RPS3AP15	TF binding region
ENSG00000243794	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
ENSG00000221602	CpG island
MIR4273	CpG island
AGGF1P3	CpG island
LINC00960	CpG island
RPS3AP15	CpG island
ENSG00000243794	CpG island
OR7E121P	CpG island
RN7SL92P	CpG island
RARRES2P1	CpG island
ENSG00000236138	CpG island
ENSG00000272710	CpG island
MIR1324	CpG island
ENSG00000212195	chromatin interactions
ENSG00000236829	chromatin interactions
ENSG00000232815	chromatin interactions
ENSG00000129925	chromatin interactions

Extended variants
information (count: 14805 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:14805 , 50 per page) page: 1 2 3 4 5 6 7 ... 297

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9873181	chr3:75568433-75568434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs13062434	chr3:75568447-75568448	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs6763623	chr3:75568453-75568454	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs9873205	chr3:75568474-75568475	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs60100987	chr3:75568480-75568481	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs56947443	chr3:75568505-75568506	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs560583234	chr3:75568508-75568509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2940508	chr3:75568511-75568512	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs186249945	chr3:75568531-75568532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35697282	chr3:75568541-75568542	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs550978810	chr3:75568563-75568564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191770720	chr3:75568581-75568582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530041894	chr3:75568594-75568595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184000327	chr3:75568597-75568598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs35353277	chr3:75568611-75568612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138226119	chr3:75568617-75568618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112486544	chr3:75568633-75568634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185173288	chr3:75568645-75568646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs36082875	chr3:75568649-75568650	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs376942376	chr3:75568650-75568651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370093069	chr3:75568651-75568652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187504902	chr3:75568658-75568659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191836693	chr3:75568675-75568676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568955800	chr3:75568686-75568687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113942655	chr3:75568725-75568726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146505556	chr3:75568730-75568731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142683426	chr3:75568731-75568732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113731768	chr3:75568767-75568768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564301401	chr3:75568776-75568777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554584948	chr3:75568790-75568791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190515321	chr3:75568793-75568794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111608659	chr3:75568807-75568808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111401278	chr3:75568828-75568829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112859209	chr3:75568833-75568834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs113797076	chr3:75568857-75568858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577083166	chr3:75568866-75568867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540896368	chr3:75568877-75568878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182225636	chr3:75568885-75568886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368615894	chr3:75568891-75568892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529624183	chr3:75568906-75568907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186457226	chr3:75568907-75568908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113843391	chr3:75568917-75568918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533417409	chr3:75568918-75568919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs60492298	chr3:75568955-75568956	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs61544587	chr3:75568975-75568976	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs60251151	chr3:75568977-75568978	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs527674460	chr3:75568997-75568998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547770206	chr3:75568998-75568999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567440038	chr3:75569005-75569006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113375313	chr3:75569018-75569019	Weak transcription	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:2820 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75562200-75574200	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr3:75567000-75571400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:75571400-75573400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:75573400-75575600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:75574200-75575800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:75575600-75575800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr3:75581000-75585800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr3:75586600-75586800	ZNF genes & repeats	Ovary	ovary
9	chr3:75586800-75587400	Weak transcription	Ovary	ovary
10	chr3:75599400-75601200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:75600600-75601200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr3:75608000-75608600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr3:75625600-75626000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr3:75625600-75628000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:75625800-75626800	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr3:75626000-75627400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr3:75626800-75628200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr3:75627400-75628200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr3:75628000-75629000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr3:75628200-75628400	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr3:75628200-75628400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr3:75628200-75628400	Bivalent Enhancer	Fetal Kidney	kidney
23	chr3:75628200-75629400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:75628400-75628600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
25	chr3:75628400-75628600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
26	chr3:75628400-75628600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr3:75628400-75628600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
28	chr3:75628400-75628600	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
29	chr3:75628400-75628600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr3:75628400-75629400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
31	chr3:75628400-75629400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
32	chr3:75628400-75629400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
33	chr3:75628400-75629400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
34	chr3:75628400-75629600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
35	chr3:75628400-75629600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
36	chr3:75628400-75629600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
37	chr3:75628400-75629600	Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr3:75628400-75629600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr3:75628400-75629800	Active TSS	Brain Cingulate Gyrus	brain
40	chr3:75628600-75628800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr3:75628600-75628800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr3:75628600-75628800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:75628600-75628800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr3:75628600-75628800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr3:75628600-75628800	Enhancers	Brain Hippocampus Middle	brain
46	chr3:75628600-75628800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr3:75628600-75629000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr3:75628600-75629000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr3:75628600-75629000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr3:75628600-75629000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland

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