Variant report

Variant	esv1840403
Chromosome Location	chr3:75545172-75796728
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5865)
CpG islands
(count:3847)
Chromatin interactive
region (count:10)
LncRNA
region (count:27)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:5865 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75693851-75694060	K562	blood:	n/a	n/a
2	ARID3A	chr3:75710663-75710916	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:75736701-75737480	K562	blood:	n/a	n/a
4	ARID3A	chr3:75693043-75693065	K562	blood:	n/a	n/a
5	ARID3A	chr3:75770122-75770154	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:75710659-75710674	K562	blood:	n/a	n/a
7	ARID3A	chr3:75717896-75719229	K562	blood:	n/a	n/a
8	ARID3A	chr3:75739156-75739286	K562	blood:	n/a	n/a
9	ARID3A	chr3:75718141-75718928	HepG2	liver:	n/a	n/a
10	ARID3A	chr3:75719697-75719867	HepG2	liver:	n/a	n/a
11	ARID3A	chr3:75601426-75601483	K562	blood:	n/a	n/a
12	ARID3A	chr3:75754843-75755270	K562	blood:	n/a	n/a
13	ARID3A	chr3:75691908-75692517	K562	blood:	n/a	n/a
14	ATF1	chr3:75728521-75728535	K562	blood:	n/a	n/a
15	ATF1	chr3:75728107-75728162	K562	blood:	n/a	n/a
16	ATF1	chr3:75783726-75784839	K562	blood:	n/a	n/a
17	ATF1	chr3:75734703-75734852	K562	blood:	n/a	n/a
18	ATF1	chr3:75690145-75690820	K562	blood:	n/a	n/a
19	ATF1	chr3:75679956-75680482	K562	blood:	n/a	n/a
20	ATF1	chr3:75685926-75686418	K562	blood:	n/a	n/a
21	ATF1	chr3:75762715-75762961	K562	blood:	n/a	n/a
22	ATF1	chr3:75736867-75738707	K562	blood:	n/a	n/a
23	ATF1	chr3:75747229-75747380	K562	blood:	n/a	n/a
24	ATF1	chr3:75769325-75769986	K562	blood:	n/a	n/a
25	ATF1	chr3:75743644-75744222	K562	blood:	n/a	n/a
26	ATF1	chr3:75754856-75755222	K562	blood:	n/a	n/a
27	ATF1	chr3:75777037-75777776	K562	blood:	n/a	n/a
28	ATF1	chr3:75760657-75761408	K562	blood:	n/a	n/a
29	ATF1	chr3:75771441-75772260	K562	blood:	n/a	n/a
30	ATF1	chr3:75789795-75794952	K562	blood:	n/a	n/a
31	ATF1	chr3:75750030-75750205	K562	blood:	n/a	n/a
32	ATF1	chr3:75763746-75764601	K562	blood:	n/a	n/a
33	ATF1	chr3:75733400-75734148	K562	blood:	n/a	n/a
34	ATF1	chr3:75726782-75726783	K562	blood:	n/a	n/a
35	ATF1	chr3:75710744-75710785	K562	blood:	n/a	n/a
36	ATF1	chr3:75730688-75730845	K562	blood:	n/a	n/a
37	ATF1	chr3:75779002-75782622	K562	blood:	n/a	n/a
38	ATF1	chr3:75755512-75756182	K562	blood:	n/a	n/a
39	ATF1	chr3:75703512-75703565	K562	blood:	n/a	n/a
40	ATF1	chr3:75735948-75736287	K562	blood:	n/a	n/a
41	ATF1	chr3:75759504-75760427	K562	blood:	n/a	n/a
42	ATF1	chr3:75745544-75745744	K562	blood:	n/a	n/a
43	ATF1	chr3:75693870-75694088	K562	blood:	n/a	n/a
44	ATF1	chr3:75778219-75778585	K562	blood:	n/a	n/a
45	ATF1	chr3:75735197-75735394	K562	blood:	n/a	n/a
46	ATF1	chr3:75740338-75740804	K562	blood:	n/a	n/a
47	ATF1	chr3:75689319-75689814	K562	blood:	n/a	n/a
48	ATF1	chr3:75695108-75700001	K562	blood:	n/a	n/a
49	ATF1	chr3:75787686-75789584	K562	blood:	n/a	n/a
50	ATF1	chr3:75773435-75776229	K562	blood:	n/a	n/a

(count:3847 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75668369-75668419	AG04449	skin:	fetal
2	chr3:75658735-75658785	A549	lung:	n/a
3	chr3:75715783-75715833	SK-N-SH	brain:	n/a
4	chr3:75657183-75657233	U87	brain:	n/a
5	chr3:75668369-75668419	AG04449	skin:	fetal
6	chr3:75658735-75658785	A549	lung:	n/a
7	chr3:75715783-75715833	SK-N-SH	brain:	n/a
8	chr3:75657183-75657233	U87	brain:	n/a
9	chr3:75707805-75707855	ovcar-3	ovarian:	n/a
10	chr3:75679024-75679074	HNPCEpiC	eye:	n/a
11	chr3:75717248-75717298	Hepatocyte	liver:	n/a
12	chr3:75671793-75671843	HCT-116	colon:	n/a
13	chr3:75668924-75668974	HCF	heart:	n/a
14	chr3:75555994-75556044	SK-N-SH_RA	brain:	n/a
15	chr3:75668369-75668419	HNPCEpiC	eye:	n/a
16	chr3:75712404-75712454	HepG2	liver:	n/a
17	chr3:75669109-75669159	HCT-116	colon:	n/a
18	chr3:75714447-75714497	NT2-D1	testis:	n/a
19	chr3:75704573-75704623	HRCEpiC	kidney:	n/a
20	chr3:75666381-75666431	HIPEpiC	eye:	n/a
21	chr3:75629039-75629089	SK-N-SH	brain:	n/a
22	chr3:75712404-75712454	AG09319	gingival:	n/a
23	chr3:75690456-75690506	PFSK-1	brain:	n/a
24	chr3:75704951-75705001	NH-A	brain:	n/a
25	chr3:75721434-75721484	MCF-7	breast:	n/a
26	chr3:75666381-75666431	PrEC	prostate:	n/a
27	chr3:75705922-75705972	IMR90	lung:	fetal
28	chr3:75707560-75707610	BJ	skin:	n/a
29	chr3:75666392-75666442	GM06990	blood:	n/a
30	chr3:75664059-75664109	GM12891	blood:	n/a
31	chr3:75707560-75707610	NH-A	brain:	n/a
32	chr3:75707990-75708040	Hepatocyte	liver:	n/a
33	chr3:75679024-75679074	AG04450	lung:	fetal
34	chr3:75668924-75668974	H1-hESC	embryonic stem cell:	embryo
35	chr3:75715783-75715833	H1-hESC	embryonic stem cell:	embryo
36	chr3:75553762-75553812	HRE	kidney:	n/a
37	chr3:75661320-75661370	AG04449	skin:	fetal
38	chr3:75628932-75628982	HepG2	liver:	n/a
39	chr3:75658410-75658460	PFSK-1	brain:	n/a
40	chr3:75714447-75714497	HAEpiC	amniotic membrane:	n/a
41	chr3:75653319-75653369	H1-hESC	embryonic stem cell:	embryo
42	chr3:75661320-75661370	BJ	skin:	n/a
43	chr3:75712404-75712454	AG04449	skin:	fetal
44	chr3:75668924-75668974	PrEC	prostate:	n/a
45	chr3:75720876-75720926	HCPEpiC	choroid plexus:	n/a
46	chr3:75664059-75664109	HCT-116	colon:	n/a
47	chr3:75714447-75714497	BE2_C	brain:	n/a
48	chr3:75556027-75556077	SAEC	small airway:	n/a
49	chr3:75659629-75659679	HAEpiC	amniotic membrane:	n/a
50	chr3:75555938-75555988	GM19239	blood:	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	chr17:56709052..56711813-chr3:75770362..75772517,2	MCF-7	breast:
3	chr3:75790783..75791412-chr6:15280318..15280818,2	MCF-7	breast:
4	chr16:436504..437180-chr3:75674246..75674764,2	MCF-7	breast:
5	chr3:75343397..75343923-chr3:75600934..75601577,2	MCF-7	breast:
6	chr3:75717548..75719836-chr9:68411784..68414340,4	MCF-7	breast:
7	chr3:75692090..75692596-chr7:138578273..138578773,2	K562	blood:
8	chr3:75693392..75694000-chr5:103852101..103852601,2	MCF-7	breast:
9	chr16:33943186..33943816-chr3:75719164..75719883,2	MCF-7	breast:
10	chr3:75718137..75719895-chr9:68411990..68414461,3	MCF-7	breast:

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

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

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
LINC00960	TF binding region
RPS3AP15	TF binding region
ENSG00000243794	TF binding region
OR7E121P	TF binding region
RARRES2P1	TF binding region
ENSG00000221602	TF binding region
AGGF1P3	TF binding region
RN7SL92P	TF binding region
ENPP7P2	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
LINC00960	CpG island
RPS3AP15	CpG island
ENSG00000243794	CpG island
OR7E121P	CpG island
RARRES2P1	CpG island
ENSG00000221602	CpG island
AGGF1P3	CpG island
RN7SL92P	CpG island
ENPP7P2	CpG island
ENSG00000236138	CpG island
ENSG00000272710	CpG island
MIR1324	CpG island
ENSG00000236829	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000129925	chromatin interactions
ENSG00000232815	chromatin interactions

Extended variants
information (count: 15715 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:15715 , 50 per page) page: 1 2 3 4 5 6 7 ... 315

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12639451	chr3:75545172-75545173	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530276451	chr3:75545173-75545174	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs139947842	chr3:75545192-75545193	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs145465223	chr3:75545196-75545197	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs531245743	chr3:75545199-75545200	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs147663833	chr3:75545208-75545209	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs377594819	chr3:75545209-75545210	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs570737334	chr3:75545234-75545235	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs149956452	chr3:75545250-75545251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185592989	chr3:75545258-75545259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34031024	chr3:75545264-75545265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs34836183	chr3:75545286-75545287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145134629	chr3:75545338-75545339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573603675	chr3:75545347-75545348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552478767	chr3:75545353-75545354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12630559	chr3:75545375-75545376	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs556761826	chr3:75545381-75545382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575163444	chr3:75545412-75545413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369606739	chr3:75545469-75545470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190164181	chr3:75545475-75545476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534927394	chr3:75545507-75545508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs75460252	chr3:75545516-75545517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs114497047	chr3:75545526-75545527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs56770995	chr3:75545529-75545530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529016434	chr3:75545532-75545533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535169612	chr3:75545547-75545548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183159285	chr3:75545562-75545563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542405671	chr3:75545564-75545565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186939247	chr3:75545603-75545604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531159385	chr3:75545616-75545617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2976052	chr3:75545713-75545714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112989372	chr3:75545775-75545776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374757009	chr3:75545802-75545803	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371483809	chr3:75545809-75545810	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528437440	chr3:75545870-75545871	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs386662458	chr3:75545879-75545880	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192130555	chr3:75545881-75545882	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11716245	chr3:75545926-75545927	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs11708230	chr3:75545941-75545942	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs567242977	chr3:75545962-75545963	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs137882499	chr3:75545997-75545998	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142397854	chr3:75546013-75546014	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368106630	chr3:75546050-75546051	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536958652	chr3:75546051-75546052	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375326475	chr3:75546052-75546053	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201273526	chr3:75546109-75546110	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535177103	chr3:75546141-75546142	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs80320059	chr3:75546147-75546148	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573095546	chr3:75546177-75546178	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533523443	chr3:75546183-75546184	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Melanoma	20877625	CNVD
Ollier disease	21235737	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:2853 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75542600-75551400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:75544400-75552000	Weak transcription	Ovary	ovary
3	chr3:75545800-75562400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:75546200-75550800	Weak transcription	Fetal Intestine Small	intestine
5	chr3:75546800-75551400	Weak transcription	Fetal Lung	lung
6	chr3:75548000-75548200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr3:75548200-75552000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr3:75549000-75551600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr3:75549200-75549800	Enhancers	Fetal Intestine Large	intestine
10	chr3:75549200-75550200	Enhancers	K562	blood
11	chr3:75549800-75550800	Weak transcription	Fetal Intestine Large	intestine
12	chr3:75550200-75550800	Weak transcription	K562	blood
13	chr3:75550200-75553600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr3:75550600-75552800	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr3:75550800-75551000	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr3:75550800-75551200	Enhancers	Fetal Heart	heart
17	chr3:75550800-75551200	Enhancers	Stomach Mucosa	stomach
18	chr3:75550800-75551400	Enhancers	Fetal Intestine Large	intestine
19	chr3:75550800-75551400	Enhancers	Fetal Intestine Small	intestine
20	chr3:75550800-75552000	Enhancers	K562	blood
21	chr3:75550800-75552800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr3:75551000-75551400	Enhancers	Small Intestine	intestine
23	chr3:75551000-75552400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr3:75551400-75551600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr3:75551400-75551600	Weak transcription	Small Intestine	intestine
26	chr3:75551400-75552000	Enhancers	Fetal Lung	lung
27	chr3:75551400-75552200	Active TSS	Fetal Heart	heart
28	chr3:75551400-75552400	Active TSS	Skeletal Muscle Female	skeletal muscle
29	chr3:75551400-75552400	Active TSS	Stomach Mucosa	stomach
30	chr3:75551400-75552600	Enhancers	H9 Cell Line	embryonic stem cell
31	chr3:75551400-75552600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr3:75551400-75552600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr3:75551400-75552600	Active TSS	Duodenum Mucosa	Duodenum
34	chr3:75551400-75552800	Active TSS	Fetal Intestine Small	intestine
35	chr3:75551400-75552800	Active TSS	Right Atrium	heart
36	chr3:75551400-75553000	Active TSS	Rectal Mucosa Donor 29	rectum
37	chr3:75551400-75554000	Active TSS	Fetal Intestine Large	intestine
38	chr3:75551600-75551800	Active TSS	Small Intestine	intestine
39	chr3:75551600-75552000	Enhancers	Fetal Muscle Leg	muscle
40	chr3:75551600-75552400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr3:75551600-75552600	Active TSS	Left Ventricle	heart
42	chr3:75551600-75552800	Active TSS	Colonic Mucosa	Colon
43	chr3:75551600-75552800	Active TSS	Duodenum Smooth Muscle	Duodenum
44	chr3:75551600-75552800	Active TSS	Rectal Smooth Muscle	rectum
45	chr3:75551600-75552800	Active TSS	Right Ventricle	heart
46	chr3:75551600-75553000	Active TSS	Rectal Mucosa Donor 31	rectum
47	chr3:75551600-75553200	Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr3:75551600-75553600	Active TSS	Brain Anterior Caudate	brain
49	chr3:75551800-75552000	Enhancers	Fetal Kidney	kidney
50	chr3:75551800-75552400	Weak transcription	Small Intestine	intestine

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