Variant report

Variant	esv2754135
Chromosome Location	chr3:75713010-76016610
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5060)
CpG islands
(count:2077)
Chromatin interactive
region (count:15)
LncRNA
region (count:15)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:5060 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

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	chr3:75719697-75719867	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:75913424-75913483	K562	blood:	n/a	n/a
4	ARID3A	chr3:75718141-75718928	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:75991836-75991901	K562	blood:	n/a	n/a
6	ARID3A	chr3:75717896-75719229	K562	blood:	n/a	n/a
7	ARID3A	chr3:75736701-75737480	K562	blood:	n/a	n/a
8	ARID3A	chr3:75770122-75770154	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:75754843-75755270	K562	blood:	n/a	n/a
10	ATF1	chr3:75913346-75913538	K562	blood:	n/a	n/a
11	ATF1	chr3:75759504-75760427	K562	blood:	n/a	n/a
12	ATF1	chr3:75985241-75985450	K562	blood:	n/a	n/a
13	ATF1	chr3:75743644-75744222	K562	blood:	n/a	n/a
14	ATF1	chr3:75762715-75762961	K562	blood:	n/a	n/a
15	ATF1	chr3:75991766-75991934	K562	blood:	n/a	n/a
16	ATF1	chr3:75848335-75848417	K562	blood:	n/a	n/a
17	ATF1	chr3:75733400-75734148	K562	blood:	n/a	n/a
18	ATF1	chr3:75735197-75735394	K562	blood:	n/a	n/a
19	ATF1	chr3:75747229-75747380	K562	blood:	n/a	n/a
20	ATF1	chr3:75779002-75782622	K562	blood:	n/a	n/a
21	ATF1	chr3:75726782-75726783	K562	blood:	n/a	n/a
22	ATF1	chr3:75986254-75986287	K562	blood:	n/a	n/a
23	ATF1	chr3:75773435-75776229	K562	blood:	n/a	n/a
24	ATF1	chr3:75760657-75761408	K562	blood:	n/a	n/a
25	ATF1	chr3:75746545-75746765	K562	blood:	n/a	n/a
26	ATF1	chr3:75777037-75777776	K562	blood:	n/a	n/a
27	ATF1	chr3:75778219-75778585	K562	blood:	n/a	n/a
28	ATF1	chr3:75842286-75842335	K562	blood:	n/a	n/a
29	ATF1	chr3:75763746-75764601	K562	blood:	n/a	n/a
30	ATF1	chr3:75728107-75728162	K562	blood:	n/a	n/a
31	ATF1	chr3:75785062-75787392	K562	blood:	n/a	n/a
32	ATF1	chr3:75728521-75728535	K562	blood:	n/a	n/a
33	ATF1	chr3:75769325-75769986	K562	blood:	n/a	n/a
34	ATF1	chr3:75754856-75755222	K562	blood:	n/a	n/a
35	ATF1	chr3:75789795-75794952	K562	blood:	n/a	n/a
36	ATF1	chr3:75736867-75738707	K562	blood:	n/a	n/a
37	ATF1	chr3:75745544-75745744	K562	blood:	n/a	n/a
38	ATF1	chr3:75730688-75730845	K562	blood:	n/a	n/a
39	ATF1	chr3:75740338-75740804	K562	blood:	n/a	n/a
40	ATF1	chr3:75834638-75834999	K562	blood:	n/a	n/a
41	ATF1	chr3:75787686-75789584	K562	blood:	n/a	n/a
42	ATF1	chr3:75783726-75784839	K562	blood:	n/a	n/a
43	ATF1	chr3:75734703-75734852	K562	blood:	n/a	n/a
44	ATF1	chr3:75755512-75756182	K562	blood:	n/a	n/a
45	ATF1	chr3:75986623-75986792	K562	blood:	n/a	n/a
46	ATF1	chr3:75761625-75762259	K562	blood:	n/a	n/a
47	ATF1	chr3:75771441-75772260	K562	blood:	n/a	n/a
48	ATF1	chr3:75998476-75998676	K562	blood:	n/a	n/a
49	ATF1	chr3:75765400-75768808	K562	blood:	n/a	n/a
50	ATF1	chr3:75750030-75750205	K562	blood:	n/a	n/a

(count:2077 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75956119-75956169	PANC-1	pancreas:	n/a
2	chr3:75834108-75834158	BE2_C	brain:	n/a
3	chr3:75719158-75719208	AoSMC	blood vessel:	n/a
4	chr3:75956119-75956169	PANC-1	pancreas:	n/a
5	chr3:75834108-75834158	BE2_C	brain:	n/a
6	chr3:75719158-75719208	AoSMC	blood vessel:	n/a
7	chr3:75834525-75834575	GM19239	blood:	n/a
8	chr3:75834381-75834431	NT2-D1	testis:	n/a
9	chr3:75838027-75838077	SKMC	muscle:	n/a
10	chr3:75834658-75834708	NT2-D1	testis:	n/a
11	chr3:75717453-75717503	AG04449	skin:	fetal
12	chr3:75721888-75721938	MCF10A-Er-Src	breast:	n/a
13	chr3:75834381-75834431	HRE	kidney:	n/a
14	chr3:75717248-75717298	AG04450	lung:	fetal
15	chr3:75833811-75833861	AG10803	skin:	n/a
16	chr3:75831181-75831231	HRPEpiC	eye:	n/a
17	chr3:75831181-75831231	NHBE	bronchial:	n/a
18	chr3:75834648-75834698	AG10803	skin:	n/a
19	chr3:75956119-75956169	U87	brain:	n/a
20	chr3:75828829-75828879	H1-hESC	embryonic stem cell:	embryo
21	chr3:75715783-75715833	NB4	blood:	n/a
22	chr3:75834381-75834431	NHDF-neo	bronchial:	n/a
23	chr3:75717248-75717298	LNCaP	prostate:	n/a
24	chr3:75955844-75955894	K562	blood:	n/a
25	chr3:75721577-75721627	Caco-2	colon:	n/a
26	chr3:75834648-75834698	HIPEpiC	eye:	n/a
27	chr3:75721434-75721484	LNCaP	prostate:	n/a
28	chr3:75834910-75834960	HL-60	blood:	n/a
29	chr3:75832003-75832053	HPAEpiC	pulmonary alveolar:	n/a
30	chr3:75956295-75956345	AoSMC	blood vessel:	n/a
31	chr3:75834658-75834708	SK-N-MC	brain:	n/a
32	chr3:75830568-75830618	HRE	kidney:	n/a
33	chr3:75834335-75834385	ovcar-3	ovarian:	n/a
34	chr3:75721434-75721484	HL-60	blood:	n/a
35	chr3:75720199-75720249	HEK293	kidney:	embryo
36	chr3:75956295-75956345	SAEC	small airway:	n/a
37	chr3:75958299-75958349	HRE	kidney:	n/a
38	chr3:75834703-75834753	SK-N-SH_RA	brain:	n/a
39	chr3:75834716-75834766	RPTEC	kidney:	n/a
40	chr3:75719158-75719208	MCF10A-Er-Src	breast:	n/a
41	chr3:75834525-75834575	RPTEC	kidney:	n/a
42	chr3:75715783-75715833	SK-N-SH	brain:	n/a
43	chr3:75721888-75721938	A549	lung:	n/a
44	chr3:75719149-75719199	HepG2	liver:	n/a
45	chr3:75830568-75830618	ovcar-3	ovarian:	n/a
46	chr3:75831226-75831276	SK-N-MC	brain:	n/a
47	chr3:75717453-75717503	MCF10A-Er-Src	breast:	n/a
48	chr3:75955844-75955894	PrEC	prostate:	n/a
49	chr3:75834648-75834698	Hepatocyte	liver:	n/a
50	chr3:75831226-75831276	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:75867624..75868149-chr3:76093803..76094658,2	MCF-7	breast:
2	chr3:75804459..75806623-chr3:75811168..75814143,2	K562	blood:
3	chr20:26208095..26209894-chr3:75988198..75990401,2	MCF-7	breast:
4	chr3:75790783..75791412-chr6:15280318..15280818,2	MCF-7	breast:
5	chr20:26206073..26206971-chr3:75991464..75992265,2	MCF-7	breast:
6	chr20:26201563..26203476-chr3:75993448..75995749,2	K562	blood:
7	chr16:33943186..33943816-chr3:75719164..75719883,2	MCF-7	breast:
8	chr1:143540009..143542435-chr3:75911879..75914281,2	MCF-7	breast:
9	chr3:75804459..75806623-chr3:75811168..75814143,2	K562	blood:
10	chr20:26199924..26201625-chr3:75995563..75997738,2	MCF-7	breast:
11	chr17:56709052..56711813-chr3:75770362..75772517,2	MCF-7	breast:
12	chr20:26208071..26209607-chr3:75987301..75988916,2	K562	blood:
13	chr20:26201915..26204776-chr3:75992954..75996738,5	MCF-7	breast:
14	chr3:75717548..75719836-chr9:68411784..68414340,4	MCF-7	breast:
15	chr3:75718137..75719895-chr9:68411990..68414461,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-1	chr3:75725119-75725776	ENSG00000242516
2	lnc-FRG2C-7	chr3:75714277-75714354	NR_037925
3	lnc-FRG2C-7	chr3:75713970-75714047	NR_037925
4	lnc-ZNF717-1	chr3:75719171-75719204	NONHSAT090540
5	lnc-CNTN3-1	chr3:75762167-75762465	NONHSAT090550
6	lnc-FRG2C-12	chr3:75955945-75956111	NONHSAT090553
7	lnc-ZNF717-1	chr3:75716700-75717742	ENSG00000234317
8	lnc-ZNF717-1	chr3:75719171-75721030	NONHSAT090545
9	lnc-FRG2C-7	chr3:75714678-75716368	NR_037925
10	lnc-ZNF717-1	chr3:75716700-75717742	NONHSAT090545
11	lnc-FRG2C-7	chr3:75713481-75713708	NR_037925
12	lnc-FRG2C-12	chr3:75986632-75986776	NONHSAT090553
13	lnc-ZNF717-1	chr3:75719171-75721122	ENSG00000234317
14	lnc-FRG2C-1	chr3:75723564-75725031	ENSG00000242516
15	lnc-ZNF717-1	chr3:75721121-75721241	NONHSAT090545

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4273	chr3:75787441-75787458	MIMAT0016903

No data

Variant related genes	Relation type
FRG2C	TF binding region
ZNF717	TF binding region
MIR4273	TF binding region
LINC00960	TF binding region
ENSG00000222883	TF binding region
RN7SL92P	TF binding region
ROBO2	TF binding region
ENSG00000236138	TF binding region
FRG2C	CpG island
ZNF717	CpG island
MIR4273	CpG island
LINC00960	CpG island
ENSG00000222883	CpG island
RN7SL92P	CpG island
ROBO2	CpG island
ENSG00000236138	CpG island
ENSG00000232815	chromatin interactions
ENSG00000212195	chromatin interactions

Extended variants
information (count: 17049 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:17049 , 50 per page) page: 1 2 3 4 5 6 7 ... 341

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202018335	chr3:75713019-75713020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs369519321	chr3:75713029-75713030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200227228	chr3:75713037-75713038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201360818	chr3:75713039-75713040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369656430	chr3:75713051-75713052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148536155	chr3:75713085-75713086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200304981	chr3:75713086-75713087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201128227	chr3:75713095-75713096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369232854	chr3:75713100-75713101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs115382887	chr3:75713104-75713105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114738172	chr3:75713105-75713106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs116378120	chr3:75713119-75713120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs73840307	chr3:75713128-75713129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115308620	chr3:75713166-75713167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs62247145	chr3:75713212-75713213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs62247146	chr3:75713238-75713239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200363775	chr3:75713239-75713240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs62247147	chr3:75713241-75713242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73840308	chr3:75713242-75713243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77152765	chr3:75713264-75713265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs80080952	chr3:75713267-75713268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs78745533	chr3:75713279-75713280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77227941	chr3:75713299-75713300	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs73840309	chr3:75713305-75713306	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs62247148	chr3:75713324-75713325	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs73840310	chr3:75713327-75713328	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs62247149	chr3:75713345-75713346	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs74780582	chr3:75713365-75713366	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs113160857	chr3:75713381-75713382	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs111998404	chr3:75713392-75713393	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs202214835	chr3:75713410-75713411	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs73840311	chr3:75713442-75713443	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs201045273	chr3:75713444-75713445	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs201980474	chr3:75713449-75713450	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs200280949	chr3:75713457-75713458	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs138624694	chr3:75713466-75713467	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs201901334	chr3:75713469-75713470	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs73840313	chr3:75713472-75713473	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs201957725	chr3:75713473-75713474	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs146207114	chr3:75713492-75713493	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs73840316	chr3:75713496-75713497	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs80271626	chr3:75713507-75713508	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs200828502	chr3:75713552-75713553	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs201844648	chr3:75713555-75713556	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs199575562	chr3:75713561-75713562	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs201362708	chr3:75713563-75713564	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs143803036	chr3:75713564-75713565	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs116151319	chr3:75713566-75713567	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs150902075	chr3:75713618-75713619	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs368803515	chr3:75713650-75713651	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Ovarian cancer	21720365	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2830 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75708400-75714800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr3:75714600-75714800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
3	chr3:75714600-75715400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr3:75714800-75715000	Bivalent Enhancer	Lung	lung
5	chr3:75714800-75715200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr3:75714800-75715400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:75715200-75715400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr3:75715200-75717000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr3:75715400-75716800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr3:75715400-75717000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr3:75716400-75717000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
12	chr3:75716400-75717200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
13	chr3:75716400-75717800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
14	chr3:75716600-75719600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr3:75716600-75722400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr3:75716800-75717000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
17	chr3:75716800-75717000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
18	chr3:75716800-75717000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
19	chr3:75716800-75717000	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr3:75716800-75717000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr3:75716800-75717000	Bivalent/Poised TSS	Adipose Nuclei	Adipose
22	chr3:75716800-75717000	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
23	chr3:75716800-75717000	Bivalent Enhancer	Lung	lung
24	chr3:75716800-75717000	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
25	chr3:75716800-75717000	ZNF genes & repeats	NH-A	brain
26	chr3:75716800-75717400	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
27	chr3:75716800-75717400	Flanking Bivalent TSS/Enh	Right Ventricle	heart
28	chr3:75716800-75717600	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr3:75716800-75718000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
30	chr3:75716800-75718200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
31	chr3:75716800-75718600	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
32	chr3:75716800-75719600	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
33	chr3:75716800-75720000	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
34	chr3:75716800-75721400	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr3:75716800-75721400	ZNF genes & repeats	HepG2	liver
36	chr3:75716800-75721600	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
37	chr3:75716800-75721800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:75716800-75721800	ZNF genes & repeats	Rectal Smooth Muscle	rectum
39	chr3:75716800-75722000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr3:75716800-75722000	ZNF genes & repeats	Pancreas	Pancrea
41	chr3:75716800-75722400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
42	chr3:75717000-75717200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
43	chr3:75717000-75717200	Flanking Bivalent TSS/Enh	H9 Cell Line	embryonic stem cell
44	chr3:75717000-75717200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr3:75717000-75717200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
46	chr3:75717000-75717200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
47	chr3:75717000-75717200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
48	chr3:75717000-75717200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
49	chr3:75717000-75717200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr3:75717000-75717200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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