Variant report

Variant	nsv876987
Chromosome Location	chr3:75682878-75826472
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5186)
CpG islands
(count:1593)
Chromatin interactive
region (count:10)
LncRNA
region (count:18)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:5186 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75718141-75718928	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:75710663-75710916	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:75739156-75739286	K562	blood:	n/a	n/a
4	ARID3A	chr3:75736701-75737480	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	chr3:75754843-75755270	K562	blood:	n/a	n/a
8	ARID3A	chr3:75693851-75694060	K562	blood:	n/a	n/a
9	ARID3A	chr3:75693043-75693065	K562	blood:	n/a	n/a
10	ARID3A	chr3:75691908-75692517	K562	blood:	n/a	n/a
11	ARID3A	chr3:75717896-75719229	K562	blood:	n/a	n/a
12	ARID3A	chr3:75770122-75770154	HepG2	liver:	n/a	n/a
13	ATF1	chr3:75728521-75728535	K562	blood:	n/a	n/a
14	ATF1	chr3:75789795-75794952	K562	blood:	n/a	n/a
15	ATF1	chr3:75787686-75789584	K562	blood:	n/a	n/a
16	ATF1	chr3:75745544-75745744	K562	blood:	n/a	n/a
17	ATF1	chr3:75778219-75778585	K562	blood:	n/a	n/a
18	ATF1	chr3:75726782-75726783	K562	blood:	n/a	n/a
19	ATF1	chr3:75730688-75730845	K562	blood:	n/a	n/a
20	ATF1	chr3:75736867-75738707	K562	blood:	n/a	n/a
21	ATF1	chr3:75769325-75769986	K562	blood:	n/a	n/a
22	ATF1	chr3:75703512-75703565	K562	blood:	n/a	n/a
23	ATF1	chr3:75754856-75755222	K562	blood:	n/a	n/a
24	ATF1	chr3:75685926-75686418	K562	blood:	n/a	n/a
25	ATF1	chr3:75743644-75744222	K562	blood:	n/a	n/a
26	ATF1	chr3:75783726-75784839	K562	blood:	n/a	n/a
27	ATF1	chr3:75755512-75756182	K562	blood:	n/a	n/a
28	ATF1	chr3:75690145-75690820	K562	blood:	n/a	n/a
29	ATF1	chr3:75740338-75740804	K562	blood:	n/a	n/a
30	ATF1	chr3:75771441-75772260	K562	blood:	n/a	n/a
31	ATF1	chr3:75691118-75692520	K562	blood:	n/a	n/a
32	ATF1	chr3:75761625-75762259	K562	blood:	n/a	n/a
33	ATF1	chr3:75728107-75728162	K562	blood:	n/a	n/a
34	ATF1	chr3:75693870-75694088	K562	blood:	n/a	n/a
35	ATF1	chr3:75763746-75764601	K562	blood:	n/a	n/a
36	ATF1	chr3:75777037-75777776	K562	blood:	n/a	n/a
37	ATF1	chr3:75689319-75689814	K562	blood:	n/a	n/a
38	ATF1	chr3:75710744-75710785	K562	blood:	n/a	n/a
39	ATF1	chr3:75747229-75747380	K562	blood:	n/a	n/a
40	ATF1	chr3:75695108-75700001	K562	blood:	n/a	n/a
41	ATF1	chr3:75762715-75762961	K562	blood:	n/a	n/a
42	ATF1	chr3:75785062-75787392	K562	blood:	n/a	n/a
43	ATF1	chr3:75765400-75768808	K562	blood:	n/a	n/a
44	ATF1	chr3:75734703-75734852	K562	blood:	n/a	n/a
45	ATF1	chr3:75773435-75776229	K562	blood:	n/a	n/a
46	ATF1	chr3:75735948-75736287	K562	blood:	n/a	n/a
47	ATF1	chr3:75750030-75750205	K562	blood:	n/a	n/a
48	ATF1	chr3:75759504-75760427	K562	blood:	n/a	n/a
49	ATF1	chr3:75779002-75782622	K562	blood:	n/a	n/a
50	ATF1	chr3:75746545-75746765	K562	blood:	n/a	n/a

(count:1593 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75707805-75707855	MCF10A-Er-Src	breast:	n/a
2	chr3:75690456-75690506	HRPEpiC	eye:	n/a
3	chr3:75721577-75721627	HRPEpiC	eye:	n/a
4	chr3:75717453-75717503	HepG2	liver:	n/a
5	chr3:75721434-75721484	HMEC	breast:	n/a
6	chr3:75704951-75705001	NH-A	brain:	n/a
7	chr3:75721888-75721938	Hela-S3	cervix:	n/a
8	chr3:75707805-75707855	MCF10A-Er-Src	breast:	n/a
9	chr3:75690456-75690506	HRPEpiC	eye:	n/a
10	chr3:75721577-75721627	HRPEpiC	eye:	n/a
11	chr3:75717453-75717503	HepG2	liver:	n/a
12	chr3:75721434-75721484	HMEC	breast:	n/a
13	chr3:75704951-75705001	NH-A	brain:	n/a
14	chr3:75721888-75721938	Hela-S3	cervix:	n/a
15	chr3:75707990-75708040	H1-hESC	embryonic stem cell:	embryo
16	chr3:75712404-75712454	ovcar-3	ovarian:	n/a
17	chr3:75707805-75707855	GM06990	blood:	n/a
18	chr3:75719149-75719199	HCM	heart:	n/a
19	chr3:75720876-75720926	HRE	kidney:	n/a
20	chr3:75721434-75721484	SKMC	muscle:	n/a
21	chr3:75708197-75708247	A549	lung:	n/a
22	chr3:75719149-75719199	NH-A	brain:	n/a
23	chr3:75719158-75719208	H1-hESC	embryonic stem cell:	embryo
24	chr3:75690456-75690506	AG10803	skin:	n/a
25	chr3:75707990-75708040	SKMC	muscle:	n/a
26	chr3:75707805-75707855	IMR90	lung:	fetal
27	chr3:75717453-75717503	Jurkat	blood:	n/a
28	chr3:75720199-75720249	Hela-S3	cervix:	n/a
29	chr3:75701993-75702043	HL-60	blood:	n/a
30	chr3:75701993-75702043	Caco-2	colon:	n/a
31	chr3:75707560-75707610	HNPCEpiC	eye:	n/a
32	chr3:75712404-75712454	GM06990	blood:	n/a
33	chr3:75715783-75715833	GM12891	blood:	n/a
34	chr3:75701993-75702043	GM19239	blood:	n/a
35	chr3:75712404-75712454	SKMC	muscle:	n/a
36	chr3:75720876-75720926	PrEC	prostate:	n/a
37	chr3:75704951-75705001	AG10803	skin:	n/a
38	chr3:75721577-75721627	GM12892	blood:	n/a
39	chr3:75704951-75705001	HUVEC	blood vessel:	n/a
40	chr3:75704824-75704874	HCF	heart:	n/a
41	chr3:75715783-75715833	U87	brain:	n/a
42	chr3:75708104-75708154	AoSMC	blood vessel:	n/a
43	chr3:75714447-75714497	GM12891	blood:	n/a
44	chr3:75720199-75720249	AG09319	gingival:	n/a
45	chr3:75704951-75705001	Jurkat	blood:	n/a
46	chr3:75707560-75707610	NHDF-neo	bronchial:	n/a
47	chr3:75704573-75704623	SAEC	small airway:	n/a
48	chr3:75705922-75705972	HCPEpiC	choroid plexus:	n/a
49	chr3:75720876-75720926	GM12891	blood:	n/a
50	chr3:75707560-75707610	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:75790783..75791412-chr6:15280318..15280818,2	MCF-7	breast:
2	chr3:75804459..75806623-chr3:75811168..75814143,2	K562	blood:
3	chr3:75718137..75719895-chr9:68411990..68414461,3	MCF-7	breast:
4	chr3:75804459..75806623-chr3:75811168..75814143,2	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	chr3:75692090..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	chr17:56709052..56711813-chr3:75770362..75772517,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF717-2	chr3:75691158-75691575	XLOC_003164
2	lnc-CNTN3-1	chr3:75762167-75762465	NONHSAT090550
3	lnc-FRG2C-7	chr3:75714678-75716368	NR_037925
4	lnc-FRG2C-7	chr3:75714277-75714354	NR_037925
5	lnc-FRG2C-10	chr3:75694930-75696049	NONHSAT090542
6	lnc-FRG2C-1	chr3:75725119-75725776	ENSG00000242516
7	lnc-FRG2C-1	chr3:75723564-75725031	ENSG00000242516
8	lnc-FRG2C-10	chr3:75691156-75691895	NONHSAT090542
9	lnc-FRG2C-7	chr3:75713481-75713708	NR_037925
10	lnc-FRG2C-7	chr3:75713970-75714047	NR_037925
11	lnc-ZNF717-2	chr3:75695572-75695597	XLOC_003164
12	lnc-ZNF717-1	chr3:75719171-75719204	NONHSAT090540
13	lnc-ZNF717-1	chr3:75719171-75721122	ENSG00000234317
14	lnc-ZNF717-1	chr3:75721121-75721241	NONHSAT090545
15	lnc-ZNF717-1	chr3:75716700-75717742	NONHSAT090545
16	lnc-ZNF717-1	chr3:75719171-75721030	NONHSAT090545
17	lnc-FRG2C-10	chr3:75687750-75688507	NONHSAT090542
18	lnc-ZNF717-1	chr3:75716700-75717742	ENSG00000234317

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

No data

Variant related genes	Relation type
FRG2C	TF binding region
MIR4273	TF binding region
AGGF1P3	TF binding region
LINC00960	TF binding region
RN7SL92P	TF binding region
RARRES2P1	TF binding region
ENSG00000236138	TF binding region
FRG2C	CpG island
MIR4273	CpG island
AGGF1P3	CpG island
LINC00960	CpG island
RN7SL92P	CpG island
RARRES2P1	CpG island
ENSG00000236138	CpG island
ENSG00000212195	chromatin interactions
ENSG00000232815	chromatin interactions

Extended variants
information (count: 14370 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:14370 , 50 per page) page: 1 2 3 4 5 6 7 ... 288

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115845905	chr3:75682878-75682879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562016608	chr3:75682893-75682894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74724175	chr3:75682895-75682896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186987895	chr3:75682899-75682900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73842078	chr3:75682900-75682901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113402215	chr3:75682918-75682919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112659566	chr3:75682920-75682921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201166695	chr3:75682931-75682932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs202033047	chr3:75682932-75682933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2077232	chr3:75682933-75682934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs62247863	chr3:75682977-75682978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs115124249	chr3:75682989-75682990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs62247864	chr3:75683032-75683033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113154833	chr3:75683036-75683037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs62247865	chr3:75683071-75683072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs202036430	chr3:75683072-75683073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200516960	chr3:75683119-75683120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374703991	chr3:75683165-75683166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75348419	chr3:75683190-75683191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375922223	chr3:75683194-75683195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111592944	chr3:75683199-75683200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs367628594	chr3:75683219-75683220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370636723	chr3:75683243-75683244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs77400822	chr3:75683249-75683250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs62247866	chr3:75683254-75683255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370172566	chr3:75683264-75683265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373392405	chr3:75683265-75683266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376310705	chr3:75683267-75683268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs62247867	chr3:75683270-75683271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113171023	chr3:75683277-75683278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369529215	chr3:75683279-75683280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376383346	chr3:75683284-75683285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377002006	chr3:75683290-75683291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs72501861	chr3:75683297-75683298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143227141	chr3:75683302-75683303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs202003148	chr3:75683312-75683313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375103862	chr3:75683319-75683320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76764884	chr3:75683327-75683328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550520085	chr3:75683331-75683332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201877900	chr3:75683349-75683350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115267920	chr3:75683350-75683351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113829989	chr3:75683355-75683356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372477280	chr3:75683380-75683381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376134509	chr3:75683399-75683400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369135046	chr3:75683416-75683417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs62247869	chr3:75683417-75683418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs56331826	chr3:75683418-75683419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs201758857	chr3:75683423-75683424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376186610	chr3:75683452-75683453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs62247871	chr3:75683456-75683457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Non-syndromic sensorineural hearing loss	21293372	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:2957 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75682400-75684200	Weak transcription	Right Ventricle	heart
2	chr3:75682400-75688200	Weak transcription	Pancreas	Pancrea
3	chr3:75682600-75683200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:75682600-75683400	Weak transcription	GM12878-XiMat	blood
5	chr3:75683400-75684200	Enhancers	GM12878-XiMat	blood
6	chr3:75683800-75684600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr3:75683800-75685000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr3:75684200-75684400	Enhancers	Right Ventricle	heart
9	chr3:75684200-75684600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr3:75684400-75690200	Weak transcription	Right Ventricle	heart
11	chr3:75684600-75684800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr3:75684600-75685000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr3:75685000-75688200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr3:75685200-75688200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr3:75687800-75688600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr3:75687800-75688600	Active TSS	Rectal Mucosa Donor 31	rectum
17	chr3:75687800-75690000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
18	chr3:75688200-75688400	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
19	chr3:75688200-75688400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr3:75688200-75688400	ZNF genes & repeats	Brain Germinal Matrix	brain
21	chr3:75688200-75688400	Bivalent/Poised TSS	Gastric	stomach
22	chr3:75688200-75688400	Flanking Bivalent TSS/Enh	Ovary	ovary
23	chr3:75688200-75688600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr3:75688200-75688600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr3:75688200-75688600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr3:75688200-75688600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr3:75688200-75688600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr3:75688200-75688600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr3:75688200-75688600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr3:75688200-75688600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
31	chr3:75688200-75688600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr3:75688200-75688600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr3:75688200-75688600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr3:75688200-75688600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr3:75688200-75688600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr3:75688200-75688600	Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr3:75688200-75688600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr3:75688200-75688600	Active TSS	Primary neutrophils fromperipheralblood	blood
39	chr3:75688200-75688600	Active TSS	Primary T cells from cord blood	blood
40	chr3:75688200-75688600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
41	chr3:75688200-75688600	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
42	chr3:75688200-75688600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr3:75688200-75688600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr3:75688200-75688600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr3:75688200-75688600	Active TSS	Muscle Satellite Cultured Cells	--
46	chr3:75688200-75688600	Bivalent/Poised TSS	Adipose Nuclei	Adipose
47	chr3:75688200-75688600	Active TSS	Liver	Liver
48	chr3:75688200-75688600	Bivalent/Poised TSS	Brain Angular Gyrus	brain
49	chr3:75688200-75688600	Active TSS	Duodenum Mucosa	Duodenum
50	chr3:75688200-75688600	ZNF genes & repeats	Esophagus	oesophagus

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