Variant report

Variant	nsv432457
Chromosome Location	chr3:75676582-75796728
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4799)
CpG islands
(count:1711)
Chromatin interactive
region (count:8)
LncRNA
region (count:19)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:4799 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

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	chr3:75710659-75710674	K562	blood:	n/a	n/a
3	ARID3A	chr3:75770122-75770154	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:75691908-75692517	K562	blood:	n/a	n/a
5	ARID3A	chr3:75736701-75737480	K562	blood:	n/a	n/a
6	ARID3A	chr3:75693043-75693065	K562	blood:	n/a	n/a
7	ARID3A	chr3:75710663-75710916	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:75719697-75719867	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:75717896-75719229	K562	blood:	n/a	n/a
10	ARID3A	chr3:75739156-75739286	K562	blood:	n/a	n/a
11	ARID3A	chr3:75754843-75755270	K562	blood:	n/a	n/a
12	ARID3A	chr3:75718141-75718928	HepG2	liver:	n/a	n/a
13	ATF1	chr3:75750030-75750205	K562	blood:	n/a	n/a
14	ATF1	chr3:75728521-75728535	K562	blood:	n/a	n/a
15	ATF1	chr3:75754856-75755222	K562	blood:	n/a	n/a
16	ATF1	chr3:75710744-75710785	K562	blood:	n/a	n/a
17	ATF1	chr3:75755512-75756182	K562	blood:	n/a	n/a
18	ATF1	chr3:75703512-75703565	K562	blood:	n/a	n/a
19	ATF1	chr3:75779002-75782622	K562	blood:	n/a	n/a
20	ATF1	chr3:75787686-75789584	K562	blood:	n/a	n/a
21	ATF1	chr3:75726782-75726783	K562	blood:	n/a	n/a
22	ATF1	chr3:75783726-75784839	K562	blood:	n/a	n/a
23	ATF1	chr3:75763746-75764601	K562	blood:	n/a	n/a
24	ATF1	chr3:75789795-75794952	K562	blood:	n/a	n/a
25	ATF1	chr3:75740338-75740804	K562	blood:	n/a	n/a
26	ATF1	chr3:75735197-75735394	K562	blood:	n/a	n/a
27	ATF1	chr3:75747229-75747380	K562	blood:	n/a	n/a
28	ATF1	chr3:75773435-75776229	K562	blood:	n/a	n/a
29	ATF1	chr3:75728107-75728162	K562	blood:	n/a	n/a
30	ATF1	chr3:75690145-75690820	K562	blood:	n/a	n/a
31	ATF1	chr3:75735948-75736287	K562	blood:	n/a	n/a
32	ATF1	chr3:75734703-75734852	K562	blood:	n/a	n/a
33	ATF1	chr3:75733400-75734148	K562	blood:	n/a	n/a
34	ATF1	chr3:75745544-75745744	K562	blood:	n/a	n/a
35	ATF1	chr3:75760657-75761408	K562	blood:	n/a	n/a
36	ATF1	chr3:75695108-75700001	K562	blood:	n/a	n/a
37	ATF1	chr3:75691118-75692520	K562	blood:	n/a	n/a
38	ATF1	chr3:75679956-75680482	K562	blood:	n/a	n/a
39	ATF1	chr3:75771441-75772260	K562	blood:	n/a	n/a
40	ATF1	chr3:75785062-75787392	K562	blood:	n/a	n/a
41	ATF1	chr3:75765400-75768808	K562	blood:	n/a	n/a
42	ATF1	chr3:75743644-75744222	K562	blood:	n/a	n/a
43	ATF1	chr3:75730688-75730845	K562	blood:	n/a	n/a
44	ATF1	chr3:75685926-75686418	K562	blood:	n/a	n/a
45	ATF1	chr3:75769325-75769986	K562	blood:	n/a	n/a
46	ATF1	chr3:75777037-75777776	K562	blood:	n/a	n/a
47	ATF1	chr3:75693870-75694088	K562	blood:	n/a	n/a
48	ATF1	chr3:75759504-75760427	K562	blood:	n/a	n/a
49	ATF1	chr3:75736867-75738707	K562	blood:	n/a	n/a
50	ATF1	chr3:75689319-75689814	K562	blood:	n/a	n/a

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75712695-75712745	HIPEpiC	eye:	n/a
2	chr3:75712695-75712745	GM06990	blood:	n/a
3	chr3:75719149-75719199	A549	lung:	n/a
4	chr3:75712695-75712745	HIPEpiC	eye:	n/a
5	chr3:75712695-75712745	GM06990	blood:	n/a
6	chr3:75719149-75719199	A549	lung:	n/a
7	chr3:75721577-75721627	SK-N-SH_RA	brain:	n/a
8	chr3:75721577-75721627	HPAEpiC	pulmonary alveolar:	n/a
9	chr3:75701993-75702043	AoSMC	blood vessel:	n/a
10	chr3:75707560-75707610	GM12878	blood:	n/a
11	chr3:75707990-75708040	GM12892	blood:	n/a
12	chr3:75708197-75708247	HUVEC	blood vessel:	n/a
13	chr3:75719158-75719208	RPTEC	kidney:	n/a
14	chr3:75719149-75719199	H1-hESC	embryonic stem cell:	embryo
15	chr3:75719158-75719208	Hela-S3	cervix:	n/a
16	chr3:75690456-75690506	GM12891	blood:	n/a
17	chr3:75704573-75704623	AG04450	lung:	fetal
18	chr3:75719158-75719208	SK-N-MC	brain:	n/a
19	chr3:75708104-75708154	AG09309	skin:	n/a
20	chr3:75704498-75704548	ECC-1	luminal epithelium:	n/a
21	chr3:75707805-75707855	CMK	blood:	n/a
22	chr3:75717248-75717298	HepG2	liver:	n/a
23	chr3:75712695-75712745	HRE	kidney:	n/a
24	chr3:75690456-75690506	HPAEpiC	pulmonary alveolar:	n/a
25	chr3:75721888-75721938	HCT-116	colon:	n/a
26	chr3:75721577-75721627	AoSMC	blood vessel:	n/a
27	chr3:75717248-75717298	A549	lung:	n/a
28	chr3:75717248-75717298	GM12891	blood:	n/a
29	chr3:75712695-75712745	SK-N-SH	brain:	n/a
30	chr3:75701993-75702043	IMR90	lung:	fetal
31	chr3:75715783-75715833	HMEC	breast:	n/a
32	chr3:75712695-75712745	HCF	heart:	n/a
33	chr3:75701993-75702043	Jurkat	blood:	n/a
34	chr3:75720876-75720926	GM12892	blood:	n/a
35	chr3:75720876-75720926	GM12891	blood:	n/a
36	chr3:75721888-75721938	HRPEpiC	eye:	n/a
37	chr3:75719158-75719208	AG09309	skin:	n/a
38	chr3:75707805-75707855	HEK293	kidney:	embryo
39	chr3:75708104-75708154	PrEC	prostate:	n/a
40	chr3:75704573-75704623	BJ	skin:	n/a
41	chr3:75721888-75721938	HCM	heart:	n/a
42	chr3:75679454-75679504	NB4	blood:	n/a
43	chr3:75708197-75708247	HCF	heart:	n/a
44	chr3:75690456-75690506	GM06990	blood:	n/a
45	chr3:75707990-75708040	HRE	kidney:	n/a
46	chr3:75707805-75707855	HepG2	liver:	n/a
47	chr3:75707560-75707610	Caco-2	colon:	n/a
48	chr3:75719158-75719208	NT2-D1	testis:	n/a
49	chr3:75701993-75702043	HCPEpiC	choroid plexus:	n/a
50	chr3:75690456-75690506	MCF10A-Er-Src	breast:	n/a

(count:8 , 50 per page) page: 1

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

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF717-1	chr3:75716700-75717742	ENSG00000234317
2	lnc-FRG2C-10	chr3:75691156-75691895	NONHSAT090542
3	lnc-ZNF717-1	chr3:75716700-75717742	NONHSAT090545
4	lnc-ZNF717-2	chr3:75695572-75695597	XLOC_003164
5	lnc-ZNF717-1	chr3:75719171-75721030	NONHSAT090545
6	lnc-FRG2C-10	chr3:75694930-75696049	NONHSAT090542
7	lnc-FRG2C-7	chr3:75713481-75713708	NR_037925
8	lnc-FRG2C-1	chr3:75723564-75725031	ENSG00000242516
9	lnc-ZNF717-1	chr3:75679231-75679352	NONHSAT090540
10	lnc-FRG2C-10	chr3:75687750-75688507	NONHSAT090542
11	lnc-FRG2C-7	chr3:75714678-75716368	NR_037925
12	lnc-ZNF717-2	chr3:75691158-75691575	XLOC_003164
13	lnc-FRG2C-7	chr3:75714277-75714354	NR_037925
14	lnc-FRG2C-7	chr3:75713970-75714047	NR_037925
15	lnc-ZNF717-1	chr3:75719171-75719204	NONHSAT090540
16	lnc-CNTN3-1	chr3:75762167-75762465	NONHSAT090550
17	lnc-ZNF717-1	chr3:75721121-75721241	NONHSAT090545
18	lnc-FRG2C-1	chr3:75725119-75725776	ENSG00000242516
19	lnc-ZNF717-1	chr3:75719171-75721122	ENSG00000234317

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
MIR4273	TF binding region
LINC00960	TF binding region
RARRES2P1	TF binding region
AGGF1P3	TF binding region
RN7SL92P	TF binding region
ENSG00000236138	TF binding region
MIR1324	TF binding region
UNC93B3	CpG island
FRG2C	CpG island
ENSG00000243422	CpG island
MIR4273	CpG island
LINC00960	CpG island
RARRES2P1	CpG island
AGGF1P3	CpG island
RN7SL92P	CpG island
ENSG00000236138	CpG island
MIR1324	CpG island
ENSG00000212195	chromatin interactions
ENSG00000232815	chromatin interactions

Extended variants
information (count: 12236 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:12236 , 50 per page) page: 1 2 3 4 5 6 7 ... 245

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116026222	chr3:75676582-75676583	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
2	rs572678129	chr3:75676610-75676611	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
3	rs200328510	chr3:75676618-75676619	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
4	rs576634608	chr3:75676621-75676622	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
5	rs114661296	chr3:75676626-75676627	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
6	rs188600917	chr3:75676644-75676645	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
7	rs557655957	chr3:75676648-75676649	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
8	rs566704387	chr3:75676689-75676690	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
9	rs201878464	chr3:75676886-75676887	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
10	rs200307433	chr3:75676955-75676956	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
11	rs12629386	chr3:75677027-75677028	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
12	rs373955016	chr3:75677067-75677068	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
13	rs79138009	chr3:75677115-75677116	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
14	rs201004042	chr3:75677340-75677341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537742083	chr3:75677342-75677343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113037044	chr3:75677394-75677395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201189637	chr3:75677487-75677488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373563700	chr3:75677597-75677598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369753002	chr3:75677630-75677631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs377009687	chr3:75677725-75677726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374495783	chr3:75677742-75677743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111646031	chr3:75677816-75677817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9812575	chr3:75677860-75677861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201534775	chr3:75677926-75677927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150002245	chr3:75677946-75677947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200596300	chr3:75677956-75677957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111610875	chr3:75677964-75677965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11710100	chr3:75678082-75678083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372244627	chr3:75678157-75678158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200113555	chr3:75678227-75678228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200735856	chr3:75678279-75678280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201969773	chr3:75678295-75678296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140734020	chr3:75678308-75678309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs202207702	chr3:75678337-75678338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200480542	chr3:75678343-75678344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201040654	chr3:75678349-75678350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182767074	chr3:75678373-75678374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201212322	chr3:75678393-75678394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201978534	chr3:75678394-75678395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138967778	chr3:75678426-75678427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200858733	chr3:75678468-75678469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74365298	chr3:75678469-75678470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200455258	chr3:75678494-75678495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201417597	chr3:75678518-75678519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs111443150	chr3:75678526-75678527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200390169	chr3:75678548-75678549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201216899	chr3:75678557-75678558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs202205739	chr3:75678572-75678573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371582220	chr3:75678627-75678628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373415369	chr3:75678651-75678652	Weak transcription	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:2302 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75672000-75679000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:75679000-75679400	Weak transcription	Gastric	stomach
3	chr3:75679000-75679400	Weak transcription	Right Atrium	heart
4	chr3:75679000-75679800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:75679000-75681200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr3:75679200-75679400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr3:75679200-75679800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
8	chr3:75679400-75679600	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr3:75679400-75679600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr3:75679400-75679600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr3:75679400-75679600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr3:75679400-75679600	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
13	chr3:75679400-75679600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr3:75679400-75679600	ZNF genes & repeats	Gastric	stomach
15	chr3:75679400-75679600	ZNF genes & repeats	Pancreas	Pancrea
16	chr3:75679400-75679600	ZNF genes & repeats	Right Atrium	heart
17	chr3:75679400-75679600	ZNF genes & repeats	Thymus	Thymus
18	chr3:75679400-75679800	ZNF genes & repeats	Lung	lung
19	chr3:75679400-75680000	Enhancers	Fetal Muscle Leg	muscle
20	chr3:75679400-75681200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr3:75679400-75681200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
22	chr3:75679400-75682600	Enhancers	GM12878-XiMat	blood
23	chr3:75679600-75680800	Weak transcription	Right Atrium	heart
24	chr3:75679600-75682000	Weak transcription	Pancreas	Pancrea
25	chr3:75680000-75680400	Bivalent Enhancer	Fetal Muscle Leg	muscle
26	chr3:75680200-75680400	ZNF genes & repeats	Spleen	Spleen
27	chr3:75680200-75681000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
28	chr3:75680200-75681200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr3:75680200-75682800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr3:75680400-75681000	Weak transcription	Spleen	Spleen
31	chr3:75680800-75681200	Strong transcription	Right Atrium	heart
32	chr3:75681000-75681200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr3:75681000-75681200	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
34	chr3:75681000-75681200	Enhancers	Spleen	Spleen
35	chr3:75681200-75682000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr3:75681200-75682000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr3:75681200-75682000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr3:75681200-75682000	Weak transcription	Right Atrium	heart
39	chr3:75681200-75682000	Weak transcription	Spleen	Spleen
40	chr3:75681800-75682200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr3:75682000-75682200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr3:75682000-75682200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:75682000-75682200	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
44	chr3:75682000-75682200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
45	chr3:75682000-75682200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
46	chr3:75682000-75682200	ZNF genes & repeats	Right Atrium	heart
47	chr3:75682000-75682400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr3:75682000-75682400	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr3:75682000-75682400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr3:75682000-75682400	ZNF genes & repeats	Pancreas	Pancrea

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