Variant report

Variant	nsv967026
Chromosome Location	chr3:75672284-75765976
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4008)
CpG islands
(count:1711)
Chromatin interactive
region (count:7)
LncRNA
region (count:20)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:4008 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75710659-75710674	K562	blood:	n/a	n/a
2	ARID3A	chr3:75717896-75719229	K562	blood:	n/a	n/a
3	ARID3A	chr3:75693851-75694060	K562	blood:	n/a	n/a
4	ARID3A	chr3:75710663-75710916	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:75718141-75718928	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:75693043-75693065	K562	blood:	n/a	n/a
7	ARID3A	chr3:75736701-75737480	K562	blood:	n/a	n/a
8	ARID3A	chr3:75754843-75755270	K562	blood:	n/a	n/a
9	ARID3A	chr3:75719697-75719867	HepG2	liver:	n/a	n/a
10	ARID3A	chr3:75691908-75692517	K562	blood:	n/a	n/a
11	ARID3A	chr3:75739156-75739286	K562	blood:	n/a	n/a
12	ATF1	chr3:75730688-75730845	K562	blood:	n/a	n/a
13	ATF1	chr3:75760657-75761408	K562	blood:	n/a	n/a
14	ATF1	chr3:75762715-75762961	K562	blood:	n/a	n/a
15	ATF1	chr3:75703512-75703565	K562	blood:	n/a	n/a
16	ATF1	chr3:75728521-75728535	K562	blood:	n/a	n/a
17	ATF1	chr3:75736867-75738707	K562	blood:	n/a	n/a
18	ATF1	chr3:75693870-75694088	K562	blood:	n/a	n/a
19	ATF1	chr3:75679956-75680482	K562	blood:	n/a	n/a
20	ATF1	chr3:75747229-75747380	K562	blood:	n/a	n/a
21	ATF1	chr3:75746545-75746765	K562	blood:	n/a	n/a
22	ATF1	chr3:75690145-75690820	K562	blood:	n/a	n/a
23	ATF1	chr3:75733400-75734148	K562	blood:	n/a	n/a
24	ATF1	chr3:75691118-75692520	K562	blood:	n/a	n/a
25	ATF1	chr3:75763746-75764601	K562	blood:	n/a	n/a
26	ATF1	chr3:75761625-75762259	K562	blood:	n/a	n/a
27	ATF1	chr3:75734703-75734852	K562	blood:	n/a	n/a
28	ATF1	chr3:75740338-75740804	K562	blood:	n/a	n/a
29	ATF1	chr3:75754856-75755222	K562	blood:	n/a	n/a
30	ATF1	chr3:75755512-75756182	K562	blood:	n/a	n/a
31	ATF1	chr3:75689319-75689814	K562	blood:	n/a	n/a
32	ATF1	chr3:75728107-75728162	K562	blood:	n/a	n/a
33	ATF1	chr3:75765400-75768808	K562	blood:	n/a	n/a
34	ATF1	chr3:75726782-75726783	K562	blood:	n/a	n/a
35	ATF1	chr3:75759504-75760427	K562	blood:	n/a	n/a
36	ATF1	chr3:75743644-75744222	K562	blood:	n/a	n/a
37	ATF1	chr3:75735948-75736287	K562	blood:	n/a	n/a
38	ATF1	chr3:75710744-75710785	K562	blood:	n/a	n/a
39	ATF1	chr3:75745544-75745744	K562	blood:	n/a	n/a
40	ATF1	chr3:75735197-75735394	K562	blood:	n/a	n/a
41	ATF1	chr3:75685926-75686418	K562	blood:	n/a	n/a
42	ATF1	chr3:75750030-75750205	K562	blood:	n/a	n/a
43	ATF1	chr3:75695108-75700001	K562	blood:	n/a	n/a
44	ATF3	chr3:75718289-75718505	K562	blood:	n/a	n/a
45	ATF3	chr3:75717987-75718165	K562	blood:	n/a	n/a
46	BACH1	chr3:75682306-75682660	K562	blood:	n/a	n/a
47	BACH1	chr3:75693848-75694086	K562	blood:	n/a	n/a
48	BACH1	chr3:75689184-75689642	K562	blood:	n/a	n/a
49	BACH1	chr3:75735200-75735345	K562	blood:	n/a	n/a
50	BACH1	chr3:75717886-75719337	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	chr3:75705922-75705972	SK-N-MC	brain:	n/a
2	chr3:75704824-75704874	AG10803	skin:	n/a
3	chr3:75721888-75721938	SAEC	small airway:	n/a
4	chr3:75705922-75705972	SK-N-MC	brain:	n/a
5	chr3:75704824-75704874	AG10803	skin:	n/a
6	chr3:75721888-75721938	SAEC	small airway:	n/a
7	chr3:75715783-75715833	ovcar-3	ovarian:	n/a
8	chr3:75707805-75707855	HepG2	liver:	n/a
9	chr3:75704824-75704874	SAEC	small airway:	n/a
10	chr3:75708104-75708154	HepG2	liver:	n/a
11	chr3:75719158-75719208	AG09319	gingival:	n/a
12	chr3:75704824-75704874	HepG2	liver:	n/a
13	chr3:75704498-75704548	GM12891	blood:	n/a
14	chr3:75719149-75719199	HCPEpiC	choroid plexus:	n/a
15	chr3:75717453-75717503	NHBE	bronchial:	n/a
16	chr3:75714447-75714497	H1-hESC	embryonic stem cell:	embryo
17	chr3:75705108-75705158	GM12878	blood:	n/a
18	chr3:75679454-75679504	HCF	heart:	n/a
19	chr3:75707560-75707610	HAEpiC	amniotic membrane:	n/a
20	chr3:75714447-75714497	HEEpiC	esophagus:	n/a
21	chr3:75719149-75719199	NHDF-neo	bronchial:	n/a
22	chr3:75717248-75717298	MCF10A-Er-Src	breast:	n/a
23	chr3:75679454-75679504	HUVEC	blood vessel:	n/a
24	chr3:75704573-75704623	Jurkat	blood:	n/a
25	chr3:75708197-75708247	HPAEpiC	pulmonary alveolar:	n/a
26	chr3:75707990-75708040	MCF-7	breast:	n/a
27	chr3:75712695-75712745	NHBE	bronchial:	n/a
28	chr3:75704498-75704548	NB4	blood:	n/a
29	chr3:75721434-75721484	HEK293	kidney:	embryo
30	chr3:75707560-75707610	ProgFib	skin:	n/a
31	chr3:75721577-75721627	H1-hESC	embryonic stem cell:	embryo
32	chr3:75720876-75720926	LNCaP	prostate:	n/a
33	chr3:75712404-75712454	BJ	skin:	n/a
34	chr3:75721577-75721627	GM06990	blood:	n/a
35	chr3:75714447-75714497	PrEC	prostate:	n/a
36	chr3:75701993-75702043	SAEC	small airway:	n/a
37	chr3:75720876-75720926	AG10803	skin:	n/a
38	chr3:75705922-75705972	AG09319	gingival:	n/a
39	chr3:75708197-75708247	U87	brain:	n/a
40	chr3:75707990-75708040	HEK293	kidney:	embryo
41	chr3:75679454-75679504	HPAEpiC	pulmonary alveolar:	n/a
42	chr3:75717248-75717298	NB4	blood:	n/a
43	chr3:75704824-75704874	AG09309	skin:	n/a
44	chr3:75717248-75717298	HUVEC	blood vessel:	n/a
45	chr3:75719149-75719199	U87	brain:	n/a
46	chr3:75712695-75712745	SAEC	small airway:	n/a
47	chr3:75705922-75705972	ProgFib	skin:	n/a
48	chr3:75720876-75720926	ECC-1	luminal epithelium:	n/a
49	chr3:75717248-75717298	AG09319	gingival:	n/a
50	chr3:75717453-75717503	SAEC	small airway:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:436504..437180-chr3:75674246..75674764,2	MCF-7	breast:
2	chr19:22025273..22026773-chr3:75695462..75697658,2	MCF-7	breast:
3	chr3:75717548..75719836-chr9:68411784..68414340,4	MCF-7	breast:
4	chr3:75718137..75719895-chr9:68411990..68414461,3	MCF-7	breast:
5	chr16:33943186..33943816-chr3:75719164..75719883,2	MCF-7	breast:
6	chr3:75692090..75692596-chr7:138578273..138578773,2	K562	blood:
7	chr3:75693392..75694000-chr5:103852101..103852601,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-7	chr3:75714678-75716368	NR_037925
2	lnc-ZNF717-1	chr3:75716700-75717742	ENSG00000234317
3	lnc-ZNF717-1	chr3:75721121-75721241	NONHSAT090545
4	lnc-ZNF717-1	chr3:75674122-75674304	NONHSAT090540
5	lnc-FRG2C-7	chr3:75713970-75714047	NR_037925
6	lnc-FRG2C-7	chr3:75713481-75713708	NR_037925
7	lnc-FRG2C-10	chr3:75694930-75696049	NONHSAT090542
8	lnc-ZNF717-2	chr3:75695572-75695597	XLOC_003164
9	lnc-ZNF717-1	chr3:75719171-75719204	NONHSAT090540
10	lnc-ZNF717-2	chr3:75691158-75691575	XLOC_003164
11	lnc-FRG2C-7	chr3:75714277-75714354	NR_037925
12	lnc-FRG2C-10	chr3:75691156-75691895	NONHSAT090542
13	lnc-ZNF717-1	chr3:75719171-75721122	ENSG00000234317
14	lnc-ZNF717-1	chr3:75716700-75717742	NONHSAT090545
15	lnc-FRG2C-1	chr3:75725119-75725776	ENSG00000242516
16	lnc-ZNF717-1	chr3:75679231-75679352	NONHSAT090540
17	lnc-ZNF717-1	chr3:75719171-75721030	NONHSAT090545
18	lnc-FRG2C-1	chr3:75723564-75725031	ENSG00000242516
19	lnc-CNTN3-1	chr3:75762167-75762465	NONHSAT090550
20	lnc-FRG2C-10	chr3:75687750-75688507	NONHSAT090542

miRNA name	Chromosome Location	mirBase accession
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
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
LINC00960	CpG island
RARRES2P1	CpG island
AGGF1P3	CpG island
RN7SL92P	CpG island
ENSG00000236138	CpG island
MIR1324	CpG island
ENSG00000236829	chromatin interactions
ENSG00000129925	chromatin interactions
ENSG00000232815	chromatin interactions

Extended variants
information (count: 8946 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:8946 , 50 per page) page: 1 2 3 4 5 6 7 ... 179

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200929173	chr3:75672433-75672434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs115367344	chr3:75672436-75672437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs115114799	chr3:75672480-75672481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375791099	chr3:75672484-75672485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs368305178	chr3:75672568-75672569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143092044	chr3:75672680-75672681	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs55805986	chr3:75672681-75672682	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369175327	chr3:75672683-75672684	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs201529149	chr3:75672689-75672690	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12495682	chr3:75672698-75672699	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150348780	chr3:75672699-75672700	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535406801	chr3:75672719-75672720	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs55949754	chr3:75672854-75672855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200130441	chr3:75672889-75672890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs200914815	chr3:75672890-75672891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375484791	chr3:75672952-75672953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs201981655	chr3:75672981-75672982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs368531989	chr3:75673022-75673023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533051307	chr3:75673034-75673035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552457690	chr3:75673061-75673062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549121821	chr3:75673089-75673090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112829397	chr3:75673105-75673106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs60808875	chr3:75673117-75673118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564743025	chr3:75673119-75673120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371326128	chr3:75673133-75673134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528780052	chr3:75673192-75673193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111912171	chr3:75673215-75673216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111396241	chr3:75673233-75673234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374680116	chr3:75673234-75673235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12630397	chr3:75673303-75673304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371566582	chr3:75673368-75673369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs56080247	chr3:75673374-75673375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200380319	chr3:75673376-75673377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111434923	chr3:75673415-75673416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1808833	chr3:75673419-75673420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371286195	chr3:75673503-75673504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200847172	chr3:75673514-75673515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12632754	chr3:75673556-75673557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200786599	chr3:75673571-75673572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs202005254	chr3:75673611-75673612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200060153	chr3:75673624-75673625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199580937	chr3:75673627-75673628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200688823	chr3:75673636-75673637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369520871	chr3:75673661-75673662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373361020	chr3:75673672-75673673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376375144	chr3:75673718-75673719	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs370454521	chr3:75673723-75673724	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs375378467	chr3:75673734-75673735	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs373617639	chr3:75673749-75673750	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs201477827	chr3:75673774-75673775	Weak transcription	TF binding region	1 gene(s)	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:1959 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75669400-75674600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr3:75672000-75679000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:75672600-75672800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
4	chr3:75672600-75672800	Enhancers	HSMM	muscle
5	chr3:75672800-75673000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr3:75673000-75675000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:75673400-75674200	Weak transcription	Psoas Muscle	Psoas
8	chr3:75673800-75674200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr3:75675000-75675200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr3:75679000-75679400	Weak transcription	Gastric	stomach
11	chr3:75679000-75679400	Weak transcription	Right Atrium	heart
12	chr3:75679000-75679800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:75679000-75681200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr3:75679200-75679400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr3:75679200-75679800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
16	chr3:75679400-75679600	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr3:75679400-75679600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr3:75679400-75679600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr3:75679400-75679600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr3:75679400-75679600	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
21	chr3:75679400-75679600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr3:75679400-75679600	ZNF genes & repeats	Gastric	stomach
23	chr3:75679400-75679600	ZNF genes & repeats	Pancreas	Pancrea
24	chr3:75679400-75679600	ZNF genes & repeats	Right Atrium	heart
25	chr3:75679400-75679600	ZNF genes & repeats	Thymus	Thymus
26	chr3:75679400-75679800	ZNF genes & repeats	Lung	lung
27	chr3:75679400-75680000	Enhancers	Fetal Muscle Leg	muscle
28	chr3:75679400-75681200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr3:75679400-75681200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
30	chr3:75679400-75682600	Enhancers	GM12878-XiMat	blood
31	chr3:75679600-75680800	Weak transcription	Right Atrium	heart
32	chr3:75679600-75682000	Weak transcription	Pancreas	Pancrea
33	chr3:75680000-75680400	Bivalent Enhancer	Fetal Muscle Leg	muscle
34	chr3:75680200-75680400	ZNF genes & repeats	Spleen	Spleen
35	chr3:75680200-75681000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
36	chr3:75680200-75681200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr3:75680200-75682800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr3:75680400-75681000	Weak transcription	Spleen	Spleen
39	chr3:75680800-75681200	Strong transcription	Right Atrium	heart
40	chr3:75681000-75681200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr3:75681000-75681200	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
42	chr3:75681000-75681200	Enhancers	Spleen	Spleen
43	chr3:75681200-75682000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr3:75681200-75682000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr3:75681200-75682000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr3:75681200-75682000	Weak transcription	Right Atrium	heart
47	chr3:75681200-75682000	Weak transcription	Spleen	Spleen
48	chr3:75681800-75682200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr3:75682000-75682200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr3:75682000-75682200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell

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