Variant report

Variant	esv1843910
Chromosome Location	chr3:75700895-75828813
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3746)
CpG islands
(count:1528)
Chromatin interactive
region (count:7)
LncRNA
region (count:13)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:3746 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

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	chr3:75710659-75710674	K562	blood:	n/a	n/a
3	ARID3A	chr3:75719697-75719867	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:75736701-75737480	K562	blood:	n/a	n/a
5	ARID3A	chr3:75718141-75718928	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:75710663-75710916	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:75770122-75770154	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:75717896-75719229	K562	blood:	n/a	n/a
9	ARID3A	chr3:75754843-75755270	K562	blood:	n/a	n/a
10	ATF1	chr3:75736867-75738707	K562	blood:	n/a	n/a
11	ATF1	chr3:75746545-75746765	K562	blood:	n/a	n/a
12	ATF1	chr3:75735197-75735394	K562	blood:	n/a	n/a
13	ATF1	chr3:75771441-75772260	K562	blood:	n/a	n/a
14	ATF1	chr3:75710744-75710785	K562	blood:	n/a	n/a
15	ATF1	chr3:75730688-75730845	K562	blood:	n/a	n/a
16	ATF1	chr3:75765400-75768808	K562	blood:	n/a	n/a
17	ATF1	chr3:75789795-75794952	K562	blood:	n/a	n/a
18	ATF1	chr3:75740338-75740804	K562	blood:	n/a	n/a
19	ATF1	chr3:75773435-75776229	K562	blood:	n/a	n/a
20	ATF1	chr3:75733400-75734148	K562	blood:	n/a	n/a
21	ATF1	chr3:75728107-75728162	K562	blood:	n/a	n/a
22	ATF1	chr3:75734703-75734852	K562	blood:	n/a	n/a
23	ATF1	chr3:75755512-75756182	K562	blood:	n/a	n/a
24	ATF1	chr3:75750030-75750205	K562	blood:	n/a	n/a
25	ATF1	chr3:75735948-75736287	K562	blood:	n/a	n/a
26	ATF1	chr3:75779002-75782622	K562	blood:	n/a	n/a
27	ATF1	chr3:75747229-75747380	K562	blood:	n/a	n/a
28	ATF1	chr3:75762715-75762961	K562	blood:	n/a	n/a
29	ATF1	chr3:75777037-75777776	K562	blood:	n/a	n/a
30	ATF1	chr3:75759504-75760427	K562	blood:	n/a	n/a
31	ATF1	chr3:75726782-75726783	K562	blood:	n/a	n/a
32	ATF1	chr3:75703512-75703565	K562	blood:	n/a	n/a
33	ATF1	chr3:75785062-75787392	K562	blood:	n/a	n/a
34	ATF1	chr3:75743644-75744222	K562	blood:	n/a	n/a
35	ATF1	chr3:75783726-75784839	K562	blood:	n/a	n/a
36	ATF1	chr3:75763746-75764601	K562	blood:	n/a	n/a
37	ATF1	chr3:75728521-75728535	K562	blood:	n/a	n/a
38	ATF1	chr3:75769325-75769986	K562	blood:	n/a	n/a
39	ATF1	chr3:75760657-75761408	K562	blood:	n/a	n/a
40	ATF1	chr3:75787686-75789584	K562	blood:	n/a	n/a
41	ATF1	chr3:75761625-75762259	K562	blood:	n/a	n/a
42	ATF1	chr3:75754856-75755222	K562	blood:	n/a	n/a
43	ATF1	chr3:75778219-75778585	K562	blood:	n/a	n/a
44	ATF1	chr3:75745544-75745744	K562	blood:	n/a	n/a
45	ATF3	chr3:75717987-75718165	K562	blood:	n/a	n/a
46	ATF3	chr3:75718289-75718505	K562	blood:	n/a	n/a
47	ATF3	chr3:75788958-75789896	K562	blood:	n/a	n/a
48	BACH1	chr3:75736972-75737792	K562	blood:	n/a	n/a
49	BACH1	chr3:75719455-75720405	H1-hESC	embryonic stem cell:	n/a	n/a
50	BACH1	chr3:75717968-75719070	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75712404-75712454	NHBE	bronchial:	n/a
2	chr3:75704824-75704874	GM12878	blood:	n/a
3	chr3:75717453-75717503	PANC-1	pancreas:	n/a
4	chr3:75712404-75712454	NHBE	bronchial:	n/a
5	chr3:75704824-75704874	GM12878	blood:	n/a
6	chr3:75717453-75717503	PANC-1	pancreas:	n/a
7	chr3:75712695-75712745	HCM	heart:	n/a
8	chr3:75721888-75721938	AG04450	lung:	fetal
9	chr3:75719149-75719199	HAEpiC	amniotic membrane:	n/a
10	chr3:75721434-75721484	SK-N-MC	brain:	n/a
11	chr3:75717248-75717298	AG09309	skin:	n/a
12	chr3:75717453-75717503	CMK	blood:	n/a
13	chr3:75717453-75717503	Caco-2	colon:	n/a
14	chr3:75717453-75717503	Hela-S3	cervix:	n/a
15	chr3:75705922-75705972	HRPEpiC	eye:	n/a
16	chr3:75704498-75704548	A549	lung:	n/a
17	chr3:75715783-75715833	SKMC	muscle:	n/a
18	chr3:75712695-75712745	NT2-D1	testis:	n/a
19	chr3:75701993-75702043	NHDF-neo	bronchial:	n/a
20	chr3:75704498-75704548	SAEC	small airway:	n/a
21	chr3:75712695-75712745	AG09309	skin:	n/a
22	chr3:75715783-75715833	SK-N-SH_RA	brain:	n/a
23	chr3:75717453-75717503	HMEC	breast:	n/a
24	chr3:75704498-75704548	ProgFib	skin:	n/a
25	chr3:75717248-75717298	HNPCEpiC	eye:	n/a
26	chr3:75717248-75717298	ECC-1	luminal epithelium:	n/a
27	chr3:75714447-75714497	GM12891	blood:	n/a
28	chr3:75714447-75714497	HUVEC	blood vessel:	n/a
29	chr3:75714447-75714497	GM06990	blood:	n/a
30	chr3:75707990-75708040	RPTEC	kidney:	n/a
31	chr3:75704573-75704623	HCM	heart:	n/a
32	chr3:75717248-75717298	HEK293	kidney:	embryo
33	chr3:75721434-75721484	Jurkat	blood:	n/a
34	chr3:75707990-75708040	NH-A	brain:	n/a
35	chr3:75707805-75707855	HAEpiC	amniotic membrane:	n/a
36	chr3:75704498-75704548	NB4	blood:	n/a
37	chr3:75721888-75721938	HPAEpiC	pulmonary alveolar:	n/a
38	chr3:75704498-75704548	HCM	heart:	n/a
39	chr3:75708104-75708154	HPAEpiC	pulmonary alveolar:	n/a
40	chr3:75712695-75712745	GM06990	blood:	n/a
41	chr3:75721434-75721484	SK-N-SH	brain:	n/a
42	chr3:75720876-75720926	GM12891	blood:	n/a
43	chr3:75720199-75720249	NB4	blood:	n/a
44	chr3:75719158-75719208	HCT-116	colon:	n/a
45	chr3:75705922-75705972	AG09319	gingival:	n/a
46	chr3:75717248-75717298	NH-A	brain:	n/a
47	chr3:75707560-75707610	HRCEpiC	kidney:	n/a
48	chr3:75708104-75708154	HRE	kidney:	n/a
49	chr3:75721577-75721627	SKMC	muscle:	n/a
50	chr3:75719158-75719208	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr3:75804459..75806623-chr3:75811168..75814143,2	K562	blood:
2	chr3:75804459..75806623-chr3:75811168..75814143,2	K562	blood:
3	chr17:56709052..56711813-chr3:75770362..75772517,2	MCF-7	breast:
4	chr3:75718137..75719895-chr9:68411990..68414461,3	MCF-7	breast:
5	chr3:75717548..75719836-chr9:68411784..68414340,4	MCF-7	breast:
6	chr16:33943186..33943816-chr3:75719164..75719883,2	MCF-7	breast:
7	chr3:75790783..75791412-chr6:15280318..15280818,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-7	chr3:75713970-75714047	NR_037925
2	lnc-ZNF717-1	chr3:75716700-75717742	NONHSAT090545
3	lnc-ZNF717-1	chr3:75719171-75719204	NONHSAT090540
4	lnc-CNTN3-1	chr3:75762167-75762465	NONHSAT090550
5	lnc-FRG2C-1	chr3:75725119-75725776	ENSG00000242516
6	lnc-ZNF717-1	chr3:75716700-75717742	ENSG00000234317
7	lnc-FRG2C-1	chr3:75723564-75725031	ENSG00000242516
8	lnc-FRG2C-7	chr3:75714678-75716368	NR_037925
9	lnc-FRG2C-7	chr3:75714277-75714354	NR_037925
10	lnc-FRG2C-7	chr3:75713481-75713708	NR_037925
11	lnc-ZNF717-1	chr3:75721121-75721241	NONHSAT090545
12	lnc-ZNF717-1	chr3:75719171-75721122	ENSG00000234317
13	lnc-ZNF717-1	chr3:75719171-75721030	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
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: 12619 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:12619 , 50 per page) page: 1 2 3 4 5 6 7 ... 253

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139519220	chr3:75700896-75700897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs201844989	chr3:75700925-75700926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372673462	chr3:75700956-75700957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368695851	chr3:75700970-75700971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113556621	chr3:75700979-75700980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112147621	chr3:75700994-75700995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112113773	chr3:75701011-75701012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs62247070	chr3:75701028-75701029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140739344	chr3:75701043-75701044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200461456	chr3:75701044-75701045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201516973	chr3:75701067-75701068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs62247071	chr3:75701081-75701082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs77086584	chr3:75701118-75701119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs77265970	chr3:75701123-75701124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139083312	chr3:75701138-75701139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79884937	chr3:75701141-75701142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs111420457	chr3:75701151-75701152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143934751	chr3:75701160-75701161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs77923534	chr3:75701181-75701182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201827289	chr3:75701216-75701217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115330496	chr3:75701223-75701224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114895353	chr3:75701246-75701247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs115536796	chr3:75701247-75701248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200043709	chr3:75701297-75701298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375248058	chr3:75701298-75701299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200980338	chr3:75701300-75701301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73122997	chr3:75701313-75701314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs72501862	chr3:75701350-75701351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs80047091	chr3:75701367-75701368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369871012	chr3:75701393-75701394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139784280	chr3:75701409-75701410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146712298	chr3:75701410-75701411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200584250	chr3:75701466-75701467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114219207	chr3:75701483-75701484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376096893	chr3:75701507-75701508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370788890	chr3:75701512-75701513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565382787	chr3:75701545-75701546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78505151	chr3:75701553-75701554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373811816	chr3:75701555-75701556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73843810	chr3:75701559-75701560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs116427549	chr3:75701565-75701566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371037811	chr3:75701574-75701575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201458008	chr3:75701582-75701583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201767753	chr3:75701600-75701601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200074981	chr3:75701607-75701608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201030099	chr3:75701615-75701616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201974511	chr3:75701620-75701621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116681292	chr3:75701629-75701630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114244261	chr3:75701640-75701641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73122998	chr3:75701642-75701643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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	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:2320 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75699400-75704600	Weak transcription	Pancreas	Pancrea
2	chr3:75699600-75704600	Weak transcription	Gastric	stomach
3	chr3:75700200-75704600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:75702600-75702800	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
5	chr3:75703400-75704600	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:75704200-75704400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
7	chr3:75704200-75704400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
8	chr3:75704200-75704600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr3:75704200-75705200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr3:75704400-75704600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr3:75704400-75705200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
12	chr3:75704400-75705200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
13	chr3:75704400-75705200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
14	chr3:75704400-75705200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
15	chr3:75704400-75705200	Bivalent Enhancer	Brain Germinal Matrix	brain
16	chr3:75704400-75705200	Bivalent Enhancer	Fetal Brain Female	brain
17	chr3:75704400-75705200	ZNF genes & repeats	Right Atrium	heart
18	chr3:75704400-75705400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
19	chr3:75704400-75705400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
20	chr3:75704400-75705400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
21	chr3:75704600-75704800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr3:75704600-75704800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
23	chr3:75704600-75704800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
24	chr3:75704600-75704800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr3:75704600-75705000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
26	chr3:75704600-75705000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr3:75704600-75705000	ZNF genes & repeats	Gastric	stomach
28	chr3:75704600-75705000	Flanking Bivalent TSS/Enh	Psoas Muscle	Psoas
29	chr3:75704600-75705000	Flanking Bivalent TSS/Enh	Right Ventricle	heart
30	chr3:75704600-75705200	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr3:75704600-75705200	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr3:75704600-75705200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr3:75704600-75705200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr3:75704600-75705200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr3:75704600-75705200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
36	chr3:75704600-75705200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr3:75704600-75705200	Bivalent Enhancer	Fetal Muscle Leg	muscle
38	chr3:75704600-75705200	Bivalent Enhancer	Left Ventricle	heart
39	chr3:75704600-75705400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr3:75704600-75705400	ZNF genes & repeats	Pancreas	Pancrea
41	chr3:75704800-75705000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
42	chr3:75704800-75705000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
43	chr3:75704800-75705000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr3:75704800-75705000	Bivalent Enhancer	Fetal Brain Male	brain
45	chr3:75704800-75705000	Bivalent Enhancer	Spleen	Spleen
46	chr3:75704800-75705200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr3:75704800-75705200	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr3:75704800-75705200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr3:75704800-75705200	Bivalent Enhancer	Fetal Stomach	stomach
50	chr3:75704800-75705200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach

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