Variant report

Variant	nsv876994
Chromosome Location	chr3:75935763-75976655
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:75955912-75956209	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr3:75936348-75936578	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr3:75955701-75956187	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr3:75945762-75945954	HepG2	liver:	n/a	chr3:75945863-75945874
5	CHD2	chr3:75955746-75956057	H1-hESC	embryonic stem cell:	n/a	chr3:75955999-75956009
6	CTBP2	chr3:75955733-75956447	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr3:75955800-75955950	NHEK	skin:	n/a	chr3:75955887-75955900
8	CTCF	chr3:75955760-75955910	WI-38	lung:	n/a	chr3:75955887-75955900
9	CTCF	chr3:75955800-75955950	AG04449	skin:	n/a	chr3:75955887-75955900
10	CTCF	chr3:75955800-75955950	HRE	kidney:	n/a	chr3:75955887-75955900
11	CTCF	chr3:75955820-75955970	HMEC	breast:	n/a	chr3:75955887-75955900
12	CTCF	chr3:75955820-75955970	AG09309	skin:	n/a	chr3:75955887-75955900
13	CTCF	chr3:75955820-75955970	AG04450	lung:	n/a	chr3:75955887-75955900
14	CTCF	chr3:75955800-75955950	SK-N-SH_RA	brain:	n/a	chr3:75955887-75955900
15	CTCF	chr3:75959676-75959745	GM20000	blood:	n/a	n/a
16	CTCF	chr3:75950773-75950826	GM10248	blood:	n/a	n/a
17	CTCF	chr3:75955720-75955870	HAc	cerebellar:	n/a	n/a
18	CTCF	chr3:75955798-75955940	LNCaP	prostate:	n/a	chr3:75955887-75955900
19	CTCF	chr3:75955745-75956011	MCF-7	breast:	n/a	chr3:75955887-75955900
20	CTCF	chr3:75955789-75955936	K562	blood:	n/a	chr3:75955887-75955900
21	CTCF	chr3:75955672-75956077	H1-hESC	embryonic stem cell:	n/a	chr3:75955887-75955900
22	CTCF	chr3:75955816-75955914	HepG2	liver:	n/a	chr3:75955887-75955900
23	CTCF	chr3:75955820-75955970	AG04449	skin:	n/a	chr3:75955887-75955900
24	CTCF	chr3:75955820-75955970	HPF	lung:	n/a	chr3:75955887-75955900
25	CTCF	chr3:75955800-75955950	HEK293	kidney:	n/a	chr3:75955887-75955900
26	CTCF	chr3:75955770-75955957	Spleen_OC	spleen:	n/a	chr3:75955887-75955900
27	CTCF	chr3:75955785-75955982	MCF-7	breast:	n/a	chr3:75955887-75955900
28	CTCF	chr3:75955780-75955930	BE2_C	brain:	n/a	chr3:75955887-75955900
29	CTCF	chr3:75955820-75955970	HCPEpiC	choroid plexus:	n/a	chr3:75955887-75955900
30	CTCF	chr3:75955820-75955970	SAEC	small airway:	n/a	chr3:75955887-75955900
31	CTCF	chr3:75955787-75955965	Medullo	brain:	n/a	chr3:75955887-75955900
32	CTCF	chr3:75947135-75947229	GM10248	blood:	n/a	n/a
33	CTCF	chr3:75955820-75955970	WERI-Rb-1	eye:	n/a	chr3:75955887-75955900
34	CTCF	chr3:75955737-75955991	MCF-7	breast:	n/a	chr3:75955887-75955900
35	CTCF	chr3:75955800-75955950	AG09309	skin:	n/a	chr3:75955887-75955900
36	CTCF	chr3:75955700-75955850	HAc	cerebellar:	n/a	n/a
37	CTCF	chr3:75955590-75956027	SK-N-SH	brain:	n/a	chr3:75955887-75955900
38	CTCF	chr3:75955880-75956030	MCF-7	breast:	n/a	chr3:75955887-75955900
39	CTCF	chr3:75955820-75955970	HEEpiC	esophagus:	n/a	chr3:75955887-75955900
40	CTCF	chr3:75955713-75956030	H1-hESC	embryonic stem cell:	n/a	chr3:75955887-75955900
41	CTCF	chr3:75955800-75955950	SAEC	small airway:	n/a	chr3:75955887-75955900
42	CTCF	chr3:75955792-75955962	MCF-7	breast:	n/a	chr3:75955887-75955900
43	CTCF	chr3:75955791-75955970	MCF-7	breast:	n/a	chr3:75955887-75955900
44	CTCF	chr3:75955719-75956023	NHEK	skin:	n/a	chr3:75955887-75955900
45	CTCF	chr3:75955707-75955899	K562	blood:	n/a	n/a
46	CTCF	chr3:75955774-75955961	SK-N-SH_RA	brain:	n/a	chr3:75955887-75955900
47	CTCF	chr3:75955709-75955990	Fibrobl	skin:	n/a	chr3:75955887-75955900
48	CTCF	chr3:75955741-75956007	ProgFib	skin:	n/a	chr3:75955887-75955900
49	CTCF	chr3:75955820-75955970	HRPEpiC	eye:	n/a	chr3:75955887-75955900
50	CTCF	chr3:75955700-75955850	HCFaa	heart:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75955844-75955894	HCT-116	colon:	n/a
2	chr3:75956119-75956169	HAEpiC	amniotic membrane:	n/a
3	chr3:75955844-75955894	HEK293	kidney:	embryo
4	chr3:75955844-75955894	T-47D	breast:	n/a
5	chr3:75956295-75956345	AG09319	gingival:	n/a
6	chr3:75956119-75956169	HUVEC	blood vessel:	n/a
7	chr3:75959386-75959436	CMK	blood:	n/a
8	chr3:75956295-75956345	Hepatocyte	liver:	n/a
9	chr3:75956295-75956345	SKMC	muscle:	n/a
10	chr3:75955844-75955894	HNPCEpiC	eye:	n/a
11	chr3:75956295-75956345	HPAEpiC	pulmonary alveolar:	n/a
12	chr3:75958299-75958349	HNPCEpiC	eye:	n/a
13	chr3:75956119-75956169	RPTEC	kidney:	n/a
14	chr3:75956119-75956169	AG09309	skin:	n/a
15	chr3:75956295-75956345	Caco-2	colon:	n/a
16	chr3:75955844-75955894	NHBE	bronchial:	n/a
17	chr3:75955844-75955894	AoSMC	blood vessel:	n/a
18	chr3:75956119-75956169	GM06990	blood:	n/a
19	chr3:75955844-75955894	MCF-7	breast:	n/a
20	chr3:75955844-75955894	MCF10A-Er-Src	breast:	n/a
21	chr3:75956119-75956169	HRCEpiC	kidney:	n/a
22	chr3:75956295-75956345	GM12891	blood:	n/a
23	chr3:75956119-75956169	MCF-7	breast:	n/a
24	chr3:75956295-75956345	K562	blood:	n/a
25	chr3:75959386-75959436	T-47D	breast:	n/a
26	chr3:75955844-75955894	HIPEpiC	eye:	n/a
27	chr3:75959386-75959436	RPTEC	kidney:	n/a
28	chr3:75956119-75956169	HCT-116	colon:	n/a
29	chr3:75958299-75958349	AoSMC	blood vessel:	n/a
30	chr3:75956295-75956345	PrEC	prostate:	n/a
31	chr3:75958299-75958349	RPTEC	kidney:	n/a
32	chr3:75959386-75959436	AG09309	skin:	n/a
33	chr3:75956295-75956345	HL-60	blood:	n/a
34	chr3:75958299-75958349	HUVEC	blood vessel:	n/a
35	chr3:75956119-75956169	LNCaP	prostate:	n/a
36	chr3:75956295-75956345	SK-N-MC	brain:	n/a
37	chr3:75956295-75956345	HRE	kidney:	n/a
38	chr3:75955844-75955894	HPAEpiC	pulmonary alveolar:	n/a
39	chr3:75956295-75956345	ProgFib	skin:	n/a
40	chr3:75959386-75959436	LNCaP	prostate:	n/a
41	chr3:75956119-75956169	AG04449	skin:	fetal
42	chr3:75955844-75955894	NB4	blood:	n/a
43	chr3:75959386-75959436	PFSK-1	brain:	n/a
44	chr3:75956119-75956169	HPAEpiC	pulmonary alveolar:	n/a
45	chr3:75956119-75956169	GM12892	blood:	n/a
46	chr3:75958299-75958349	SK-N-MC	brain:	n/a
47	chr3:75955844-75955894	HRCEpiC	kidney:	n/a
48	chr3:75955844-75955894	NHDF-neo	bronchial:	n/a
49	chr3:75956119-75956169	AG10803	skin:	n/a
50	chr3:75959386-75959436	ovcar-3	ovarian:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-12	chr3:75955945-75956111	NONHSAT090553

Variant related genes	Relation type
ROBO2	TF binding region
ROBO2	CpG island

Extended variants
information (count: 378 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2137509	chr3:75935763-75935764	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530455127	chr3:75935783-75935784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146977541	chr3:75935797-75935798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563858268	chr3:75935801-75935802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528142477	chr3:75935828-75935829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547980527	chr3:75935857-75935858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559645872	chr3:75935885-75935886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79241044	chr3:75936000-75936001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548643050	chr3:75936032-75936033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570315268	chr3:75936074-75936075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544171447	chr3:75936178-75936179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559279416	chr3:75936219-75936220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188963039	chr3:75936224-75936225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537472175	chr3:75936259-75936260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556368296	chr3:75936302-75936303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552569424	chr3:75936313-75936314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570965474	chr3:75936358-75936359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535073087	chr3:75936359-75936360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564363158	chr3:75936395-75936396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533076720	chr3:75936411-75936412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs193115711	chr3:75936424-75936425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550098969	chr3:75936429-75936430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557000776	chr3:75936461-75936462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72503585	chr3:75936472-75936473	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs1828654	chr3:75936494-75936495	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs116147036	chr3:75936499-75936500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532381646	chr3:75936562-75936563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573293797	chr3:75936583-75936584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185529287	chr3:75936616-75936617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540002453	chr3:75936633-75936634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561812450	chr3:75936634-75936635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530264863	chr3:75936677-75936678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375073989	chr3:75936716-75936717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563995102	chr3:75936751-75936752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138048877	chr3:75936760-75936761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143487107	chr3:75936786-75936787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570904224	chr3:75936832-75936833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370045654	chr3:75936919-75936920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528326810	chr3:75936976-75936977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535007746	chr3:75937001-75937002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114999214	chr3:75937022-75937023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548170470	chr3:75937023-75937024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540657197	chr3:75937033-75937034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373493625	chr3:75937035-75937036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112232532	chr3:75937120-75937121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145791890	chr3:75937140-75937141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534358026	chr3:75937153-75937154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575183827	chr3:75937163-75937164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539303219	chr3:75937185-75937186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557630655	chr3:75937202-75937203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	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
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	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:163 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75933400-75936200	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr3:75933800-75940400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr3:75936200-75936400	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr3:75939600-75940200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr3:75940200-75940800	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr3:75940400-75940600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr3:75940800-75941000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr3:75941200-75941600	Enhancers	H1 Cell Line	embryonic stem cell
9	chr3:75954800-75955000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
10	chr3:75954800-75955000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr3:75954800-75955400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
12	chr3:75954800-75955400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
13	chr3:75954800-75955600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
14	chr3:75955000-75955600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:75955200-75955400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr3:75955200-75955600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr3:75955400-75955600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr3:75955400-75955600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
19	chr3:75955400-75955600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
20	chr3:75955400-75955600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
21	chr3:75955400-75955600	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr3:75955400-75955600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr3:75955400-75955600	Active TSS	Brain Anterior Caudate	brain
24	chr3:75955400-75955600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr3:75955400-75955800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
26	chr3:75955400-75955800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr3:75955400-75955800	Active TSS	Brain Germinal Matrix	brain
28	chr3:75955400-75956400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
29	chr3:75955400-75956400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
30	chr3:75955400-75956800	Active TSS	Fetal Brain Male	brain
31	chr3:75955400-75958400	Active TSS	Fetal Brain Female	brain
32	chr3:75955600-75955800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
33	chr3:75955600-75955800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr3:75955600-75955800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr3:75955600-75955800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr3:75955600-75955800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
37	chr3:75955600-75955800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr3:75955600-75955800	Active TSS	Adipose Nuclei	Adipose
39	chr3:75955600-75955800	Active TSS	Brain Cingulate Gyrus	brain
40	chr3:75955600-75955800	Flanking Bivalent TSS/Enh	Brain Inferior Temporal Lobe	brain
41	chr3:75955600-75955800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
42	chr3:75955600-75955800	Flanking Active TSS	Fetal Muscle Trunk	muscle
43	chr3:75955600-75955800	Active TSS	Fetal Muscle Leg	muscle
44	chr3:75955600-75955800	Active TSS	Fetal Stomach	stomach
45	chr3:75955600-75955800	Enhancers	Pancreas	Pancrea
46	chr3:75955600-75955800	Enhancers	Psoas Muscle	Psoas
47	chr3:75955600-75955800	Bivalent/Poised TSS	Right Ventricle	heart
48	chr3:75955600-75956000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr3:75955600-75956000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr3:75955600-75956000	Bivalent/Poised TSS	Brain Anterior Caudate	brain

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