Variant report

Variant	nsv3670
Chromosome Location	chr3:222480-248778
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:129)
CpG islands
(count:1160)
Chromatin interactive
region (count:1)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:129 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:238302-238499	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr3:238826-240389	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr3:238979-239034	K562	blood:	n/a	n/a
4	CEBPB	chr3:242454-242771	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr3:242488-242808	A549	lung:	n/a	n/a
6	CEBPB	chr3:242447-242817	IMR90	lung:	n/a	n/a
7	CEBPB	chr3:242440-242811	HepG2	liver:	n/a	n/a
8	CEBPB	chr3:243949-244303	HepG2	liver:	n/a	chr3:244109-244120
9	CEBPB	chr3:243976-244300	IMR90	lung:	n/a	chr3:244109-244120
10	CEBPB	chr3:244050-244226	H1-hESC	embryonic stem cell:	n/a	chr3:244109-244120
11	CEBPB	chr3:242500-242742	K562	blood:	n/a	n/a
12	CEBPB	chr3:243974-244307	A549	lung:	n/a	chr3:244109-244120
13	CHD1	chr3:238324-238476	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD1	chr3:239219-239240	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr3:239582-239589	GM12878	blood:	n/a	n/a
16	CHD2	chr3:238225-238590	GM12878	blood:	n/a	n/a
17	CTBP2	chr3:238125-240202	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr3:239180-239330	GM12871	blood:	n/a	n/a
19	CTCF	chr3:239800-239950	GM12866	blood:	n/a	n/a
20	CTCF	chr3:237400-237550	HEK293	kidney:	n/a	n/a
21	CTCF	chr3:239720-239870	GM12866	blood:	n/a	chr3:239796-239809
22	CTCF	chr3:237440-237590	GM12873	blood:	n/a	n/a
23	CTCF	chr3:237340-237490	BE2_C	brain:	n/a	n/a
24	CTCF	chr3:237420-237570	GM12867	blood:	n/a	n/a
25	CTCF	chr3:239660-239810	GM12871	blood:	n/a	chr3:239796-239809
26	CTCF	chr3:237400-237550	HPF	lung:	n/a	n/a
27	CTCF	chr3:239660-239810	GM12875	blood:	n/a	chr3:239796-239809
28	CTCF	chr3:239700-239850	GM12868	blood:	n/a	chr3:239796-239809
29	CTCF	chr3:239600-239750	GM12867	blood:	n/a	n/a
30	CTCF	chr3:239860-240010	GM12867	blood:	n/a	n/a
31	CTCF	chr3:239520-239670	GM12873	blood:	n/a	n/a
32	CTCF	chr3:237380-237530	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr3:238820-238970	GM12868	blood:	n/a	n/a
34	CTCF	chr3:237440-237590	GM12874	blood:	n/a	n/a
35	CTCF	chr3:237402-237596	GM12878	blood:	n/a	n/a
36	CTCF	chr3:237320-237470	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr3:239854-239957	GM19239	blood:	n/a	n/a
38	CTCF	chr3:237400-237550	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr3:239600-239750	GM12869	blood:	n/a	n/a
40	CTCF	chr3:237420-237570	GM12874	blood:	n/a	n/a
41	CTCF	chr3:238520-238670	GM12874	blood:	n/a	n/a
42	CTCF	chr3:237460-237610	HRE	kidney:	n/a	n/a
43	CTCF	chr3:239140-239290	GM12866	blood:	n/a	n/a
44	CTCF	chr3:237480-237630	GM12872	blood:	n/a	n/a
45	CTCF	chr3:239640-239790	GM12872	blood:	n/a	n/a
46	CTCF	chr3:237466-237556	H1-hESC	embryonic stem cell:	n/a	n/a
47	E2F6	chr3:238259-238732	H1-hESC	embryonic stem cell:	n/a	n/a
48	E2F6	chr3:234185-234722	H1-hESC	embryonic stem cell:	n/a	n/a
49	E2F6	chr3:238188-239306	H1-hESC	embryonic stem cell:	n/a	n/a
50	E2F6	chr3:239630-240243	H1-hESC	embryonic stem cell:	n/a	chr3:239843-239855 chr3:240073-240082 chr3:239831-239843 chr3:240028-240042 chr3:239843-239852 chr3:240020-240029

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:241182-241232	AG04449	skin:	fetal
2	chr3:241182-241232	AG04449	skin:	fetal
3	chr3:239506-239556	T-47D	breast:	n/a
4	chr3:238611-238661	T-47D	breast:	n/a
5	chr3:238618-238668	AG09309	skin:	n/a
6	chr3:238931-238981	SK-N-MC	brain:	n/a
7	chr3:239188-239238	LNCaP	prostate:	n/a
8	chr3:239188-239238	T-47D	breast:	n/a
9	chr3:238496-238546	SAEC	small airway:	n/a
10	chr3:238611-238661	HMEC	breast:	n/a
11	chr3:241182-241232	HCT-116	colon:	n/a
12	chr3:238611-238661	K562	blood:	n/a
13	chr3:239733-239783	ProgFib	skin:	n/a
14	chr3:238048-238098	GM12892	blood:	n/a
15	chr3:241182-241232	AG10803	skin:	n/a
16	chr3:239229-239279	NB4	blood:	n/a
17	chr3:239665-239715	HEEpiC	esophagus:	n/a
18	chr3:238161-238211	NHBE	bronchial:	n/a
19	chr3:238611-238661	Hela-S3	cervix:	n/a
20	chr3:238931-238981	HIPEpiC	eye:	n/a
21	chr3:238931-238981	HCPEpiC	choroid plexus:	n/a
22	chr3:240139-240189	NHBE	bronchial:	n/a
23	chr3:238618-238668	HMEC	breast:	n/a
24	chr3:238048-238098	ECC-1	luminal epithelium:	n/a
25	chr3:238318-238368	HCF	heart:	n/a
26	chr3:238618-238668	ovcar-3	ovarian:	n/a
27	chr3:239207-239257	GM12878	blood:	n/a
28	chr3:239506-239556	AG09309	skin:	n/a
29	chr3:239229-239279	MCF-7	breast:	n/a
30	chr3:239506-239556	PANC-1	pancreas:	n/a
31	chr3:236078-236128	HEEpiC	esophagus:	n/a
32	chr3:238496-238546	ProgFib	skin:	n/a
33	chr3:238931-238981	RPTEC	kidney:	n/a
34	chr3:243996-244046	BE2_C	brain:	n/a
35	chr3:238611-238661	HNPCEpiC	eye:	n/a
36	chr3:239665-239715	HIPEpiC	eye:	n/a
37	chr3:239188-239238	AG04450	lung:	fetal
38	chr3:238161-238211	NB4	blood:	n/a
39	chr3:240139-240189	MCF-7	breast:	n/a
40	chr3:241182-241232	HRPEpiC	eye:	n/a
41	chr3:241182-241232	SK-N-MC	brain:	n/a
42	chr3:239188-239238	HPAEpiC	pulmonary alveolar:	n/a
43	chr3:238931-238981	HRE	kidney:	n/a
44	chr3:238048-238098	NH-A	brain:	n/a
45	chr3:238618-238668	BE2_C	brain:	n/a
46	chr3:236078-236128	GM12891	blood:	n/a
47	chr3:238618-238668	HUVEC	blood vessel:	n/a
48	chr3:238161-238211	HNPCEpiC	eye:	n/a
49	chr3:238161-238211	HCT-116	colon:	n/a
50	chr3:238618-238668	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:217250..219144-chr3:222760..225297,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL5RA-6	chr3:238650-239024	ENSG00000224318.1
2	lnc-CNTN6-7	chr3:239697-239775	NONHSAT087562
3	lnc-IL5RA-6	chr3:237679-237723	NONHSAT087559
4	lnc-IL5RA-6	chr3:238139-238386	NONHSAT087559
5	lnc-IL5RA-6	chr3:237540-237597	NONHSAT087559
6	lnc-IL5RA-6	chr3:237441-237597	ENSG00000224318.1
7	lnc-CNTN6-7	chr3:238454-238746	NONHSAT087560
8	lnc-IL5RA-6	chr3:238290-238385	ENSG00000224318.1
9	lnc-IL5RA-6	chr3:237441-237597	ENSG00000224318.1
10	lnc-IL5RA-6	chr3:237679-237723	ENSG00000224318.1
11	lnc-IL5RA-6	chr3:238650-238882	ENSG00000224318.1
12	lnc-IL5RA-6	chr3:238139-238191	ENSG00000224318.1
13	lnc-IL5RA-6	chr3:237679-237723	ENSG00000224318.1
14	lnc-IL5RA-6	chr3:238290-238542	ENSG00000224318.1
15	lnc-IL5RA-6	chr3:237441-237597	ENSG00000224318.1
16	lnc-IL5RA-6	chr3:238139-238191	ENSG00000224318.1
17	lnc-CNTN6-7	chr3:239326-239775	NONHSAT087561
18	lnc-IL5RA-6	chr3:237679-237723	ENSG00000224318.1
19	lnc-IL5RA-6	chr3:238139-238191	ENSG00000224318.1

No data

Variant related genes	Relation type
CHL1-AS2	TF binding region
CHL1	TF binding region
CHL1-AS2	CpG island
CHL1	CpG island

Extended variants
information (count: 771 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370191847	chr3:225266-225267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs3946790	chr3:225296-225297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563441225	chr3:225298-225299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181529959	chr3:225321-225322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141665501	chr3:225346-225347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564078510	chr3:225355-225356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2839803	chr3:225361-225362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs561494290	chr3:225368-225369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs186229595	chr3:225369-225370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546935843	chr3:225372-225373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145237184	chr3:225402-225403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs529120525	chr3:225421-225422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs73086725	chr3:225429-225430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs79058949	chr3:225460-225461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570455725	chr3:225470-225471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2173496	chr3:225473-225474	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs534272811	chr3:225517-225518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552220617	chr3:225535-225536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570535067	chr3:225545-225546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189340578	chr3:225585-225586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs137903269	chr3:225590-225591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141633818	chr3:225595-225596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs9846093	chr3:226603-226604	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs190204611	chr3:226629-226630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182825543	chr3:226635-226636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs56935729	chr3:226646-226647	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs544794685	chr3:226650-226651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs33973117	chr3:226652-226653	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs528582709	chr3:226694-226695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547033647	chr3:226700-226701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs568376356	chr3:226717-226718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529257239	chr3:226719-226720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs373336464	chr3:226729-226730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs58544565	chr3:226733-226734	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs74619414	chr3:226808-226809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs9819270	chr3:226861-226862	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs187430698	chr3:226888-226889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs59080621	chr3:226899-226900	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs145493379	chr3:226913-226914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565828779	chr3:233612-233613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs527394707	chr3:233653-233654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536499007	chr3:233676-233677	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs554808861	chr3:233678-233679	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs569827349	chr3:233687-233688	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs191197208	chr3:233713-233714	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs147742006	chr3:233736-233737	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs368812162	chr3:233744-233745	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs73814162	chr3:233747-233748	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs577995689	chr3:233758-233759	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs545063805	chr3:233818-233819	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Cancer	20164920	CNVD
Lung cancer	16618734	CNVD
Autism	18349135	CNVD
Breast cancer	20409316	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Intellectual disability	22045946	CNVD
Squamous cell cancer	19607727	CNVD
Gastric adenocarcinoma	19115996	CNVD
sporadic birth defects	19047251	CNVD
Mental retardation	17124404	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Sudden cardiac death	19188705	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	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
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
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Autism	22543975	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Tetralogy of Fallot	22912587	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:225200-225600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:226600-227000	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr3:233600-233800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr3:233600-234400	Enhancers	Primary B cells from peripheral blood	blood
5	chr3:233800-235000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr3:234200-234800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
7	chr3:234600-234800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
8	chr3:235000-235200	Enhancers	Fetal Brain Female	brain
9	chr3:235000-236000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr3:235200-236000	Weak transcription	Fetal Brain Female	brain
11	chr3:235400-236600	Enhancers	Fetal Brain Male	brain
12	chr3:235800-236000	Enhancers	Adipose Nuclei	Adipose
13	chr3:235800-236400	Enhancers	Spleen	Spleen
14	chr3:235800-237000	Enhancers	Ovary	ovary
15	chr3:236000-236200	Flanking Active TSS	Adipose Nuclei	Adipose
16	chr3:236000-236400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr3:236000-236600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
18	chr3:236000-236800	Enhancers	Fetal Brain Female	brain
19	chr3:236200-236400	Enhancers	Brain Cingulate Gyrus	brain
20	chr3:236200-236400	Enhancers	Brain Substantia Nigra	brain
21	chr3:236200-237800	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr3:236400-237000	Enhancers	Brain Germinal Matrix	brain
23	chr3:236400-237400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr3:236400-238200	Weak transcription	Spleen	Spleen
25	chr3:236600-237200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr3:236600-237200	Flanking Active TSS	Fetal Brain Male	brain
27	chr3:236800-238000	Active TSS	Fetal Brain Female	brain
28	chr3:237000-237200	Active TSS	Brain Germinal Matrix	brain
29	chr3:237000-237800	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr3:237000-237800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr3:237000-240400	Active TSS	Ovary	ovary
32	chr3:237200-237400	Flanking Active TSS	Brain Germinal Matrix	brain
33	chr3:237200-237600	Active TSS	Brain Cingulate Gyrus	brain
34	chr3:237200-237800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr3:237200-240000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr3:237200-240200	Active TSS	Brain Anterior Caudate	brain
37	chr3:237200-241000	Active TSS	Brain Angular Gyrus	brain
38	chr3:237200-241000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr3:237200-241000	Active TSS	Fetal Brain Male	brain
40	chr3:237400-237600	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
41	chr3:237400-241200	Active TSS	Brain Inferior Temporal Lobe	brain
42	chr3:237600-237800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
43	chr3:237600-237800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
44	chr3:237600-240000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
45	chr3:237600-240200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
46	chr3:237600-241200	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
47	chr3:237800-238000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
48	chr3:237800-238000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr3:237800-238000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr3:237800-238000	Active TSS	Brain Substantia Nigra	brain

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