Variant report

Variant	nsv1010140
Chromosome Location	chr3:84997012-85034281
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:572)
CpG islands
(count:1160)
Chromatin interactive
region (count:4)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:572 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr3:85014321-85014662	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF3	chr3:85014281-85014577	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr3:85011727-85011885	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:85007700-85007990	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:85008844-85009156	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr3:85007545-85007619	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr3:85016899-85017319	Hela-S3	cervix:	n/a	chr3:85017262-85017273
8	CEBPB	chr3:85014267-85014637	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr3:85014296-85014633	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr3:85016947-85017327	H1-hESC	embryonic stem cell:	n/a	chr3:85017262-85017273
11	CEBPB	chr3:85010675-85010724	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD1	chr3:85016866-85017054	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD1	chr3:85007333-85007372	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD1	chr3:85009160-85009452	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr3:85008169-85008877	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr3:85007777-85007910	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr3:85008771-85009363	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr3:85007816-85008169	HepG2	liver:	n/a	n/a
19	CHD2	chr3:85007823-85008268	GM12878	blood:	n/a	n/a
20	CHD2	chr3:85007748-85008250	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr3:85007701-85008149	K562	blood:	n/a	n/a
22	CHD2	chr3:85007616-85008518	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr3:85007924-85008243	A549	lung:	n/a	n/a
24	CREB1	chr3:85014249-85014675	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr3:85014243-85014716	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTBP2	chr3:85008265-85009372	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr3:85014346-85014523	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr3:85007690-85007927	ProgFib	skin:	n/a	chr3:85007805-85007821 chr3:85007804-85007822 chr3:85007806-85007819
29	CTCF	chr3:85008420-85008570	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr3:85023580-85023730	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr3:85012360-85012510	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr3:85007720-85007870	AG09319	gingival:	n/a	chr3:85007805-85007821 chr3:85007804-85007822 chr3:85007806-85007819
33	CTCF	chr3:85014376-85014546	MCF-7	breast:	n/a	n/a
34	CTCF	chr3:85014410-85014481	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr3:85023588-85023794	LNCaP	prostate:	n/a	n/a
36	CTCF	chr3:85007600-85007750	NHLF	lung:	n/a	n/a
37	CTCF	chr3:85007740-85007890	HCM	heart:	n/a	chr3:85007805-85007821 chr3:85007804-85007822 chr3:85007806-85007819
38	CTCF	chr3:85007780-85007930	HEK293	kidney:	n/a	chr3:85007919-85007928 chr3:85007805-85007821 chr3:85007804-85007822 chr3:85007806-85007819
39	CTCF	chr3:85014297-85014531	HepG2	liver:	n/a	n/a
40	CTCF	chr3:85014380-85014530	HPF	lung:	n/a	n/a
41	CTCF	chr3:85007720-85007870	HFF-Myc	foreskin:	n/a	chr3:85007805-85007821 chr3:85007804-85007822 chr3:85007806-85007819
42	CTCF	chr3:85007720-85007870	SAEC	small airway:	n/a	chr3:85007805-85007821 chr3:85007804-85007822 chr3:85007806-85007819
43	CTCF	chr3:85008420-85008570	HAc	cerebellar:	n/a	n/a
44	CTCF	chr3:85007780-85007930	GM12869	blood:	n/a	chr3:85007919-85007928 chr3:85007805-85007821 chr3:85007804-85007822 chr3:85007806-85007819
45	CTCF	chr3:85008420-85008570	HPF	lung:	n/a	n/a
46	CTCF	chr3:85023640-85023790	HMEC	breast:	n/a	n/a
47	CTCF	chr3:85014348-85014528	HepG2	liver:	n/a	n/a
48	CTCF	chr3:85007780-85007930	HCPEpiC	choroid plexus:	n/a	chr3:85007919-85007928 chr3:85007805-85007821 chr3:85007804-85007822 chr3:85007806-85007819
49	CTCF	chr3:85008900-85009050	BE2_C	brain:	n/a	chr3:85008956-85008969
50	CTCF	chr3:85014780-85014930	BE2_C	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:85008991-85009041	AG09309	skin:	n/a
2	chr3:85008991-85009041	AG09309	skin:	n/a
3	chr3:85010677-85010727	HRCEpiC	kidney:	n/a
4	chr3:85007894-85007944	Hepatocyte	liver:	n/a
5	chr3:85007732-85007782	SAEC	small airway:	n/a
6	chr3:85007894-85007944	HCT-116	colon:	n/a
7	chr3:85008678-85008728	HRPEpiC	eye:	n/a
8	chr3:85010606-85010656	GM12892	blood:	n/a
9	chr3:85007894-85007944	HCPEpiC	choroid plexus:	n/a
10	chr3:85007894-85007944	SK-N-SH_RA	brain:	n/a
11	chr3:85008061-85008111	NH-A	brain:	n/a
12	chr3:85017543-85017593	HRE	kidney:	n/a
13	chr3:85017543-85017593	MCF10A-Er-Src	breast:	n/a
14	chr3:85008678-85008728	A549	lung:	n/a
15	chr3:85007817-85007867	SAEC	small airway:	n/a
16	chr3:85007992-85008042	BE2_C	brain:	n/a
17	chr3:85017543-85017593	SKMC	muscle:	n/a
18	chr3:85008991-85009041	MCF-7	breast:	n/a
19	chr3:85007817-85007867	NB4	blood:	n/a
20	chr3:85007959-85008009	SKMC	muscle:	n/a
21	chr3:85008786-85008836	PFSK-1	brain:	n/a
22	chr3:85008105-85008155	GM12892	blood:	n/a
23	chr3:85008587-85008637	LNCaP	prostate:	n/a
24	chr3:85008828-85008878	GM12892	blood:	n/a
25	chr3:85007732-85007782	BE2_C	brain:	n/a
26	chr3:85010677-85010727	U87	brain:	n/a
27	chr3:85010606-85010656	MCF-7	breast:	n/a
28	chr3:85007959-85008009	HEEpiC	esophagus:	n/a
29	chr3:85007959-85008009	BJ	skin:	n/a
30	chr3:85008156-85008206	U87	brain:	n/a
31	chr3:85008991-85009041	Caco-2	colon:	n/a
32	chr3:85006115-85006165	HL-60	blood:	n/a
33	chr3:85008156-85008206	ProgFib	skin:	n/a
34	chr3:85006115-85006165	HCT-116	colon:	n/a
35	chr3:85010606-85010656	SKMC	muscle:	n/a
36	chr3:85007992-85008042	SK-N-SH	brain:	n/a
37	chr3:85008678-85008728	K562	blood:	n/a
38	chr3:85008156-85008206	AG10803	skin:	n/a
39	chr3:85005177-85005227	SK-N-MC	brain:	n/a
40	chr3:85006115-85006165	RPTEC	kidney:	n/a
41	chr3:85005177-85005227	MCF10A-Er-Src	breast:	n/a
42	chr3:85010677-85010727	HCT-116	colon:	n/a
43	chr3:85008678-85008728	Hepatocyte	liver:	n/a
44	chr3:85008156-85008206	T-47D	breast:	n/a
45	chr3:85008587-85008637	SKMC	muscle:	n/a
46	chr3:85008991-85009041	GM12892	blood:	n/a
47	chr3:85008156-85008206	CMK	blood:	n/a
48	chr3:85007732-85007782	HIPEpiC	eye:	n/a
49	chr3:85010606-85010656	PFSK-1	brain:	n/a
50	chr3:85010677-85010727	HEEpiC	esophagus:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:85029590..85031359-chr3:85035312..85037118,2	K562	blood:
2	chr3:85011548..85014009-chr3:85014905..85018347,3	MCF-7	breast:
3	chr3:85011548..85014009-chr3:85014905..85018347,3	MCF-7	breast:
4	chr3:85023240..85023756-chr3:85409642..85410352,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VGLL3-9	chr3:85000744-85000865	ucscGeneNc_uc003dqi_2
2	lnc-VGLL3-9	chr3:85000439-85000509	ucscGeneNc_uc003dqi_2
3	lnc-CHMP2B-6	chr3:85008741-85008787	NONHSAT090657
4	lnc-VGLL3-9	chr3:85001119-85001416	ucscGeneNc_uc003dqi_2
5	lnc-CHMP2B-6	chr3:85009248-85009589	NONHSAT090658
6	lnc-CHMP2B-6	chr3:85008140-85008643	NONHSAT090657
7	lnc-CHMP2B-6	chr3:85008156-85008819	NONHSAT090658

No data

Variant related genes	Relation type
CADM2	TF binding region
CADM2	CpG island

Extended variants
information (count: 1042 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1042 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532331122	chr3:85000462-85000463	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs548146784	chr3:85000804-85000805	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs200420211	chr3:85000807-85000808	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs550322281	chr3:85000808-85000809	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs371755364	chr3:85000826-85000827	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs527935838	chr3:85000830-85000831	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs552834999	chr3:85000831-85000832	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs570999104	chr3:85000841-85000842	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs569051559	chr3:85000854-85000855	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs556653856	chr3:85000861-85000862	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs182847999	chr3:85001137-85001138	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs557587893	chr3:85001206-85001207	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs577219350	chr3:85001280-85001281	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs560334084	chr3:85001305-85001306	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs371788668	chr3:85003552-85003553	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs114870497	chr3:85003598-85003599	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs200714259	chr3:85003607-85003608	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs12490121	chr3:85003612-85003613	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs549332628	chr3:85003625-85003626	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs568023671	chr3:85003630-85003631	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs529141903	chr3:85003646-85003647	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs375450271	chr3:85003701-85003702	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs547373759	chr3:85003708-85003709	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs76487636	chr3:85003709-85003710	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs565906034	chr3:85003710-85003711	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs193219214	chr3:85003711-85003712	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs558311508	chr3:85003731-85003732	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs534964293	chr3:85003744-85003745	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs570136835	chr3:85003760-85003761	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs117755938	chr3:85003775-85003776	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs371877713	chr3:85003784-85003785	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs534243655	chr3:85003831-85003832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73137632	chr3:85003857-85003858	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs535289331	chr3:85003873-85003874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147670461	chr3:85003913-85003914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79173002	chr3:85003961-85003962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112942681	chr3:85003973-85003974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs578146907	chr3:85003981-85003982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151292049	chr3:85004012-85004013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563856371	chr3:85004218-85004219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560254095	chr3:85004227-85004228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536680605	chr3:85004262-85004263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561887013	chr3:85004297-85004298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531265771	chr3:85004379-85004380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554415581	chr3:85004389-85004390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140567247	chr3:85004402-85004403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528873395	chr3:85004440-85004441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1248863	chr3:85004452-85004453	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs375978984	chr3:85004487-85004488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559362665	chr3:85004494-85004495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
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
Acute myeloid leukemia	20729466	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
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
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Autism	22102821	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:804 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:85003600-85007600	Weak transcription	Fetal Brain Male	brain
2	chr3:85004800-85005000	Active TSS	Primary T helper naive cells from peripheral blood	blood
3	chr3:85005000-85007600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr3:85005200-85005800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:85005800-85006200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:85006200-85006600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr3:85006400-85006600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr3:85006400-85007000	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr3:85006400-85007200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr3:85006400-85007200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr3:85006600-85007200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr3:85006600-85007200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr3:85006600-85007600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:85006800-85007200	Enhancers	H1 Cell Line	embryonic stem cell
15	chr3:85006800-85007200	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr3:85006800-85007200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr3:85007000-85007200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr3:85007000-85007200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr3:85007000-85007200	Enhancers	Brain Anterior Caudate	brain
20	chr3:85007200-85007400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr3:85007200-85007400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr3:85007200-85007400	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr3:85007200-85007400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
24	chr3:85007200-85007400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
25	chr3:85007200-85007400	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr3:85007200-85007400	Enhancers	Brain Angular Gyrus	brain
27	chr3:85007200-85007400	Enhancers	Brain Hippocampus Middle	brain
28	chr3:85007200-85007400	Enhancers	Brain Substantia Nigra	brain
29	chr3:85007200-85007400	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr3:85007200-85007600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
31	chr3:85007200-85007600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
32	chr3:85007200-85007600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
33	chr3:85007200-85007600	Flanking Active TSS	Brain Anterior Caudate	brain
34	chr3:85007200-85007600	Bivalent Enhancer	Fetal Kidney	kidney
35	chr3:85007200-85007800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr3:85007200-85008800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
37	chr3:85007200-85009600	Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr3:85007200-85011800	Active TSS	H1 Cell Line	embryonic stem cell
39	chr3:85007200-85012400	Active TSS	Brain Inferior Temporal Lobe	brain
40	chr3:85007200-85012600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr3:85007400-85007600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr3:85007400-85007600	Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr3:85007400-85007600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
44	chr3:85007400-85007600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
45	chr3:85007400-85007600	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
46	chr3:85007400-85007600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr3:85007400-85007600	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr3:85007400-85007600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr3:85007400-85007600	Enhancers	Adipose Nuclei	Adipose
50	chr3:85007400-85007600	Enhancers	Liver	Liver

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