Variant report

Variant	nsv590895
Chromosome Location	chr3:84838638-84940927
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:188)
CpG islands
(count:366)
Chromatin interactive
region (count:0)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:188 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:84886062-84886466	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr3:84930983-84931198	A549	lung:	n/a	n/a
3	CEBPB	chr3:84930981-84931137	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr3:84874694-84874997	HepG2	liver:	n/a	chr3:84874822-84874833 chr3:84874824-84874833
5	CEBPB	chr3:84886070-84886388	HepG2	liver:	n/a	n/a
6	CEBPB	chr3:84870916-84871443	HepG2	liver:	n/a	chr3:84871286-84871297
7	CEBPB	chr3:84858168-84858322	H1-hESC	embryonic stem cell:	n/a	chr3:84858283-84858294
8	CEBPB	chr3:84858191-84858414	HepG2	liver:	n/a	chr3:84858283-84858294
9	CEBPB	chr3:84886005-84886347	MCF-7	breast:	n/a	n/a
10	CEBPB	chr3:84886127-84886390	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr3:84886016-84886489	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr3:84886026-84886697	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr3:84875044-84875284	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr3:84875088-84875247	Medullo	brain:	n/a	n/a
15	CTCF	chr3:84875076-84875261	MCF-7	breast:	n/a	n/a
16	CTCF	chr3:84929620-84929667	Spleen_OC	spleen:	n/a	n/a
17	CTCF	chr3:84875099-84875207	HepG2	liver:	n/a	n/a
18	CTCF	chr3:84875120-84875172	MCF-7	breast:	n/a	n/a
19	CTCF	chr3:84875054-84875261	LNCaP	prostate:	n/a	n/a
20	CTCF	chr3:84875040-84875190	MCF-7	breast:	n/a	n/a
21	CTCF	chr3:84875080-84875230	BE2_C	brain:	n/a	n/a
22	CTCF	chr3:84875081-84875257	LNCaP	prostate:	n/a	n/a
23	CTCF	chr3:84876629-84876686	GM10248	blood:	n/a	n/a
24	CTCF	chr3:84875047-84875264	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr3:84855235-84855296	GM20000	blood:	n/a	n/a
26	CTCF	chr3:84875013-84875326	GM12878	blood:	n/a	n/a
27	CTCF	chr3:84875105-84875213	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr3:84934950-84934956	LNCaP	prostate:	n/a	n/a
29	CTCF	chr3:84875040-84875190	BE2_C	brain:	n/a	n/a
30	CTCF	chr3:84875120-84875270	MCF-7	breast:	n/a	n/a
31	CTCF	chr3:84875060-84875210	HEK293	kidney:	n/a	n/a
32	CTCF	chr3:84875120-84875270	A549	lung:	n/a	n/a
33	CTCF	chr3:84875122-84875217	GM10248	blood:	n/a	n/a
34	CTCF	chr3:84875080-84875230	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr3:84875100-84875250	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr3:84875127-84875191	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr3:84875057-84875202	HepG2	liver:	n/a	n/a
38	CTCF	chr3:84875080-84875230	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr3:84875080-84875230	HepG2	liver:	n/a	n/a
40	CTCF	chr3:84923877-84923947	Lung_OC	lung:	n/a	n/a
41	CTCF	chr3:84875020-84875170	GM12868	blood:	n/a	n/a
42	CTCF	chr3:84875098-84875231	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:84875120-84875270	Caco-2	colon:	n/a	n/a
44	CTCF	chr3:84901608-84901641	GM20000	blood:	n/a	n/a
45	CTCF	chr3:84874941-84875303	MCF-7	breast:	n/a	n/a
46	CTCF	chr3:84920920-84921070	MCF-7	breast:	n/a	chr3:84921010-84921028
47	E2F4	chr3:84874880-84875132	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr3:84906725-84906921	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr3:84854886-84854939	MCF10A-Er-Src	breast:	n/a	n/a
50	ELK1	chr3:84870296-84870325	Hela-S3	cervix:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:84919226-84919276	SK-N-MC	brain:	n/a
2	chr3:84919438-84919488	HNPCEpiC	eye:	n/a
3	chr3:84919226-84919276	T-47D	breast:	n/a
4	chr3:84919438-84919488	NHBE	bronchial:	n/a
5	chr3:84885990-84886040	HRE	kidney:	n/a
6	chr3:84884069-84884119	AG04449	skin:	fetal
7	chr3:84884069-84884119	Caco-2	colon:	n/a
8	chr3:84884069-84884119	BE2_C	brain:	n/a
9	chr3:84919438-84919488	ProgFib	skin:	n/a
10	chr3:84884069-84884119	SAEC	small airway:	n/a
11	chr3:84909261-84909311	HCT-116	colon:	n/a
12	chr3:84919226-84919276	NT2-D1	testis:	n/a
13	chr3:84909261-84909311	CMK	blood:	n/a
14	chr3:84919226-84919276	ovcar-3	ovarian:	n/a
15	chr3:84884069-84884119	RPTEC	kidney:	n/a
16	chr3:84919226-84919276	SKMC	muscle:	n/a
17	chr3:84919438-84919488	GM12892	blood:	n/a
18	chr3:84909261-84909311	NB4	blood:	n/a
19	chr3:84885990-84886040	BJ	skin:	n/a
20	chr3:84851738-84851788	HCT-116	colon:	n/a
21	chr3:84919226-84919276	ProgFib	skin:	n/a
22	chr3:84885990-84886040	HRPEpiC	eye:	n/a
23	chr3:84885990-84886040	AG09309	skin:	n/a
24	chr3:84919438-84919488	SK-N-SH	brain:	n/a
25	chr3:84909261-84909311	HIPEpiC	eye:	n/a
26	chr3:84919438-84919488	PrEC	prostate:	n/a
27	chr3:84919438-84919488	HPAEpiC	pulmonary alveolar:	n/a
28	chr3:84885990-84886040	AoSMC	blood vessel:	n/a
29	chr3:84884069-84884119	HRE	kidney:	n/a
30	chr3:84909261-84909311	GM19239	blood:	n/a
31	chr3:84851738-84851788	SAEC	small airway:	n/a
32	chr3:84909261-84909311	AG04450	lung:	fetal
33	chr3:84851738-84851788	AG04450	lung:	fetal
34	chr3:84884069-84884119	ProgFib	skin:	n/a
35	chr3:84885990-84886040	HCF	heart:	n/a
36	chr3:84919438-84919488	HEEpiC	esophagus:	n/a
37	chr3:84851738-84851788	GM12892	blood:	n/a
38	chr3:84851738-84851788	ECC-1	luminal epithelium:	n/a
39	chr3:84851738-84851788	HEEpiC	esophagus:	n/a
40	chr3:84919226-84919276	AoSMC	blood vessel:	n/a
41	chr3:84909261-84909311	AG09309	skin:	n/a
42	chr3:84885990-84886040	HAEpiC	amniotic membrane:	n/a
43	chr3:84919226-84919276	SAEC	small airway:	n/a
44	chr3:84851738-84851788	LNCaP	prostate:	n/a
45	chr3:84851738-84851788	HAEpiC	amniotic membrane:	n/a
46	chr3:84885990-84886040	MCF10A-Er-Src	breast:	n/a
47	chr3:84885990-84886040	GM12892	blood:	n/a
48	chr3:84851738-84851788	AG09319	gingival:	n/a
49	chr3:84909261-84909311	NT2-D1	testis:	n/a
50	chr3:84885990-84886040	GM06990	blood:	n/a

No data

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VGLL3-6	chr3:84912367-84912587	NONHSAT090649
2	lnc-VGLL3-6	chr3:84908966-84909074	ENSG00000242641.1
3	lnc-VGLL3-6	chr3:84918054-84918175	ENSG00000242641.1
4	lnc-VGLL3-6	chr3:84917749-84917819	NONHSAT090652
5	lnc-VGLL3-6	chr3:84841319-84841442	NONHSAT090649
6	lnc-CADM2-1	chr3:84934087-84934274	XLOC_002723
7	lnc-VGLL3-6	chr3:84912857-84913156	NONHSAT090649
8	lnc-VGLL3-6	chr3:84917933-84917994	ENSG00000242641.1
9	lnc-VGLL3-6	chr3:84912367-84912587	ENSG00000242641.1
10	lnc-VGLL3-6	chr3:84912387-84912587	NONHSAT090652
11	lnc-VGLL3-9	chr3:84877886-84878178	ucscGeneNc_uc003dqi_2
12	lnc-VGLL3-6	chr3:84911874-84911972	NONHSAT090649
13	lnc-VGLL3-6	chr3:84911874-84911972	ENSG00000242641.1
14	lnc-VGLL3-6	chr3:84838789-84838923	ENSG00000242641.1
15	lnc-VGLL3-6	chr3:84917279-84917406	ENSG00000242641.1
16	lnc-VGLL3-6	chr3:84841319-84841442	ENSG00000242641.1
17	lnc-VGLL3-6	chr3:84918054-84918175	NONHSAT090652
18	lnc-VGLL3-6	chr3:84912857-84913156	ENSG00000242641.1
19	lnc-VGLL3-6	chr3:84917749-84917819	ENSG00000242641.1
20	lnc-VGLL3-6	chr3:84918054-84918175	ENSG00000242641.1
21	lnc-VGLL3-6	chr3:84917749-84917819	ENSG00000242641.1
22	lnc-VGLL3-6	chr3:84851600-84851903	ENSG00000242641.1
23	lnc-CADM2-1	chr3:84934086-84934274	NONHSAT090654
24	lnc-VGLL3-6	chr3:84908966-84909074	NONHSAT090649
25	lnc-VGLL3-6	chr3:84917749-84917819	NONHSAT090649
26	lnc-VGLL3-6	chr3:84918054-84918175	NONHSAT090649
27	lnc-VGLL3-6	chr3:84918429-84918726	NONHSAT090649
28	lnc-VGLL3-6	chr3:84918429-84918637	NONHSAT090652
29	lnc-VGLL3-6	chr3:84917749-84917819	ENSG00000242641.1
30	lnc-VGLL3-6	chr3:84918742-84918779	ENSG00000242641.1
31	lnc-VGLL3-9	chr3:84921479-84921613	ucscGeneNc_uc003dqi_2
32	lnc-VGLL3-6	chr3:84838789-84838923	NONHSAT090649
33	lnc-VGLL3-9	chr3:84924009-84924132	ucscGeneNc_uc003dqi_2
34	lnc-VGLL3-6	chr3:84903093-84903166	NONHSAT090649
35	lnc-VGLL3-6	chr3:84918429-84918726	ENSG00000242641.1
36	lnc-VGLL3-6	chr3:84930640-84930830	ENSG00000242641.1
37	lnc-VGLL3-6	chr3:84903093-84903166	ENSG00000242641.1

No data

Variant related genes	Relation type
ENSG00000242339	TF binding region
LINC00971	TF binding region
ENSG00000242339	CpG island
LINC00971	CpG island
TCEAL1	miRNA target sites

Extended variants
information (count: 1518 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1518 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs980332	chr3:84838638-84838639	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565244364	chr3:84838658-84838659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573684205	chr3:84838662-84838663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75211100	chr3:84838664-84838665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs140893704	chr3:84838668-84838669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs376464091	chr3:84838682-84838683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs980331	chr3:84838697-84838698	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs188088160	chr3:84838720-84838721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528543826	chr3:84838731-84838732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575052449	chr3:84838751-84838752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192881312	chr3:84838755-84838756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561220340	chr3:84838764-84838765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs72911321	chr3:84838775-84838776	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs567939355	chr3:84838780-84838781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565309405	chr3:84838802-84838803	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs532572167	chr3:84838817-84838818	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs7611577	chr3:84838828-84838829	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs115629390	chr3:84838848-84838849	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs536796921	chr3:84838927-84838928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562647121	chr3:84838933-84838934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548811793	chr3:84839010-84839011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561143998	chr3:84839047-84839048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567242332	chr3:84839111-84839112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs34311844	chr3:84839143-84839144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373737424	chr3:84839144-84839145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552673984	chr3:84839187-84839188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs3948003	chr3:84839194-84839195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577191852	chr3:84839206-84839207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538254981	chr3:84839264-84839265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144827993	chr3:84839274-84839275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs190057404	chr3:84839275-84839276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529838000	chr3:84839301-84839302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575191879	chr3:84839317-84839318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs542401840	chr3:84839339-84839340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575506726	chr3:84841334-84841335	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs529645188	chr3:84841364-84841365	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs148324536	chr3:84841376-84841377	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs1901986	chr3:84841407-84841408	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs570333714	chr3:84841410-84841411	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs533878733	chr3:84841414-84841415	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs6777273	chr3:84842407-84842408	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs143204261	chr3:84842408-84842409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552856934	chr3:84842430-84842431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551305167	chr3:84842432-84842433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs187738210	chr3:84842450-84842451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs527243818	chr3:84842480-84842481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545819598	chr3:84842498-84842499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564360345	chr3:84842499-84842500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531667549	chr3:84842506-84842507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs549924290	chr3:84842551-84842552	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Schizophrenia	23813976	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Autism	22102821	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:84837800-84839400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:84838200-84839400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr3:84842400-84843200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr3:84845200-84856400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr3:84850800-84851400	Enhancers	H9 Cell Line	embryonic stem cell
6	chr3:84850800-84851400	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr3:84850800-84851800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr3:84850800-84851800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr3:84850800-84851800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr3:84851000-84851400	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr3:84851000-84851400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr3:84851000-84851600	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr3:84856400-84856600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr3:84856600-84856800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr3:84864600-84865000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
16	chr3:84864600-84865000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr3:84877600-84880000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr3:84882000-84884800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr3:84883200-84887200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr3:84883400-84884000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
21	chr3:84883400-84884200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
22	chr3:84884000-84885800	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr3:84884200-84884600	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr3:84884600-84885200	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr3:84884600-84885400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr3:84884600-84886800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr3:84884600-84886800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr3:84884600-84886800	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr3:84884600-84887200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr3:84884800-84886800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr3:84885200-84885600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr3:84885400-84885800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr3:84885600-84886800	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr3:84885800-84886000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr3:84885800-84886200	Enhancers	H9 Cell Line	embryonic stem cell
36	chr3:84885800-84886200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr3:84885800-84886800	Enhancers	H1 Cell Line	embryonic stem cell
38	chr3:84886000-84886200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr3:84886000-84886800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:84886200-84886400	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr3:84886200-84886600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr3:84886200-84886600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr3:84886200-84890600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr3:84886400-84886800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr3:84886600-84886800	Enhancers	H9 Cell Line	embryonic stem cell
46	chr3:84886800-84889000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr3:84886800-84890600	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr3:84886800-84890600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr3:84886800-84891000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr3:84886800-84891000	Weak transcription	H9 Cell Line	embryonic stem cell

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