Variant report

Variant	esv2752870
Chromosome Location	chr3:82014410-82050310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:277)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:277 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:82035096-82035370	HepG2	liver:	n/a	n/a
2	BATF	chr3:82030000-82030292	GM12878	blood:	n/a	chr3:82030159-82030170
3	BRCA1	chr3:82024002-82024104	GM12878	blood:	n/a	n/a
4	CBX3	chr3:82035076-82035563	HCT-116	colon:	n/a	n/a
5	CBX3	chr3:82029976-82030443	HCT-116	colon:	n/a	n/a
6	CEBPB	chr3:82049628-82049796	H1-hESC	embryonic stem cell:	n/a	chr3:82049682-82049693
7	CEBPB	chr3:82049665-82049820	A549	lung:	n/a	chr3:82049682-82049693
8	CEBPB	chr3:82049515-82049844	HepG2	liver:	n/a	chr3:82049682-82049693
9	CEBPZ	chr3:82044198-82044217	HepG2	liver:	n/a	n/a
10	CHD2	chr3:82035150-82035359	HepG2	liver:	n/a	n/a
11	CTCF	chr3:82035100-82035250	HCT-116	colon:	n/a	n/a
12	CTCF	chr3:82044543-82044794	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr3:82044620-82044770	HMEC	breast:	n/a	n/a
14	CTCF	chr3:82044680-82044830	RPTEC	kidney:	n/a	n/a
15	CTCF	chr3:82035135-82035302	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr3:82044580-82044730	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr3:82044580-82044730	HA-sp	spinal cord:	n/a	n/a
18	CTCF	chr3:82044559-82044797	LNCaP	prostate:	n/a	n/a
19	CTCF	chr3:82044580-82044730	GM12873	blood:	n/a	n/a
20	CTCF	chr3:82044660-82044810	A549	lung:	n/a	n/a
21	CTCF	chr3:82044580-82044730	BE2_C	brain:	n/a	n/a
22	CTCF	chr3:82044600-82044750	A549	lung:	n/a	n/a
23	CTCF	chr3:82044560-82044710	GM12865	blood:	n/a	n/a
24	CTCF	chr3:82044608-82044787	NHEK	skin:	n/a	n/a
25	CTCF	chr3:82044623-82044697	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr3:82035100-82035250	K562	blood:	n/a	n/a
27	CTCF	chr3:82044506-82044819	GM12878	blood:	n/a	n/a
28	CTCF	chr3:82044519-82044793	MCF-7	breast:	n/a	n/a
29	CTCF	chr3:82044560-82044710	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr3:82035185-82035258	Gliobla	brain:	n/a	n/a
31	CTCF	chr3:82044580-82044730	HCT-116	colon:	n/a	n/a
32	CTCF	chr3:82035120-82035270	GM12873	blood:	n/a	n/a
33	CTCF	chr3:82035134-82035302	HepG2	liver:	n/a	n/a
34	CTCF	chr3:82035120-82035270	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr3:82044580-82044730	MCF-7	breast:	n/a	n/a
36	CTCF	chr3:82038600-82038750	HepG2	liver:	n/a	n/a
37	CTCF	chr3:82044580-82044730	AG09309	skin:	n/a	n/a
38	CTCF	chr3:82034960-82035110	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr3:82044540-82044690	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr3:82035120-82035270	HEK293	kidney:	n/a	n/a
41	CTCF	chr3:82035000-82035150	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr3:82044672-82044723	Fibrobl	skin:	n/a	n/a
43	CTCF	chr3:82044655-82044770	MCF-7	breast:	n/a	n/a
44	CTCF	chr3:82044620-82044770	GM12875	blood:	n/a	n/a
45	CTCF	chr3:82044600-82044750	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr3:82035080-82035230	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:82044580-82044730	Caco-2	colon:	n/a	n/a
48	CTCF	chr3:82044620-82044770	HEK293	kidney:	n/a	n/a
49	CTCF	chr3:82044480-82044630	HFF	foreskin:	n/a	n/a
50	CTCF	chr3:82035100-82035250	Hela-S3	cervix:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:82035330-82035380	NT2-D1	testis:	n/a
2	chr3:82035330-82035380	HCF	heart:	n/a
3	chr3:82035330-82035380	HIPEpiC	eye:	n/a
4	chr3:82035330-82035380	PFSK-1	brain:	n/a
5	chr3:82035330-82035380	ProgFib	skin:	n/a
6	chr3:82035330-82035380	SAEC	small airway:	n/a
7	chr3:82035330-82035380	SKMC	muscle:	n/a
8	chr3:82035330-82035380	NH-A	brain:	n/a
9	chr3:82035330-82035380	Caco-2	colon:	n/a
10	chr3:82035330-82035380	NHDF-neo	bronchial:	n/a
11	chr3:82035330-82035380	RPTEC	kidney:	n/a
12	chr3:82035330-82035380	LNCaP	prostate:	n/a
13	chr3:82035330-82035380	AG04450	lung:	fetal
14	chr3:82035330-82035380	MCF-7	breast:	n/a
15	chr3:82035330-82035380	IMR90	lung:	fetal
16	chr3:82035330-82035380	HNPCEpiC	eye:	n/a
17	chr3:82035330-82035380	GM19239	blood:	n/a
18	chr3:82035330-82035380	AG09309	skin:	n/a
19	chr3:82035330-82035380	HCM	heart:	n/a
20	chr3:82035330-82035380	NB4	blood:	n/a
21	chr3:82035330-82035380	ECC-1	luminal epithelium:	n/a
22	chr3:82035330-82035380	Jurkat	blood:	n/a
23	chr3:82035330-82035380	Hepatocyte	liver:	n/a
24	chr3:82035330-82035380	U87	brain:	n/a
25	chr3:82035330-82035380	HAEpiC	amniotic membrane:	n/a
26	chr3:82035330-82035380	HL-60	blood:	n/a
27	chr3:82035330-82035380	HepG2	liver:	n/a
28	chr3:82035330-82035380	HEK293	kidney:	embryo
29	chr3:82035330-82035380	AG09319	gingival:	n/a
30	chr3:82035330-82035380	HRE	kidney:	n/a
31	chr3:82035330-82035380	AoSMC	blood vessel:	n/a
32	chr3:82035330-82035380	K562	blood:	n/a
33	chr3:82035330-82035380	SK-N-MC	brain:	n/a
34	chr3:82035330-82035380	HRPEpiC	eye:	n/a
35	chr3:82035330-82035380	GM06990	blood:	n/a
36	chr3:82035330-82035380	HUVEC	blood vessel:	n/a
37	chr3:82035330-82035380	HRCEpiC	kidney:	n/a
38	chr3:82035330-82035380	CMK	blood:	n/a
39	chr3:82035330-82035380	BJ	skin:	n/a
40	chr3:82035330-82035380	BE2_C	brain:	n/a
41	chr3:82035330-82035380	HCPEpiC	choroid plexus:	n/a
42	chr3:82035330-82035380	Hela-S3	cervix:	n/a
43	chr3:82035330-82035380	MCF10A-Er-Src	breast:	n/a
44	chr3:82035330-82035380	GM12878	blood:	n/a
45	chr3:82035330-82035380	HCT-116	colon:	n/a
46	chr3:82035330-82035380	A549	lung:	n/a
47	chr3:82035330-82035380	HMEC	breast:	n/a
48	chr3:82035330-82035380	PrEC	prostate:	n/a
49	chr3:82035330-82035380	GM12891	blood:	n/a
50	chr3:82035330-82035380	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:82044423..82045130-chr3:82182277..82182777,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CADM2-6	chr3:82035303-82035532	ENSG00000239440
2	lnc-GBE1-2	chr3:82026048-82026638	XLOC_003171
3	lnc-GBE1-2	chr3:82020171-82020208	NONHSAT090625
4	lnc-GBE1-2	chr3:82025796-82026250	NONHSAT090625
5	lnc-GBE1-2	chr3:82025722-82025860	XLOC_003171
6	lnc-CADM2-6	chr3:82035289-82035532	ENSG00000239440

No data

Variant related genes	Relation type
ENSG00000239440	TF binding region
ENSG00000239440	CpG island
ADAMTS9	miRNA target sites
DSC3	miRNA target sites

Extended variants
information (count: 1351 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1351 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9309883	chr3:82014428-82014429	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs143861040	chr3:82014451-82014452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529343800	chr3:82014477-82014478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542675544	chr3:82014478-82014479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562507549	chr3:82014565-82014566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531914047	chr3:82014645-82014646	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs72895805	chr3:82014674-82014675	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs571555883	chr3:82014686-82014687	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs527869971	chr3:82014743-82014744	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs547929382	chr3:82014768-82014769	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs569432594	chr3:82014814-82014815	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs148647750	chr3:82014826-82014827	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs539675564	chr3:82014834-82014835	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs190035604	chr3:82014907-82014908	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs549547209	chr3:82014927-82014928	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs569647932	chr3:82015020-82015021	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs538982191	chr3:82015029-82015030	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs551849975	chr3:82015030-82015031	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs558196319	chr3:82015074-82015075	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs181691114	chr3:82015091-82015092	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs572332317	chr3:82015123-82015124	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs534523286	chr3:82015228-82015229	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs554719935	chr3:82015253-82015254	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs574064005	chr3:82015262-82015263	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs543089674	chr3:82015272-82015273	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs115381094	chr3:82015298-82015299	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs4389498	chr3:82015395-82015396	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs11915669	chr3:82015441-82015442	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs545333242	chr3:82015487-82015488	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs369144495	chr3:82015489-82015490	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs185420464	chr3:82015493-82015494	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs527938874	chr3:82015505-82015506	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs190295545	chr3:82015543-82015544	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs561517539	chr3:82015621-82015622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181979431	chr3:82015648-82015649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143289124	chr3:82015656-82015657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569710998	chr3:82015696-82015697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538650979	chr3:82015749-82015750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185166233	chr3:82015757-82015758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs7427000	chr3:82015818-82015819	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs369853898	chr3:82015823-82015824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189876822	chr3:82015829-82015830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10433514	chr3:82015839-82015840	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs574550949	chr3:82015870-82015871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146687322	chr3:82015928-82015929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs79813421	chr3:82015993-82015994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576087424	chr3:82016047-82016048	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs79400691	chr3:82016059-82016060	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs564906816	chr3:82016071-82016072	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs572685731	chr3:82016100-82016101	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Splenic marginal zone lymphoma	21957467	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
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Autism	20808228	CNVD
Urothelial carcinoma	21177765	CNVD
Neurodevelopmental disorder	22521361	CNVD

Chromatin state (count:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:82013000-82014600	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr3:82013200-82015200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr3:82013200-82018600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr3:82013600-82015800	Enhancers	Brain Germinal Matrix	brain
5	chr3:82013600-82017400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr3:82013800-82016400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr3:82014000-82014600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr3:82014000-82014600	Enhancers	H9 Cell Line	embryonic stem cell
9	chr3:82014000-82016200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr3:82014200-82014600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr3:82014200-82016200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr3:82014200-82018400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr3:82014400-82017600	Weak transcription	Fetal Heart	heart
14	chr3:82014600-82015200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr3:82014600-82015800	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr3:82014600-82017400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr3:82014600-82018000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr3:82014800-82015000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr3:82015000-82015400	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr3:82015000-82017600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr3:82015200-82015600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr3:82015200-82016000	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr3:82015600-82018200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr3:82015800-82016200	Enhancers	H9 Cell Line	embryonic stem cell
25	chr3:82015800-82017600	Weak transcription	Brain Germinal Matrix	brain
26	chr3:82016000-82016200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr3:82016200-82016800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr3:82016200-82017400	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr3:82016200-82017600	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr3:82016200-82017800	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr3:82016400-82017400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr3:82016800-82017200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr3:82017200-82018400	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr3:82017400-82018000	Enhancers	H9 Cell Line	embryonic stem cell
35	chr3:82017400-82018000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr3:82017400-82018200	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr3:82017400-82018400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr3:82017400-82018600	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr3:82017600-82017800	Enhancers	Brain Germinal Matrix	brain
40	chr3:82017600-82018000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr3:82017600-82018400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr3:82017600-82018400	Enhancers	Fetal Heart	heart
43	chr3:82017800-82018200	Enhancers	H1 Cell Line	embryonic stem cell
44	chr3:82017800-82018200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr3:82018000-82018400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr3:82018200-82019000	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr3:82018200-82023800	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr3:82018400-82020600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr3:82018400-82023400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr3:82018400-82023800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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