Variant report

Variant	nsv460300
Chromosome Location	chr3:82010-185281
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:481)
CpG islands
(count:122)
Chromatin interactive
region (count:14)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:481 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:86873-86900	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:84683-85432	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:104725-105176	HepG2	liver:	n/a	n/a
4	ATF1	chr3:128118-128267	K562	blood:	n/a	n/a
5	BACH1	chr3:165624-165661	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:166561-166841	GM12878	blood:	n/a	chr3:166679-166690 chr3:166653-166662
7	BATF	chr3:166548-166773	GM12878	blood:	n/a	chr3:166679-166690 chr3:166653-166662
8	BHLHE40	chr3:152996-153196	A549	lung:	n/a	n/a
9	BHLHE40	chr3:84678-84869	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:150637-150664	A549	lung:	n/a	n/a
11	BRCA1	chr3:85112-85127	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr3:84696-84876	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr3:85095-85318	HepG2	liver:	n/a	chr3:85237-85250 chr3:85237-85248
14	CEBPB	chr3:110019-110065	A549	lung:	n/a	n/a
15	CEBPB	chr3:88330-88522	HepG2	liver:	n/a	chr3:88338-88349 chr3:88336-88349 chr3:88336-88347
16	CEBPB	chr3:130437-130508	A549	lung:	n/a	n/a
17	CEBPB	chr3:99754-100055	HepG2	liver:	n/a	n/a
18	CEBPB	chr3:137940-138307	HepG2	liver:	n/a	chr3:138113-138124 chr3:138111-138128
19	CEBPB	chr3:85080-85291	HepG2	liver:	n/a	chr3:85237-85250 chr3:85237-85248 chr3:85092-85105
20	CEBPB	chr3:111396-111753	Hela-S3	cervix:	n/a	chr3:111564-111575 chr3:111563-111574
21	CEBPB	chr3:104930-105426	HepG2	liver:	n/a	chr3:105311-105324
22	CEBPB	chr3:99766-99979	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr3:111431-111722	HepG2	liver:	n/a	chr3:111564-111575 chr3:111563-111574
24	CEBPB	chr3:157534-157826	IMR90	lung:	n/a	chr3:157561-157572 chr3:157692-157703
25	CEBPB	chr3:85051-85419	HepG2	liver:	n/a	chr3:85237-85250 chr3:85237-85248 chr3:85092-85105
26	CEBPB	chr3:86201-86402	HepG2	liver:	n/a	n/a
27	CEBPB	chr3:86185-86385	IMR90	lung:	n/a	n/a
28	CEBPB	chr3:162469-162671	A549	lung:	n/a	n/a
29	CEBPB	chr3:169853-170053	A549	lung:	n/a	n/a
30	CEBPB	chr3:157527-157838	HepG2	liver:	n/a	chr3:157561-157572 chr3:157692-157703
31	CEBPD	chr3:85139-85291	HepG2	liver:	n/a	chr3:85238-85249
32	CHD2	chr3:166635-166663	GM12878	blood:	n/a	n/a
33	CHD2	chr3:105065-105090	HepG2	liver:	n/a	n/a
34	CTCF	chr3:108256-108265	GM20000	blood:	n/a	n/a
35	CTCF	chr3:82200-82350	GM12873	blood:	n/a	n/a
36	CTCF	chr3:82200-82350	GM06990	blood:	n/a	n/a
37	CTCF	chr3:96080-96230	GM12868	blood:	n/a	n/a
38	CTCF	chr3:84620-84770	HRE	kidney:	n/a	chr3:84742-84763 chr3:84740-84758 chr3:84743-84756
39	CTCF	chr3:84660-84810	GM12868	blood:	n/a	chr3:84742-84763 chr3:84740-84758 chr3:84743-84756
40	CTCF	chr3:108297-108309	GM20000	blood:	n/a	n/a
41	CTCF	chr3:178240-178390	HepG2	liver:	n/a	n/a
42	CTCF	chr3:84600-84750	HAc	cerebellar:	n/a	n/a
43	CTCF	chr3:96040-96190	GM12870	blood:	n/a	n/a
44	CTCF	chr3:84558-84919	A549	lung:	n/a	chr3:84742-84763 chr3:84740-84758 chr3:84743-84756
45	CTCF	chr3:82180-82330	RPTEC	kidney:	n/a	n/a
46	CTCF	chr3:84640-84790	SK-N-SH_RA	brain:	n/a	chr3:84742-84763 chr3:84740-84758 chr3:84743-84756
47	CTCF	chr3:108292-108360	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr3:84660-84810	GM12869	blood:	n/a	chr3:84742-84763 chr3:84740-84758 chr3:84743-84756
49	CTCF	chr3:96140-96290	HAc	cerebellar:	n/a	n/a
50	CTCF	chr3:82200-82350	GM12874	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:114243-114293	AoSMC	blood vessel:	n/a
2	chr3:153242-153292	CMK	blood:	n/a
3	chr3:114243-114293	HCM	heart:	n/a
4	chr3:153242-153292	SK-N-MC	brain:	n/a
5	chr3:114243-114293	HCPEpiC	choroid plexus:	n/a
6	chr3:153242-153292	MCF-7	breast:	n/a
7	chr3:114243-114293	HL-60	blood:	n/a
8	chr3:153242-153292	HEK293	kidney:	embryo
9	chr3:153242-153292	NB4	blood:	n/a
10	chr3:153242-153292	Hela-S3	cervix:	n/a
11	chr3:153242-153292	HEEpiC	esophagus:	n/a
12	chr3:153242-153292	SKMC	muscle:	n/a
13	chr3:153242-153292	PrEC	prostate:	n/a
14	chr3:153242-153292	HAEpiC	amniotic membrane:	n/a
15	chr3:114243-114293	AG04449	skin:	fetal
16	chr3:153242-153292	GM12892	blood:	n/a
17	chr3:153242-153292	PFSK-1	brain:	n/a
18	chr3:114243-114293	NT2-D1	testis:	n/a
19	chr3:153242-153292	AG04449	skin:	fetal
20	chr3:153242-153292	SK-N-SH	brain:	n/a
21	chr3:114243-114293	LNCaP	prostate:	n/a
22	chr3:114243-114293	GM12891	blood:	n/a
23	chr3:153242-153292	H1-hESC	embryonic stem cell:	embryo
24	chr3:114243-114293	BE2_C	brain:	n/a
25	chr3:153242-153292	HPAEpiC	pulmonary alveolar:	n/a
26	chr3:114243-114293	Caco-2	colon:	n/a
27	chr3:114243-114293	GM19239	blood:	n/a
28	chr3:114243-114293	U87	brain:	n/a
29	chr3:114243-114293	HRPEpiC	eye:	n/a
30	chr3:153242-153292	GM12878	blood:	n/a
31	chr3:153242-153292	AG10803	skin:	n/a
32	chr3:153242-153292	HCM	heart:	n/a
33	chr3:114243-114293	NB4	blood:	n/a
34	chr3:114243-114293	GM06990	blood:	n/a
35	chr3:153242-153292	BE2_C	brain:	n/a
36	chr3:114243-114293	SK-N-SH_RA	brain:	n/a
37	chr3:153242-153292	RPTEC	kidney:	n/a
38	chr3:114243-114293	AG09319	gingival:	n/a
39	chr3:153242-153292	AG09319	gingival:	n/a
40	chr3:114243-114293	PANC-1	pancreas:	n/a
41	chr3:114243-114293	HPAEpiC	pulmonary alveolar:	n/a
42	chr3:114243-114293	AG09309	skin:	n/a
43	chr3:114243-114293	Hela-S3	cervix:	n/a
44	chr3:153242-153292	SK-N-SH_RA	brain:	n/a
45	chr3:114243-114293	HRE	kidney:	n/a
46	chr3:114243-114293	ECC-1	luminal epithelium:	n/a
47	chr3:153242-153292	AoSMC	blood vessel:	n/a
48	chr3:153242-153292	HepG2	liver:	n/a
49	chr3:114243-114293	CMK	blood:	n/a
50	chr3:153242-153292	HNPCEpiC	eye:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:84119..86199-chr3:87586..89599,2	K562	blood:
2	chr3:169328..170327-chr3:184848..185564,2	MCF-7	breast:
3	chr3:84468..85168-chr3:395782..396503,2	MCF-7	breast:
4	chr11:73160067..73160822-chr3:118894..119482,2	MCF-7	breast:
5	chr3:131415..134151-chr3:136022..137906,2	MCF-7	breast:
6	chr3:84119..86199-chr3:87586..89599,2	K562	blood:
7	chr3:169328..170327-chr3:184848..185564,2	MCF-7	breast:
8	chr3:163984..165661-chr3:172610..174560,2	K562	blood:
9	chr3:84540..85233-chr3:395143..396665,5	MCF-7	breast:
10	chr3:131415..134151-chr3:136022..137906,2	MCF-7	breast:
11	chr3:86365..87356-chr3:395941..396726,2	MCF-7	breast:
12	chr3:84682..85249-chr3:418773..419384,2	MCF-7	breast:
13	chr14:56081549..56082133-chr3:97763..98653,2	MCF-7	breast:
14	chr3:163984..165661-chr3:172610..174560,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL5RA-16	chr3:153782-154143	NONHSAT087554
2	lnc-IL5RA-7	chr3:95976-96029	XLOC_003014
3	lnc-CHL1-1	chr3:109310-109435	XLOC_002563
4	lnc-CHL1-1	chr3:109008-109196	XLOC_002563
5	lnc-CHL1-1	chr3:111531-111980	XLOC_002563
6	lnc-CHL1-1	chr3:95888-96275	XLOC_002563
7	lnc-IL5RA-16	chr3:172879-173007	NONHSAT087554
8	lnc-IL5RA-17	chr3:147014-147245	l_2301_chr3:147013-148034_heart
9	lnc-IL5RA-16	chr3:153927-154143	NONHSAT087555
10	lnc-CHL1-4	chr3:86531-87048	l_2300_chr3:84309-87048_testes
11	lnc-CHL1-1	chr3:95888-96275	XLOC_002563
12	lnc-CHL1-4	chr3:84310-84695	l_2300_chr3:84309-87048_testes
13	lnc-IL5RA-17	chr3:147879-148034	l_2301_chr3:147013-148034_heart
14	lnc-IL5RA-16	chr3:157540-157620	NONHSAT087554
15	lnc-CHL1-1	chr3:109008-109196	XLOC_002563
16	lnc-CHL1-1	chr3:109310-109695	XLOC_002563
17	lnc-IL5RA-16	chr3:157540-157624	NONHSAT087555
18	lnc-CHL1-1	chr3:111531-111663	XLOC_002563
19	lnc-CHL1-1	chr3:109401-109695	XLOC_002563
20	lnc-IL5RA-7	chr3:95031-95375	XLOC_003014

No data

Variant related genes	Relation type
ENSG00000224918	TF binding region
ENSG00000224918	CpG island

Extended variants
information (count: 3861 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3861 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533573840	chr3:84020-84021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548556509	chr3:84034-84035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184333600	chr3:84050-84051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs5001134	chr3:84054-84055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs5001133	chr3:84060-84061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200257115	chr3:84061-84062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs5001132	chr3:84064-84065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs58721708	chr3:84088-84089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs58759780	chr3:84092-84093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs35353500	chr3:84097-84098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201480653	chr3:84098-84099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538136781	chr3:84123-84124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188024273	chr3:84152-84153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143262540	chr3:84163-84164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539564833	chr3:84170-84171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558254166	chr3:84202-84203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573353535	chr3:84203-84204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540665344	chr3:84216-84217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs115968896	chr3:84220-84221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113784275	chr3:84297-84298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs376951330	chr3:84299-84300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370406035	chr3:84309-84310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs17075489	chr3:84316-84317	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs374939005	chr3:84342-84343	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs562958343	chr3:84350-84351	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs533544632	chr3:84381-84382	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs146227594	chr3:84385-84386	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs557070854	chr3:84421-84422	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs559853462	chr3:84431-84432	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs527373840	chr3:84436-84437	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs7615980	chr3:84486-84487	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs569709057	chr3:84493-84494	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs184093982	chr3:84522-84523	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs188816350	chr3:84523-84524	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs537251404	chr3:84559-84560	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs571373652	chr3:84575-84576	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs538855433	chr3:84578-84579	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs542016157	chr3:84588-84589	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs374934017	chr3:84589-84590	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs139071047	chr3:84596-84597	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs377504883	chr3:84665-84666	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs567017833	chr3:84675-84676	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs534238793	chr3:84687-84688	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs558543512	chr3:84700-84701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573945919	chr3:84715-84716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs57680071	chr3:84741-84742	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs556846343	chr3:84756-84757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144901807	chr3:84777-84778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181583432	chr3:84784-84785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549785487	chr3:84803-84804	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Ependymoma	20639864	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
early-passage human iPS cells	21368824	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22495311	CNVD
Autism	20685689	CNVD

Chromatin state (count:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:84000-84400	Enhancers	Fetal Brain Male	brain
2	chr3:84200-84600	Enhancers	Fetal Brain Female	brain
3	chr3:84400-85400	Weak transcription	Fetal Brain Male	brain
4	chr3:84800-85200	Enhancers	Brain Germinal Matrix	brain
5	chr3:84800-85200	Active TSS	Fetal Brain Female	brain
6	chr3:84800-85400	Enhancers	Liver	Liver
7	chr3:85200-85800	Enhancers	Fetal Brain Female	brain
8	chr3:85200-85800	Enhancers	HepG2	liver
9	chr3:85400-86000	Flanking Active TSS	Liver	Liver
10	chr3:85400-86200	Enhancers	Fetal Brain Male	brain
11	chr3:85600-85800	Flanking Active TSS	Gastric	stomach
12	chr3:85600-86000	Bivalent Enhancer	Fetal Kidney	kidney
13	chr3:85800-86000	ZNF genes & repeats	Gastric	stomach
14	chr3:85800-86200	Flanking Active TSS	HepG2	liver
15	chr3:86000-86800	Enhancers	Liver	Liver
16	chr3:86200-86800	Enhancers	HepG2	liver
17	chr3:86800-87800	Weak transcription	HepG2	liver
18	chr3:88000-88200	Enhancers	HepG2	liver
19	chr3:88000-89000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr3:88000-90400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr3:88200-89800	Enhancers	Adipose Nuclei	Adipose
22	chr3:95000-95600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr3:95000-96600	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr3:95600-104600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr3:97400-97600	Enhancers	Brain Hippocampus Middle	brain
26	chr3:97600-98000	Enhancers	Fetal Brain Male	brain
27	chr3:97800-98200	Active TSS	Fetal Brain Female	brain
28	chr3:98000-98600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr3:98000-104800	Weak transcription	Fetal Brain Male	brain
30	chr3:98200-98600	Enhancers	Fetal Brain Female	brain
31	chr3:103600-104400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr3:103800-104200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:104200-104400	Enhancers	Gastric	stomach
34	chr3:104400-104800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr3:104400-105000	Weak transcription	Gastric	stomach
36	chr3:104400-105400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr3:104400-105400	Enhancers	HepG2	liver
38	chr3:104400-105600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr3:104600-104800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr3:104600-104800	Enhancers	Adipose Nuclei	Adipose
41	chr3:104600-104800	Enhancers	Brain Substantia Nigra	brain
42	chr3:104600-105600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr3:104600-105600	Enhancers	Fetal Lung	lung
44	chr3:104800-105000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr3:104800-105000	Active TSS	Brain Germinal Matrix	brain
46	chr3:104800-105000	Enhancers	Stomach Mucosa	stomach
47	chr3:104800-105200	Enhancers	Fetal Brain Male	brain
48	chr3:104800-105400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr3:104800-105400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr3:104800-105400	Flanking Active TSS	Adipose Nuclei	Adipose

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