Variant report

Variant	nsv1004215
Chromosome Location	chr3:86204-172906
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:275)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:275 , 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	chr3:104725-105176	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:86873-86900	HepG2	liver:	n/a	n/a
3	ATF1	chr3:128118-128267	K562	blood:	n/a	n/a
4	BACH1	chr3:165624-165661	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr3:166561-166841	GM12878	blood:	n/a	chr3:166679-166690 chr3:166653-166662
6	BATF	chr3:166548-166773	GM12878	blood:	n/a	chr3:166679-166690 chr3:166653-166662
7	BHLHE40	chr3:152996-153196	A549	lung:	n/a	n/a
8	BHLHE40	chr3:150637-150664	A549	lung:	n/a	n/a
9	CEBPB	chr3:130437-130508	A549	lung:	n/a	n/a
10	CEBPB	chr3:111396-111753	Hela-S3	cervix:	n/a	chr3:111564-111575 chr3:111563-111574
11	CEBPB	chr3:99766-99979	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr3:137940-138307	HepG2	liver:	n/a	chr3:138113-138124 chr3:138111-138128
13	CEBPB	chr3:157527-157838	HepG2	liver:	n/a	chr3:157561-157572 chr3:157692-157703
14	CEBPB	chr3:99754-100055	HepG2	liver:	n/a	n/a
15	CEBPB	chr3:157534-157826	IMR90	lung:	n/a	chr3:157561-157572 chr3:157692-157703
16	CEBPB	chr3:162469-162671	A549	lung:	n/a	n/a
17	CEBPB	chr3:169853-170053	A549	lung:	n/a	n/a
18	CEBPB	chr3:110019-110065	A549	lung:	n/a	n/a
19	CEBPB	chr3:104930-105426	HepG2	liver:	n/a	chr3:105311-105324
20	CEBPB	chr3:86201-86402	HepG2	liver:	n/a	n/a
21	CEBPB	chr3:88330-88522	HepG2	liver:	n/a	chr3:88338-88349 chr3:88336-88349 chr3:88336-88347
22	CEBPB	chr3:111431-111722	HepG2	liver:	n/a	chr3:111564-111575 chr3:111563-111574
23	CEBPB	chr3:86185-86385	IMR90	lung:	n/a	n/a
24	CHD2	chr3:166635-166663	GM12878	blood:	n/a	n/a
25	CHD2	chr3:105065-105090	HepG2	liver:	n/a	n/a
26	CTCF	chr3:96060-96210	HMF	breast:	n/a	n/a
27	CTCF	chr3:95980-96130	GM12872	blood:	n/a	n/a
28	CTCF	chr3:96000-96150	GM12864	blood:	n/a	n/a
29	CTCF	chr3:108277-108402	LNCaP	prostate:	n/a	n/a
30	CTCF	chr3:108234-108390	MCF-7	breast:	n/a	n/a
31	CTCF	chr3:96080-96230	GM12875	blood:	n/a	n/a
32	CTCF	chr3:88280-88430	MCF-7	breast:	n/a	n/a
33	CTCF	chr3:128198-128255	GM19239	blood:	n/a	n/a
34	CTCF	chr3:96060-96210	GM12866	blood:	n/a	n/a
35	CTCF	chr3:108309-108354	GM12878	blood:	n/a	n/a
36	CTCF	chr3:96140-96290	HAc	cerebellar:	n/a	n/a
37	CTCF	chr3:165953-165988	GM13976	blood:	n/a	n/a
38	CTCF	chr3:96060-96210	GM12865	blood:	n/a	n/a
39	CTCF	chr3:96040-96190	GM12873	blood:	n/a	n/a
40	CTCF	chr3:108215-108426	MCF-7	breast:	n/a	n/a
41	CTCF	chr3:155789-155867	Lung_OC	lung:	n/a	n/a
42	CTCF	chr3:145560-145710	GM12872	blood:	n/a	n/a
43	CTCF	chr3:97159-97300	MCF-7	breast:	n/a	n/a
44	CTCF	chr3:96000-96150	HEK293	kidney:	n/a	n/a
45	CTCF	chr3:96040-96190	GM12867	blood:	n/a	n/a
46	CTCF	chr3:96080-96230	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:96060-96210	SAEC	small airway:	n/a	n/a
48	CTCF	chr3:96040-96190	NHEK	skin:	n/a	n/a
49	CTCF	chr3:96040-96190	GM12869	blood:	n/a	n/a
50	CTCF	chr3:96040-96190	GM12864	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	HIPEpiC	eye:	n/a
2	chr3:153242-153292	BE2_C	brain:	n/a
3	chr3:153242-153292	SK-N-SH	brain:	n/a
4	chr3:153242-153292	AG04449	skin:	fetal
5	chr3:114243-114293	Jurkat	blood:	n/a
6	chr3:114243-114293	AoSMC	blood vessel:	n/a
7	chr3:153242-153292	GM12892	blood:	n/a
8	chr3:114243-114293	GM12892	blood:	n/a
9	chr3:153242-153292	AG10803	skin:	n/a
10	chr3:114243-114293	T-47D	breast:	n/a
11	chr3:153242-153292	PrEC	prostate:	n/a
12	chr3:153242-153292	AG04450	lung:	fetal
13	chr3:114243-114293	HCM	heart:	n/a
14	chr3:153242-153292	NH-A	brain:	n/a
15	chr3:114243-114293	ProgFib	skin:	n/a
16	chr3:153242-153292	NT2-D1	testis:	n/a
17	chr3:114243-114293	PANC-1	pancreas:	n/a
18	chr3:114243-114293	HCT-116	colon:	n/a
19	chr3:153242-153292	ECC-1	luminal epithelium:	n/a
20	chr3:114243-114293	U87	brain:	n/a
21	chr3:153242-153292	H1-hESC	embryonic stem cell:	embryo
22	chr3:114243-114293	HAEpiC	amniotic membrane:	n/a
23	chr3:114243-114293	HL-60	blood:	n/a
24	chr3:153242-153292	HIPEpiC	eye:	n/a
25	chr3:153242-153292	HCF	heart:	n/a
26	chr3:153242-153292	Jurkat	blood:	n/a
27	chr3:114243-114293	RPTEC	kidney:	n/a
28	chr3:153242-153292	LNCaP	prostate:	n/a
29	chr3:114243-114293	HRPEpiC	eye:	n/a
30	chr3:114243-114293	HUVEC	blood vessel:	n/a
31	chr3:153242-153292	MCF10A-Er-Src	breast:	n/a
32	chr3:153242-153292	PFSK-1	brain:	n/a
33	chr3:153242-153292	AoSMC	blood vessel:	n/a
34	chr3:114243-114293	SAEC	small airway:	n/a
35	chr3:153242-153292	AG09319	gingival:	n/a
36	chr3:153242-153292	MCF-7	breast:	n/a
37	chr3:114243-114293	AG09309	skin:	n/a
38	chr3:153242-153292	BJ	skin:	n/a
39	chr3:114243-114293	NB4	blood:	n/a
40	chr3:153242-153292	AG09309	skin:	n/a
41	chr3:114243-114293	GM19239	blood:	n/a
42	chr3:153242-153292	A549	lung:	n/a
43	chr3:114243-114293	HMEC	breast:	n/a
44	chr3:153242-153292	HL-60	blood:	n/a
45	chr3:153242-153292	HMEC	breast:	n/a
46	chr3:153242-153292	T-47D	breast:	n/a
47	chr3:114243-114293	A549	lung:	n/a
48	chr3:153242-153292	SK-N-MC	brain:	n/a
49	chr3:114243-114293	HEEpiC	esophagus:	n/a
50	chr3:114243-114293	H1-hESC	embryonic stem cell:	embryo

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:169328..170327-chr3:184848..185564,2	MCF-7	breast:
2	chr3:84119..86199-chr3:87586..89599,2	K562	blood:
3	chr14:56081549..56082133-chr3:97763..98653,2	MCF-7	breast:
4	chr3:86365..87356-chr3:395941..396726,2	MCF-7	breast:
5	chr3:131415..134151-chr3:136022..137906,2	MCF-7	breast:
6	chr3:163984..165661-chr3:172610..174560,2	K562	blood:
7	chr3:131415..134151-chr3:136022..137906,2	MCF-7	breast:
8	chr3:163984..165661-chr3:172610..174560,2	K562	blood:
9	chr11:73160067..73160822-chr3:118894..119482,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 3610 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3610 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1949341	chr3:86204-86205	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376446869	chr3:86205-86206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs144189523	chr3:86248-86249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs77792366	chr3:86256-86257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559390901	chr3:86265-86266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187205344	chr3:86298-86299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114084337	chr3:86319-86320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191930154	chr3:86344-86345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184182218	chr3:86431-86432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530589966	chr3:86461-86462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569355216	chr3:86464-86465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545954952	chr3:86518-86519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187527917	chr3:86520-86521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs373853956	chr3:86538-86539	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs532459908	chr3:86548-86549	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs138666658	chr3:86572-86573	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs191366226	chr3:86619-86620	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs13087728	chr3:86625-86626	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs548573300	chr3:86632-86633	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs146209326	chr3:86648-86649	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs75837458	chr3:86669-86670	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs570580977	chr3:86676-86677	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs1516324	chr3:86691-86692	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs534913468	chr3:86696-86697	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs1516325	chr3:86722-86723	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs559096202	chr3:86726-86727	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs374688574	chr3:86773-86774	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs570605534	chr3:86776-86777	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs1516326	chr3:86801-86802	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs182403057	chr3:86846-86847	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs187038118	chr3:86849-86850	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs574444943	chr3:86866-86867	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs1516327	chr3:86871-86872	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs111572308	chr3:86882-86883	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs542131617	chr3:86887-86888	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs185165120	chr3:86891-86892	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs190409823	chr3:86935-86936	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs142564328	chr3:86961-86962	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs563936560	chr3:86993-86994	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs369987169	chr3:86995-86996	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs193075999	chr3:87000-87001	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs556755501	chr3:87010-87011	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs185809704	chr3:87034-87035	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs530067812	chr3:87045-87046	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs575316755	chr3:87066-87067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188176262	chr3:87115-87116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531231770	chr3:87134-87135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529496360	chr3:87139-87140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78473435	chr3:87145-87146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201336541	chr3:87150-87151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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

Chromatin state (count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:86000-86800	Enhancers	Liver	Liver
2	chr3:86200-86800	Enhancers	HepG2	liver
3	chr3:86800-87800	Weak transcription	HepG2	liver
4	chr3:88000-88200	Enhancers	HepG2	liver
5	chr3:88000-89000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr3:88000-90400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr3:88200-89800	Enhancers	Adipose Nuclei	Adipose
8	chr3:95000-95600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr3:95000-96600	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr3:95600-104600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr3:97400-97600	Enhancers	Brain Hippocampus Middle	brain
12	chr3:97600-98000	Enhancers	Fetal Brain Male	brain
13	chr3:97800-98200	Active TSS	Fetal Brain Female	brain
14	chr3:98000-98600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr3:98000-104800	Weak transcription	Fetal Brain Male	brain
16	chr3:98200-98600	Enhancers	Fetal Brain Female	brain
17	chr3:103600-104400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr3:103800-104200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:104200-104400	Enhancers	Gastric	stomach
20	chr3:104400-104800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr3:104400-105000	Weak transcription	Gastric	stomach
22	chr3:104400-105400	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr3:104400-105400	Enhancers	HepG2	liver
24	chr3:104400-105600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr3:104600-104800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr3:104600-104800	Enhancers	Adipose Nuclei	Adipose
27	chr3:104600-104800	Enhancers	Brain Substantia Nigra	brain
28	chr3:104600-105600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr3:104600-105600	Enhancers	Fetal Lung	lung
30	chr3:104800-105000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr3:104800-105000	Active TSS	Brain Germinal Matrix	brain
32	chr3:104800-105000	Enhancers	Stomach Mucosa	stomach
33	chr3:104800-105200	Enhancers	Fetal Brain Male	brain
34	chr3:104800-105400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr3:104800-105400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr3:104800-105400	Flanking Active TSS	Adipose Nuclei	Adipose
37	chr3:104800-105400	Enhancers	Brain Angular Gyrus	brain
38	chr3:104800-105400	Active TSS	Brain Inferior Temporal Lobe	brain
39	chr3:104800-105600	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr3:104800-105600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr3:104800-105600	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr3:104800-105600	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr3:104800-105600	Enhancers	Brain Hippocampus Middle	brain
44	chr3:104800-105600	Flanking Active TSS	Brain Substantia Nigra	brain
45	chr3:104800-105600	Enhancers	Fetal Brain Female	brain
46	chr3:104800-105600	Enhancers	Psoas Muscle	Psoas
47	chr3:104800-105800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr3:105000-105200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr3:105000-105200	Enhancers	Liver	Liver
50	chr3:105000-105400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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