Variant report

Variant	esv3507650
Chromosome Location	chr3:88348625-88460502
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:250)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:250 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:88434387-88434629	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr3:88438892-88438979	K562	blood:	n/a	n/a
3	CEBPB	chr3:88434165-88434583	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr3:88370833-88371190	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr3:88396623-88396919	HepG2	liver:	n/a	chr3:88396754-88396765
6	CEBPB	chr3:88396713-88396914	Hela-S3	cervix:	n/a	chr3:88396754-88396765
7	CEBPB	chr3:88378823-88378968	HepG2	liver:	n/a	chr3:88378941-88378952
8	CEBPB	chr3:88427165-88427365	H1-hESC	embryonic stem cell:	n/a	chr3:88427292-88427305
9	CEBPB	chr3:88396706-88396908	A549	lung:	n/a	chr3:88396754-88396765
10	CEBPB	chr3:88369030-88369230	A549	lung:	n/a	n/a
11	CEBPB	chr3:88378808-88379094	IMR90	lung:	n/a	chr3:88378941-88378952
12	CHD1	chr3:88357026-88357066	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr3:88366689-88366822	GM12891	blood:	n/a	n/a
14	CTCF	chr3:88396440-88396590	RPTEC	kidney:	n/a	n/a
15	CTCF	chr3:88383460-88383610	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr3:88428300-88428450	MCF-7	breast:	n/a	chr3:88428421-88428434 chr3:88428419-88428437 chr3:88428414-88428435
17	CTCF	chr3:88412093-88412153	MCF-7	breast:	n/a	n/a
18	CTCF	chr3:88366736-88366740	GM12878	blood:	n/a	n/a
19	CTCF	chr3:88366654-88366767	MCF-7	breast:	n/a	n/a
20	CTCF	chr3:88391615-88391656	HepG2	liver:	n/a	n/a
21	CTCF	chr3:88366668-88366851	MCF-7	breast:	n/a	n/a
22	CTCF	chr3:88354695-88354777	LNCaP	prostate:	n/a	n/a
23	CTCF	chr3:88366680-88366797	MCF-7	breast:	n/a	n/a
24	CTCF	chr3:88366721-88366814	GM13977	blood:	n/a	n/a
25	CTCF	chr3:88366714-88366804	GM19238	blood:	n/a	n/a
26	CTCF	chr3:88366675-88366780	MCF-7	breast:	n/a	n/a
27	CTCF	chr3:88356440-88356590	AG09319	gingival:	n/a	n/a
28	CTCF	chr3:88366660-88366810	HepG2	liver:	n/a	n/a
29	CTCF	chr3:88449307-88449344	GM20000	blood:	n/a	n/a
30	CTCF	chr3:88366722-88366803	HepG2	liver:	n/a	n/a
31	CTCF	chr3:88428358-88428558	GM12878	blood:	n/a	chr3:88428421-88428434 chr3:88428419-88428437 chr3:88428414-88428435
32	CTCF	chr3:88351660-88351810	GM12870	blood:	n/a	n/a
33	CTCF	chr3:88372984-88373041	MCF-7	breast:	n/a	n/a
34	CTCF	chr3:88366639-88366827	A549	lung:	n/a	n/a
35	CTCF	chr3:88383440-88383590	HCM	heart:	n/a	n/a
36	CTCF	chr3:88366673-88366774	MCF-7	breast:	n/a	n/a
37	CTCF	chr3:88428380-88428530	GM12865	blood:	n/a	chr3:88428421-88428434 chr3:88428419-88428437 chr3:88428414-88428435
38	CTCF	chr3:88366679-88366802	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr3:88366726-88366760	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr3:88366675-88366727	GM12878	blood:	n/a	n/a
41	CTCF	chr3:88366706-88366789	ProgFib	skin:	n/a	n/a
42	CTCF	chr3:88366691-88366812	HepG2	liver:	n/a	n/a
43	CTCF	chr3:88366691-88366794	GM12892	blood:	n/a	n/a
44	CTCF	chr3:88366712-88366739	Gliobla	brain:	n/a	n/a
45	E2F4	chr3:88398054-88398133	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr3:88412425-88412431	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr3:88371620-88371836	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr3:88349180-88349380	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr3:88396640-88396749	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr3:88361780-88361868	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:88352696-88352746	AG09309	skin:	n/a
2	chr3:88352696-88352746	HMEC	breast:	n/a
3	chr3:88352696-88352746	AG04449	skin:	fetal
4	chr3:88352696-88352746	PFSK-1	brain:	n/a
5	chr3:88352696-88352746	RPTEC	kidney:	n/a
6	chr3:88352696-88352746	AG10803	skin:	n/a
7	chr3:88352696-88352746	HCT-116	colon:	n/a
8	chr3:88352696-88352746	HAEpiC	amniotic membrane:	n/a
9	chr3:88352696-88352746	AG04450	lung:	fetal
10	chr3:88352696-88352746	HRPEpiC	eye:	n/a
11	chr3:88352696-88352746	IMR90	lung:	fetal
12	chr3:88352696-88352746	GM19239	blood:	n/a
13	chr3:88352696-88352746	HEK293	kidney:	embryo
14	chr3:88352696-88352746	NHDF-neo	bronchial:	n/a
15	chr3:88352696-88352746	SK-N-MC	brain:	n/a
16	chr3:88352696-88352746	BJ	skin:	n/a
17	chr3:88352696-88352746	LNCaP	prostate:	n/a
18	chr3:88352696-88352746	HRE	kidney:	n/a
19	chr3:88352696-88352746	HRCEpiC	kidney:	n/a
20	chr3:88352696-88352746	A549	lung:	n/a
21	chr3:88352696-88352746	T-47D	breast:	n/a
22	chr3:88352696-88352746	HL-60	blood:	n/a
23	chr3:88352696-88352746	SKMC	muscle:	n/a
24	chr3:88352696-88352746	AG09319	gingival:	n/a
25	chr3:88352696-88352746	Hepatocyte	liver:	n/a
26	chr3:88352696-88352746	GM06990	blood:	n/a
27	chr3:88352696-88352746	NT2-D1	testis:	n/a
28	chr3:88352696-88352746	HCF	heart:	n/a
29	chr3:88352696-88352746	ovcar-3	ovarian:	n/a
30	chr3:88352696-88352746	HUVEC	blood vessel:	n/a
31	chr3:88352696-88352746	H1-hESC	embryonic stem cell:	embryo
32	chr3:88352696-88352746	NB4	blood:	n/a
33	chr3:88352696-88352746	SK-N-SH_RA	brain:	n/a
34	chr3:88352696-88352746	MCF10A-Er-Src	breast:	n/a
35	chr3:88352696-88352746	HEEpiC	esophagus:	n/a
36	chr3:88352696-88352746	ECC-1	luminal epithelium:	n/a
37	chr3:88352696-88352746	CMK	blood:	n/a
38	chr3:88352696-88352746	PrEC	prostate:	n/a
39	chr3:88352696-88352746	SK-N-SH	brain:	n/a
40	chr3:88352696-88352746	BE2_C	brain:	n/a
41	chr3:88352696-88352746	HepG2	liver:	n/a
42	chr3:88352696-88352746	HIPEpiC	eye:	n/a
43	chr3:88352696-88352746	AoSMC	blood vessel:	n/a
44	chr3:88352696-88352746	HNPCEpiC	eye:	n/a
45	chr3:88352696-88352746	U87	brain:	n/a
46	chr3:88352696-88352746	PANC-1	pancreas:	n/a
47	chr3:88352696-88352746	MCF-7	breast:	n/a
48	chr3:88352696-88352746	Caco-2	colon:	n/a
49	chr3:88352696-88352746	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:88352696-88352746	Jurkat	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:88377277..88378950-chr3:88387834..88390220,2	MCF-7	breast:
2	chr3:88356773..88358838-chr3:88359447..88361325,2	K562	blood:
3	chr3:88348034..88350434-chr3:88355298..88358101,2	MCF-7	breast:
4	chr3:88348034..88350434-chr3:88355298..88358101,2	MCF-7	breast:
5	chr3:88443258..88445795-chr3:88448224..88450369,2	K562	blood:
6	chr3:88356773..88358838-chr3:88359447..88361325,2	K562	blood:
7	chr3:88377277..88378950-chr3:88387834..88390220,2	MCF-7	breast:
8	chr3:88443258..88445795-chr3:88448224..88450369,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C3orf38-2	chr3:88387572-88387793	NONHSAT090703
2	lnc-C3orf38-2	chr3:88431734-88431938	NONHSAT090703
3	lnc-C3orf38-2	chr3:88387573-88387793	XLOC_002727
4	lnc-C3orf38-2	chr3:88392302-88392435	XLOC_002727
5	lnc-C3orf38-2	chr3:88392301-88392435	NONHSAT090703
6	lnc-C3orf38-2	chr3:88387591-88387793	XLOC_002727
7	lnc-C3orf38-2	chr3:88418571-88418634	XLOC_002727
8	lnc-C3orf38-2	chr3:88387573-88387793	XLOC_002727
9	lnc-C3orf38-2	chr3:88431735-88431938	XLOC_002727
10	lnc-C3orf38-2	chr3:88431735-88431938	XLOC_002727

No data

Variant related genes	Relation type
ABCF2P1	TF binding region
ABCF2P1	CpG island
E2F8	miRNA target sites
BLCAP	miRNA target sites
HCCS	miRNA target sites
VLDLR	miRNA target sites
ECE1	miRNA target sites

Extended variants
information (count: 1303 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1303 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565919696	chr3:88348627-88348628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373749085	chr3:88348630-88348631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs377581725	chr3:88348634-88348635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10560482	chr3:88348635-88348636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140156646	chr3:88348638-88348639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557807074	chr3:88348646-88348647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs74267747	chr3:88348665-88348666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs71131574	chr3:88348668-88348669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200805266	chr3:88348681-88348682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140541692	chr3:88348682-88348683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201824783	chr3:88348683-88348684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575956330	chr3:88348688-88348689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572029846	chr3:88348693-88348694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543445198	chr3:88348700-88348701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369997509	chr3:88348706-88348707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555399989	chr3:88348729-88348730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140709439	chr3:88348758-88348759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184344776	chr3:88348763-88348764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560552228	chr3:88348776-88348777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548151558	chr3:88348786-88348787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571593971	chr3:88348804-88348805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs6776335	chr3:88348808-88348809	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs143834841	chr3:88348813-88348814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564566433	chr3:88348843-88348844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549633235	chr3:88348850-88348851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188403206	chr3:88348853-88348854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181882917	chr3:88348861-88348862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369264928	chr3:88348877-88348878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148080057	chr3:88348920-88348921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75971332	chr3:88348937-88348938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184778193	chr3:88348970-88348971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189552040	chr3:88348990-88348991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375962791	chr3:88348991-88348992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539509391	chr3:88349001-88349002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs56999350	chr3:88349027-88349028	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs537122076	chr3:88349040-88349041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573331317	chr3:88349086-88349087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555433151	chr3:88349095-88349096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373026132	chr3:88349103-88349104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78298002	chr3:88349137-88349138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534936272	chr3:88349146-88349147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553255192	chr3:88349148-88349149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs80057962	chr3:88349246-88349247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545231743	chr3:88349331-88349332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555674312	chr3:88349398-88349399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7637010	chr3:88349410-88349411	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs576511746	chr3:88349411-88349412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141849601	chr3:88349426-88349427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543751463	chr3:88349453-88349454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7634615	chr3:88349484-88349485	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:72)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
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
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Soft tissue tumor	16732325	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22522925	CNVD
Lung cancer	19547694	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:88347800-88350000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr3:88348600-88350000	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr3:88350000-88351000	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr3:88350000-88352000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr3:88351000-88358600	Weak transcription	Right Atrium	heart
6	chr3:88352200-88352800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr3:88355200-88360000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr3:88355400-88357400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr3:88355600-88357000	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr3:88355600-88359000	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr3:88355600-88359800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr3:88355800-88359400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr3:88356000-88356200	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr3:88356000-88356200	Enhancers	H1 Cell Line	embryonic stem cell
15	chr3:88356200-88356800	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr3:88356200-88358400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr3:88356800-88357000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr3:88356800-88357200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr3:88356800-88357200	Enhancers	Brain Germinal Matrix	brain
20	chr3:88356800-88357200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
21	chr3:88356800-88357200	Enhancers	Pancreas	Pancrea
22	chr3:88356800-88357600	Enhancers	H1 Cell Line	embryonic stem cell
23	chr3:88357000-88357200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr3:88357000-88357400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
25	chr3:88357000-88357800	Enhancers	H9 Cell Line	embryonic stem cell
26	chr3:88357400-88358000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr3:88357400-88358800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr3:88358000-88359000	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr3:88358400-88359200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr3:88359000-88361000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr3:88360800-88362200	Enhancers	Fetal Lung	lung
32	chr3:88361000-88361200	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr3:88361000-88361800	Enhancers	Fetal Stomach	stomach
34	chr3:88365000-88366000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:88370400-88371200	Enhancers	Hela-S3	cervix
36	chr3:88370600-88370800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr3:88370800-88371000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr3:88371000-88371200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr3:88371200-88371400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr3:88373800-88374800	Enhancers	HepG2	liver
41	chr3:88374000-88374400	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr3:88374200-88374400	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr3:88383600-88384000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr3:88399800-88400200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr3:88405600-88406000	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr3:88406200-88406600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr3:88411200-88411800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr3:88411400-88412200	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr3:88411600-88411800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr3:88418000-88419200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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