Variant report

Variant	nsv876297
Chromosome Location	chr3:516255-597064
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:534692-534822	HepG2	liver:	n/a	n/a
2	BACH1	chr3:516562-516874	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr3:541423-541496	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:577662-577951	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr3:543200-543216	GM12878	blood:	n/a	n/a
6	CEBPB	chr3:575781-576057	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr3:560575-560880	HepG2	liver:	n/a	chr3:560731-560742
8	CEBPB	chr3:534354-535027	Hela-S3	cervix:	n/a	chr3:534767-534778
9	CEBPB	chr3:544942-545225	HepG2	liver:	n/a	chr3:545063-545076 chr3:545064-545075
10	CEBPB	chr3:544910-545217	Hela-S3	cervix:	n/a	chr3:545063-545076 chr3:545064-545075
11	CEBPB	chr3:545112-545116	K562	blood:	n/a	n/a
12	CEBPB	chr3:544911-545212	IMR90	lung:	n/a	chr3:545063-545076 chr3:545064-545075
13	CEBPB	chr3:526407-526558	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr3:544957-545231	H1-hESC	embryonic stem cell:	n/a	chr3:545063-545076 chr3:545064-545075
15	CEBPB	chr3:560581-560882	A549	lung:	n/a	chr3:560731-560742
16	CEBPB	chr3:526427-526685	HepG2	liver:	n/a	n/a
17	CEBPB	chr3:544919-545200	A549	lung:	n/a	chr3:545063-545076 chr3:545064-545075
18	CEBPB	chr3:555007-555386	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:591255-591764	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr3:534600-534964	HepG2	liver:	n/a	chr3:534767-534778
21	CHD2	chr3:577375-577868	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr3:523500-523609	ProgFib	skin:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
23	CTCF	chr3:577614-578025	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr3:577733-577941	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr3:577760-577910	RPTEC	kidney:	n/a	n/a
26	CTCF	chr3:523512-523516	GM10248	blood:	n/a	n/a
27	CTCF	chr3:523374-523745	GM12878	blood:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
28	CTCF	chr3:523480-523630	GM12878	blood:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
29	CTCF	chr3:584280-584430	HVMF	connective:	n/a	n/a
30	CTCF	chr3:523480-523630	WERI-Rb-1	eye:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
31	CTCF	chr3:523420-523570	HEEpiC	esophagus:	n/a	chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
32	CTCF	chr3:523500-523650	GM12868	blood:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
33	CTCF	chr3:523540-523690	NHEK	skin:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
34	CTCF	chr3:523420-523570	GM12865	blood:	n/a	chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
35	CTCF	chr3:532405-532434	K562	blood:	n/a	n/a
36	CTCF	chr3:523480-523630	GM12874	blood:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
37	CTCF	chr3:523519-523624	HepG2	liver:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
38	CTCF	chr3:577720-577870	GM12875	blood:	n/a	n/a
39	CTCF	chr3:523458-523669	GM12878	blood:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
40	CTCF	chr3:523500-523650	HPF	lung:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
41	CTCF	chr3:523440-523590	GM12864	blood:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
42	CTCF	chr3:523540-523690	GM12865	blood:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
43	CTCF	chr3:577780-577930	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr3:523500-523650	RPTEC	kidney:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
45	CTCF	chr3:577787-577953	Lung_OC	lung:	n/a	n/a
46	CTCF	chr3:523380-523530	HCM	heart:	n/a	n/a
47	CTCF	chr3:577740-577890	HAc	cerebellar:	n/a	n/a
48	CTCF	chr3:587000-587150	GM12871	blood:	n/a	n/a
49	CTCF	chr3:523500-523650	HMF	breast:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
50	CTCF	chr3:523453-523652	MCF-7	breast:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:577629-577679	GM12891	blood:	n/a
2	chr3:577629-577679	NH-A	brain:	n/a
3	chr3:577629-577679	Jurkat	blood:	n/a
4	chr3:523375-523425	HRCEpiC	kidney:	n/a
5	chr3:577821-577871	BE2_C	brain:	n/a
6	chr3:577629-577679	A549	lung:	n/a
7	chr3:577964-578014	HMEC	breast:	n/a
8	chr3:577964-578014	CMK	blood:	n/a
9	chr3:523375-523425	CMK	blood:	n/a
10	chr3:577964-578014	ovcar-3	ovarian:	n/a
11	chr3:577821-577871	K562	blood:	n/a
12	chr3:523012-523062	ECC-1	luminal epithelium:	n/a
13	chr3:523012-523062	NH-A	brain:	n/a
14	chr3:577821-577871	AG04449	skin:	fetal
15	chr3:577629-577679	PFSK-1	brain:	n/a
16	chr3:523375-523425	U87	brain:	n/a
17	chr3:523012-523062	RPTEC	kidney:	n/a
18	chr3:523012-523062	AG04449	skin:	fetal
19	chr3:577821-577871	NT2-D1	testis:	n/a
20	chr3:523375-523425	GM12878	blood:	n/a
21	chr3:577821-577871	Hela-S3	cervix:	n/a
22	chr3:523012-523062	HepG2	liver:	n/a
23	chr3:523012-523062	SKMC	muscle:	n/a
24	chr3:523012-523062	HRE	kidney:	n/a
25	chr3:577964-578014	SK-N-MC	brain:	n/a
26	chr3:577629-577679	HIPEpiC	eye:	n/a
27	chr3:523012-523062	AG09319	gingival:	n/a
28	chr3:577964-578014	IMR90	lung:	fetal
29	chr3:577629-577679	K562	blood:	n/a
30	chr3:577964-578014	HIPEpiC	eye:	n/a
31	chr3:577821-577871	AG10803	skin:	n/a
32	chr3:523375-523425	BE2_C	brain:	n/a
33	chr3:577629-577679	HRE	kidney:	n/a
34	chr3:577964-578014	Caco-2	colon:	n/a
35	chr3:577964-578014	HRE	kidney:	n/a
36	chr3:577821-577871	PFSK-1	brain:	n/a
37	chr3:523012-523062	ovcar-3	ovarian:	n/a
38	chr3:523012-523062	BE2_C	brain:	n/a
39	chr3:577629-577679	Hepatocyte	liver:	n/a
40	chr3:523375-523425	PANC-1	pancreas:	n/a
41	chr3:577629-577679	LNCaP	prostate:	n/a
42	chr3:577821-577871	HIPEpiC	eye:	n/a
43	chr3:523012-523062	CMK	blood:	n/a
44	chr3:523012-523062	NHBE	bronchial:	n/a
45	chr3:523012-523062	GM12891	blood:	n/a
46	chr3:577629-577679	AG09309	skin:	n/a
47	chr3:523012-523062	GM12892	blood:	n/a
48	chr3:523012-523062	AG10803	skin:	n/a
49	chr3:577964-578014	NB4	blood:	n/a
50	chr3:577821-577871	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:565796..568589-chr3:571178..572728,2	K562	blood:
2	chr3:522873..523625-chr3:674344..674995,2	MCF-7	breast:
3	chr3:554700..557337-chr3:557649..560284,2	K562	blood:
4	chr3:571404..573075-chr3:573790..576325,2	MCF-7	breast:
5	chr3:556350..557928-chr3:558208..559835,2	MCF-7	breast:
6	chr3:556350..557928-chr3:558208..559835,2	MCF-7	breast:
7	chr3:571404..573075-chr3:573790..576325,2	MCF-7	breast:
8	chr3:512741..514299-chr3:528430..530623,2	K562	blood:
9	chr3:565796..568589-chr3:571178..572728,2	K562	blood:
10	chr3:554700..557337-chr3:557649..560284,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHL1-3	chr3:577936-578010	ENSG00000224957
2	lnc-CHL1-6	chr3:552914-553010	ucscGeneNc_uc003boy_1
3	lnc-CHL1-3	chr3:577941-579275	NONHSAT087570

Variant related genes	Relation type
ENSG00000224957	TF binding region
ENSG00000224957	CpG island
DCBLD2	miRNA target sites

Extended variants
information (count: 2303 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2303 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548987927	chr3:517804-517805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs567231946	chr3:517861-517862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs199766043	chr3:517889-517890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368927196	chr3:517918-517919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537984725	chr3:517963-517964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189884336	chr3:517979-517980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371439156	chr3:517987-517988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182050938	chr3:517999-518000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142189869	chr3:518010-518011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546457637	chr3:518019-518020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557995081	chr3:518053-518054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573509919	chr3:518059-518060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75294428	chr3:518070-518071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185311546	chr3:518074-518075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190549668	chr3:518090-518091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570248510	chr3:518102-518103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182327677	chr3:518111-518112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544673124	chr3:518148-518149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184916400	chr3:518230-518231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533128759	chr3:518256-518257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548204288	chr3:518297-518298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189724715	chr3:518339-518340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560163234	chr3:518340-518341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149985822	chr3:518359-518360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145598828	chr3:518365-518366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs386657280	chr3:518412-518413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs1529762	chr3:518414-518415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139432502	chr3:518417-518418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs144086609	chr3:518421-518422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539623395	chr3:518503-518504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181091186	chr3:518546-518547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140894679	chr3:518551-518552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs143104917	chr3:518568-518569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555790546	chr3:518596-518597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573939845	chr3:518653-518654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536721111	chr3:518665-518666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs78240571	chr3:518701-518702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544636284	chr3:518715-518716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs59762189	chr3:518720-518721	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs376041232	chr3:518728-518729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570674437	chr3:518747-518748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs578161129	chr3:518757-518758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs115992670	chr3:518800-518801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140053753	chr3:518818-518819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs62229764	chr3:518828-518829	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs115713305	chr3:518836-518837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561034626	chr3:518866-518867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185530510	chr3:518869-518870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566915632	chr3:518885-518886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549387303	chr3:518914-518915	Weak transcription	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
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
Acute lymphoblastic leukemia	20435627	CNVD
Autism	20685689	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:230 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:517800-522600	Weak transcription	Ovary	ovary
2	chr3:519000-520000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:522400-522600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr3:522400-524000	Enhancers	Hela-S3	cervix
5	chr3:522600-523000	Enhancers	Ovary	ovary
6	chr3:522600-523200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr3:522800-523000	Enhancers	Aorta	Aorta
8	chr3:522800-523000	Enhancers	Fetal Stomach	stomach
9	chr3:522800-524000	Enhancers	Fetal Lung	lung
10	chr3:523000-524200	Weak transcription	Aorta	Aorta
11	chr3:523000-525400	Weak transcription	Ovary	ovary
12	chr3:523200-523400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr3:523400-526000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr3:523800-524400	Enhancers	Fetal Brain Male	brain
15	chr3:524000-525400	Weak transcription	Fetal Lung	lung
16	chr3:524000-526200	Weak transcription	Hela-S3	cervix
17	chr3:524200-524400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr3:524200-524400	Enhancers	Aorta	Aorta
19	chr3:524200-524400	Bivalent Enhancer	Fetal Stomach	stomach
20	chr3:524200-524400	Flanking Bivalent TSS/Enh	Lung	lung
21	chr3:524200-524400	Enhancers	Right Atrium	heart
22	chr3:524200-524600	ZNF genes & repeats	Left Ventricle	heart
23	chr3:524400-525200	Weak transcription	Aorta	Aorta
24	chr3:524600-525600	Weak transcription	Left Ventricle	heart
25	chr3:525200-525600	Active TSS	Right Atrium	heart
26	chr3:525200-526800	Active TSS	Aorta	Aorta
27	chr3:525400-525600	Enhancers	Fetal Stomach	stomach
28	chr3:525400-525600	Weak transcription	Lung	lung
29	chr3:525400-525800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr3:525400-525800	Enhancers	Ovary	ovary
31	chr3:525400-526000	Enhancers	Fetal Lung	lung
32	chr3:525400-526000	Active TSS	NHDF-Ad	bronchial
33	chr3:525400-526000	Active TSS	NHLF	lung
34	chr3:525600-525800	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr3:525600-525800	Active TSS	Brain Anterior Caudate	brain
36	chr3:525600-525800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr3:525600-525800	Enhancers	Left Ventricle	heart
38	chr3:525600-525800	Enhancers	Pancreas	Pancrea
39	chr3:525600-525800	Flanking Active TSS	Right Atrium	heart
40	chr3:525600-526000	Enhancers	Brain Hippocampus Middle	brain
41	chr3:525600-526000	Enhancers	Lung	lung
42	chr3:525800-526000	Flanking Active TSS	Brain Anterior Caudate	brain
43	chr3:525800-526000	Enhancers	Brain Substantia Nigra	brain
44	chr3:525800-526600	Enhancers	Fetal Muscle Leg	muscle
45	chr3:525800-529200	Weak transcription	Ovary	ovary
46	chr3:526000-526800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr3:526000-527200	Weak transcription	NHLF	lung
48	chr3:526200-526800	Enhancers	Hela-S3	cervix
49	chr3:526200-527000	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr3:526800-533800	Weak transcription	Hela-S3	cervix

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