Variant report

Variant	esv3336986
Chromosome Location	chr5:89450723-89482244
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	CEBPB	chr5:89478585-89478897	Hela-S3	cervix:	n/a	chr5:89478732-89478745 chr5:89478734-89478745 chr5:89478732-89478743
2	CEBPB	chr5:89478743-89478746	K562	blood:	n/a	n/a
3	CEBPB	chr5:89479193-89479407	HepG2	liver:	n/a	chr5:89479325-89479336
4	CEBPB	chr5:89478395-89479106	MCF-7	breast:	n/a	chr5:89478732-89478745 chr5:89478734-89478745 chr5:89478732-89478743
5	CEBPB	chr5:89478598-89478876	HepG2	liver:	n/a	chr5:89478732-89478745 chr5:89478734-89478745 chr5:89478732-89478743
6	CEBPB	chr5:89478677-89478896	A549	lung:	n/a	chr5:89478732-89478745 chr5:89478734-89478745 chr5:89478732-89478743
7	CEBPB	chr5:89478490-89479052	MCF-7	breast:	n/a	chr5:89478732-89478745 chr5:89478734-89478745 chr5:89478732-89478743
8	CEBPB	chr5:89480125-89480178	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr5:89479145-89479330	K562	blood:	n/a	n/a
10	CTCF	chr5:89457400-89457550	HA-sp	spinal cord:	n/a	chr5:89457504-89457522 chr5:89457506-89457519 chr5:89457499-89457520
11	CTCF	chr5:89457380-89457530	GM06990	blood:	n/a	chr5:89457504-89457522 chr5:89457506-89457519 chr5:89457499-89457520
12	CTCF	chr5:89481220-89481370	GM12866	blood:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
13	CTCF	chr5:89460020-89460170	HA-sp	spinal cord:	n/a	n/a
14	CTCF	chr5:89481280-89481430	RPTEC	kidney:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
15	CTCF	chr5:89457400-89457550	GM12867	blood:	n/a	chr5:89457504-89457522 chr5:89457506-89457519 chr5:89457499-89457520
16	CTCF	chr5:89481142-89481533	GM12878	blood:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
17	CTCF	chr5:89481240-89481390	HPF	lung:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
18	CTCF	chr5:89481280-89481430	GM12867	blood:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
19	CTCF	chr5:89481160-89481310	A549	lung:	n/a	n/a
20	CTCF	chr5:89460020-89460170	HCFaa	heart:	n/a	n/a
21	CTCF	chr5:89481273-89481408	MCF-7	breast:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
22	CTCF	chr5:89457340-89457490	GM12873	blood:	n/a	n/a
23	CTCF	chr5:89457304-89457666	H1-hESC	embryonic stem cell:	n/a	chr5:89457504-89457522 chr5:89457506-89457519 chr5:89457499-89457520
24	CTCF	chr5:89481260-89481410	HMF	breast:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
25	CTCF	chr5:89457380-89457530	HepG2	liver:	n/a	chr5:89457504-89457522 chr5:89457506-89457519 chr5:89457499-89457520
26	CTCF	chr5:89481240-89481390	BJ	skin:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
27	CTCF	chr5:89457400-89457550	HCFaa	heart:	n/a	chr5:89457504-89457522 chr5:89457506-89457519 chr5:89457499-89457520
28	CTCF	chr5:89457420-89457570	HepG2	liver:	n/a	chr5:89457504-89457522 chr5:89457506-89457519 chr5:89457499-89457520
29	CTCF	chr5:89481240-89481390	SAEC	small airway:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
30	CTCF	chr5:89457440-89457590	AG10803	skin:	n/a	chr5:89457504-89457522 chr5:89457506-89457519 chr5:89457499-89457520
31	CTCF	chr5:89481260-89481410	HA-sp	spinal cord:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
32	CTCF	chr5:89481260-89481410	GM12873	blood:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
33	CTCF	chr5:89457400-89457550	GM12865	blood:	n/a	chr5:89457504-89457522 chr5:89457506-89457519 chr5:89457499-89457520
34	CTCF	chr5:89457431-89457533	GM13976	blood:	n/a	chr5:89457504-89457522 chr5:89457506-89457519 chr5:89457499-89457520
35	CTCF	chr5:89481240-89481390	BE2_C	brain:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
36	CTCF	chr5:89481500-89481650	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr5:89457400-89457550	GM12866	blood:	n/a	chr5:89457504-89457522 chr5:89457506-89457519 chr5:89457499-89457520
38	CTCF	chr5:89457351-89457521	SK-N-SH_RA	brain:	n/a	chr5:89457506-89457519 chr5:89457499-89457520
39	CTCF	chr5:89460080-89460230	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr5:89481220-89481370	HA-sp	spinal cord:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
41	CTCF	chr5:89481200-89481350	GM12865	blood:	n/a	n/a
42	CTCF	chr5:89457363-89457560	NHEK	skin:	n/a	chr5:89457504-89457522 chr5:89457506-89457519 chr5:89457499-89457520
43	CTCF	chr5:89457480-89457630	NHLF	lung:	n/a	chr5:89457504-89457522 chr5:89457506-89457519 chr5:89457499-89457520
44	CTCF	chr5:89457360-89457510	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr5:89481562-89481660	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:89481234-89481386	SK-N-SH_RA	brain:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
47	CTCF	chr5:89457340-89457490	HCM	heart:	n/a	n/a
48	CTCF	chr5:89481240-89481390	GM12864	blood:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
49	CTCF	chr5:89481240-89481390	AG09319	gingival:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
50	CTCF	chr5:89460020-89460170	AG10803	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:89458394-89458444	GM12878	blood:	n/a
2	chr5:89458394-89458444	GM12878	blood:	n/a
3	chr5:89458394-89458444	HCF	heart:	n/a
4	chr5:89458394-89458444	ProgFib	skin:	n/a
5	chr5:89458394-89458444	SK-N-SH_RA	brain:	n/a
6	chr5:89458394-89458444	HEEpiC	esophagus:	n/a
7	chr5:89458394-89458444	HAEpiC	amniotic membrane:	n/a
8	chr5:89458394-89458444	SKMC	muscle:	n/a
9	chr5:89458394-89458444	NH-A	brain:	n/a
10	chr5:89458394-89458444	MCF-7	breast:	n/a
11	chr5:89458394-89458444	BJ	skin:	n/a
12	chr5:89458394-89458444	HL-60	blood:	n/a
13	chr5:89458394-89458444	AG10803	skin:	n/a
14	chr5:89458394-89458444	SK-N-SH	brain:	n/a
15	chr5:89458394-89458444	Caco-2	colon:	n/a
16	chr5:89458394-89458444	AG04450	lung:	fetal
17	chr5:89458394-89458444	NHDF-neo	bronchial:	n/a
18	chr5:89458394-89458444	BE2_C	brain:	n/a
19	chr5:89458394-89458444	HCPEpiC	choroid plexus:	n/a
20	chr5:89458394-89458444	IMR90	lung:	fetal
21	chr5:89458394-89458444	HCM	heart:	n/a
22	chr5:89458394-89458444	RPTEC	kidney:	n/a
23	chr5:89458394-89458444	AG09319	gingival:	n/a
24	chr5:89458394-89458444	HPAEpiC	pulmonary alveolar:	n/a
25	chr5:89458394-89458444	MCF10A-Er-Src	breast:	n/a
26	chr5:89458394-89458444	HEK293	kidney:	embryo
27	chr5:89458394-89458444	HRPEpiC	eye:	n/a
28	chr5:89458394-89458444	AoSMC	blood vessel:	n/a
29	chr5:89458394-89458444	PFSK-1	brain:	n/a
30	chr5:89458394-89458444	PrEC	prostate:	n/a
31	chr5:89458394-89458444	CMK	blood:	n/a
32	chr5:89458394-89458444	ECC-1	luminal epithelium:	n/a
33	chr5:89458394-89458444	HRE	kidney:	n/a
34	chr5:89458394-89458444	HCT-116	colon:	n/a
35	chr5:89458394-89458444	HIPEpiC	eye:	n/a
36	chr5:89458394-89458444	PANC-1	pancreas:	n/a
37	chr5:89458394-89458444	Hepatocyte	liver:	n/a
38	chr5:89458394-89458444	SK-N-MC	brain:	n/a
39	chr5:89458394-89458444	T-47D	breast:	n/a
40	chr5:89458394-89458444	NHBE	bronchial:	n/a
41	chr5:89458394-89458444	NT2-D1	testis:	n/a
42	chr5:89458394-89458444	HRCEpiC	kidney:	n/a
43	chr5:89458394-89458444	HNPCEpiC	eye:	n/a
44	chr5:89458394-89458444	HMEC	breast:	n/a
45	chr5:89458394-89458444	AG09309	skin:	n/a
46	chr5:89458394-89458444	HUVEC	blood vessel:	n/a
47	chr5:89458394-89458444	ovcar-3	ovarian:	n/a
48	chr5:89458394-89458444	HepG2	liver:	n/a
49	chr5:89458394-89458444	Hela-S3	cervix:	n/a
50	chr5:89458394-89458444	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:88025172..88025905-chr5:89457296..89457865,2	MCF-7	breast:
2	chr5:89464195..89466496-chr5:89478759..89480447,2	MCF-7	breast:
3	chr5:89478001..89478682-chr5:89560766..89561737,2	MCF-7	breast:
4	chr5:88023266..88024159-chr5:89481181..89482220,3	MCF-7	breast:
5	chr5:89450263..89452091-chr5:89459803..89462765,2	K562	blood:
6	chr5:89225139..89225642-chr5:89457055..89457700,2	MCF-7	breast:
7	chr5:89424577..89427181-chr5:89477384..89480232,2	MCF-7	breast:
8	chr5:89431785..89432445-chr5:89480883..89481450,2	MCF-7	breast:
9	chr5:89478930..89481287-chr5:89704809..89706837,2	MCF-7	breast:
10	chr5:89478032..89480920-chr5:89706398..89708148,2	K562	blood:
11	chr5:89450263..89452091-chr5:89459803..89462765,2	K562	blood:
12	chr5:89464195..89466496-chr5:89478759..89480447,2	MCF-7	breast:
13	chr19:47452350..47452852-chr5:89481098..89481635,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CETN3-3	chr5:89456346-89456450	ENSG00000248555
2	lnc-CETN3-3	chr5:89454173-89454336	ENSG00000248555
3	lnc-CETN3-3	chr5:89454156-89454336	ENSG00000248555
4	lnc-CETN3-3	chr5:89456346-89456406	ENSG00000248555
5	lnc-CETN3-3	chr5:89456346-89456406	ENSG00000248555
6	lnc-CETN3-3	chr5:89455806-89455940	ENSG00000248555

Variant related genes	Relation type
ENSG00000248555	TF binding region
ENSG00000248555	CpG island
ENSG00000255647	chromatin interactions
ENSG00000153140	chromatin interactions
ENSG00000081189	chromatin interactions

Extended variants
information (count: 814 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:814 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576714922	chr5:89450723-89450724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542457429	chr5:89450731-89450732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555672709	chr5:89450758-89450759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs199941133	chr5:89450767-89450768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200200974	chr5:89450768-89450769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371023117	chr5:89450782-89450783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529734497	chr5:89450798-89450799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549759956	chr5:89450819-89450820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147543919	chr5:89450832-89450833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532387737	chr5:89450841-89450842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552183678	chr5:89450892-89450893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567609803	chr5:89450946-89450947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187756361	chr5:89450961-89450962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565905927	chr5:89450996-89450997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534502094	chr5:89451016-89451017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548305364	chr5:89451026-89451027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192586336	chr5:89451029-89451030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182863867	chr5:89451030-89451031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140283029	chr5:89451076-89451077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577473322	chr5:89451097-89451098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144246770	chr5:89451120-89451121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188694363	chr5:89451143-89451144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs114673873	chr5:89451194-89451195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542026559	chr5:89451218-89451219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111538223	chr5:89451246-89451247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147797775	chr5:89451247-89451248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543442930	chr5:89451269-89451270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563319025	chr5:89451284-89451285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572139661	chr5:89451330-89451331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148417665	chr5:89451344-89451345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552479255	chr5:89451352-89451353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35583166	chr5:89451355-89451356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184867693	chr5:89451399-89451400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11960542	chr5:89451504-89451505	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs528310822	chr5:89451547-89451548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532730858	chr5:89451573-89451574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568225540	chr5:89451695-89451696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150974274	chr5:89451766-89451767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550659403	chr5:89451779-89451780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375128313	chr5:89451809-89451810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77161046	chr5:89451814-89451815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199505621	chr5:89451815-89451816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs57730306	chr5:89451822-89451823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs60672552	chr5:89451824-89451825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140840498	chr5:89451829-89451830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573420859	chr5:89451832-89451833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545856367	chr5:89451868-89451869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538698226	chr5:89451874-89451875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553600465	chr5:89451932-89451933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73772619	chr5:89451946-89451947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89443400-89457000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:89452000-89452200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:89452200-89454200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:89452800-89454400	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr5:89453200-89454000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr5:89453800-89454400	Enhancers	Colon Smooth Muscle	Colon
7	chr5:89454000-89454400	Enhancers	GM12878-XiMat	blood
8	chr5:89454200-89454400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:89454200-89454800	Enhancers	Ovary	ovary
10	chr5:89454200-89454800	Enhancers	HSMMtube	muscle
11	chr5:89454800-89456800	Weak transcription	Ovary	ovary
12	chr5:89456400-89457200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:89456800-89457600	Enhancers	Ovary	ovary
14	chr5:89456800-89457600	Enhancers	Stomach Mucosa	stomach
15	chr5:89457000-89457200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr5:89457000-89457600	Enhancers	Pancreas	Pancrea
17	chr5:89457000-89457600	Enhancers	Right Atrium	heart
18	chr5:89457000-89457600	Enhancers	Spleen	Spleen
19	chr5:89457200-89457400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr5:89457200-89457600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr5:89457200-89457600	Enhancers	Adipose Nuclei	Adipose
22	chr5:89457200-89458400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:89457200-89460000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr5:89457400-89458000	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr5:89457600-89458000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr5:89457600-89459800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr5:89457600-89464600	Weak transcription	Right Atrium	heart
28	chr5:89458000-89458400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr5:89458000-89459400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr5:89458400-89458600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr5:89458400-89458800	Enhancers	H1 Cell Line	embryonic stem cell
32	chr5:89458400-89459000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:89458400-89460000	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr5:89458400-89460400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr5:89458600-89459200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr5:89458600-89459800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr5:89458600-89460000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr5:89459000-89459200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:89459200-89459400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr5:89459400-89459600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:89459400-89459800	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr5:89459600-89460000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:89459800-89460200	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr5:89459800-89461000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr5:89464000-89464800	Enhancers	Primary B cells from peripheral blood	blood
46	chr5:89464200-89464800	Enhancers	Aorta	Aorta
47	chr5:89464400-89464800	Enhancers	Fetal Muscle Leg	muscle
48	chr5:89464400-89464800	Enhancers	Psoas Muscle	Psoas
49	chr5:89464400-89466600	Enhancers	Stomach Mucosa	stomach
50	chr5:89464400-89467200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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