Variant report

Variant	nsv523593
Chromosome Location	chr5:104090636-104254580
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	BACH1	chr5:104223199-104223207	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr5:104246667-104246983	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr5:104136117-104136616	MCF-7	breast:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
4	CEBPB	chr5:104136188-104136569	K562	blood:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
5	CEBPB	chr5:104136032-104136689	MCF-7	breast:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
6	CEBPB	chr5:104171648-104171720	HepG2	liver:	n/a	n/a
7	CEBPB	chr5:104195073-104195449	IMR90	lung:	n/a	chr5:104195252-104195263
8	CEBPB	chr5:104136209-104136550	A549	lung:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
9	CEBPB	chr5:104177422-104177540	K562	blood:	n/a	n/a
10	CEBPB	chr5:104136178-104136571	HepG2	liver:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
11	CEBPB	chr5:104136228-104136514	Hela-S3	cervix:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
12	CEBPB	chr5:104136061-104136624	A549	lung:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
13	CEBPB	chr5:104195064-104195524	A549	lung:	n/a	chr5:104195252-104195263
14	CEBPB	chr5:104136186-104136537	K562	blood:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
15	CEBPB	chr5:104195099-104195433	H1-hESC	embryonic stem cell:	n/a	chr5:104195252-104195263
16	CEBPB	chr5:104090393-104090670	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr5:104136225-104136497	HepG2	liver:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
18	CEBPB	chr5:104195083-104195431	A549	lung:	n/a	chr5:104195252-104195263
19	CEBPB	chr5:104102566-104102783	HepG2	liver:	n/a	chr5:104102656-104102667
20	CEBPB	chr5:104136123-104136646	HCT-116	colon:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
21	CEBPB	chr5:104195080-104195455	K562	blood:	n/a	chr5:104195252-104195263
22	CEBPB	chr5:104195089-104195447	ECC-1	luminal epithelium:	n/a	chr5:104195252-104195263
23	CEBPB	chr5:104195095-104195389	MCF-7	breast:	n/a	chr5:104195252-104195263
24	CEBPB	chr5:104195078-104195490	Hela-S3	cervix:	n/a	chr5:104195252-104195263
25	CEBPB	chr5:104195135-104195333	K562	blood:	n/a	chr5:104195252-104195263
26	CEBPB	chr5:104136181-104136567	HepG2	liver:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
27	CEBPB	chr5:104102501-104102787	A549	lung:	n/a	chr5:104102656-104102667
28	CEBPB	chr5:104195098-104195441	HepG2	liver:	n/a	chr5:104195252-104195263
29	CEBPB	chr5:104136190-104136565	H1-hESC	embryonic stem cell:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
30	CEBPB	chr5:104136224-104136540	IMR90	lung:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
31	CEBPB	chr5:104246629-104247018	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr5:104195172-104195487	MCF-7	breast:	n/a	chr5:104195252-104195263
33	CEBPB	chr5:104136255-104136426	K562	blood:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
34	CEBPB	chr5:104136258-104136502	HepG2	liver:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
35	CEBPB	chr5:104136136-104136548	A549	lung:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
36	CEBPD	chr5:104179642-104179910	K562	blood:	n/a	n/a
37	CEBPD	chr5:104136280-104136473	HepG2	liver:	n/a	n/a
38	CHD2	chr5:104246611-104246974	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr5:104136300-104136450	AG04449	skin:	n/a	n/a
40	CTCF	chr5:104136260-104136410	K562	blood:	n/a	n/a
41	CTCF	chr5:104136280-104136430	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr5:104136260-104136410	GM12872	blood:	n/a	n/a
43	CTCF	chr5:104136249-104136464	K562	blood:	n/a	n/a
44	CTCF	chr5:104195892-104195968	LNCaP	prostate:	n/a	n/a
45	CTCF	chr5:104136220-104136370	NHEK	skin:	n/a	n/a
46	CTCF	chr5:104136240-104136390	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr5:104136260-104136410	HEK293	kidney:	n/a	n/a
48	CTCF	chr5:104136300-104136450	RPTEC	kidney:	n/a	n/a
49	CTCF	chr5:104145880-104146030	GM12875	blood:	n/a	n/a
50	CTCF	chr5:104136280-104136430	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:104234931..104236476-chr5:104238248..104241105,2	MCF-7	breast:
2	chr5:104223049..104225474-chr5:104235768..104238593,2	MCF-7	breast:
3	chr17:57939158..57941470-chr5:104246724..104248724,2	MCF-7	breast:
4	chr5:104246978..104249905-chr5:104251799..104254646,2	MCF-7	breast:
5	chr5:104091669..104093962-chr5:104097846..104099466,2	MCF-7	breast:
6	chr5:104091669..104093962-chr5:104097846..104099466,2	MCF-7	breast:
7	chr5:104246978..104249905-chr5:104251799..104254646,2	MCF-7	breast:
8	chr5:104239889..104241844-chr5:104241951..104244541,2	MCF-7	breast:
9	chr5:104227529..104229773-chr5:104240979..104242491,2	MCF-7	breast:
10	chr5:104226367..104227906-chr5:104228376..104230821,2	MCF-7	breast:
11	chr5:104086946..104088891-chr5:104090048..104092847,2	MCF-7	breast:
12	chr5:104223049..104225474-chr5:104235768..104238593,2	MCF-7	breast:
13	chr5:104248370..104250240-chr5:104261197..104262793,2	MCF-7	breast:
14	chr5:104239889..104241844-chr5:104241951..104244541,2	MCF-7	breast:
15	chr5:104226367..104227906-chr5:104228376..104230821,2	MCF-7	breast:
16	chr5:104234931..104236476-chr5:104238248..104241105,2	MCF-7	breast:
17	chr5:104227529..104229773-chr5:104240979..104242491,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
2	lnc-NUDT12-5	chr5:104098981-104099084	NONHSAT103081
3	lnc-NUDT12-6	chr5:104222559-104222676	ENSG00000251574
4	lnc-NUDT12-6	chr5:104222559-104222676	ENSG00000251574
5	lnc-NUDT12-5	chr5:104109314-104109361	ENSG00000251574
6	lnc-NUDT12-6	chr5:104246363-104246434	ENSG00000251574
7	lnc-NUDT12-5	chr5:104109314-104109485	ENSG00000251574
8	lnc-NUDT12-13	chr5:104103132-104103235	l_2988_chr5:104103131-104137422_testes
9	lnc-NUDT12-7	chr5:104253193-104253599	ENSG00000253584
10	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
11	lnc-NUDT12-5	chr5:104098932-104099084	ENSG00000251574
12	lnc-NUDT12-5	chr5:104109314-104109397	ENSG00000251574
13	lnc-NUDT12-5	chr5:104109314-104109524	NONHSAT103088
14	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
15	lnc-NUDT12-5	chr5:104109314-104109492	ENSG00000251574
16	lnc-NUDT12-13	chr5:104118423-104118445	l_2988_chr5:104103131-104137422_testes
17	lnc-C5orf30-2	chr5:104098977-104099084	XLOC_004497
18	lnc-C5orf30-3	chr5:104135007-104135473	ENSG00000253776
19	lnc-C5orf30-3	chr5:104109342-104109441	ENSG00000253776
20	lnc-NUDT12-5	chr5:104109434-104109524	NONHSAT103081
21	lnc-NUDT12-13	chr5:104137254-104137422	l_2988_chr5:104103131-104137422_testes
22	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
23	lnc-NUDT12-5	chr5:104109434-104109523	ENSG00000251574
24	lnc-NUDT12-5	chr5:104098981-104099084	NONHSAT103082
25	lnc-NUDT12-5	chr5:104109314-104109524	NONHSAT103082

Variant related genes	Relation type
ENSG00000253776	TF binding region
RNU6-334P	TF binding region
ENSG00000251574	TF binding region
CREB3L2	miRNA target sites

Extended variants
information (count: 2323 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2323 , 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	rs325492	chr5:104090636-104090637	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs533554946	chr5:104090724-104090725	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs553827336	chr5:104090837-104090838	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs77682640	chr5:104090855-104090856	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs545971798	chr5:104090879-104090880	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs556367071	chr5:104090953-104090954	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs144349065	chr5:104090982-104090983	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs542475948	chr5:104091001-104091002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562255770	chr5:104091059-104091060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527639739	chr5:104091072-104091073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573784936	chr5:104091084-104091085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541115896	chr5:104091085-104091086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs112366394	chr5:104091089-104091090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192034286	chr5:104091148-104091149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376987247	chr5:104091191-104091192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533490966	chr5:104091212-104091213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550317774	chr5:104091222-104091223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs140765038	chr5:104091223-104091224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34211343	chr5:104091237-104091238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35909731	chr5:104091240-104091241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370330505	chr5:104091254-104091255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs34563303	chr5:104091259-104091260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572657977	chr5:104091314-104091315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548416509	chr5:104091315-104091316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544378309	chr5:104091324-104091325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568309569	chr5:104091336-104091337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562508624	chr5:104091393-104091394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533773075	chr5:104091394-104091395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs144729580	chr5:104091399-104091400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182091427	chr5:104091409-104091410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374503802	chr5:104091424-104091425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186679886	chr5:104091425-104091426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576191160	chr5:104091467-104091468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542062995	chr5:104091469-104091470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs161776	chr5:104091478-104091479	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs572693299	chr5:104091494-104091495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541402999	chr5:104091630-104091631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564442792	chr5:104091645-104091646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533377326	chr5:104091647-104091648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10057262	chr5:104091652-104091653	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs373986831	chr5:104091659-104091660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111981803	chr5:104091660-104091661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563772666	chr5:104091680-104091681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376446608	chr5:104091682-104091683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576432824	chr5:104091683-104091684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556408832	chr5:104091686-104091687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189911828	chr5:104091723-104091724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs55864875	chr5:104091724-104091725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75904032	chr5:104091727-104091728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531529291	chr5:104091767-104091768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
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	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
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	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
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Obesity	20622171	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104089600-104090800	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr5:104089800-104091200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr5:104089800-104091200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr5:104089800-104091200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr5:104089800-104091200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr5:104089800-104091400	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr5:104090200-104091000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:104090400-104090800	Active TSS	HUES6 Cell Line	embryonic stem cell
9	chr5:104090600-104090800	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr5:104090800-104091000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr5:104091200-104092600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr5:104091400-104095000	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr5:104095000-104095800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr5:104112400-104113000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr5:104112600-104113000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr5:104124800-104125400	Enhancers	Duodenum Smooth Muscle	Duodenum
17	chr5:104124800-104125400	Enhancers	Rectal Smooth Muscle	rectum
18	chr5:104124800-104125600	Enhancers	Fetal Lung	lung
19	chr5:104124800-104126400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr5:104126400-104130000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr5:104127800-104129000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:104128400-104129800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr5:104128600-104129000	Enhancers	Fetal Intestine Small	intestine
24	chr5:104128600-104129000	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr5:104128600-104129200	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr5:104128600-104129400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr5:104128600-104129400	Enhancers	Rectal Mucosa Donor 29	rectum
28	chr5:104128600-104130000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
29	chr5:104128600-104130200	Enhancers	Fetal Intestine Large	intestine
30	chr5:104128800-104129200	Enhancers	NH-A	brain
31	chr5:104129000-104129400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
32	chr5:104129000-104129400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr5:104129200-104129400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
34	chr5:104129200-104130000	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr5:104130000-104130200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
36	chr5:104130000-104130200	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr5:104130000-104132000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr5:104136200-104136400	ZNF genes & repeats	Aorta	Aorta
39	chr5:104137600-104138400	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr5:104150800-104151200	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr5:104151200-104154800	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr5:104157200-104157800	Enhancers	Fetal Intestine Large	intestine
43	chr5:104157200-104159600	Enhancers	Fetal Intestine Small	intestine
44	chr5:104173200-104173400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr5:104173200-104173400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr5:104173200-104173400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr5:104173200-104173400	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr5:104173200-104173400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr5:104173200-104173400	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr5:104173400-104179600	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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