Variant report

Variant	nsv589858
Chromosome Location	chr3:20388105-20480253
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:183)
Chromatin interactive
region (count:10)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:216 , 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	ARID3A	chr3:20394102-20394581	K562	blood:	n/a	n/a
2	ATF3	chr3:20394287-20394634	K562	blood:	n/a	n/a
3	BACH1	chr3:20394371-20394578	K562	blood:	n/a	n/a
4	BACH1	chr3:20394395-20394609	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr3:20416798-20417091	GM12878	blood:	n/a	n/a
6	BHLHE40	chr3:20394266-20394730	K562	blood:	n/a	n/a
7	CBX3	chr3:20394150-20394723	K562	blood:	n/a	chr3:20394644-20394655
8	CCNT2	chr3:20394423-20394638	K562	blood:	n/a	n/a
9	CEBPB	chr3:20394100-20394376	HepG2	liver:	n/a	chr3:20394224-20394235
10	CEBPB	chr3:20421949-20421971	HepG2	liver:	n/a	n/a
11	CEBPB	chr3:20393995-20394652	K562	blood:	n/a	chr3:20394224-20394235
12	CEBPB	chr3:20442866-20443121	HepG2	liver:	n/a	chr3:20442974-20442985
13	CEBPB	chr3:20394121-20394364	A549	lung:	n/a	chr3:20394224-20394235
14	CEBPB	chr3:20421835-20421992	K562	blood:	n/a	n/a
15	CEBPB	chr3:20405252-20405383	K562	blood:	n/a	n/a
16	CEBPB	chr3:20439795-20440063	K562	blood:	n/a	n/a
17	CEBPB	chr3:20394124-20394372	IMR90	lung:	n/a	chr3:20394224-20394235
18	CEBPB	chr3:20439757-20440083	IMR90	lung:	n/a	n/a
19	CEBPB	chr3:20394114-20394325	K562	blood:	n/a	chr3:20394224-20394235
20	CEBPB	chr3:20417034-20417209	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr3:20416950-20417260	K562	blood:	n/a	n/a
22	CEBPB	chr3:20439770-20440049	A549	lung:	n/a	n/a
23	CEBPB	chr3:20447358-20447747	HepG2	liver:	n/a	chr3:20447481-20447492
24	CEBPB	chr3:20439732-20440080	HepG2	liver:	n/a	n/a
25	CEBPB	chr3:20394053-20394628	K562	blood:	n/a	chr3:20394224-20394235
26	CEBPB	chr3:20439832-20440032	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPD	chr3:20394123-20394654	K562	blood:	n/a	n/a
28	CEBPD	chr3:20394035-20394664	K562	blood:	n/a	n/a
29	CTCF	chr3:20423900-20424050	GM12866	blood:	n/a	n/a
30	CTCF	chr3:20425961-20426058	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr3:20440798-20440832	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr3:20413920-20414070	K562	blood:	n/a	n/a
33	CTCF	chr3:20421429-20421486	GM13976	blood:	n/a	n/a
34	CTCF	chr3:20448200-20448350	GM12871	blood:	n/a	n/a
35	CTCF	chr3:20468507-20468543	Lung_OC	lung:	n/a	n/a
36	CTCF	chr3:20413924-20414242	K562	blood:	n/a	n/a
37	CTCF	chr3:20473944-20474006	GM20000	blood:	n/a	n/a
38	CTCF	chr3:20476860-20477010	GM12869	blood:	n/a	n/a
39	CTCF	chr3:20411488-20411559	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr3:20414039-20414139	K562	blood:	n/a	n/a
41	CUX1	chr3:20401199-20401265	K562	blood:	n/a	n/a
42	CUX1	chr3:20394275-20394601	K562	blood:	n/a	n/a
43	CUX1	chr3:20419922-20420115	K562	blood:	n/a	n/a
44	E2F4	chr3:20478080-20478220	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr3:20447363-20447582	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr3:20419428-20419437	MCF10A-Er-Src	breast:	n/a	n/a
47	EBF1	chr3:20409751-20410037	GM12878	blood:	n/a	n/a
48	EBF1	chr3:20417008-20417208	GM12878	blood:	n/a	chr3:20417095-20417106
49	EBF1	chr3:20409792-20410035	GM12878	blood:	n/a	n/a
50	EP300	chr3:20394048-20394247	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:20412342-20412392	Hela-S3	cervix:	n/a
2	chr3:20412342-20412392	GM19239	blood:	n/a
3	chr3:20448283-20448333	RPTEC	kidney:	n/a
4	chr3:20418856-20418906	AG04449	skin:	fetal
5	chr3:20418856-20418906	PrEC	prostate:	n/a
6	chr3:20448283-20448333	A549	lung:	n/a
7	chr3:20448283-20448333	Hepatocyte	liver:	n/a
8	chr3:20412342-20412392	MCF-7	breast:	n/a
9	chr3:20418856-20418906	NT2-D1	testis:	n/a
10	chr3:20418856-20418906	SAEC	small airway:	n/a
11	chr3:20412342-20412392	HEEpiC	esophagus:	n/a
12	chr3:20448283-20448333	GM06990	blood:	n/a
13	chr3:20412342-20412392	SK-N-SH	brain:	n/a
14	chr3:20448283-20448333	NT2-D1	testis:	n/a
15	chr3:20418856-20418906	NB4	blood:	n/a
16	chr3:20448283-20448333	Jurkat	blood:	n/a
17	chr3:20418856-20418906	HUVEC	blood vessel:	n/a
18	chr3:20448283-20448333	GM19239	blood:	n/a
19	chr3:20418856-20418906	HCPEpiC	choroid plexus:	n/a
20	chr3:20412342-20412392	LNCaP	prostate:	n/a
21	chr3:20418856-20418906	HNPCEpiC	eye:	n/a
22	chr3:20412342-20412392	NH-A	brain:	n/a
23	chr3:20448283-20448333	AG09309	skin:	n/a
24	chr3:20412342-20412392	CMK	blood:	n/a
25	chr3:20448283-20448333	GM12878	blood:	n/a
26	chr3:20418856-20418906	BE2_C	brain:	n/a
27	chr3:20412342-20412392	HEK293	kidney:	embryo
28	chr3:20448283-20448333	NB4	blood:	n/a
29	chr3:20412342-20412392	HCF	heart:	n/a
30	chr3:20448283-20448333	ProgFib	skin:	n/a
31	chr3:20412342-20412392	HCT-116	colon:	n/a
32	chr3:20412342-20412392	T-47D	breast:	n/a
33	chr3:20418856-20418906	GM19239	blood:	n/a
34	chr3:20418856-20418906	RPTEC	kidney:	n/a
35	chr3:20418856-20418906	Hela-S3	cervix:	n/a
36	chr3:20448283-20448333	HAEpiC	amniotic membrane:	n/a
37	chr3:20448283-20448333	HRCEpiC	kidney:	n/a
38	chr3:20418856-20418906	GM06990	blood:	n/a
39	chr3:20412342-20412392	NHDF-neo	bronchial:	n/a
40	chr3:20448283-20448333	HCF	heart:	n/a
41	chr3:20412342-20412392	U87	brain:	n/a
42	chr3:20418856-20418906	GM12891	blood:	n/a
43	chr3:20448283-20448333	AG09319	gingival:	n/a
44	chr3:20418856-20418906	HCM	heart:	n/a
45	chr3:20412342-20412392	GM12892	blood:	n/a
46	chr3:20412342-20412392	GM12891	blood:	n/a
47	chr3:20418856-20418906	PFSK-1	brain:	n/a
48	chr3:20418856-20418906	T-47D	breast:	n/a
49	chr3:20448283-20448333	H1-hESC	embryonic stem cell:	embryo
50	chr3:20418856-20418906	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:20413525..20416049-chr3:20420124..20421856,2	K562	blood:
2	chr3:20436330..20438604-chr3:20439437..20442062,2	MCF-7	breast:
3	chr3:20460438..20462411-chr3:20516734..20518648,2	MCF-7	breast:
4	chr3:20451777..20453884-chr3:20476566..20478123,2	K562	blood:
5	chr3:20436330..20438604-chr3:20439437..20442062,2	MCF-7	breast:
6	chr3:20447764..20450202-chr3:20450641..20452829,2	MCF-7	breast:
7	chr3:20451777..20453884-chr3:20476566..20478123,2	K562	blood:
8	chr3:20447764..20450202-chr3:20450641..20452829,2	MCF-7	breast:
9	chr3:20384572..20387306-chr3:20389164..20391622,2	K562	blood:
10	chr3:20413525..20416049-chr3:20420124..20421856,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-3	chr3:20429741-20432054	ENSG00000261734.1
2	lnc-KAT2B-2	chr3:20389489-20389501	XLOC_002595
3	lnc-KAT2B-2	chr3:20389489-20389581	XLOC_002595
4	lnc-KAT2B-2	chr3:20392207-20392420	XLOC_002595
5	lnc-KAT2B-2	chr3:20389488-20389501	NONHSAT088622

No data

Variant related genes	Relation type
ENSG00000261734	TF binding region
ENSG00000261734	CpG island

Extended variants
information (count: 2975 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2975 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11719694	chr3:20388105-20388106	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553594539	chr3:20388149-20388150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78600729	chr3:20388173-20388174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145359692	chr3:20388250-20388251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568865723	chr3:20388251-20388252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539493071	chr3:20388253-20388254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551418316	chr3:20388286-20388287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146649716	chr3:20388307-20388308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533753629	chr3:20388339-20388340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555423308	chr3:20388349-20388350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573870929	chr3:20388395-20388396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537654747	chr3:20388427-20388428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556277969	chr3:20388477-20388478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551032703	chr3:20388503-20388504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577739225	chr3:20388554-20388555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76799962	chr3:20388599-20388600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186402021	chr3:20388600-20388601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75725943	chr3:20388648-20388649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190691893	chr3:20388725-20388726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561464142	chr3:20388730-20388731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149220008	chr3:20388733-20388734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550108148	chr3:20388749-20388750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143371144	chr3:20388755-20388756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35296277	chr3:20388765-20388766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533075148	chr3:20388794-20388795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551534519	chr3:20388805-20388806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs180762626	chr3:20388814-20388815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575914703	chr3:20388873-20388874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533813831	chr3:20388881-20388882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75372003	chr3:20388886-20388887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78917586	chr3:20388903-20388904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538118340	chr3:20388926-20388927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115636030	chr3:20388932-20388933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577451596	chr3:20388975-20388976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538426815	chr3:20388989-20388990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs939297	chr3:20389023-20389024	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs17006896	chr3:20389045-20389046	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs148354283	chr3:20389046-20389047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141505661	chr3:20389048-20389049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576685930	chr3:20389049-20389050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544059894	chr3:20389055-20389056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547832729	chr3:20389068-20389069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73185181	chr3:20389097-20389098	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs76476027	chr3:20389139-20389140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs367610386	chr3:20389145-20389146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376784264	chr3:20389170-20389171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527333942	chr3:20389201-20389202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567579049	chr3:20389234-20389235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs150436314	chr3:20389239-20389240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs79145056	chr3:20389278-20389279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	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
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
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20382200-20390000	Weak transcription	Pancreas	Pancrea
2	chr3:20382400-20394600	Weak transcription	Aorta	Aorta
3	chr3:20387000-20394200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr3:20390000-20390400	ZNF genes & repeats	Pancreas	Pancrea
5	chr3:20390400-20401200	Weak transcription	Pancreas	Pancrea
6	chr3:20394200-20394800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr3:20394200-20395000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr3:20394200-20395000	Enhancers	K562	blood
9	chr3:20394400-20394800	Enhancers	H1 Cell Line	embryonic stem cell
10	chr3:20394400-20394800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr3:20394400-20394800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr3:20401200-20401600	ZNF genes & repeats	Pancreas	Pancrea
13	chr3:20401600-20406400	Weak transcription	Pancreas	Pancrea
14	chr3:20402200-20403600	Enhancers	K562	blood
15	chr3:20403000-20403200	Enhancers	Fetal Intestine Small	intestine
16	chr3:20403200-20405200	Weak transcription	Fetal Intestine Small	intestine
17	chr3:20403600-20405200	Weak transcription	K562	blood
18	chr3:20405200-20405400	Enhancers	Fetal Intestine Small	intestine
19	chr3:20405200-20405400	Enhancers	K562	blood
20	chr3:20405200-20405600	Enhancers	Fetal Intestine Large	intestine
21	chr3:20405200-20406000	Enhancers	Duodenum Mucosa	Duodenum
22	chr3:20405400-20405800	Weak transcription	K562	blood
23	chr3:20405400-20408000	Weak transcription	Fetal Intestine Small	intestine
24	chr3:20405800-20406200	Enhancers	K562	blood
25	chr3:20408000-20408200	ZNF genes & repeats	Fetal Intestine Small	intestine
26	chr3:20408200-20415600	Weak transcription	Fetal Intestine Small	intestine
27	chr3:20410800-20411000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr3:20411600-20411800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:20415600-20415800	Enhancers	Fetal Intestine Large	intestine
30	chr3:20415600-20417200	Enhancers	Fetal Intestine Small	intestine
31	chr3:20415800-20416000	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr3:20415800-20417000	Weak transcription	Fetal Intestine Large	intestine
33	chr3:20416000-20418400	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr3:20417000-20420000	Enhancers	Fetal Intestine Large	intestine
35	chr3:20417200-20418200	Weak transcription	Fetal Intestine Small	intestine
36	chr3:20418200-20419400	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr3:20418200-20420200	Enhancers	Fetal Intestine Small	intestine
38	chr3:20418400-20419000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr3:20418400-20419200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:20418400-20419600	Enhancers	H9 Cell Line	embryonic stem cell
41	chr3:20418400-20420000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr3:20418400-20420000	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr3:20418400-20420400	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr3:20418600-20420200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr3:20418600-20420200	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr3:20419000-20419800	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr3:20419200-20419400	Enhancers	Small Intestine	intestine
48	chr3:20419200-20419800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:20419200-20420400	Enhancers	Duodenum Mucosa	Duodenum
50	chr3:20419400-20420000	Enhancers	Duodenum Smooth Muscle	Duodenum

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