Variant report

Variant	nsv969776
Chromosome Location	chr9:92946057-92998706
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:488)
CpG islands
(count:183)
Chromatin interactive
region (count:8)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:92951642-92951847	GM12878	blood:	n/a	n/a
2	BACH1	chr9:92989234-92989338	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr9:92989140-92989405	GM12878	blood:	n/a	n/a
4	BATF	chr9:92965282-92965468	GM12878	blood:	n/a	n/a
5	BATF	chr9:92989064-92989394	GM12878	blood:	n/a	n/a
6	BCL11A	chr9:92951650-92951969	GM12878	blood:	n/a	n/a
7	BCL11A	chr9:92951613-92951890	GM12878	blood:	n/a	n/a
8	BCL3	chr9:92989044-92989494	A549	lung:	n/a	n/a
9	BCL3	chr9:92988991-92989508	A549	lung:	n/a	n/a
10	BHLHE40	chr9:92951617-92952004	GM12878	blood:	n/a	n/a
11	BHLHE40	chr9:92989171-92989351	GM12878	blood:	n/a	n/a
12	CEBPB	chr9:92960940-92961231	HepG2	liver:	n/a	chr9:92961075-92961086 chr9:92961211-92961224 chr9:92961211-92961222 chr9:92961077-92961088 chr9:92961075-92961088
13	CEBPB	chr9:92960908-92961245	IMR90	lung:	n/a	chr9:92961075-92961086 chr9:92961211-92961224 chr9:92961211-92961222 chr9:92961077-92961088 chr9:92961075-92961088
14	CEBPB	chr9:92962033-92962255	HepG2	liver:	n/a	chr9:92962129-92962140
15	CEBPB	chr9:92989382-92989579	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr9:92960993-92961257	A549	lung:	n/a	chr9:92961075-92961086 chr9:92961211-92961224 chr9:92961211-92961222 chr9:92961077-92961088 chr9:92961075-92961088
17	CEBPB	chr9:92980940-92981132	A549	lung:	n/a	n/a
18	CHD2	chr9:92989233-92989362	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr9:92989106-92989444	A549	lung:	n/a	n/a
20	CTCF	chr9:92989100-92989250	MCF-7	breast:	n/a	n/a
21	CTCF	chr9:92989160-92989311	MCF-7	breast:	n/a	n/a
22	CTCF	chr9:92989102-92989304	HepG2	liver:	n/a	n/a
23	CTCF	chr9:92989495-92989663	GM12892	blood:	n/a	n/a
24	CTCF	chr9:92989420-92989570	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr9:92989127-92989306	GM10248	blood:	n/a	n/a
26	CTCF	chr9:92989380-92989530	HVMF	connective:	n/a	n/a
27	CTCF	chr9:92989060-92989210	GM12864	blood:	n/a	n/a
28	CTCF	chr9:92989420-92989570	NB4	blood:	n/a	n/a
29	CTCF	chr9:92989060-92989210	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr9:92989060-92989210	AG09309	skin:	n/a	n/a
31	CTCF	chr9:92981881-92982132	GM12878	blood:	n/a	n/a
32	CTCF	chr9:92989080-92989230	HMEC	breast:	n/a	n/a
33	CTCF	chr9:92989360-92989510	GM12873	blood:	n/a	n/a
34	CTCF	chr9:92989083-92989291	HCT-116	colon:	n/a	n/a
35	CTCF	chr9:92981865-92982138	A549	lung:	n/a	n/a
36	CTCF	chr9:92988843-92988966	GM19238	blood:	n/a	n/a
37	CTCF	chr9:92981937-92982083	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr9:92989020-92989378	A549	lung:	n/a	n/a
39	CTCF	chr9:92989100-92989250	HCT-116	colon:	n/a	n/a
40	CTCF	chr9:92981862-92982140	GM12892	blood:	n/a	n/a
41	CTCF	chr9:92989044-92989414	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr9:92989400-92989550	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr9:92989124-92989376	ECC-1	luminal epithelium:	n/a	n/a
44	CTCF	chr9:92989380-92989530	HMF	breast:	n/a	n/a
45	CTCF	chr9:92981840-92982089	T-47D	breast:	n/a	n/a
46	CTCF	chr9:92989100-92989250	GM12867	blood:	n/a	n/a
47	CTCF	chr9:92966420-92966570	GM12869	blood:	n/a	n/a
48	CTCF	chr9:92989400-92989550	GM12873	blood:	n/a	n/a
49	CTCF	chr9:92989538-92989604	GM10266	blood:	n/a	n/a
50	CTCF	chr9:92988855-92989019	GM10266	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	chr9:92981825-92981875	AoSMC	blood vessel:	n/a
2	chr9:92981825-92981875	U87	brain:	n/a
3	chr9:92982316-92982366	A549	lung:	n/a
4	chr9:92983726-92983776	HRCEpiC	kidney:	n/a
5	chr9:92983726-92983776	GM12891	blood:	n/a
6	chr9:92983726-92983776	NHDF-neo	bronchial:	n/a
7	chr9:92982316-92982366	HepG2	liver:	n/a
8	chr9:92981825-92981875	GM06990	blood:	n/a
9	chr9:92982316-92982366	HCM	heart:	n/a
10	chr9:92983726-92983776	H1-hESC	embryonic stem cell:	embryo
11	chr9:92982316-92982366	K562	blood:	n/a
12	chr9:92981825-92981875	GM12878	blood:	n/a
13	chr9:92983726-92983776	Hepatocyte	liver:	n/a
14	chr9:92982316-92982366	HIPEpiC	eye:	n/a
15	chr9:92982316-92982366	AG09309	skin:	n/a
16	chr9:92981825-92981875	HCT-116	colon:	n/a
17	chr9:92983726-92983776	HAEpiC	amniotic membrane:	n/a
18	chr9:92983726-92983776	ProgFib	skin:	n/a
19	chr9:92983726-92983776	BE2_C	brain:	n/a
20	chr9:92982316-92982366	PrEC	prostate:	n/a
21	chr9:92981825-92981875	CMK	blood:	n/a
22	chr9:92982316-92982366	GM06990	blood:	n/a
23	chr9:92982316-92982366	PANC-1	pancreas:	n/a
24	chr9:92981825-92981875	HRCEpiC	kidney:	n/a
25	chr9:92983726-92983776	Caco-2	colon:	n/a
26	chr9:92981825-92981875	SK-N-SH_RA	brain:	n/a
27	chr9:92982316-92982366	GM12892	blood:	n/a
28	chr9:92981825-92981875	MCF-7	breast:	n/a
29	chr9:92983726-92983776	HRE	kidney:	n/a
30	chr9:92981825-92981875	NHDF-neo	bronchial:	n/a
31	chr9:92983726-92983776	U87	brain:	n/a
32	chr9:92983726-92983776	HMEC	breast:	n/a
33	chr9:92983726-92983776	MCF10A-Er-Src	breast:	n/a
34	chr9:92982316-92982366	SKMC	muscle:	n/a
35	chr9:92981825-92981875	HEEpiC	esophagus:	n/a
36	chr9:92981825-92981875	ovcar-3	ovarian:	n/a
37	chr9:92982316-92982366	HL-60	blood:	n/a
38	chr9:92981825-92981875	SK-N-SH	brain:	n/a
39	chr9:92982316-92982366	AG04450	lung:	fetal
40	chr9:92982316-92982366	LNCaP	prostate:	n/a
41	chr9:92982316-92982366	HRCEpiC	kidney:	n/a
42	chr9:92983726-92983776	HCF	heart:	n/a
43	chr9:92981825-92981875	NHBE	bronchial:	n/a
44	chr9:92981825-92981875	GM19239	blood:	n/a
45	chr9:92983726-92983776	AG09319	gingival:	n/a
46	chr9:92982316-92982366	Hepatocyte	liver:	n/a
47	chr9:92983726-92983776	GM12878	blood:	n/a
48	chr9:92983726-92983776	HCPEpiC	choroid plexus:	n/a
49	chr9:92983726-92983776	Jurkat	blood:	n/a
50	chr9:92983726-92983776	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr9:92904573..92905325-chr9:92981766..92982487,4	MCF-7	breast:
2	chr9:92936090..92938700-chr9:92964176..92966160,2	MCF-7	breast:
3	chr9:92904585..92905563-chr9:92981517..92982470,9	MCF-7	breast:
4	chr9:92906459..92907062-chr9:92981976..92982746,2	MCF-7	breast:
5	chr9:92903793..92904418-chr9:92981541..92982063,2	MCF-7	breast:
6	chr9:92905785..92906382-chr9:92981694..92982360,2	MCF-7	breast:
7	chr9:92989065..92989678-chr9:93404924..93405630,3	MCF-7	breast:
8	chr9:92918798..92921681-chr9:92947393..92950211,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SYK-11	chr9:92964974-92967679	NONHSAT132996
2	lnc-DIRAS2-11	chr9:92965108-92965190	NONHSAT132995
3	lnc-SYK-11	chr9:92961872-92961910	NONHSAT132996

No data

Variant related genes	Relation type
OR7E116P	TF binding region
OR7E31P	TF binding region
OR7E116P	CpG island
OR7E31P	CpG island
ENSG00000165023	chromatin interactions

Extended variants
information (count: 1554 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1554 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184797713	chr9:92950002-92950003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs536077152	chr9:92950055-92950056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4358907	chr9:92950076-92950077	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs566303156	chr9:92950100-92950101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs77016923	chr9:92950107-92950108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs4506347	chr9:92950130-92950131	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs4506348	chr9:92950140-92950141	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs145434190	chr9:92950141-92950142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs111340900	chr9:92950164-92950165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147256410	chr9:92950167-92950168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536550827	chr9:92950172-92950173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556051720	chr9:92950195-92950196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575866938	chr9:92950196-92950197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35417762	chr9:92950228-92950229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2380283	chr9:92950229-92950230	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs541557074	chr9:92950236-92950237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545758657	chr9:92950247-92950248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565571848	chr9:92950262-92950263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189571692	chr9:92950263-92950264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550938031	chr9:92950264-92950265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1539519	chr9:92950272-92950273	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs181436257	chr9:92950284-92950285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546643669	chr9:92950309-92950310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139690699	chr9:92950313-92950314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149759317	chr9:92950336-92950337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558607089	chr9:92950365-92950366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145870503	chr9:92950369-92950370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185286987	chr9:92950387-92950388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554568747	chr9:92950401-92950402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2380284	chr9:92950402-92950403	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs540337967	chr9:92950412-92950413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115480761	chr9:92950425-92950426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573526012	chr9:92950453-92950454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147923397	chr9:92950465-92950466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs176191	chr9:92950500-92950501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545599156	chr9:92950536-92950537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs366237	chr9:92950576-92950577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs425462	chr9:92950579-92950580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538795528	chr9:92950585-92950586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2150797	chr9:92950618-92950619	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs148997822	chr9:92950652-92950653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529535911	chr9:92950658-92950659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149925458	chr9:92950663-92950664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs430772	chr9:92950686-92950687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7867907	chr9:92950714-92950715	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs206213	chr9:92950724-92950725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs530026571	chr9:92950772-92950773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs546735978	chr9:92950789-92950790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560191564	chr9:92950810-92950811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563055286	chr9:92950874-92950875	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Glioma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	17133270	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:92950000-92951000	Enhancers	Primary B cells from cord blood	blood
2	chr9:92950000-92951200	Enhancers	Primary B cells from peripheral blood	blood
3	chr9:92950200-92951800	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr9:92950200-92952000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr9:92950400-92951000	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr9:92950600-92952000	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr9:92950800-92951400	Enhancers	Primary T cells from cord blood	blood
8	chr9:92951000-92951200	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr9:92951000-92951400	Enhancers	Dnd41	blood
10	chr9:92951000-92951600	Flanking Active TSS	GM12878-XiMat	blood
11	chr9:92951000-92951800	Flanking Active TSS	Primary B cells from cord blood	blood
12	chr9:92951000-92951800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr9:92951000-92951800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr9:92951000-92951800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
15	chr9:92951000-92951800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr9:92951000-92951800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr9:92951000-92951800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr9:92951000-92952200	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr9:92951200-92951600	Flanking Active TSS	Primary B cells from peripheral blood	blood
20	chr9:92951200-92951600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
21	chr9:92951200-92951600	Enhancers	Adipose Nuclei	Adipose
22	chr9:92951400-92951800	Enhancers	Primary hematopoietic stem cells	blood
23	chr9:92951400-92954400	Weak transcription	Primary T cells from cord blood	blood
24	chr9:92951600-92953000	Enhancers	Primary B cells from peripheral blood	blood
25	chr9:92951800-92952200	Active TSS	Monocytes-CD14+_RO01746	blood
26	chr9:92951800-92954400	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr9:92951800-92954800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr9:92951800-92955000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr9:92952000-92954400	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr9:92953000-92954400	Weak transcription	Primary B cells from peripheral blood	blood
31	chr9:92954400-92955000	Enhancers	Primary T cells from cord blood	blood
32	chr9:92954400-92955200	Enhancers	Primary T cells fromperipheralblood	blood
33	chr9:92954400-92955400	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr9:92954400-92955400	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr9:92954400-92955800	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr9:92954400-92956000	Enhancers	Primary B cells from peripheral blood	blood
37	chr9:92954600-92955000	Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr9:92954600-92955400	Enhancers	Colonic Mucosa	Colon
39	chr9:92954800-92955000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
40	chr9:92955000-92955200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
41	chr9:92955000-92955600	Enhancers	Stomach Mucosa	stomach
42	chr9:92960600-92961800	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr9:92960800-92961600	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr9:92963400-92963600	Enhancers	Primary B cells from cord blood	blood
45	chr9:92963400-92964200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr9:92963600-92964400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr9:92963800-92964200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr9:92963800-92964200	Enhancers	Fetal Intestine Large	intestine
49	chr9:92963800-92965800	Weak transcription	Primary B cells from cord blood	blood
50	chr9:92964000-92964400	Enhancers	Duodenum Mucosa	Duodenum

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