Variant report

Variant	esv2756469
Chromosome Location	chr5:94323268-94400017
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:356)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:94343956-94344333	GM12878	blood:	n/a	n/a
2	ATF2	chr5:94343810-94344354	GM12878	blood:	n/a	n/a
3	BACH1	chr5:94388000-94388142	K562	blood:	n/a	n/a
4	BATF	chr5:94365307-94365655	GM12878	blood:	n/a	n/a
5	BATF	chr5:94343946-94344239	GM12878	blood:	n/a	n/a
6	BATF	chr5:94363432-94363746	GM12878	blood:	n/a	n/a
7	BATF	chr5:94348400-94348787	GM12878	blood:	n/a	n/a
8	BATF	chr5:94343952-94344260	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:94343910-94344291	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:94365371-94365683	GM12878	blood:	n/a	n/a
11	BCL11A	chr5:94343909-94344283	GM12878	blood:	n/a	n/a
12	BCLAF1	chr5:94358634-94359027	GM12878	blood:	n/a	n/a
13	BHLHE40	chr5:94365308-94365687	GM12878	blood:	n/a	n/a
14	BHLHE40	chr5:94348687-94348704	GM12878	blood:	n/a	n/a
15	BHLHE40	chr5:94343764-94344368	GM12878	blood:	n/a	n/a
16	CEBPB	chr5:94382993-94383009	A549	lung:	n/a	n/a
17	CEBPB	chr5:94382818-94383105	HepG2	liver:	n/a	chr5:94382984-94383001
18	CEBPB	chr5:94326702-94326902	HepG2	liver:	n/a	chr5:94326803-94326814
19	CHD1	chr5:94343675-94343894	GM12878	blood:	n/a	n/a
20	CHD1	chr5:94344142-94344178	GM12878	blood:	n/a	n/a
21	CHD1	chr5:94362322-94362340	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr5:94365583-94365592	GM12878	blood:	n/a	n/a
23	CHD2	chr5:94365378-94365695	GM12878	blood:	n/a	n/a
24	CHD2	chr5:94362223-94362334	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr5:94393421-94393516	GM12878	blood:	n/a	n/a
26	CHD2	chr5:94343872-94344304	GM12878	blood:	n/a	n/a
27	CTCF	chr5:94359163-94359293	Gliobla	brain:	n/a	n/a
28	CTCF	chr5:94399620-94399770	GM12864	blood:	n/a	n/a
29	CTCF	chr5:94382940-94383090	GM12867	blood:	n/a	n/a
30	CTCF	chr5:94387120-94387270	GM12872	blood:	n/a	n/a
31	CTCF	chr5:94341440-94341590	AG10803	skin:	n/a	n/a
32	CTCF	chr5:94350678-94350732	Lung_OC	lung:	n/a	n/a
33	CTCF	chr5:94387040-94387190	MCF-7	breast:	n/a	n/a
34	CTCF	chr5:94324861-94324918	GM20000	blood:	n/a	n/a
35	CTCF	chr5:94399375-94399447	MCF-7	breast:	n/a	n/a
36	CTCF	chr5:94399402-94399432	MCF-7	breast:	n/a	n/a
37	CTCF	chr5:94337540-94337690	MCF-7	breast:	n/a	n/a
38	CTCF	chr5:94387000-94387150	GM12866	blood:	n/a	n/a
39	CTCF	chr5:94359061-94359328	GM12878	blood:	n/a	n/a
40	CTCF	chr5:94399371-94399438	GM12891	blood:	n/a	n/a
41	CTCF	chr5:94387020-94387170	GM12870	blood:	n/a	n/a
42	CTCF	chr5:94399398-94399401	MCF-7	breast:	n/a	n/a
43	CTCF	chr5:94363697-94363735	GM19239	blood:	n/a	n/a
44	CTCF	chr5:94399370-94399457	GM19239	blood:	n/a	n/a
45	CTCF	chr5:94329980-94330130	GM12873	blood:	n/a	n/a
46	CTCF	chr5:94399391-94399461	MCF-7	breast:	n/a	n/a
47	CUX1	chr5:94343877-94344268	GM12878	blood:	n/a	n/a
48	CUX1	chr5:94356189-94356517	GM12878	blood:	n/a	n/a
49	EBF1	chr5:94343713-94344252	GM12878	blood:	n/a	n/a
50	EBF1	chr5:94365275-94365754	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:94330872-94330922	AG04450	lung:	fetal
2	chr5:94330872-94330922	GM06990	blood:	n/a
3	chr5:94330872-94330922	PFSK-1	brain:	n/a
4	chr5:94330872-94330922	HCT-116	colon:	n/a
5	chr5:94330872-94330922	SK-N-SH_RA	brain:	n/a
6	chr5:94330872-94330922	ovcar-3	ovarian:	n/a
7	chr5:94330872-94330922	NHBE	bronchial:	n/a
8	chr5:94330872-94330922	PANC-1	pancreas:	n/a
9	chr5:94330872-94330922	NHDF-neo	bronchial:	n/a
10	chr5:94330872-94330922	MCF-7	breast:	n/a
11	chr5:94330872-94330922	H1-hESC	embryonic stem cell:	embryo
12	chr5:94330872-94330922	U87	brain:	n/a
13	chr5:94330872-94330922	HRE	kidney:	n/a
14	chr5:94330872-94330922	BE2_C	brain:	n/a
15	chr5:94330872-94330922	AG10803	skin:	n/a
16	chr5:94330872-94330922	A549	lung:	n/a
17	chr5:94330872-94330922	AG04449	skin:	fetal
18	chr5:94330872-94330922	RPTEC	kidney:	n/a
19	chr5:94330872-94330922	GM19239	blood:	n/a
20	chr5:94330872-94330922	SK-N-MC	brain:	n/a
21	chr5:94330872-94330922	HUVEC	blood vessel:	n/a
22	chr5:94330872-94330922	HPAEpiC	pulmonary alveolar:	n/a
23	chr5:94330872-94330922	AoSMC	blood vessel:	n/a
24	chr5:94330872-94330922	PrEC	prostate:	n/a
25	chr5:94330872-94330922	SAEC	small airway:	n/a
26	chr5:94330872-94330922	HepG2	liver:	n/a
27	chr5:94330872-94330922	NT2-D1	testis:	n/a
28	chr5:94330872-94330922	K562	blood:	n/a
29	chr5:94330872-94330922	HEEpiC	esophagus:	n/a
30	chr5:94330872-94330922	NB4	blood:	n/a
31	chr5:94330872-94330922	GM12878	blood:	n/a
32	chr5:94330872-94330922	MCF10A-Er-Src	breast:	n/a
33	chr5:94330872-94330922	AG09309	skin:	n/a
34	chr5:94330872-94330922	T-47D	breast:	n/a
35	chr5:94330872-94330922	SKMC	muscle:	n/a
36	chr5:94330872-94330922	HRCEpiC	kidney:	n/a
37	chr5:94330872-94330922	HIPEpiC	eye:	n/a
38	chr5:94330872-94330922	Caco-2	colon:	n/a
39	chr5:94330872-94330922	HCM	heart:	n/a
40	chr5:94330872-94330922	BJ	skin:	n/a
41	chr5:94330872-94330922	SK-N-SH	brain:	n/a
42	chr5:94330872-94330922	HNPCEpiC	eye:	n/a
43	chr5:94330872-94330922	HCPEpiC	choroid plexus:	n/a
44	chr5:94330872-94330922	GM12892	blood:	n/a
45	chr5:94330872-94330922	GM12891	blood:	n/a
46	chr5:94330872-94330922	HRPEpiC	eye:	n/a
47	chr5:94330872-94330922	AG09319	gingival:	n/a
48	chr5:94330872-94330922	HMEC	breast:	n/a
49	chr5:94330872-94330922	HEK293	kidney:	embryo
50	chr5:94330872-94330922	IMR90	lung:	fetal

No data

Variant related genes	Relation type
MCTP1	TF binding region
MCTP1	CpG island

Extended variants
information (count: 2717 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2717 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13360791	chr5:94323268-94323269	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570071711	chr5:94323307-94323308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs10043872	chr5:94323373-94323374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370314510	chr5:94323420-94323421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373821718	chr5:94323454-94323455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539160596	chr5:94323467-94323468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200859447	chr5:94323479-94323480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112639664	chr5:94323505-94323506	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73138010	chr5:94323506-94323507	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs540112696	chr5:94323539-94323540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560149893	chr5:94323560-94323561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182531004	chr5:94323565-94323566	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139795975	chr5:94323570-94323571	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548344000	chr5:94323602-94323603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs295209	chr5:94323604-94323605	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs537378606	chr5:94323645-94323646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554857572	chr5:94323652-94323653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs977578	chr5:94323708-94323709	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs570800591	chr5:94323719-94323720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539783327	chr5:94323730-94323731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553195206	chr5:94323747-94323748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189240261	chr5:94323760-94323761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145693874	chr5:94323772-94323773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372100309	chr5:94323773-94323774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370853480	chr5:94323832-94323833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191972035	chr5:94323856-94323857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs998822	chr5:94323906-94323907	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs143179235	chr5:94323940-94323941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542731290	chr5:94323960-94323961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183246559	chr5:94323998-94323999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577102472	chr5:94324016-94324017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs397998768	chr5:94324025-94324026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187560827	chr5:94324062-94324063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192073178	chr5:94324091-94324092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574901966	chr5:94324137-94324138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs977577	chr5:94324180-94324181	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs184295591	chr5:94324213-94324214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560010798	chr5:94324219-94324220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528919653	chr5:94324264-94324265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542297677	chr5:94324265-94324266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530808906	chr5:94324301-94324302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373479775	chr5:94324302-94324303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs79868969	chr5:94324320-94324321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561994069	chr5:94324343-94324344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531002470	chr5:94324413-94324414	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187945966	chr5:94324424-94324425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374081995	chr5:94324442-94324443	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571081768	chr5:94324466-94324467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75182050	chr5:94324483-94324484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs67223139	chr5:94324500-94324501	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:80)

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	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
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
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
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
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Williams Syndrome	20824207	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:507 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94301200-94337600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:94313800-94337000	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr5:94314000-94325400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr5:94319800-94346600	Weak transcription	HUVEC	blood vessel
5	chr5:94320400-94348000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:94321400-94323800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:94322400-94334200	Weak transcription	Gastric	stomach
8	chr5:94323000-94324000	Strong transcription	Primary hematopoietic stem cells	blood
9	chr5:94323200-94324400	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr5:94323200-94326200	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr5:94323800-94325800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr5:94324000-94324600	Weak transcription	Primary hematopoietic stem cells	blood
13	chr5:94324400-94326000	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr5:94324600-94327200	Strong transcription	Primary hematopoietic stem cells	blood
15	chr5:94325200-94326200	ZNF genes & repeats	GM12878-XiMat	blood
16	chr5:94325400-94325600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr5:94325600-94337600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr5:94325800-94337400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr5:94326000-94339400	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr5:94326200-94328000	Weak transcription	GM12878-XiMat	blood
21	chr5:94326200-94329600	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr5:94327000-94339200	Weak transcription	Primary T cells from cord blood	blood
23	chr5:94327200-94339000	Weak transcription	Primary hematopoietic stem cells	blood
24	chr5:94328000-94328400	Enhancers	GM12878-XiMat	blood
25	chr5:94328200-94328400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr5:94328400-94329200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr5:94328400-94331000	Weak transcription	GM12878-XiMat	blood
28	chr5:94329200-94330000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr5:94329200-94330400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:94329400-94330000	Enhancers	Stomach Mucosa	stomach
31	chr5:94329600-94330400	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr5:94330000-94330600	Weak transcription	Stomach Mucosa	stomach
33	chr5:94330000-94331200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr5:94330000-94331600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr5:94330200-94330400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr5:94330200-94332200	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr5:94330400-94331200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr5:94330400-94334200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr5:94330400-94336600	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr5:94330600-94331000	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr5:94330600-94331200	Active TSS	Stomach Mucosa	stomach
42	chr5:94330600-94331600	Enhancers	H1 Cell Line	embryonic stem cell
43	chr5:94330800-94331400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr5:94330800-94332200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr5:94331000-94331200	Enhancers	GM12878-XiMat	blood
46	chr5:94331000-94331400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr5:94331000-94332200	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr5:94331200-94331600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr5:94331200-94332000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr5:94331200-94333000	Weak transcription	Stomach Mucosa	stomach

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