Variant report

Variant	esv3451067
Chromosome Location	chr7:56435658-56443956
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:477)
CpG islands
(count:244)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:477 , 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	BATF	chr7:56440976-56442496	GM12878	blood:	n/a	n/a
2	BATF	chr7:56438226-56439458	GM12878	blood:	n/a	n/a
3	BATF	chr7:56439727-56440134	GM12878	blood:	n/a	n/a
4	BATF	chr7:56438872-56439456	GM12878	blood:	n/a	n/a
5	BATF	chr7:56442645-56442830	GM12878	blood:	n/a	n/a
6	BATF	chr7:56440170-56440754	GM12878	blood:	n/a	n/a
7	BATF	chr7:56438429-56438836	GM12878	blood:	n/a	n/a
8	BATF	chr7:56441021-56441428	GM12878	blood:	n/a	n/a
9	BATF	chr7:56441464-56441866	GM12878	blood:	n/a	n/a
10	BATF	chr7:56437428-56437607	GM12878	blood:	n/a	n/a
11	BATF	chr7:56439524-56440756	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:56437865-56440812	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:56440941-56442557	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:56437836-56440868	GM12878	blood:	n/a	chr7:56437839-56437852
15	BCL11A	chr7:56435572-56435743	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:56440912-56442515	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:56437350-56437622	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:56438197-56439314	HepG2	liver:	n/a	n/a
19	BHLHE40	chr7:56439495-56440612	HepG2	liver:	n/a	n/a
20	BHLHE40	chr7:56442086-56442477	HepG2	liver:	n/a	n/a
21	BHLHE40	chr7:56440907-56441906	HepG2	liver:	n/a	n/a
22	BRCA1	chr7:56441064-56441264	GM12878	blood:	n/a	n/a
23	CBX3	chr7:56441554-56442520	K562	blood:	n/a	n/a
24	CBX3	chr7:56440971-56442559	K562	blood:	n/a	n/a
25	CBX3	chr7:56440964-56441418	K562	blood:	n/a	n/a
26	CBX3	chr7:56437915-56438800	K562	blood:	n/a	n/a
27	CBX3	chr7:56437959-56440105	K562	blood:	n/a	n/a
28	CBX3	chr7:56438827-56440837	K562	blood:	n/a	n/a
29	CBX3	chr7:56440162-56440822	K562	blood:	n/a	n/a
30	CEBPB	chr7:56436551-56436928	K562	blood:	n/a	n/a
31	CEBPB	chr7:56436722-56436761	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:56436638-56436845	K562	blood:	n/a	n/a
33	CHD1	chr7:56441237-56441247	GM12878	blood:	n/a	n/a
34	CHD2	chr7:56441229-56441247	K562	blood:	n/a	n/a
35	CHD2	chr7:56441230-56441262	GM12878	blood:	n/a	n/a
36	CTCF	chr7:56441100-56441250	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr7:56441160-56441310	GM12869	blood:	n/a	n/a
38	CTCF	chr7:56438891-56440131	K562	blood:	n/a	n/a
39	CTCF	chr7:56441100-56441250	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr7:56441100-56441250	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr7:56441180-56441330	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr7:56441140-56441290	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr7:56441100-56441250	SAEC	small airway:	n/a	n/a
44	CTCF	chr7:56439580-56439730	GM12866	blood:	n/a	n/a
45	CTCF	chr7:56441100-56441250	GM12878	blood:	n/a	n/a
46	CTCF	chr7:56441706-56441799	LNCaP	prostate:	n/a	n/a
47	CTCF	chr7:56441566-56441838	K562	blood:	n/a	n/a
48	CTCF	chr7:56441736-56441819	LNCaP	prostate:	n/a	n/a
49	CTCF	chr7:56441100-56441250	HL-60	blood:	n/a	n/a
50	CTCF	chr7:56441221-56441277	Gliobla	brain:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:56442537-56442587	SK-N-SH_RA	brain:	n/a
2	chr7:56437009-56437059	K562	blood:	n/a
3	chr7:56437009-56437059	HNPCEpiC	eye:	n/a
4	chr7:56439703-56439753	H1-hESC	embryonic stem cell:	embryo
5	chr7:56442537-56442587	HepG2	liver:	n/a
6	chr7:56437009-56437059	HCPEpiC	choroid plexus:	n/a
7	chr7:56442537-56442587	Jurkat	blood:	n/a
8	chr7:56437009-56437059	HEEpiC	esophagus:	n/a
9	chr7:56437009-56437059	AoSMC	blood vessel:	n/a
10	chr7:56439703-56439753	NB4	blood:	n/a
11	chr7:56439703-56439753	AG09309	skin:	n/a
12	chr7:56437009-56437059	GM12878	blood:	n/a
13	chr7:56442537-56442587	HPAEpiC	pulmonary alveolar:	n/a
14	chr7:56442537-56442587	CMK	blood:	n/a
15	chr7:56437746-56437796	HIPEpiC	eye:	n/a
16	chr7:56437009-56437059	T-47D	breast:	n/a
17	chr7:56437009-56437059	HepG2	liver:	n/a
18	chr7:56442537-56442587	GM12878	blood:	n/a
19	chr7:56437009-56437059	NT2-D1	testis:	n/a
20	chr7:56437746-56437796	Caco-2	colon:	n/a
21	chr7:56439703-56439753	AG10803	skin:	n/a
22	chr7:56437746-56437796	SK-N-SH	brain:	n/a
23	chr7:56437746-56437796	U87	brain:	n/a
24	chr7:56437009-56437059	HRPEpiC	eye:	n/a
25	chr7:56437746-56437796	HCM	heart:	n/a
26	chr7:56439703-56439753	ECC-1	luminal epithelium:	n/a
27	chr7:56439703-56439753	NT2-D1	testis:	n/a
28	chr7:56437746-56437796	HL-60	blood:	n/a
29	chr7:56442537-56442587	NH-A	brain:	n/a
30	chr7:56439703-56439753	CMK	blood:	n/a
31	chr7:56439703-56439753	RPTEC	kidney:	n/a
32	chr7:56437009-56437059	A549	lung:	n/a
33	chr7:56437009-56437059	Caco-2	colon:	n/a
34	chr7:56437746-56437796	GM12878	blood:	n/a
35	chr7:56439703-56439753	MCF10A-Er-Src	breast:	n/a
36	chr7:56442537-56442587	PANC-1	pancreas:	n/a
37	chr7:56437746-56437796	AG04449	skin:	fetal
38	chr7:56439703-56439753	PANC-1	pancreas:	n/a
39	chr7:56442537-56442587	K562	blood:	n/a
40	chr7:56442537-56442587	HUVEC	blood vessel:	n/a
41	chr7:56442537-56442587	HIPEpiC	eye:	n/a
42	chr7:56442537-56442587	BE2_C	brain:	n/a
43	chr7:56437009-56437059	GM06990	blood:	n/a
44	chr7:56439703-56439753	AG04449	skin:	fetal
45	chr7:56442537-56442587	AG04450	lung:	fetal
46	chr7:56439703-56439753	HCF	heart:	n/a
47	chr7:56442537-56442587	GM06990	blood:	n/a
48	chr7:56442537-56442587	ProgFib	skin:	n/a
49	chr7:56437009-56437059	BE2_C	brain:	n/a
50	chr7:56437009-56437059	HRE	kidney:	n/a

No data

Variant related genes	Relation type
ENSG00000224370	TF binding region
ENSG00000224370	CpG island

Extended variants
information (count: 553 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:553 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537615017	chr7:56435660-56435661	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs372920774	chr7:56435679-56435680	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555914353	chr7:56435693-56435694	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567640141	chr7:56435700-56435701	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375746226	chr7:56435701-56435702	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs367753450	chr7:56435705-56435706	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs11768612	chr7:56435709-56435710	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553089155	chr7:56435710-56435711	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11762027	chr7:56435721-56435722	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551023406	chr7:56435722-56435723	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185402138	chr7:56435726-56435727	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545700994	chr7:56435730-56435731	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11765582	chr7:56435734-56435735	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570957275	chr7:56435754-56435755	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139388710	chr7:56435768-56435769	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543177228	chr7:56435773-56435774	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561478278	chr7:56435774-56435775	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528957969	chr7:56435777-56435778	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541065952	chr7:56435798-56435799	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559098033	chr7:56435800-56435801	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532896670	chr7:56435804-56435805	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552127566	chr7:56435814-56435815	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371316762	chr7:56435815-56435816	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531165353	chr7:56435816-56435817	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149255642	chr7:56435818-56435819	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567795400	chr7:56435826-56435827	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534799600	chr7:56435854-56435855	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547031347	chr7:56435869-56435870	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571554236	chr7:56435873-56435874	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369338337	chr7:56435876-56435877	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557644937	chr7:56435899-56435900	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575914667	chr7:56435908-56435909	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536872124	chr7:56435912-56435913	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555266380	chr7:56435917-56435918	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573718828	chr7:56435928-56435929	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs71528889	chr7:56435929-56435930	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs71528890	chr7:56435932-56435933	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs74793499	chr7:56435943-56435944	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540774569	chr7:56435944-56435945	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78813900	chr7:56435946-56435947	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76197044	chr7:56435958-56435959	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191825187	chr7:56435976-56435977	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144440074	chr7:56435978-56435979	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
44	rs369421306	chr7:56435979-56435980	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371931596	chr7:56435990-56435991	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374710040	chr7:56435991-56435992	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201743572	chr7:56435992-56435993	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531228824	chr7:56436010-56436011	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369058997	chr7:56436017-56436018	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536625905	chr7:56436019-56436020	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Wilms tumour	21544195	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Biliary cancer	19435499	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Esophageal cancer	21851588	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Intracranial ependymoma	16609018	CNVD
Lung cancer	21911935	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17925434	CNVD
Glioma	24330732	CNVD
Lung adenocarcinoma	23938291	CNVD
Glioma	17634744	CNVD
Oral squamous cell carcinoma	19276369	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Lung cancer	20031968	CNVD
Glioblastoma	17090523	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Glioma	17123091	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Medullary thyroid carcinoma	18765511	CNVD
small cell lung cancer	20016488	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:56434200-56439400	Weak transcription	Right Atrium	heart
2	chr7:56434800-56436400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:56436200-56436800	ZNF genes & repeats	Colonic Mucosa	Colon
4	chr7:56439000-56439600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:56439400-56439800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
6	chr7:56439400-56439800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:56439400-56439800	ZNF genes & repeats	Pancreas	Pancrea
8	chr7:56439400-56439800	ZNF genes & repeats	Right Atrium	heart
9	chr7:56439400-56439800	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
10	chr7:56439400-56439800	ZNF genes & repeats	Spleen	Spleen
11	chr7:56439600-56439800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
12	chr7:56439600-56439800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr7:56439600-56439800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr7:56439600-56439800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr7:56439600-56439800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr7:56439600-56439800	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
17	chr7:56439600-56439800	ZNF genes & repeats	Aorta	Aorta
18	chr7:56439600-56439800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
19	chr7:56439600-56439800	ZNF genes & repeats	Esophagus	oesophagus
20	chr7:56439600-56439800	ZNF genes & repeats	Fetal Stomach	stomach
21	chr7:56439600-56439800	ZNF genes & repeats	Gastric	stomach
22	chr7:56439600-56439800	ZNF genes & repeats	Left Ventricle	heart
23	chr7:56439600-56439800	ZNF genes & repeats	Lung	lung
24	chr7:56439600-56439800	ZNF genes & repeats	Ovary	ovary
25	chr7:56439600-56439800	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 31	rectum
26	chr7:56439600-56439800	ZNF genes & repeats	Right Ventricle	heart
27	chr7:56439600-56439800	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
28	chr7:56439600-56439800	ZNF genes & repeats	Thymus	Thymus
29	chr7:56439600-56439800	ZNF genes & repeats	Dnd41	blood
30	chr7:56439800-56441000	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr7:56439800-56441000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr7:56439800-56441000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr7:56439800-56441000	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr7:56439800-56441000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr7:56439800-56441000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr7:56439800-56441000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr7:56439800-56441000	Weak transcription	Aorta	Aorta
38	chr7:56439800-56441000	Weak transcription	Duodenum Mucosa	Duodenum
39	chr7:56439800-56441000	Weak transcription	Fetal Stomach	stomach
40	chr7:56439800-56441000	Weak transcription	Gastric	stomach
41	chr7:56439800-56441000	Weak transcription	Left Ventricle	heart
42	chr7:56439800-56441000	Weak transcription	Lung	lung
43	chr7:56439800-56441000	Weak transcription	Ovary	ovary
44	chr7:56439800-56441000	Weak transcription	Right Ventricle	heart
45	chr7:56439800-56441000	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr7:56439800-56441000	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr7:56439800-56441000	Weak transcription	Thymus	Thymus
48	chr7:56439800-56441000	Weak transcription	Spleen	Spleen
49	chr7:56439800-56441000	Weak transcription	Dnd41	blood
50	chr7:56439800-56442800	Weak transcription	Right Atrium	heart

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