Variant report

Variant	nsv1013586
Chromosome Location	chr2:73848777-73906844
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:602)
CpG islands
(count:1037)
Chromatin interactive
region (count:12)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:602 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:73857942-73858125	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:73869857-73870120	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:73867690-73868035	HepG2	liver:	n/a	n/a
4	ATF2	chr2:73901924-73902346	GM12878	blood:	n/a	n/a
5	ATF3	chr2:73903390-73903706	K562	blood:	n/a	n/a
6	BACH1	chr2:73857107-73857303	K562	blood:	n/a	n/a
7	BATF	chr2:73901777-73902343	GM12878	blood:	n/a	n/a
8	BATF	chr2:73851278-73851536	GM12878	blood:	n/a	chr2:73851419-73851430
9	BATF	chr2:73851315-73851489	GM12878	blood:	n/a	chr2:73851419-73851430
10	BATF	chr2:73901924-73902350	GM12878	blood:	n/a	n/a
11	BATF	chr2:73855647-73855936	GM12878	blood:	n/a	n/a
12	BCL11A	chr2:73855638-73856013	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:73901938-73902290	GM12878	blood:	n/a	chr2:73902211-73902220 chr2:73902210-73902219
14	BHLHE40	chr2:73871815-73871977	K562	blood:	n/a	n/a
15	CBX3	chr2:73865650-73865822	K562	blood:	n/a	n/a
16	CEBPB	chr2:73867603-73868071	MCF-7	breast:	n/a	chr2:73867845-73867858
17	CEBPB	chr2:73903414-73903663	A549	lung:	n/a	chr2:73903539-73903550
18	CEBPB	chr2:73877771-73878092	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:73903375-73903643	IMR90	lung:	n/a	chr2:73903539-73903550
20	CEBPB	chr2:73903437-73903637	H1-hESC	embryonic stem cell:	n/a	chr2:73903539-73903550
21	CEBPB	chr2:73903402-73903602	Hela-S3	cervix:	n/a	chr2:73903539-73903550
22	CEBPB	chr2:73865645-73865764	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr2:73877646-73878600	HepG2	liver:	n/a	chr2:73878449-73878460
24	CEBPB	chr2:73877660-73878170	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:73903410-73903643	K562	blood:	n/a	chr2:73903539-73903550
26	CEBPB	chr2:73903357-73903734	K562	blood:	n/a	chr2:73903539-73903550
27	CEBPB	chr2:73867840-73867965	A549	lung:	n/a	chr2:73867845-73867858
28	CEBPB	chr2:73877667-73878169	A549	lung:	n/a	n/a
29	CEBPB	chr2:73903369-73903615	HepG2	liver:	n/a	chr2:73903539-73903550
30	CEBPB	chr2:73869936-73870184	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:73869472-73869730	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:73859061-73859298	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:73869492-73869669	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:73903365-73903683	K562	blood:	n/a	chr2:73903539-73903550
35	CEBPB	chr2:73877993-73878055	K562	blood:	n/a	n/a
36	CEBPB	chr2:73900871-73900878	A549	lung:	n/a	n/a
37	CEBPB	chr2:73900813-73900977	K562	blood:	n/a	chr2:73900873-73900886
38	CEBPB	chr2:73867630-73868101	MCF-7	breast:	n/a	chr2:73867845-73867858
39	CEBPB	chr2:73867669-73868041	HepG2	liver:	n/a	chr2:73867845-73867858
40	CHD2	chr2:73869804-73870074	HepG2	liver:	n/a	n/a
41	CTCF	chr2:73878940-73879090	RPTEC	kidney:	n/a	n/a
42	CTCF	chr2:73857840-73857990	GM12870	blood:	n/a	n/a
43	CTCF	chr2:73851860-73852010	SAEC	small airway:	n/a	n/a
44	CTCF	chr2:73851829-73852065	Medullo	brain:	n/a	n/a
45	CTCF	chr2:73851700-73852160	A549	lung:	n/a	n/a
46	CTCF	chr2:73857940-73858090	AG04449	skin:	n/a	chr2:73857989-73858007 chr2:73857992-73858005 chr2:73857994-73858002 chr2:73857991-73858012 chr2:73857990-73858006
47	CTCF	chr2:73857851-73858108	NHEK	skin:	n/a	chr2:73857989-73858007 chr2:73857992-73858005 chr2:73857994-73858002 chr2:73857991-73858012 chr2:73857990-73858006
48	CTCF	chr2:73857840-73857990	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr2:73857760-73858273	SK-N-SH	brain:	n/a	chr2:73857989-73858007 chr2:73857992-73858005 chr2:73857994-73858002 chr2:73857991-73858012 chr2:73857990-73858006
50	CTCF	chr2:73858060-73858210	NHEK	skin:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:73870105-73870155	HNPCEpiC	eye:	n/a
2	chr2:73870105-73870155	ProgFib	skin:	n/a
3	chr2:73871849-73871899	HCF	heart:	n/a
4	chr2:73869666-73869716	LNCaP	prostate:	n/a
5	chr2:73871942-73871992	HCM	heart:	n/a
6	chr2:73867196-73867246	HCPEpiC	choroid plexus:	n/a
7	chr2:73870294-73870344	ProgFib	skin:	n/a
8	chr2:73870105-73870155	AG09319	gingival:	n/a
9	chr2:73871855-73871905	ECC-1	luminal epithelium:	n/a
10	chr2:73871782-73871832	K562	blood:	n/a
11	chr2:73871230-73871280	HCT-116	colon:	n/a
12	chr2:73871782-73871832	BE2_C	brain:	n/a
13	chr2:73870294-73870344	PrEC	prostate:	n/a
14	chr2:73871855-73871905	ProgFib	skin:	n/a
15	chr2:73868736-73868786	ECC-1	luminal epithelium:	n/a
16	chr2:73867196-73867246	AG09319	gingival:	n/a
17	chr2:73871855-73871905	HPAEpiC	pulmonary alveolar:	n/a
18	chr2:73868917-73868967	HEK293	kidney:	embryo
19	chr2:73870653-73870703	GM12892	blood:	n/a
20	chr2:73871942-73871992	BJ	skin:	n/a
21	chr2:73871942-73871992	Hepatocyte	liver:	n/a
22	chr2:73870294-73870344	NHDF-neo	bronchial:	n/a
23	chr2:73871849-73871899	SK-N-SH_RA	brain:	n/a
24	chr2:73871855-73871905	HEK293	kidney:	embryo
25	chr2:73869516-73869566	HCM	heart:	n/a
26	chr2:73868917-73868967	GM19239	blood:	n/a
27	chr2:73870294-73870344	HCM	heart:	n/a
28	chr2:73869666-73869716	BE2_C	brain:	n/a
29	chr2:73870294-73870344	BJ	skin:	n/a
30	chr2:73870294-73870344	GM06990	blood:	n/a
31	chr2:73869516-73869566	GM06990	blood:	n/a
32	chr2:73867196-73867246	ovcar-3	ovarian:	n/a
33	chr2:73871309-73871359	T-47D	breast:	n/a
34	chr2:73869666-73869716	HEK293	kidney:	embryo
35	chr2:73870105-73870155	HepG2	liver:	n/a
36	chr2:73868919-73868969	HPAEpiC	pulmonary alveolar:	n/a
37	chr2:73868917-73868967	HCT-116	colon:	n/a
38	chr2:73868736-73868786	NHBE	bronchial:	n/a
39	chr2:73868736-73868786	SK-N-SH	brain:	n/a
40	chr2:73869966-73870016	CMK	blood:	n/a
41	chr2:73869516-73869566	SKMC	muscle:	n/a
42	chr2:73871230-73871280	SAEC	small airway:	n/a
43	chr2:73869516-73869566	HCT-116	colon:	n/a
44	chr2:73869666-73869716	MCF-7	breast:	n/a
45	chr2:73871230-73871280	IMR90	lung:	fetal
46	chr2:73868919-73868969	HCT-116	colon:	n/a
47	chr2:73871782-73871832	HMEC	breast:	n/a
48	chr2:73870105-73870155	HRE	kidney:	n/a
49	chr2:73871309-73871359	BJ	skin:	n/a
50	chr2:73868917-73868967	ProgFib	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:73906056..73907836-chr2:74356105..74358909,2	MCF-7	breast:
2	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
3	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
4	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
5	chr2:73863562..73865457-chr2:73866043..73867971,2	MCF-7	breast:
6	chr2:73850004..73850829-chr2:73907369..73907993,2	K562	blood:
7	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
8	chr2:73868945..73872912-chr2:73927731..73932752,4	MCF-7	breast:
9	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
10	chr2:73857783..73858474-chr2:73917561..73918197,2	MCF-7	breast:
11	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
12	chr2:73863562..73865457-chr2:73866043..73867971,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALMS1-3	chr2:73900940-73901123	NR_003683
2	lnc-ALMS1-2	chr2:73868076-73868755	NONHSAT071625
3	lnc-ALMS1-3	chr2:73899935-73900177	NR_003683
4	lnc-ALMS1-3	chr2:73901969-73902032	NR_003683
5	lnc-ALMS1-3	chr2:73899436-73899622	NR_003683
6	lnc-ALMS1-3	chr2:73898207-73898277	NR_003683
7	lnc-ALMS1-3	chr2:73872046-73872281	NR_003683

No data

Variant related genes	Relation type
ALMS1P	TF binding region
NAT8	TF binding region
ALMS1P	CpG island
NAT8	CpG island
ENSG00000204872	chromatin interactions

Extended variants
information (count: 2061 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2061 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183977321	chr2:73848782-73848783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs76702813	chr2:73848817-73848818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557531529	chr2:73848852-73848853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566580596	chr2:73848863-73848864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374202692	chr2:73848875-73848876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs13416622	chr2:73848890-73848891	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs554930228	chr2:73848895-73848896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145655145	chr2:73848900-73848901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573344056	chr2:73848901-73848902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544501961	chr2:73848922-73848923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs13391258	chr2:73848933-73848934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs578080681	chr2:73849022-73849023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545599719	chr2:73849029-73849030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560551042	chr2:73849123-73849124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527770110	chr2:73849138-73849139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543183517	chr2:73849139-73849140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs6705977	chr2:73849170-73849171	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs531738048	chr2:73849206-73849207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550559435	chr2:73849284-73849285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569146049	chr2:73849286-73849287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532953002	chr2:73849290-73849291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373811001	chr2:73849314-73849315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551534050	chr2:73849338-73849339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186822464	chr2:73849382-73849383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533635995	chr2:73849403-73849404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570398785	chr2:73849431-73849432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555092201	chr2:73849435-73849436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192793652	chr2:73849472-73849473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537833130	chr2:73849494-73849495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537458272	chr2:73849510-73849511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574045259	chr2:73849521-73849522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556547212	chr2:73849531-73849532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139861711	chr2:73849532-73849533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545410350	chr2:73849562-73849563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554333538	chr2:73849600-73849601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114765026	chr2:73849701-73849702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373978049	chr2:73849715-73849716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561374801	chr2:73849734-73849735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576467817	chr2:73849759-73849760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11899455	chr2:73849810-73849811	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs565161321	chr2:73849814-73849815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367828071	chr2:73849820-73849821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533241877	chr2:73849837-73849838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145495374	chr2:73849843-73849844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6546861	chr2:73849861-73849862	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs527488550	chr2:73849877-73849878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548628335	chr2:73849906-73849907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs76562012	chr2:73849925-73849926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184338155	chr2:73849941-73849942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549734200	chr2:73849947-73849948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Hepatocellular carcinoma	16750200	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:227 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73830600-73854800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr2:73836400-73852600	Weak transcription	Ovary	ovary
3	chr2:73838400-73852600	Weak transcription	Right Ventricle	heart
4	chr2:73838600-73852600	Weak transcription	Pancreas	Pancrea
5	chr2:73838800-73849600	Weak transcription	Brain Germinal Matrix	brain
6	chr2:73842600-73852600	Weak transcription	Left Ventricle	heart
7	chr2:73844000-73854800	Weak transcription	Fetal Brain Female	brain
8	chr2:73844200-73848800	Weak transcription	Aorta	Aorta
9	chr2:73850000-73850200	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr2:73850200-73852400	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr2:73850800-73851400	Enhancers	GM12878-XiMat	blood
12	chr2:73851400-73853000	Weak transcription	GM12878-XiMat	blood
13	chr2:73852000-73852600	Enhancers	HepG2	liver
14	chr2:73852400-73852600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr2:73852400-73854000	Enhancers	Liver	Liver
16	chr2:73852400-73857400	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr2:73852600-73852800	Enhancers	Fetal Intestine Large	intestine
18	chr2:73852600-73852800	Enhancers	Left Ventricle	heart
19	chr2:73852600-73852800	Flanking Active TSS	HepG2	liver
20	chr2:73852600-73853000	Enhancers	Colonic Mucosa	Colon
21	chr2:73852600-73853200	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr2:73852600-73853200	Enhancers	Duodenum Mucosa	Duodenum
23	chr2:73852600-73853200	Enhancers	Pancreas	Pancrea
24	chr2:73852600-73853200	Enhancers	Right Ventricle	heart
25	chr2:73852600-73853800	Enhancers	Ovary	ovary
26	chr2:73852600-73854000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr2:73852600-73854200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr2:73852600-73854400	Enhancers	Primary hematopoietic stem cells	blood
29	chr2:73852600-73855000	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr2:73852800-73853000	Enhancers	HepG2	liver
31	chr2:73852800-73853200	Enhancers	A549	lung
32	chr2:73852800-73853200	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr2:73853000-73853200	Flanking Active TSS	HepG2	liver
34	chr2:73853000-73853400	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr2:73853000-73854000	Enhancers	GM12878-XiMat	blood
36	chr2:73853200-73853600	Enhancers	HepG2	liver
37	chr2:73853400-73853600	Enhancers	Fetal Intestine Large	intestine
38	chr2:73853800-73854000	Weak transcription	Ovary	ovary
39	chr2:73854000-73854200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr2:73854000-73858000	Weak transcription	Liver	Liver
41	chr2:73854800-73855000	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr2:73855600-73857000	Enhancers	GM12878-XiMat	blood
43	chr2:73856600-73857000	Weak transcription	HSMMtube	muscle
44	chr2:73857000-73857200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
45	chr2:73857000-73857200	Active TSS	Primary B cells from cord blood	blood
46	chr2:73857000-73857200	Active TSS	NHLF	lung
47	chr2:73857000-73857400	Active TSS	GM12878-XiMat	blood
48	chr2:73857000-73857400	Active TSS	HSMM	muscle
49	chr2:73857000-73857400	ZNF genes & repeats	HSMMtube	muscle
50	chr2:73857400-73858800	Weak transcription	HSMMtube	muscle

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