Variant report

Variant	nsv583194
Chromosome Location	chr2:141409166-141471725
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:141454048-141454388	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr2:141412222-141412454	GM12878	blood:	n/a	chr2:141412251-141412260
3	CBX3	chr2:141452720-141453189	HCT-116	colon:	n/a	n/a
4	CCNT2	chr2:141438605-141438793	K562	blood:	n/a	n/a
5	CEBPB	chr2:141422596-141422881	A549	lung:	n/a	chr2:141422733-141422742 chr2:141422733-141422742 chr2:141422733-141422744 chr2:141422733-141422742 chr2:141422731-141422742 chr2:141422733-141422742
6	CEBPB	chr2:141436115-141436374	IMR90	lung:	n/a	n/a
7	CEBPB	chr2:141452591-141453111	HCT-116	colon:	n/a	n/a
8	CEBPB	chr2:141452735-141453068	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:141413028-141413295	A549	lung:	n/a	chr2:141413158-141413169
10	CEBPB	chr2:141412955-141414108	Hela-S3	cervix:	n/a	chr2:141413719-141413730 chr2:141413158-141413169 chr2:141414049-141414060 chr2:141414049-141414060
11	CEBPB	chr2:141452680-141453086	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr2:141456315-141456644	HepG2	liver:	n/a	chr2:141456478-141456489
13	CEBPB	chr2:141413019-141413303	A549	lung:	n/a	chr2:141413158-141413169
14	CEBPB	chr2:141415225-141415654	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr2:141452510-141453235	HCT-116	colon:	n/a	n/a
16	CEBPB	chr2:141456329-141456621	IMR90	lung:	n/a	chr2:141456478-141456489
17	CEBPB	chr2:141419274-141419355	A549	lung:	n/a	n/a
18	CEBPB	chr2:141438062-141438277	H1-hESC	embryonic stem cell:	n/a	chr2:141438204-141438215 chr2:141438204-141438217
19	CEBPB	chr2:141422574-141422887	IMR90	lung:	n/a	chr2:141422733-141422742 chr2:141422733-141422742 chr2:141422733-141422744 chr2:141422733-141422742 chr2:141422731-141422742 chr2:141422733-141422742
20	CEBPB	chr2:141452764-141453058	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:141436083-141436351	A549	lung:	n/a	n/a
22	CEBPB	chr2:141413012-141413302	IMR90	lung:	n/a	chr2:141413158-141413169
23	CEBPB	chr2:141438136-141438309	K562	blood:	n/a	chr2:141438284-141438296 chr2:141438204-141438215 chr2:141438204-141438217
24	CEBPB	chr2:141456328-141456626	A549	lung:	n/a	chr2:141456478-141456489
25	CEBPB	chr2:141436201-141436313	K562	blood:	n/a	n/a
26	CEBPB	chr2:141412904-141413446	A549	lung:	n/a	chr2:141413158-141413169
27	CEBPB	chr2:141438056-141438368	IMR90	lung:	n/a	chr2:141438284-141438296 chr2:141438204-141438215 chr2:141438204-141438217
28	CEBPB	chr2:141436092-141436417	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:141438025-141438380	HepG2	liver:	n/a	chr2:141438284-141438296 chr2:141438204-141438215 chr2:141438204-141438217
30	CEBPB	chr2:141413032-141413293	HepG2	liver:	n/a	chr2:141413158-141413169
31	CEBPB	chr2:141422561-141422890	HepG2	liver:	n/a	chr2:141422733-141422742 chr2:141422733-141422742 chr2:141422733-141422744 chr2:141422733-141422742 chr2:141422731-141422742 chr2:141422733-141422742
32	CEBPB	chr2:141436168-141436280	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr2:141438069-141438295	A549	lung:	n/a	chr2:141438204-141438215 chr2:141438204-141438217
34	CHD2	chr2:141415287-141415565	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr2:141452880-141453030	HMEC	breast:	n/a	chr2:141452968-141452984 chr2:141452967-141452985 chr2:141452969-141452990
36	CTCF	chr2:141429068-141429341	GM12878	blood:	n/a	n/a
37	CTCF	chr2:141454180-141454330	HEK293	kidney:	n/a	n/a
38	CTCF	chr2:141454100-141454250	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr2:141452880-141453030	AG10803	skin:	n/a	chr2:141452968-141452984 chr2:141452967-141452985 chr2:141452969-141452990
40	CTCF	chr2:141454160-141454310	GM12871	blood:	n/a	n/a
41	CTCF	chr2:141454200-141454350	GM12866	blood:	n/a	n/a
42	CTCF	chr2:141454119-141454314	GM19238	blood:	n/a	n/a
43	CTCF	chr2:141452940-141453090	AoAF	blood vessel:	n/a	chr2:141452968-141452984 chr2:141452967-141452985 chr2:141452969-141452990
44	CTCF	chr2:141429120-141429241	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr2:141454118-141454337	A549	lung:	n/a	n/a
46	CTCF	chr2:141452886-141453043	MCF-7	breast:	n/a	chr2:141452968-141452984 chr2:141452967-141452985 chr2:141452969-141452990
47	CTCF	chr2:141454293-141454334	GM20000	blood:	n/a	n/a
48	CTCF	chr2:141454119-141454345	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr2:141454168-141454270	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr2:141454140-141454290	WERI-Rb-1	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:141441408-141441458	HRCEpiC	kidney:	n/a
2	chr2:141441408-141441458	Jurkat	blood:	n/a
3	chr2:141441408-141441458	H1-hESC	embryonic stem cell:	embryo
4	chr2:141441408-141441458	MCF-7	breast:	n/a
5	chr2:141441408-141441458	HepG2	liver:	n/a
6	chr2:141441479-141441529	Jurkat	blood:	n/a
7	chr2:141441479-141441529	SAEC	small airway:	n/a
8	chr2:141441479-141441529	GM06990	blood:	n/a
9	chr2:141441479-141441529	ProgFib	skin:	n/a
10	chr2:141441479-141441529	HRE	kidney:	n/a
11	chr2:141441408-141441458	Hela-S3	cervix:	n/a
12	chr2:141441408-141441458	ovcar-3	ovarian:	n/a
13	chr2:141441479-141441529	SK-N-SH_RA	brain:	n/a
14	chr2:141441479-141441529	H1-hESC	embryonic stem cell:	embryo
15	chr2:141441479-141441529	Hepatocyte	liver:	n/a
16	chr2:141441408-141441458	IMR90	lung:	fetal
17	chr2:141441479-141441529	ECC-1	luminal epithelium:	n/a
18	chr2:141441479-141441529	SK-N-SH	brain:	n/a
19	chr2:141441479-141441529	MCF-7	breast:	n/a
20	chr2:141441479-141441529	IMR90	lung:	fetal
21	chr2:141441479-141441529	SK-N-MC	brain:	n/a
22	chr2:141441479-141441529	SKMC	muscle:	n/a
23	chr2:141441479-141441529	RPTEC	kidney:	n/a
24	chr2:141441408-141441458	AG04450	lung:	fetal
25	chr2:141441479-141441529	BE2_C	brain:	n/a
26	chr2:141441408-141441458	GM12892	blood:	n/a
27	chr2:141441479-141441529	CMK	blood:	n/a
28	chr2:141441408-141441458	HCPEpiC	choroid plexus:	n/a
29	chr2:141441479-141441529	AG04450	lung:	fetal
30	chr2:141441479-141441529	GM12892	blood:	n/a
31	chr2:141441479-141441529	HUVEC	blood vessel:	n/a
32	chr2:141441408-141441458	NT2-D1	testis:	n/a
33	chr2:141441479-141441529	Hela-S3	cervix:	n/a
34	chr2:141441408-141441458	SK-N-SH	brain:	n/a
35	chr2:141441479-141441529	AG09309	skin:	n/a
36	chr2:141441479-141441529	HCPEpiC	choroid plexus:	n/a
37	chr2:141441479-141441529	ovcar-3	ovarian:	n/a
38	chr2:141441408-141441458	HCT-116	colon:	n/a
39	chr2:141441408-141441458	NB4	blood:	n/a
40	chr2:141441479-141441529	HRCEpiC	kidney:	n/a
41	chr2:141441408-141441458	HEEpiC	esophagus:	n/a
42	chr2:141441408-141441458	SKMC	muscle:	n/a
43	chr2:141441408-141441458	SK-N-SH_RA	brain:	n/a
44	chr2:141441479-141441529	GM12878	blood:	n/a
45	chr2:141441479-141441529	PANC-1	pancreas:	n/a
46	chr2:141441408-141441458	AG04449	skin:	fetal
47	chr2:141441479-141441529	HCT-116	colon:	n/a
48	chr2:141441479-141441529	HCF	heart:	n/a
49	chr2:141441479-141441529	HEEpiC	esophagus:	n/a
50	chr2:141441479-141441529	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:141422971..141423545-chr20:53166808..53167673,2	MCF-7	breast:
2	chr2:141432163..141433732-chr2:141435544..141437895,2	MCF-7	breast:
3	chr2:141466926..141469105-chr2:141480476..141482979,2	MCF-7	breast:
4	chr2:141462311..141465013-chr2:141470003..141471554,2	K562	blood:
5	chr2:141462311..141465013-chr2:141470003..141471554,2	K562	blood:
6	chr2:141425529..141427088-chr2:141449758..141451483,2	MCF-7	breast:
7	chr2:141469791..141471888-chr2:141475142..141477938,2	MCF-7	breast:
8	chr2:141425529..141427088-chr2:141449758..141451483,2	MCF-7	breast:
9	chr2:141432163..141433732-chr2:141435544..141437895,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000236440	TF binding region
ENSG00000236440	CpG island

Extended variants
information (count: 966 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:966 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs514478	chr2:141409166-141409167	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575234747	chr2:141409179-141409180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561225491	chr2:141409256-141409257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs116406740	chr2:141409288-141409289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs367684384	chr2:141409292-141409293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77966117	chr2:141409295-141409296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577880711	chr2:141409298-141409299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566207080	chr2:141409306-141409307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540496752	chr2:141409326-141409327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538800106	chr2:141409357-141409358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560421092	chr2:141409379-141409380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10496851	chr2:141409383-141409384	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs6760190	chr2:141409411-141409412	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs375181608	chr2:141409419-141409420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115249634	chr2:141409525-141409526	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs180838298	chr2:141409528-141409529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550723899	chr2:141409531-141409532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150198744	chr2:141409603-141409604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138926503	chr2:141409610-141409611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185141397	chr2:141409622-141409623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566772388	chr2:141409628-141409629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536139060	chr2:141409630-141409631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113645605	chr2:141409635-141409636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34949572	chr2:141409673-141409674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34696444	chr2:141409698-141409699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549513470	chr2:141409719-141409720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568863331	chr2:141409757-141409758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537917486	chr2:141409772-141409773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113457479	chr2:141409773-141409774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530724293	chr2:141409781-141409782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537152518	chr2:141409843-141409844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112230047	chr2:141409851-141409852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191965455	chr2:141409918-141409919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370974275	chr2:141409961-141409962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577045995	chr2:141409976-141409977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542955	chr2:141409996-141409997	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs573943077	chr2:141410002-141410003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542849333	chr2:141410011-141410012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562677830	chr2:141410025-141410026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575667908	chr2:141410066-141410067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544677138	chr2:141410077-141410078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182273858	chr2:141410127-141410128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs115674223	chr2:141410149-141410150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76329660	chr2:141410153-141410154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114482549	chr2:141410168-141410169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34984492	chr2:141410211-141410212	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs569397	chr2:141410231-141410232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545482	chr2:141410232-141410233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553137356	chr2:141410235-141410236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545494	chr2:141410239-141410240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	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
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma	21080181	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Autism	22543975	CNVD
Cancer	20164920	CNVD
Hypertension	22686481	CNVD
Hypospadia	22686481	CNVD
Intellectual disability	22686481	CNVD
Omphalocele	22686481	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141408600-141412200	Weak transcription	Hela-S3	cervix
2	chr2:141408800-141409200	Weak transcription	HUVEC	blood vessel
3	chr2:141408800-141410000	Enhancers	A549	lung
4	chr2:141409200-141409400	Enhancers	HUVEC	blood vessel
5	chr2:141409400-141413000	Weak transcription	HUVEC	blood vessel
6	chr2:141410000-141412000	Weak transcription	A549	lung
7	chr2:141411800-141412600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:141412000-141412400	Flanking Active TSS	A549	lung
9	chr2:141412000-141412600	Enhancers	Fetal Brain Female	brain
10	chr2:141412200-141412400	Enhancers	Hela-S3	cervix
11	chr2:141412400-141413000	Weak transcription	Hela-S3	cervix
12	chr2:141412400-141414000	Active TSS	A549	lung
13	chr2:141413000-141413200	Flanking Active TSS	HUVEC	blood vessel
14	chr2:141413000-141413800	Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr2:141413000-141413800	Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr2:141413000-141417400	Enhancers	Hela-S3	cervix
17	chr2:141413200-141413600	Active TSS	HUVEC	blood vessel
18	chr2:141413600-141413800	Flanking Active TSS	HUVEC	blood vessel
19	chr2:141413800-141417200	Enhancers	HUVEC	blood vessel
20	chr2:141414000-141416400	Enhancers	A549	lung
21	chr2:141414200-141418200	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr2:141415400-141415600	Enhancers	Fetal Lung	lung
23	chr2:141416200-141417000	Enhancers	Fetal Kidney	kidney
24	chr2:141416400-141416600	Flanking Active TSS	A549	lung
25	chr2:141416600-141416800	Enhancers	A549	lung
26	chr2:141416800-141417400	Flanking Active TSS	A549	lung
27	chr2:141417000-141420800	Weak transcription	Fetal Kidney	kidney
28	chr2:141417400-141418000	Enhancers	A549	lung
29	chr2:141420400-141421200	Enhancers	Adipose Nuclei	Adipose
30	chr2:141420800-141421200	Enhancers	Fetal Kidney	kidney
31	chr2:141421200-141422000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr2:141422000-141424400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr2:141424000-141424800	Enhancers	Dnd41	blood
34	chr2:141424000-141425800	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr2:141424400-141424800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:141424400-141425200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr2:141425800-141426400	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr2:141426400-141426600	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr2:141452000-141454200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr2:141452400-141453400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr2:141452600-141453000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr2:141452800-141453200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr2:141461400-141461800	Enhancers	Brain Angular Gyrus	brain
44	chr2:141461400-141462200	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr2:141469800-141470200	Active TSS	Skeletal Muscle Male	skeletal muscle
46	chr2:141470000-141470600	Active TSS	Skeletal Muscle Female	skeletal muscle
47	chr2:141470600-141471200	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr2:141471200-141471400	Active TSS	Skeletal Muscle Female	skeletal muscle
49	chr2:141471400-141472200	Weak transcription	Skeletal Muscle Female	skeletal muscle

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