Variant report

Variant	nsv461352
Chromosome Location	chr4:45448030-45587299
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	ATF1	chr4:45508139-45508307	K562	blood:	n/a	n/a
2	BACH1	chr4:45524358-45524446	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr4:45541453-45541711	GM12878	blood:	n/a	n/a
4	BATF	chr4:45486851-45487086	GM12878	blood:	n/a	n/a
5	BATF	chr4:45541459-45541692	GM12878	blood:	n/a	n/a
6	BCL11A	chr4:45462244-45462401	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr4:45462236-45462503	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr4:45462306-45462563	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr4:45505432-45505750	HepG2	liver:	n/a	chr4:45505570-45505581
10	CEBPB	chr4:45453007-45453183	K562	blood:	n/a	n/a
11	CEBPB	chr4:45455291-45455635	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr4:45455290-45455630	HepG2	liver:	n/a	n/a
13	CEBPB	chr4:45571706-45572005	A549	lung:	n/a	chr4:45571827-45571838 chr4:45571829-45571838 chr4:45571827-45571840 chr4:45571829-45571838 chr4:45571829-45571838 chr4:45571827-45571840 chr4:45571829-45571838 chr4:45571829-45571840
14	CEBPB	chr4:45529206-45529550	HepG2	liver:	n/a	chr4:45529359-45529368 chr4:45529357-45529368 chr4:45529359-45529368 chr4:45529398-45529409 chr4:45529357-45529370 chr4:45529397-45529408 chr4:45529359-45529368 chr4:45529357-45529370
15	CEBPB	chr4:45456959-45457177	IMR90	lung:	n/a	chr4:45457112-45457123
16	CEBPB	chr4:45529204-45529541	IMR90	lung:	n/a	chr4:45529359-45529368 chr4:45529357-45529368 chr4:45529359-45529368 chr4:45529398-45529409 chr4:45529357-45529370 chr4:45529397-45529408 chr4:45529359-45529368 chr4:45529357-45529370
17	CEBPB	chr4:45456973-45457165	A549	lung:	n/a	chr4:45457112-45457123
18	CEBPB	chr4:45529211-45529537	H1-hESC	embryonic stem cell:	n/a	chr4:45529359-45529368 chr4:45529357-45529368 chr4:45529359-45529368 chr4:45529398-45529409 chr4:45529357-45529370 chr4:45529397-45529408 chr4:45529359-45529368 chr4:45529357-45529370
19	CEBPB	chr4:45571650-45572022	HepG2	liver:	n/a	chr4:45571827-45571838 chr4:45571829-45571838 chr4:45571827-45571840 chr4:45571829-45571838 chr4:45571829-45571838 chr4:45571827-45571840 chr4:45571829-45571838 chr4:45571829-45571840
20	CEBPB	chr4:45529200-45529545	K562	blood:	n/a	chr4:45529359-45529368 chr4:45529357-45529368 chr4:45529359-45529368 chr4:45529398-45529409 chr4:45529357-45529370 chr4:45529397-45529408 chr4:45529359-45529368 chr4:45529357-45529370
21	CEBPB	chr4:45571671-45572012	IMR90	lung:	n/a	chr4:45571827-45571838 chr4:45571829-45571838 chr4:45571827-45571840 chr4:45571829-45571838 chr4:45571829-45571838 chr4:45571827-45571840 chr4:45571829-45571838 chr4:45571829-45571840
22	CEBPB	chr4:45455343-45455563	MCF-7	breast:	n/a	n/a
23	CEBPB	chr4:45505487-45505729	H1-hESC	embryonic stem cell:	n/a	chr4:45505570-45505581
24	CEBPB	chr4:45571678-45572010	K562	blood:	n/a	chr4:45571827-45571838 chr4:45571829-45571838 chr4:45571827-45571840 chr4:45571829-45571838 chr4:45571829-45571838 chr4:45571827-45571840 chr4:45571829-45571838 chr4:45571829-45571840
25	CEBPB	chr4:45456984-45457234	HepG2	liver:	n/a	chr4:45457193-45457204 chr4:45457112-45457123
26	CEBPB	chr4:45485401-45485861	Hela-S3	cervix:	n/a	chr4:45485740-45485753
27	CEBPB	chr4:45505412-45505759	IMR90	lung:	n/a	chr4:45505570-45505581
28	CEBPB	chr4:45571765-45571965	H1-hESC	embryonic stem cell:	n/a	chr4:45571827-45571838 chr4:45571829-45571838 chr4:45571827-45571840 chr4:45571829-45571838 chr4:45571829-45571838 chr4:45571827-45571840 chr4:45571829-45571838 chr4:45571829-45571840
29	CEBPB	chr4:45455286-45455634	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr4:45455318-45455545	T-47D	breast:	n/a	n/a
31	CTCF	chr4:45552801-45553115	GM12878	blood:	n/a	n/a
32	CTCF	chr4:45520990-45521134	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr4:45455340-45455490	K562	blood:	n/a	n/a
34	CTCF	chr4:45455326-45455541	GM10266	blood:	n/a	n/a
35	CTCF	chr4:45455275-45455589	Medullo	brain:	n/a	n/a
36	CTCF	chr4:45455286-45455545	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr4:45455380-45455530	BE2_C	brain:	n/a	n/a
38	CTCF	chr4:45455380-45455530	HMEC	breast:	n/a	n/a
39	CTCF	chr4:45455380-45455530	GM12872	blood:	n/a	n/a
40	CTCF	chr4:45552960-45553110	RPTEC	kidney:	n/a	n/a
41	CTCF	chr4:45518528-45518559	LNCaP	prostate:	n/a	n/a
42	CTCF	chr4:45520978-45521136	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:45451680-45451713	GM13977	blood:	n/a	n/a
44	CTCF	chr4:45455340-45455490	HL-60	blood:	n/a	n/a
45	CTCF	chr4:45455224-45455623	HepG2	liver:	n/a	n/a
46	CTCF	chr4:45455380-45455530	GM12868	blood:	n/a	n/a
47	CTCF	chr4:45455300-45455450	GM12868	blood:	n/a	n/a
48	CTCF	chr4:45520960-45521110	HEK293	kidney:	n/a	n/a
49	CTCF	chr4:45455323-45455550	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr4:45455421-45455523	GM19239	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:45459308-45459358	A549	lung:	n/a
2	chr4:45459545-45459595	AG10803	skin:	n/a
3	chr4:45459308-45459358	MCF-7	breast:	n/a
4	chr4:45459418-45459468	HCPEpiC	choroid plexus:	n/a
5	chr4:45459545-45459595	MCF-7	breast:	n/a
6	chr4:45459308-45459358	IMR90	lung:	fetal
7	chr4:45459308-45459358	HAEpiC	amniotic membrane:	n/a
8	chr4:45459418-45459468	Jurkat	blood:	n/a
9	chr4:45459308-45459358	SAEC	small airway:	n/a
10	chr4:45459545-45459595	GM19239	blood:	n/a
11	chr4:45459308-45459358	T-47D	breast:	n/a
12	chr4:45459545-45459595	Jurkat	blood:	n/a
13	chr4:45459418-45459468	PANC-1	pancreas:	n/a
14	chr4:45459418-45459468	NB4	blood:	n/a
15	chr4:45459308-45459358	U87	brain:	n/a
16	chr4:45459308-45459358	ECC-1	luminal epithelium:	n/a
17	chr4:45459418-45459468	HCM	heart:	n/a
18	chr4:45459308-45459358	Hela-S3	cervix:	n/a
19	chr4:45459545-45459595	SK-N-SH	brain:	n/a
20	chr4:45459418-45459468	HRCEpiC	kidney:	n/a
21	chr4:45459308-45459358	HUVEC	blood vessel:	n/a
22	chr4:45459418-45459468	IMR90	lung:	fetal
23	chr4:45459545-45459595	NT2-D1	testis:	n/a
24	chr4:45459308-45459358	Caco-2	colon:	n/a
25	chr4:45459545-45459595	Hela-S3	cervix:	n/a
26	chr4:45459418-45459468	HEEpiC	esophagus:	n/a
27	chr4:45459308-45459358	H1-hESC	embryonic stem cell:	embryo
28	chr4:45459308-45459358	HCF	heart:	n/a
29	chr4:45459545-45459595	PrEC	prostate:	n/a
30	chr4:45459545-45459595	NB4	blood:	n/a
31	chr4:45459308-45459358	HIPEpiC	eye:	n/a
32	chr4:45459308-45459358	Hepatocyte	liver:	n/a
33	chr4:45459418-45459468	HPAEpiC	pulmonary alveolar:	n/a
34	chr4:45459418-45459468	A549	lung:	n/a
35	chr4:45459418-45459468	PrEC	prostate:	n/a
36	chr4:45459418-45459468	GM06990	blood:	n/a
37	chr4:45459418-45459468	SAEC	small airway:	n/a
38	chr4:45459418-45459468	MCF-7	breast:	n/a
39	chr4:45459308-45459358	BJ	skin:	n/a
40	chr4:45459308-45459358	K562	blood:	n/a
41	chr4:45459545-45459595	H1-hESC	embryonic stem cell:	embryo
42	chr4:45459418-45459468	HNPCEpiC	eye:	n/a
43	chr4:45459418-45459468	AoSMC	blood vessel:	n/a
44	chr4:45459308-45459358	NHDF-neo	bronchial:	n/a
45	chr4:45459308-45459358	PrEC	prostate:	n/a
46	chr4:45459545-45459595	AG04450	lung:	fetal
47	chr4:45459545-45459595	HEK293	kidney:	embryo
48	chr4:45459418-45459468	HCT-116	colon:	n/a
49	chr4:45459545-45459595	GM12878	blood:	n/a
50	chr4:45459545-45459595	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:45552524..45553420-chr4:45743730..45744526,2	MCF-7	breast:
2	chr4:44929522..44930049-chr4:45454935..45455917,3	MCF-7	breast:

Variant related genes	Relation type
RNU6-931P	TF binding region
RNU6-931P	CpG island

Extended variants
information (count: 1140 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1140 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191155276	chr4:45448233-45448234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs182277229	chr4:45448246-45448247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187686374	chr4:45448284-45448285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150834929	chr4:45448292-45448293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139407195	chr4:45448302-45448303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs10025670	chr4:45448314-45448315	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs193285203	chr4:45448324-45448325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145689583	chr4:45448327-45448328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147715299	chr4:45448389-45448390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539392939	chr4:45448403-45448404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185124239	chr4:45448420-45448421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs190412810	chr4:45448445-45448446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs569706835	chr4:45448490-45448491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537738227	chr4:45448530-45448531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140936983	chr4:45448561-45448562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574136676	chr4:45448566-45448567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549312171	chr4:45448568-45448569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535236965	chr4:45448569-45448570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567596973	chr4:45448632-45448633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528500666	chr4:45448658-45448659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192904285	chr4:45448673-45448674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs144275464	chr4:45448676-45448677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs370727605	chr4:45448699-45448700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184004338	chr4:45448723-45448724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563337996	chr4:45448740-45448741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs147798432	chr4:45448769-45448770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188737379	chr4:45448773-45448774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs180755606	chr4:45448799-45448800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546553636	chr4:45448814-45448815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547572132	chr4:45448836-45448837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571668616	chr4:45448864-45448865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533049889	chr4:45448875-45448876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs117450349	chr4:45448883-45448884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539075103	chr4:45448911-45448912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148861233	chr4:45448957-45448958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113614425	chr4:45448983-45448984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368064286	chr4:45449007-45449008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557676033	chr4:45449012-45449013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534861260	chr4:45449083-45449084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185420003	chr4:45449090-45449091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571550077	chr4:45449132-45449133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538723290	chr4:45449147-45449148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs71611936	chr4:45449149-45449150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189433065	chr4:45449155-45449156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150938758	chr4:45449163-45449164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs116223854	chr4:45449180-45449181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182596345	chr4:45449189-45449190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115702732	chr4:45449225-45449226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573887338	chr4:45449248-45449249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541007302	chr4:45449284-45449285	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Olfactory neuroblastoma	18408657	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	16616336	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	20164919	CNVD
Renal cell carcinoma	18765545	CNVD
Gastric cancer	16891809	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:45448200-45449000	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr4:45448600-45449600	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr4:45452600-45453000	Enhancers	Fetal Heart	heart
4	chr4:45470200-45470800	Enhancers	Fetal Heart	heart
5	chr4:45473400-45473800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:45473400-45474800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:45473400-45474800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:45474600-45474800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:45477000-45478200	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr4:45477200-45478200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr4:45477400-45478200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr4:45477600-45478000	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr4:45477600-45478200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr4:45479400-45479800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr4:45479400-45480000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:45480000-45480600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:45484600-45485000	Enhancers	Fetal Lung	lung
18	chr4:45526000-45526200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr4:45526200-45532200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:45532200-45532600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr4:45532200-45532800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:45550800-45551400	Enhancers	Rectal Smooth Muscle	rectum
23	chr4:45553000-45553200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr4:45553800-45554400	Enhancers	Fetal Lung	lung
25	chr4:45554400-45557800	Weak transcription	Fetal Lung	lung
26	chr4:45556400-45557400	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr4:45556600-45557400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:45557000-45557400	Enhancers	Rectal Smooth Muscle	rectum
29	chr4:45557000-45558000	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr4:45557200-45557600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr4:45557200-45557800	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr4:45557200-45558000	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr4:45557400-45557800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr4:45557400-45558000	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr4:45557800-45558000	Enhancers	Fetal Lung	lung
36	chr4:45566600-45567400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr4:45567000-45567400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr4:45581000-45582800	Enhancers	Fetal Heart	heart
39	chr4:45582000-45582600	Enhancers	Fetal Lung	lung
40	chr4:45582400-45585200	Enhancers	Stomach Mucosa	stomach
41	chr4:45582800-45583200	Weak transcription	Fetal Heart	heart
42	chr4:45583200-45583600	Enhancers	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links