Variant report

Variant	nsv874478
Chromosome Location	chr2:87281373-87361162
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:725)
CpG islands
(count:674)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:725 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:87303415-87304067	K562	blood:	n/a	n/a
2	BATF	chr2:87303894-87304136	GM12878	blood:	n/a	n/a
3	BATF	chr2:87359687-87360006	GM12878	blood:	n/a	n/a
4	BATF	chr2:87303340-87303849	GM12878	blood:	n/a	n/a
5	BATF	chr2:87355904-87356145	GM12878	blood:	n/a	n/a
6	BATF	chr2:87299212-87299437	GM12878	blood:	n/a	n/a
7	BATF	chr2:87359765-87360029	GM12878	blood:	n/a	n/a
8	BATF	chr2:87355800-87356278	GM12878	blood:	n/a	n/a
9	BCL11A	chr2:87359754-87359999	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:87303316-87304131	GM12878	blood:	n/a	chr2:87303874-87303883
11	BCL11A	chr2:87359379-87359570	GM12878	blood:	n/a	n/a
12	BCL11A	chr2:87303323-87303874	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:87359630-87360025	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:87304285-87304456	GM12878	blood:	n/a	n/a
15	BHLHE40	chr2:87303382-87303879	HepG2	liver:	n/a	n/a
16	BHLHE40	chr2:87303369-87303773	A549	lung:	n/a	n/a
17	BHLHE40	chr2:87302885-87304239	GM12878	blood:	n/a	n/a
18	BHLHE40	chr2:87303069-87304197	K562	blood:	n/a	n/a
19	BHLHE40	chr2:87303347-87304264	HepG2	liver:	n/a	n/a
20	BHLHE40	chr2:87297693-87297913	K562	blood:	n/a	n/a
21	BHLHE40	chr2:87297701-87297910	GM12878	blood:	n/a	n/a
22	BRCA1	chr2:87303521-87304094	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr2:87313277-87313606	K562	blood:	n/a	n/a
24	CBX3	chr2:87313232-87313648	K562	blood:	n/a	n/a
25	CBX3	chr2:87303363-87304521	K562	blood:	n/a	n/a
26	CBX3	chr2:87303436-87304358	K562	blood:	n/a	n/a
27	CEBPB	chr2:87297550-87297867	IMR90	lung:	n/a	chr2:87297725-87297738
28	CEBPB	chr2:87300068-87300417	K562	blood:	n/a	n/a
29	CEBPB	chr2:87310975-87311245	K562	blood:	n/a	n/a
30	CEBPB	chr2:87297696-87297950	K562	blood:	n/a	chr2:87297725-87297738
31	CEBPB	chr2:87290711-87290954	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:87297689-87297891	H1-hESC	embryonic stem cell:	n/a	chr2:87297725-87297738
33	CEBPB	chr2:87289997-87290210	K562	blood:	n/a	n/a
34	CEBPB	chr2:87303428-87303729	Hela-S3	cervix:	n/a	n/a
35	CEBPD	chr2:87303387-87303646	HepG2	liver:	n/a	n/a
36	CEBPD	chr2:87303388-87303588	HepG2	liver:	n/a	n/a
37	CHD1	chr2:87303114-87304272	H1-hESC	embryonic stem cell:	n/a	chr2:87303892-87303902 chr2:87303553-87303563
38	CHD1	chr2:87302960-87303809	IMR90	lung:	n/a	chr2:87303553-87303563
39	CHD1	chr2:87303119-87304348	GM12878	blood:	n/a	chr2:87303892-87303902 chr2:87303553-87303563
40	CHD2	chr2:87303061-87304270	Hela-S3	cervix:	n/a	chr2:87303892-87303902 chr2:87303553-87303563
41	CHD2	chr2:87303378-87303736	HepG2	liver:	n/a	chr2:87303553-87303563
42	CHD2	chr2:87303408-87304053	K562	blood:	n/a	chr2:87303892-87303902 chr2:87303553-87303563
43	CHD2	chr2:87303399-87304194	GM12878	blood:	n/a	chr2:87303892-87303902 chr2:87303553-87303563
44	CTCF	chr2:87303095-87303113	Fibrobl	skin:	n/a	n/a
45	CTCF	chr2:87302540-87302690	GM12871	blood:	n/a	n/a
46	CTCF	chr2:87302560-87302710	GM06990	blood:	n/a	n/a
47	CTCF	chr2:87302660-87302810	BJ	skin:	n/a	chr2:87302699-87302712
48	CTCF	chr2:87303151-87303191	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr2:87302560-87302710	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr2:87333091-87333142	Kidney_OC	kidney:	n/a	n/a

(count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:87304894-87304944	HAEpiC	amniotic membrane:	n/a
2	chr2:87304894-87304944	T-47D	breast:	n/a
3	chr2:87302855-87302905	AG10803	skin:	n/a
4	chr2:87304894-87304944	HAEpiC	amniotic membrane:	n/a
5	chr2:87304894-87304944	T-47D	breast:	n/a
6	chr2:87302855-87302905	AG10803	skin:	n/a
7	chr2:87304015-87304065	PrEC	prostate:	n/a
8	chr2:87302643-87302693	GM12891	blood:	n/a
9	chr2:87304105-87304155	PANC-1	pancreas:	n/a
10	chr2:87308486-87308536	AG04450	lung:	fetal
11	chr2:87304216-87304266	AG04449	skin:	fetal
12	chr2:87304197-87304247	Jurkat	blood:	n/a
13	chr2:87304216-87304266	NHDF-neo	bronchial:	n/a
14	chr2:87304105-87304155	HepG2	liver:	n/a
15	chr2:87304197-87304247	HCT-116	colon:	n/a
16	chr2:87304216-87304266	HEK293	kidney:	embryo
17	chr2:87304197-87304247	GM12892	blood:	n/a
18	chr2:87308486-87308536	SAEC	small airway:	n/a
19	chr2:87303632-87303682	SK-N-SH_RA	brain:	n/a
20	chr2:87303632-87303682	AG09319	gingival:	n/a
21	chr2:87304894-87304944	H1-hESC	embryonic stem cell:	embryo
22	chr2:87304015-87304065	NB4	blood:	n/a
23	chr2:87304015-87304065	GM12878	blood:	n/a
24	chr2:87308486-87308536	SK-N-SH	brain:	n/a
25	chr2:87305913-87305963	SK-N-MC	brain:	n/a
26	chr2:87302855-87302905	CMK	blood:	n/a
27	chr2:87304105-87304155	NB4	blood:	n/a
28	chr2:87302162-87302212	AG09319	gingival:	n/a
29	chr2:87304105-87304155	GM19239	blood:	n/a
30	chr2:87304894-87304944	AG09309	skin:	n/a
31	chr2:87304894-87304944	AG04450	lung:	fetal
32	chr2:87302855-87302905	GM12878	blood:	n/a
33	chr2:87305913-87305963	SAEC	small airway:	n/a
34	chr2:87304197-87304247	H1-hESC	embryonic stem cell:	embryo
35	chr2:87304197-87304247	HPAEpiC	pulmonary alveolar:	n/a
36	chr2:87303632-87303682	NB4	blood:	n/a
37	chr2:87308486-87308536	T-47D	breast:	n/a
38	chr2:87303632-87303682	HRCEpiC	kidney:	n/a
39	chr2:87308486-87308536	K562	blood:	n/a
40	chr2:87308486-87308536	NHBE	bronchial:	n/a
41	chr2:87304105-87304155	HCT-116	colon:	n/a
42	chr2:87304197-87304247	NHDF-neo	bronchial:	n/a
43	chr2:87302643-87302693	SK-N-MC	brain:	n/a
44	chr2:87308486-87308536	HCM	heart:	n/a
45	chr2:87304105-87304155	GM12892	blood:	n/a
46	chr2:87302162-87302212	HNPCEpiC	eye:	n/a
47	chr2:87304105-87304155	IMR90	lung:	fetal
48	chr2:87304197-87304247	Hepatocyte	liver:	n/a
49	chr2:87302162-87302212	BE2_C	brain:	n/a
50	chr2:87303632-87303682	AG04450	lung:	fetal

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:87281176..87283798-chr2:87302577..87304633,2	MCF-7	breast:
2	chr2:87281176..87283798-chr2:87302577..87304633,2	MCF-7	breast:
3	chr2:86789024..86791664-chr2:87302659..87304185,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000230395	TF binding region
ENSG00000266931	TF binding region
ENSG00000231259	TF binding region
ENSG00000204745	TF binding region
ENSG00000230395	CpG island
ENSG00000266931	CpG island
ENSG00000231259	CpG island
ENSG00000204745	CpG island
ENSG00000266931	chromatin interactions
ENSG00000231259	chromatin interactions
ENSG00000115561	chromatin interactions
ENSG00000228363	chromatin interactions

Extended variants
information (count: 771 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548433772	chr2:87281446-87281447	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs566727268	chr2:87281458-87281459	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs372218212	chr2:87281513-87281514	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs567027211	chr2:87281536-87281537	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs375543688	chr2:87281537-87281538	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs534099355	chr2:87281556-87281557	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs558801523	chr2:87281588-87281589	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs570909832	chr2:87281765-87281766	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs537883557	chr2:87281781-87281782	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs111749055	chr2:87281816-87281817	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs556515329	chr2:87282000-87282001	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs575647241	chr2:87282001-87282002	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs542951538	chr2:87282029-87282030	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs554855826	chr2:87282030-87282031	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs573094817	chr2:87282125-87282126	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs540387509	chr2:87282132-87282133	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs564863662	chr2:87282140-87282141	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs532211172	chr2:87282271-87282272	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs564116078	chr2:87282290-87282291	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs543911565	chr2:87282331-87282332	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs562154092	chr2:87282340-87282341	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs200658351	chr2:87282454-87282455	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529597734	chr2:87282661-87282662	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs548493746	chr2:87282776-87282777	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs566791072	chr2:87282820-87282821	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs75961009	chr2:87282893-87282894	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs552718230	chr2:87282978-87282979	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs570906843	chr2:87283039-87283040	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs568192518	chr2:87283082-87283083	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs538325576	chr2:87283094-87283095	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs201342610	chr2:87283164-87283165	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs368858512	chr2:87283388-87283389	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs371286883	chr2:87283406-87283407	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs200075040	chr2:87283946-87283947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533000941	chr2:87284238-87284239	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs201210105	chr2:87284447-87284448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556339787	chr2:87284843-87284844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373718147	chr2:87284896-87284897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568466559	chr2:87284905-87284906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535819106	chr2:87284928-87284929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554918216	chr2:87285148-87285149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573157197	chr2:87285294-87285295	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs540081669	chr2:87285296-87285297	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs374831055	chr2:87285383-87285384	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs369157469	chr2:87285568-87285569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558714370	chr2:87285639-87285640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576923139	chr2:87285808-87285809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544298375	chr2:87286125-87286126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562217601	chr2:87286141-87286142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529657261	chr2:87286161-87286162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	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
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Bipolar disorder	19114987	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:87258800-87283200	Weak transcription	Fetal Intestine Small	intestine
2	chr2:87259200-87281600	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr2:87271800-87282200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr2:87275200-87283000	Weak transcription	Fetal Muscle Leg	muscle
5	chr2:87275600-87284000	Weak transcription	Fetal Stomach	stomach
6	chr2:87275600-87302000	Weak transcription	Duodenum Mucosa	Duodenum
7	chr2:87276000-87281400	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr2:87276200-87285200	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr2:87276400-87282400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr2:87276400-87283400	Weak transcription	Fetal Muscle Trunk	muscle
11	chr2:87276400-87283800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr2:87276400-87285000	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr2:87276400-87295400	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr2:87276400-87295400	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr2:87276600-87283000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr2:87276600-87302000	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr2:87277200-87284800	Weak transcription	Thymus	Thymus
18	chr2:87277800-87287400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr2:87278000-87283800	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr2:87279000-87285200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr2:87279200-87282800	Weak transcription	Fetal Thymus	thymus
22	chr2:87279200-87283800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:87279200-87285000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr2:87279200-87287400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr2:87279200-87302000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr2:87279600-87284800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr2:87280000-87287400	Weak transcription	Spleen	Spleen
28	chr2:87280600-87295200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr2:87280800-87281800	Strong transcription	Dnd41	blood
30	chr2:87280800-87282200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr2:87281400-87281800	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr2:87281600-87281800	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr2:87281800-87299600	Weak transcription	Dnd41	blood
34	chr2:87281800-87300600	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr2:87282200-87290800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr2:87284800-87285000	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr2:87284800-87285000	Enhancers	Liver	Liver
38	chr2:87285000-87290800	Weak transcription	Liver	Liver
39	chr2:87285200-87285400	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr2:87287000-87287600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr2:87287400-87287600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr2:87287400-87287600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
43	chr2:87287400-87287600	Enhancers	Muscle Satellite Cultured Cells	--
44	chr2:87287400-87287600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr2:87287400-87287600	Enhancers	Pancreas	Pancrea
46	chr2:87287400-87287600	Enhancers	Spleen	Spleen
47	chr2:87287400-87287800	Enhancers	Adipose Nuclei	Adipose
48	chr2:87287600-87288600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr2:87287800-87297000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr2:87287800-87302000	Weak transcription	Adipose Nuclei	Adipose

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links