Variant report

Variant	nsv962059
Chromosome Location	chr2:11447027-11450757
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:29)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:29 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:11450386-11450720	HepG2	liver:	n/a	n/a
2	CEBPB	chr2:11450380-11450774	Hela-S3	cervix:	n/a	chr2:11450557-11450568
3	CEBPB	chr2:11450421-11450738	IMR90	lung:	n/a	chr2:11450557-11450568
4	CEBPB	chr2:11448316-11448388	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr2:11450381-11450756	HepG2	liver:	n/a	chr2:11450557-11450568
6	CEBPB	chr2:11450389-11450745	A549	lung:	n/a	chr2:11450557-11450568
7	CEBPB	chr2:11450406-11450682	K562	blood:	n/a	chr2:11450557-11450568
8	CEBPB	chr2:11450442-11450763	MCF-7	breast:	n/a	chr2:11450557-11450568
9	CTCF	chr2:11448706-11448731	GM20000	blood:	n/a	n/a
10	CTCF	chr2:11448702-11448807	GM10266	blood:	n/a	n/a
11	E2F4	chr2:11450314-11450718	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr2:11450418-11450735	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr2:11450430-11450652	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr2:11450499-11450699	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr2:11449957-11450157	MCF10A-Er-Src	breast:	n/a	n/a
16	FOXA2	chr2:11450309-11450719	HepG2	liver:	n/a	n/a
17	MYC	chr2:11449982-11450673	MCF10A-Er-Src	breast:	n/a	chr2:11450367-11450378
18	MYC	chr2:11450353-11450739	MCF10A-Er-Src	breast:	n/a	chr2:11450367-11450378
19	POLR2A	chr2:11447950-11448197	A549	lung:	n/a	n/a
20	POLR2A	chr2:11449875-11449897	A549	lung:	n/a	n/a
21	POLR2A	chr2:11449390-11449615	ProgFib	skin:	n/a	n/a
22	POLR2A	chr2:11448122-11448222	GM12878	blood:	n/a	n/a
23	POLR2A	chr2:11449926-11450067	A549	lung:	n/a	n/a
24	STAT3	chr2:11450423-11450750	MCF10A-Er-Src	breast:	n/a	n/a
25	STAT3	chr2:11447005-11447205	MCF10A-Er-Src	breast:	n/a	n/a
26	STAT3	chr2:11450408-11450752	MCF10A-Er-Src	breast:	n/a	n/a
27	STAT3	chr2:11450328-11450798	MCF10A-Er-Src	breast:	n/a	n/a
28	STAT3	chr2:11450415-11450751	MCF10A-Er-Src	breast:	n/a	n/a
29	STAT3	chr2:11450445-11451023	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:11447160-11447210	BE2_C	brain:	n/a
2	chr2:11447160-11447210	HCPEpiC	choroid plexus:	n/a
3	chr2:11447160-11447210	U87	brain:	n/a
4	chr2:11447160-11447210	GM12878	blood:	n/a
5	chr2:11447160-11447210	GM19239	blood:	n/a
6	chr2:11447160-11447210	AG09309	skin:	n/a
7	chr2:11447160-11447210	SK-N-SH	brain:	n/a
8	chr2:11447160-11447210	HCT-116	colon:	n/a
9	chr2:11447160-11447210	SK-N-MC	brain:	n/a
10	chr2:11447160-11447210	GM06990	blood:	n/a
11	chr2:11447160-11447210	HUVEC	blood vessel:	n/a
12	chr2:11447160-11447210	AG09319	gingival:	n/a
13	chr2:11447160-11447210	AG04450	lung:	fetal
14	chr2:11447160-11447210	ovcar-3	ovarian:	n/a
15	chr2:11447160-11447210	SK-N-SH_RA	brain:	n/a
16	chr2:11447160-11447210	HEK293	kidney:	embryo
17	chr2:11447160-11447210	MCF-7	breast:	n/a
18	chr2:11447160-11447210	HRPEpiC	eye:	n/a
19	chr2:11447160-11447210	H1-hESC	embryonic stem cell:	embryo
20	chr2:11447160-11447210	NB4	blood:	n/a
21	chr2:11447160-11447210	HAEpiC	amniotic membrane:	n/a
22	chr2:11447160-11447210	HIPEpiC	eye:	n/a
23	chr2:11447160-11447210	SAEC	small airway:	n/a
24	chr2:11447160-11447210	Jurkat	blood:	n/a
25	chr2:11447160-11447210	GM12892	blood:	n/a
26	chr2:11447160-11447210	K562	blood:	n/a
27	chr2:11447160-11447210	PrEC	prostate:	n/a
28	chr2:11447160-11447210	HepG2	liver:	n/a
29	chr2:11447160-11447210	HMEC	breast:	n/a
30	chr2:11447160-11447210	A549	lung:	n/a
31	chr2:11447160-11447210	HCM	heart:	n/a
32	chr2:11447160-11447210	HRE	kidney:	n/a
33	chr2:11447160-11447210	HNPCEpiC	eye:	n/a
34	chr2:11447160-11447210	AG10803	skin:	n/a
35	chr2:11447160-11447210	HRCEpiC	kidney:	n/a
36	chr2:11447160-11447210	LNCaP	prostate:	n/a
37	chr2:11447160-11447210	MCF10A-Er-Src	breast:	n/a
38	chr2:11447160-11447210	HEEpiC	esophagus:	n/a
39	chr2:11447160-11447210	GM12891	blood:	n/a
40	chr2:11447160-11447210	SKMC	muscle:	n/a
41	chr2:11447160-11447210	ProgFib	skin:	n/a
42	chr2:11447160-11447210	AG04449	skin:	fetal
43	chr2:11447160-11447210	HL-60	blood:	n/a
44	chr2:11447160-11447210	PANC-1	pancreas:	n/a
45	chr2:11447160-11447210	T-47D	breast:	n/a
46	chr2:11447160-11447210	PFSK-1	brain:	n/a
47	chr2:11447160-11447210	Hela-S3	cervix:	n/a
48	chr2:11447160-11447210	IMR90	lung:	fetal
49	chr2:11447160-11447210	Hepatocyte	liver:	n/a
50	chr2:11447160-11447210	NHDF-neo	bronchial:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:11443856..11445730-chr2:11445772..11448144,2	K562	blood:
2	chr2:11444512..11447438-chr2:11450182..11452688,2	K562	blood:
3	chr2:11450066..11451573-chr2:11455094..11457155,2	MCF-7	breast:
4	chr2:11444512..11447438-chr2:11450182..11452688,2	K562	blood:
5	chr2:11444757..11447160-chr2:11453898..11455416,2	MCF-7	breast:
6	chr2:11446328..11449302-chr2:11482839..11485533,2	MCF-7	breast:
7	chr2:11437773..11439523-chr2:11445218..11447388,2	K562	blood:
8	chr2:11449416..11451875-chr2:11454672..11457949,3	K562	blood:
9	chr2:11435287..11437143-chr2:11445238..11447670,2	K562	blood:
10	chr2:11422735..11425372-chr2:11448792..11450664,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-E2F6-1	chr2:11447834-11447944	NONHSAT069155

No data

Variant related genes	Relation type
ENSG00000230154	TF binding region
ENSG00000230154	CpG island
ENSG00000134318	chromatin interactions

Extended variants
information (count: 163 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:163 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541550309	chr2:11447029-11447030	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs183761211	chr2:11447042-11447043	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs574932069	chr2:11447162-11447163	Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs116069807	chr2:11447186-11447187	Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs576749868	chr2:11447192-11447193	Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs188385426	chr2:11447215-11447216	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs73915159	chr2:11447226-11447227	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs575934965	chr2:11447246-11447247	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs530329846	chr2:11447280-11447281	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs574443937	chr2:11447286-11447287	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs541474753	chr2:11447306-11447307	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs191694523	chr2:11447326-11447327	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs527288817	chr2:11447330-11447331	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560498534	chr2:11447384-11447385	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs552096053	chr2:11447463-11447464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs564024874	chr2:11447464-11447465	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs531432627	chr2:11447478-11447479	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549536645	chr2:11447498-11447499	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs568477755	chr2:11447520-11447521	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs535902404	chr2:11447524-11447525	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs559641579	chr2:11447539-11447540	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs111433649	chr2:11447547-11447548	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs184229629	chr2:11447565-11447566	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs558521688	chr2:11447573-11447574	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs576786542	chr2:11447585-11447586	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs546342349	chr2:11447605-11447606	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs537660045	chr2:11447659-11447660	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs188990274	chr2:11447681-11447682	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs574453537	chr2:11447685-11447686	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs530430242	chr2:11447718-11447719	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs367801405	chr2:11447727-11447728	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs571745433	chr2:11447775-11447776	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs116137719	chr2:11447800-11447801	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs564063585	chr2:11447814-11447815	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs531468877	chr2:11447880-11447881	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs113512830	chr2:11447887-11447888	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs112667563	chr2:11447942-11447943	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs561874534	chr2:11447946-11447947	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs371991313	chr2:11447953-11447954	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs113813923	chr2:11447965-11447966	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs547909137	chr2:11447979-11447980	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs117583048	chr2:11447990-11447991	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs35265359	chr2:11448000-11448001	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs539867085	chr2:11448008-11448009	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs76066525	chr2:11448010-11448011	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs111987525	chr2:11448011-11448012	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs537697218	chr2:11448020-11448021	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs369318439	chr2:11448040-11448041	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs555784380	chr2:11448044-11448045	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs567893440	chr2:11448045-11448046	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11424800-11455200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr2:11433600-11448000	Weak transcription	Right Ventricle	heart
3	chr2:11439200-11453000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:11442800-11447800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr2:11443400-11447200	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr2:11443400-11447200	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr2:11443800-11449400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:11444000-11447400	Enhancers	Colon Smooth Muscle	Colon
9	chr2:11444000-11449800	Weak transcription	Aorta	Aorta
10	chr2:11444000-11458600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:11444200-11447400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr2:11444600-11447800	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr2:11444800-11447600	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr2:11444800-11448000	Enhancers	NHDF-Ad	bronchial
15	chr2:11444800-11454600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr2:11445000-11465200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr2:11445200-11450200	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr2:11445400-11447200	Enhancers	Muscle Satellite Cultured Cells	--
19	chr2:11445400-11447200	Enhancers	HSMM	muscle
20	chr2:11445400-11460200	Weak transcription	Left Ventricle	heart
21	chr2:11445600-11447200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr2:11445600-11447200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr2:11445600-11447200	Enhancers	Osteobl	bone
24	chr2:11445600-11447400	Enhancers	NHLF	lung
25	chr2:11445600-11447600	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr2:11445800-11447200	Enhancers	Fetal Stomach	stomach
27	chr2:11445800-11448800	Weak transcription	NHEK	skin
28	chr2:11445800-11449800	Weak transcription	Lung	lung
29	chr2:11446000-11447200	Enhancers	Stomach Smooth Muscle	stomach
30	chr2:11446000-11447200	Enhancers	A549	lung
31	chr2:11446000-11448400	Enhancers	HepG2	liver
32	chr2:11446000-11448800	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr2:11446200-11447200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr2:11446200-11453200	Weak transcription	K562	blood
35	chr2:11446400-11447200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr2:11446400-11447200	Enhancers	Liver	Liver
37	chr2:11446800-11447200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr2:11446800-11447200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr2:11446800-11447200	Enhancers	Duodenum Smooth Muscle	Duodenum
40	chr2:11446800-11448200	Enhancers	Psoas Muscle	Psoas
41	chr2:11446800-11449800	Weak transcription	HMEC	breast
42	chr2:11447000-11449800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr2:11447000-11449800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr2:11447000-11449800	Weak transcription	Adipose Nuclei	Adipose
45	chr2:11447000-11449800	Weak transcription	Fetal Intestine Small	intestine
46	chr2:11447000-11450200	Weak transcription	Brain Cingulate Gyrus	brain
47	chr2:11447000-11450400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr2:11447000-11450600	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr2:11447000-11450600	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr2:11447000-11451400	Weak transcription	Small Intestine	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links