Variant report

Variant	rs535392840
Chromosome Location	chr11:64491293-64491294
allele	A/G
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	RAD21	chr11:64490853-64491309	H1-hESC	embryonic stem cell:	n/a	chr11:64490998-64491007 chr11:64491101-64491120 chr11:64491103-64491115 chr11:64491105-64491119
2	RAD21	chr11:64490818-64491324	SK-N-SH_RA	brain:	n/a	chr11:64490998-64491007 chr11:64491101-64491120 chr11:64491103-64491115 chr11:64491105-64491119
3	RAD21	chr11:64490612-64491458	HCT-116	colon:	n/a	chr11:64490998-64491007 chr11:64491101-64491120 chr11:64491103-64491115 chr11:64491105-64491119
4	CTCF	chr11:64490904-64491322	K562	blood:	n/a	chr11:64491104-64491120 chr11:64491122-64491131 chr11:64491105-64491118 chr11:64490999-64491007 chr11:64491098-64491119 chr11:64491105-64491118 chr11:64491103-64491121
5	RELA	chr11:64490949-64491577	GM12892	blood:	n/a	chr11:64491351-64491360 chr11:64491351-64491360
6	TBL1XR1	chr11:64490724-64491450	GM12878	blood:	n/a	n/a
7	SPI1	chr11:64491254-64491493	GM12878	blood:	n/a	chr11:64491267-64491274
8	RELA	chr11:64491041-64491752	GM18505	blood:	n/a	chr11:64491351-64491360 chr11:64491351-64491360
9	CTCF	chr11:64490833-64491359	A549	lung:	n/a	chr11:64491104-64491120 chr11:64491122-64491131 chr11:64491105-64491118 chr11:64490999-64491007 chr11:64491098-64491119 chr11:64491105-64491118 chr11:64491103-64491121
10	STAT5A	chr11:64490921-64491352	GM12878	blood:	n/a	n/a
11	ZNF143	chr11:64490689-64491302	GM12878	blood:	n/a	chr11:64491215-64491233
12	CTCF	chr11:64490929-64491508	GM12891	blood:	n/a	chr11:64491104-64491120 chr11:64491122-64491131 chr11:64491105-64491118 chr11:64490999-64491007 chr11:64491098-64491119 chr11:64491105-64491118 chr11:64491103-64491121
13	ZBTB7A	chr11:64490723-64491486	ECC-1	luminal epithelium:	n/a	chr11:64490954-64490961 chr11:64490875-64490883 chr11:64491104-64491113
14	RELA	chr11:64490787-64491982	GM12891	blood:	n/a	chr11:64491351-64491360 chr11:64491351-64491360
15	RAD21	chr11:64490765-64491344	ECC-1	luminal epithelium:	n/a	chr11:64490998-64491007 chr11:64491101-64491120 chr11:64491103-64491115 chr11:64491105-64491119
16	CTCF	chr11:64490816-64491609	GM12892	blood:	n/a	chr11:64491104-64491120 chr11:64491122-64491131 chr11:64491105-64491118 chr11:64490999-64491007 chr11:64491098-64491119 chr11:64491105-64491118 chr11:64491103-64491121
17	RELA	chr11:64490948-64491525	GM18526	blood:	n/a	chr11:64491351-64491360 chr11:64491351-64491360
18	CTCF	chr11:64490874-64491384	MCF-7	breast:	n/a	chr11:64491104-64491120 chr11:64491122-64491131 chr11:64491105-64491118 chr11:64490999-64491007 chr11:64491098-64491119 chr11:64491105-64491118 chr11:64491103-64491121
19	MAX	chr11:64490506-64491373	A549	lung:	n/a	n/a
20	CTCF	chr11:64490856-64491304	H1-hESC	embryonic stem cell:	n/a	chr11:64491104-64491120 chr11:64491122-64491131 chr11:64491105-64491118 chr11:64490999-64491007 chr11:64491098-64491119 chr11:64491105-64491118 chr11:64491103-64491121
21	ATF2	chr11:64490741-64491376	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr11:64490486-64491306	GM12878	blood:	n/a	n/a
23	REST	chr11:64489384-64491458	H1-neurons	neurons:	n/a	chr11:64491102-64491115 chr11:64490832-64490842 chr11:64489578-64489591 chr11:64490990-64491003 chr11:64489854-64489862 chr11:64490679-64490699
24	FOXM1	chr11:64490731-64491358	GM12878	blood:	n/a	n/a
25	EBF1	chr11:64490975-64491903	GM12878	blood:	n/a	chr11:64491367-64491378
26	RAD21	chr11:64490579-64491425	HCT-116	colon:	n/a	chr11:64490998-64491007 chr11:64491101-64491120 chr11:64491103-64491115 chr11:64491105-64491119
27	NR2F2	chr11:64490830-64491295	K562	blood:	n/a	n/a
28	YY1	chr11:64490910-64491331	GM12892	blood:	n/a	chr11:64491101-64491115
29	MAZ	chr11:64490415-64491598	IMR90	lung:	n/a	n/a
30	FOXM1	chr11:64490883-64491333	GM12878	blood:	n/a	n/a
31	SMC3	chr11:64490912-64491515	GM12878	blood:	n/a	chr11:64491105-64491119
32	EBF1	chr11:64491191-64491557	GM12878	blood:	n/a	chr11:64491367-64491378
33	TCF12	chr11:64490797-64491319	A549	lung:	n/a	n/a
34	CHD2	chr11:64490569-64491391	H1-hESC	embryonic stem cell:	n/a	chr11:64490636-64490646 chr11:64490942-64490952 chr11:64490949-64490959 chr11:64490732-64490742
35	CTCF	chr11:64490719-64491433	GM12878	blood:	n/a	chr11:64491104-64491120 chr11:64491122-64491131 chr11:64491105-64491118 chr11:64490999-64491007 chr11:64491098-64491119 chr11:64491105-64491118 chr11:64491103-64491121
36	RELA	chr11:64490956-64491676	GM18951	blood:	n/a	chr11:64491351-64491360 chr11:64491351-64491360
37	JUND	chr11:64490741-64491300	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr11:64490676-64491421	K562	blood:	n/a	chr11:64491104-64491120 chr11:64491122-64491131 chr11:64491105-64491118 chr11:64490999-64491007 chr11:64491098-64491119 chr11:64491105-64491118 chr11:64491103-64491121
39	RAD21	chr11:64490445-64492076	SK-N-SH	brain:	n/a	chr11:64490998-64491007 chr11:64491101-64491120 chr11:64490457-64490471 chr11:64491103-64491115 chr11:64491105-64491119
40	RAD21	chr11:64490896-64491318	IMR90	lung:	n/a	chr11:64490998-64491007 chr11:64491101-64491120 chr11:64491103-64491115 chr11:64491105-64491119
41	BHLHE40	chr11:64490970-64491570	GM12878	blood:	n/a	n/a
42	CTCF	chr11:64490797-64491311	K562	blood:	n/a	chr11:64491104-64491120 chr11:64491122-64491131 chr11:64491105-64491118 chr11:64490999-64491007 chr11:64491098-64491119 chr11:64491105-64491118 chr11:64491103-64491121
43	RUNX3	chr11:64490852-64491824	GM12878	blood:	n/a	n/a
44	CTCF	chr11:64490871-64491332	H1-hESC	embryonic stem cell:	n/a	chr11:64491104-64491120 chr11:64491122-64491131 chr11:64491105-64491118 chr11:64490999-64491007 chr11:64491098-64491119 chr11:64491105-64491118 chr11:64491103-64491121
45	ELF1	chr11:64490573-64491444	GM12878	blood:	n/a	chr11:64490639-64490651
46	EP300	chr11:64490408-64492176	SK-N-SH	brain:	n/a	chr11:64490825-64490841 chr11:64490790-64490803
47	CTCF	chr11:64491280-64491430	WERI-Rb-1	eye:	n/a	n/a
48	RELA	chr11:64491004-64491773	GM19099	blood:	n/a	chr11:64491351-64491360 chr11:64491351-64491360
49	CTCF	chr11:64490548-64491494	A549	lung:	n/a	chr11:64491104-64491120 chr11:64491122-64491131 chr11:64491105-64491118 chr11:64490999-64491007 chr11:64491098-64491119 chr11:64491105-64491118 chr11:64491103-64491121
50	CTCF	chr11:64490929-64491494	GM19238	blood:	n/a	chr11:64491104-64491120 chr11:64491122-64491131 chr11:64491105-64491118 chr11:64490999-64491007 chr11:64491098-64491119 chr11:64491105-64491118 chr11:64491103-64491121

No.	Distal block	Cell Line	Cell type
1	chr11:64489616..64492284-chr11:64509871..64511516,3	K562	blood:
2	chr11:64490193..64492198-chr11:64544563..64546459,2	MCF-7	breast:
3	chr11:64489296..64491902-chr11:64644473..64646300,2	MCF-7	breast:
4	chr11:64478255..64481463-chr11:64489766..64492365,3	K562	blood:
5	chr11:64418420..64419024-chr11:64490995..64491544,2	MCF-7	breast:
6	chr11:64490664..64492722-chr11:64991494..64993936,2	MCF-7	breast:
7	chr11:64491144..64492732-chr11:64505276..64507287,3	K562	blood:
8	chr11:64420274..64420985-chr11:64490663..64491460,2	K562	blood:
9	chr11:64489351..64492621-chr11:64507509..64512935,5	K562	blood:

Variant related genes	Relation type
NRXN2	TF binding region
ENSG00000068831	Chromatin interaction
ENSG00000110076	Chromatin interaction
ENSG00000168066	Chromatin interaction
ENSG00000269038	Chromatin interaction
ENSG00000110047	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv468596	chr11:64334114-64527080	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv555195	chr11:64334114-64527080	Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv897694	chr11:64334114-64584959	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
4	nsv818842	chr11:64345448-64546391	Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
5	nsv528506	chr11:64345448-64701030	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
6	nsv555196	chr11:64357072-64559898	Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
7	nsv897695	chr11:64357072-64701030	Weak transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
8	nsv1051350	chr11:64372906-64533632	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv555198	chr11:64373899-64573589	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
10	esv1804443	chr11:64386453-64534785	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
11	nsv897697	chr11:64447420-64584959	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
12	nsv897698	chr11:64447420-64621573	Active TSS Bivalent Enhancer Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
13	nsv897699	chr11:64447420-64638041	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
14	nsv897700	chr11:64447420-64701030	Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1071 gene(s)	inside rSNPs	diseases
15	nsv359	chr11:64477008-64502873	Bivalent/Poised TSS Flanking Active TSS Genic enhancers Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
16	nsv555202	chr11:64477050-64573589	Strong transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
17	nsv468597	chr11:64477050-64584959	Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
18	nsv468598	chr11:64477050-64584959	Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
19	nsv555203	chr11:64477050-64584959	Strong transcription Genic enhancers Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
20	nsv1049744	chr11:64486615-64630149	Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
21	nsv832189	chr11:64487183-64620199	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
22	esv3324432	chr11:64489201-64492249	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
23	esv3409975	chr11:64489426-64491724	Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64490000-64491400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
2	chr11:64490200-64491400	Active TSS	iPS-15b Cell Line	embryonic stem cell
3	chr11:64490600-64491400	Active TSS	Duodenum Smooth Muscle	Duodenum
4	chr11:64490600-64491400	Active TSS	K562	blood
5	chr11:64490600-64492000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr11:64490800-64491400	Flanking Active TSS	Primary B cells from cord blood	blood
7	chr11:64490800-64491400	Flanking Active TSS	Primary B cells from peripheral blood	blood
8	chr11:64490800-64491400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:64490800-64491400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
10	chr11:64490800-64491400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr11:64490800-64491400	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
12	chr11:64490800-64491400	Flanking Active TSS	Dnd41	blood
13	chr11:64490800-64491400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
14	chr11:64490800-64491600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr11:64490800-64491600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:64490800-64491800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr11:64490800-64491800	Flanking Active TSS	GM12878-XiMat	blood
18	chr11:64490800-64492200	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr11:64490800-64498000	Enhancers	Liver	Liver
20	chr11:64491000-64491400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
21	chr11:64491000-64491400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
22	chr11:64491000-64491400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
23	chr11:64491000-64491400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr11:64491000-64491400	Flanking Active TSS	Brain Germinal Matrix	brain
25	chr11:64491000-64491400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
26	chr11:64491000-64491600	Flanking Active TSS	Spleen	Spleen
27	chr11:64491000-64494200	Enhancers	Fetal Brain Male	brain
28	chr11:64491000-64502200	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr11:64491200-64491400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
30	chr11:64491200-64491400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr11:64491200-64491400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr11:64491200-64491400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
33	chr11:64491200-64491400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr11:64491200-64491400	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr11:64491200-64491400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
36	chr11:64491200-64491400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr11:64491200-64491400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr11:64491200-64491400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr11:64491200-64491400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr11:64491200-64491400	Enhancers	Adipose Nuclei	Adipose
41	chr11:64491200-64491400	Enhancers	Brain Angular Gyrus	brain
42	chr11:64491200-64491400	Flanking Active TSS	Brain Anterior Caudate	brain
43	chr11:64491200-64491400	Flanking Active TSS	Brain Cingulate Gyrus	brain
44	chr11:64491200-64491400	Flanking Active TSS	Brain Hippocampus Middle	brain
45	chr11:64491200-64491400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
46	chr11:64491200-64491400	Bivalent Enhancer	Colonic Mucosa	Colon
47	chr11:64491200-64491400	Enhancers	Colon Smooth Muscle	Colon
48	chr11:64491200-64491400	Weak transcription	Esophagus	oesophagus
49	chr11:64491200-64491400	Enhancers	Fetal Muscle Leg	muscle
50	chr11:64491200-64491400	Enhancers	Pancreas	Pancrea

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links