Variant report

Variant	rs569307763
Chromosome Location	chr8:11706610-11706611
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:86)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:86 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr8:11700476-11706879	K562	blood:	n/a	n/a
2	POLR2A	chr8:11703953-11706886	K562	blood:	n/a	n/a
3	POLR2A	chr8:11706542-11706689	MCF-7	breast:	n/a	n/a
4	POLR2A	chr8:11706319-11706871	GM12878	blood:	n/a	n/a
5	CTCF	chr8:11706560-11706710	NB4	blood:	n/a	n/a
6	POLR2A	chr8:11706479-11706854	K562	blood:	n/a	n/a
7	MYC	chr8:11706546-11706610	MCF-7	breast:	n/a	n/a
8	POLR2A	chr8:11706393-11706812	H1-neurons	neurons:	n/a	n/a
9	HEY1	chr8:11701242-11707121	HepG2	liver:	n/a	n/a
10	MYBL2	chr8:11706547-11707094	HepG2	liver:	n/a	n/a
11	POLR2A	chr8:11703908-11707605	SK-N-MC	brain:	n/a	n/a
12	POLR2A	chr8:11703992-11706940	U87	brain:	n/a	n/a
13	POLR2A	chr8:11704627-11706739	HepG2	liver:	n/a	n/a
14	CTCF	chr8:11706540-11706690	HFF	foreskin:	n/a	n/a
15	POLR2A	chr8:11700572-11707656	HepG2	liver:	n/a	n/a
16	POLR2A	chr8:11704074-11706942	GM19193	blood:	n/a	n/a
17	POLR2A	chr8:11706385-11706786	A549	lung:	n/a	n/a
18	POLR2A	chr8:11703717-11706821	GM12878	blood:	n/a	n/a
19	POLR2A	chr8:11703999-11706821	GM18505	blood:	n/a	n/a
20	POLR2A	chr8:11704425-11707068	ECC-1	luminal epithelium:	n/a	n/a
21	POLR2A	chr8:11700562-11707759	HepG2	liver:	n/a	n/a
22	POLR2A	chr8:11704086-11706958	GM18951	blood:	n/a	n/a
23	POLR2A	chr8:11706521-11706683	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr8:11700619-11706983	K562	blood:	n/a	n/a
25	POLR2A	chr8:11706018-11706801	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr8:11700648-11706836	K562	blood:	n/a	n/a
27	POLR2A	chr8:11706425-11708174	K562	blood:	n/a	n/a
28	POLR2A	chr8:11705032-11706934	U87	brain:	n/a	n/a
29	BRCA1	chr8:11706580-11706662	HepG2	liver:	n/a	n/a
30	POLR2A	chr8:11700677-11707213	HepG2	liver:	n/a	n/a
31	POLR2A	chr8:11700786-11707123	GM12891	blood:	n/a	n/a
32	POLR2A	chr8:11706491-11706735	A549	lung:	n/a	n/a
33	POLR2A	chr8:11706321-11706872	H1-neurons	neurons:	n/a	n/a
34	HMGN3	chr8:11706410-11706770	K562	blood:	n/a	n/a
35	POLR2A	chr8:11676833-11707731	K562	blood:	n/a	n/a
36	POLR2A	chr8:11706594-11707247	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr8:11701607-11706997	HUVEC	blood vessel:	n/a	n/a
38	MYC	chr8:11706572-11706623	MCF-7	breast:	n/a	n/a
39	POLR2A	chr8:11706268-11706814	GM12878	blood:	n/a	n/a
40	CHD2	chr8:11706516-11706612	Hela-S3	cervix:	n/a	n/a
41	MAFK	chr8:11706538-11706705	HepG2	liver:	n/a	n/a
42	POLR2A	chr8:11706451-11706950	A549	lung:	n/a	n/a
43	POLR2A	chr8:11700782-11707757	HepG2	liver:	n/a	n/a
44	RAD21	chr8:11706535-11707005	H1-hESC	embryonic stem cell:	n/a	chr8:11706791-11706801 chr8:11706786-11706805
45	POLR2A	chr8:11700506-11713198	SK-N-MC	brain:	n/a	n/a
46	POLR2A	chr8:11701922-11707022	HL-60	blood:	n/a	n/a
47	POLR2A	chr8:11706351-11706800	GM12891	blood:	n/a	n/a
48	CCNT2	chr8:11706290-11706696	K562	blood:	n/a	n/a
49	POLR2A	chr8:11705832-11706881	HepG2	liver:	n/a	n/a
50	POLR2A	chr8:11706456-11706724	A549	lung:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:11662566..11665636-chr8:11705504..11707081,3	K562	blood:
2	chr8:11706290..11708186-chr8:11724044..11726922,3	MCF-7	breast:
3	chr8:11706164..11707709-chr8:11709253..11711783,2	K562	blood:
4	chr8:11664303..11666890-chr8:11705423..11707941,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000269899	TF binding region
CTSB	TF binding region
ENSG00000079459	Chromatin interaction
ENSG00000164733	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1018978	chr8:11438267-11858466	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv917963	chr8:11540723-11751798	Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1027378	chr8:11541739-11858466	Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv1028229	chr8:11575762-11805961	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv539475	chr8:11575762-11805961	Flanking Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv428514	chr8:11580381-11765706	Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
8	nsv1034014	chr8:11602337-11858466	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
9	nsv1023803	chr8:11623570-11721655	Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	nsv539476	chr8:11623570-11721655	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	nsv890361	chr8:11625808-11755513	Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
12	nsv890362	chr8:11625808-11771089	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
13	nsv1032739	chr8:11643803-11716473	Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv1034132	chr8:11657033-12198242	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
15	nsv890365	chr8:11666451-11735641	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
16	nsv890366	chr8:11666451-11900847	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
17	nsv1031158	chr8:11666558-11759064	Bivalent Enhancer Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
18	nsv539477	chr8:11666558-11759064	Enhancers Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
19	nsv1018042	chr8:11667496-11882385	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
20	nsv890367	chr8:11668153-11793529	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
21	nsv890368	chr8:11671041-11718528	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
22	nsv890369	chr8:11671041-11840011	Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
23	nsv1016952	chr8:11679271-11849955	Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
24	nsv1029093	chr8:11679271-11858466	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
25	nsv539478	chr8:11679271-11858466	Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
26	nsv1017334	chr8:11688534-11732949	Enhancers Active TSS Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
27	nsv539479	chr8:11688534-11732949	Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
28	nsv1019738	chr8:11696393-11732949	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
29	nsv539480	chr8:11696393-11732949	Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
30	nsv1031972	chr8:11696393-11805961	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
31	nsv539481	chr8:11696393-11805961	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
32	esv34042	chr8:11698337-11726817	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
33	nsv610293	chr8:11698747-11929734	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
34	nsv516685	chr8:11698747-12570199	Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	74 gene(s)	inside rSNPs	diseases
35	nsv972525	chr8:11706325-11714357	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11667000-11711000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr8:11669400-11708000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:11675200-11707000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:11675800-11712600	Strong transcription	Dnd41	blood
5	chr8:11677600-11708200	Strong transcription	Cortex derived primary cultured neurospheres	brain
6	chr8:11677600-11710600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:11677600-11711800	Strong transcription	Fetal Brain Female	brain
8	chr8:11678000-11707400	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr8:11678200-11706800	Strong transcription	H1 Cell Line	embryonic stem cell
10	chr8:11678600-11708600	Strong transcription	HUVEC	blood vessel
11	chr8:11679000-11715200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr8:11679200-11710400	Strong transcription	NHDF-Ad	bronchial
13	chr8:11679200-11710800	Strong transcription	Fetal Stomach	stomach
14	chr8:11682200-11713000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr8:11682400-11712600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr8:11683000-11713200	Strong transcription	Primary B cells from peripheral blood	blood
17	chr8:11683200-11710000	Strong transcription	NH-A	brain
18	chr8:11683400-11711600	Strong transcription	Brain Germinal Matrix	brain
19	chr8:11683600-11708600	Strong transcription	Primary hematopoietic stem cells	blood
20	chr8:11683600-11712600	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr8:11685600-11710600	Strong transcription	HSMM	muscle
22	chr8:11690400-11710200	Strong transcription	Fetal Intestine Large	intestine
23	chr8:11691600-11710600	Strong transcription	Pancreas	Pancrea
24	chr8:11691600-11711200	Strong transcription	Spleen	Spleen
25	chr8:11691800-11710600	Strong transcription	HSMMtube	muscle
26	chr8:11691800-11711000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr8:11692000-11711000	Strong transcription	Fetal Muscle Leg	muscle
28	chr8:11692000-11711200	Strong transcription	Fetal Thymus	thymus
29	chr8:11692200-11711000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr8:11692400-11710600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr8:11693400-11710400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr8:11693800-11708600	Strong transcription	Aorta	Aorta
33	chr8:11695400-11710600	Strong transcription	Osteobl	bone
34	chr8:11698600-11716600	Strong transcription	Primary T cells from cord blood	blood
35	chr8:11698800-11711000	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr8:11699000-11708800	Strong transcription	Ovary	ovary
37	chr8:11699000-11710800	Strong transcription	Primary T helper cells PMA-I stimulated	--
38	chr8:11699200-11710600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr8:11699200-11710600	Strong transcription	Muscle Satellite Cultured Cells	--
40	chr8:11699400-11710400	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr8:11700000-11711200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr8:11700600-11721200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr8:11701200-11710400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr8:11702000-11707000	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr8:11702000-11707600	Genic enhancers	HMEC	breast
46	chr8:11702200-11706800	Genic enhancers	Gastric	stomach
47	chr8:11702200-11707000	Genic enhancers	Esophagus	oesophagus
48	chr8:11702200-11707800	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr8:11702200-11710400	Weak transcription	Hela-S3	cervix
50	chr8:11702400-11710000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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