Variant report

Variant	esv3322866
Chromosome Location	chr2:98205270-98206468
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	BATF	chr2:98206281-98206755	GM12878	blood:	n/a	n/a
2	BCL11A	chr2:98205341-98205570	GM12878	blood:	n/a	n/a
3	BCL11A	chr2:98206444-98207010	GM12878	blood:	n/a	chr2:98206849-98206862 chr2:98206762-98206775
4	BHLHE40	chr2:98206228-98206632	HepG2	liver:	n/a	n/a
5	BHLHE40	chr2:98206179-98206453	K562	blood:	n/a	n/a
6	BHLHE40	chr2:98206265-98206289	GM12878	blood:	n/a	n/a
7	CBX3	chr2:98206082-98206466	K562	blood:	n/a	n/a
8	CBX3	chr2:98206107-98207533	K562	blood:	n/a	n/a
9	CCNT2	chr2:98206271-98206359	K562	blood:	n/a	n/a
10	CEBPD	chr2:98206159-98206391	HepG2	liver:	n/a	n/a
11	CHD2	chr2:98206306-98206498	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr2:98206243-98206454	K562	blood:	n/a	n/a
13	CHD2	chr2:98206316-98206476	HepG2	liver:	n/a	n/a
14	CTCF	chr2:98206384-98206448	Lung_OC	lung:	n/a	n/a
15	CTCF	chr2:98206303-98207014	A549	lung:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
16	CTCF	chr2:98206227-98207748	K562	blood:	n/a	chr2:98207475-98207496 chr2:98206933-98206946 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98206828-98206841 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
17	CTCF	chr2:98206228-98206552	K562	blood:	n/a	n/a
18	CTCF	chr2:98206237-98207868	A549	lung:	n/a	chr2:98207475-98207496 chr2:98206933-98206946 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98206828-98206841 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
19	CTCF	chr2:98206452-98206634	GM10248	blood:	n/a	n/a
20	CTCF	chr2:98206238-98207749	A549	lung:	n/a	chr2:98207475-98207496 chr2:98206933-98206946 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98206828-98206841 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
21	CTCF	chr2:98206254-98206601	Spleen_OC	spleen:	n/a	n/a
22	CTCF	chr2:98206435-98206533	Pancreas_OC	pancreas:	n/a	n/a
23	E2F4	chr2:98206318-98206347	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F6	chr2:98206135-98206716	K562	blood:	n/a	n/a
25	E2F6	chr2:98206059-98206473	K562	blood:	n/a	n/a
26	E2F6	chr2:98206085-98206389	A549	lung:	n/a	n/a
27	E2F6	chr2:98206042-98206392	H1-hESC	embryonic stem cell:	n/a	n/a
28	E2F6	chr2:98206245-98206490	K562	blood:	n/a	n/a
29	E2F6	chr2:98206002-98206382	H1-hESC	embryonic stem cell:	n/a	n/a
30	EBF1	chr2:98206134-98207466	GM12878	blood:	n/a	n/a
31	EBF1	chr2:98206252-98207004	GM12878	blood:	n/a	n/a
32	EP300	chr2:98206267-98206282	GM12878	blood:	n/a	n/a
33	EP300	chr2:98206265-98206465	K562	blood:	n/a	n/a
34	EP300	chr2:98205334-98205572	GM12878	blood:	n/a	n/a
35	FOSL2	chr2:98206119-98206625	HepG2	liver:	n/a	n/a
36	FOSL2	chr2:98205823-98207635	HepG2	liver:	n/a	n/a
37	FOSL2	chr2:98205324-98205645	HepG2	liver:	n/a	n/a
38	FOXA1	chr2:98206169-98206479	HepG2	liver:	n/a	n/a
39	FOXA2	chr2:98206086-98207149	A549	lung:	n/a	n/a
40	FOXM1	chr2:98206461-98207049	GM12878	blood:	n/a	n/a
41	FOXM1	chr2:98206029-98206469	GM12878	blood:	n/a	n/a
42	FOXP2	chr2:98206353-98206743	PFSK-1	brain:	n/a	n/a
43	FOXP2	chr2:98206126-98206498	SK-N-MC	brain:	n/a	n/a
44	GTF2F1	chr2:98206104-98206375	K562	blood:	n/a	n/a
45	HA-E2F1	chr2:98206042-98206734	MCF-7	breast:	n/a	n/a
46	HA-E2F1	chr2:98206240-98207330	Hela-S3	cervix:	n/a	chr2:98206915-98206925 chr2:98206770-98206780
47	HCFC1	chr2:98206286-98206287	K562	blood:	n/a	n/a
48	HEY1	chr2:98205872-98207524	K562	blood:	n/a	chr2:98207206-98207215 chr2:98207186-98207201 chr2:98206456-98206471 chr2:98206874-98206889 chr2:98206922-98206937 chr2:98206458-98206473
49	HEY1	chr2:98205870-98207627	HepG2	liver:	n/a	chr2:98207206-98207215 chr2:98207186-98207201 chr2:98206456-98206471 chr2:98206874-98206889 chr2:98206922-98206937 chr2:98206458-98206473
50	HEY1	chr2:98205876-98207375	K562	blood:	n/a	chr2:98207206-98207215 chr2:98207186-98207201 chr2:98206456-98206471 chr2:98206874-98206889 chr2:98206922-98206937 chr2:98206458-98206473

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:98206249-98206299	SKMC	muscle:	n/a
2	chr2:98205903-98205953	AG09309	skin:	n/a
3	chr2:98205903-98205953	AG04449	skin:	fetal
4	chr2:98206095-98206145	ProgFib	skin:	n/a
5	chr2:98206095-98206145	ECC-1	luminal epithelium:	n/a
6	chr2:98206175-98206225	SKMC	muscle:	n/a
7	chr2:98206249-98206299	GM19239	blood:	n/a
8	chr2:98205903-98205953	HCPEpiC	choroid plexus:	n/a
9	chr2:98206095-98206145	HepG2	liver:	n/a
10	chr2:98206095-98206145	LNCaP	prostate:	n/a
11	chr2:98206095-98206145	AoSMC	blood vessel:	n/a
12	chr2:98206095-98206145	U87	brain:	n/a
13	chr2:98206249-98206299	BE2_C	brain:	n/a
14	chr2:98206175-98206225	NHBE	bronchial:	n/a
15	chr2:98206095-98206145	NT2-D1	testis:	n/a
16	chr2:98206249-98206299	HepG2	liver:	n/a
17	chr2:98206095-98206145	AG04450	lung:	fetal
18	chr2:98206175-98206225	AoSMC	blood vessel:	n/a
19	chr2:98205903-98205953	HAEpiC	amniotic membrane:	n/a
20	chr2:98206175-98206225	PANC-1	pancreas:	n/a
21	chr2:98206175-98206225	HCPEpiC	choroid plexus:	n/a
22	chr2:98206175-98206225	SK-N-MC	brain:	n/a
23	chr2:98206175-98206225	MCF10A-Er-Src	breast:	n/a
24	chr2:98206249-98206299	SK-N-MC	brain:	n/a
25	chr2:98206175-98206225	SK-N-SH	brain:	n/a
26	chr2:98205903-98205953	AG04450	lung:	fetal
27	chr2:98205903-98205953	PFSK-1	brain:	n/a
28	chr2:98206249-98206299	Hepatocyte	liver:	n/a
29	chr2:98206095-98206145	AG09309	skin:	n/a
30	chr2:98206095-98206145	HRE	kidney:	n/a
31	chr2:98206175-98206225	RPTEC	kidney:	n/a
32	chr2:98205903-98205953	HepG2	liver:	n/a
33	chr2:98206095-98206145	HEEpiC	esophagus:	n/a
34	chr2:98206095-98206145	AG09319	gingival:	n/a
35	chr2:98206175-98206225	PrEC	prostate:	n/a
36	chr2:98206249-98206299	HNPCEpiC	eye:	n/a
37	chr2:98206175-98206225	HL-60	blood:	n/a
38	chr2:98206095-98206145	A549	lung:	n/a
39	chr2:98206249-98206299	NHDF-neo	bronchial:	n/a
40	chr2:98205903-98205953	U87	brain:	n/a
41	chr2:98206175-98206225	HAEpiC	amniotic membrane:	n/a
42	chr2:98206249-98206299	HRPEpiC	eye:	n/a
43	chr2:98206095-98206145	GM12878	blood:	n/a
44	chr2:98205903-98205953	GM12891	blood:	n/a
45	chr2:98206249-98206299	HCF	heart:	n/a
46	chr2:98206249-98206299	NHBE	bronchial:	n/a
47	chr2:98206175-98206225	MCF-7	breast:	n/a
48	chr2:98205903-98205953	Hepatocyte	liver:	n/a
49	chr2:98206175-98206225	ProgFib	skin:	n/a
50	chr2:98205903-98205953	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:98205848..98207835-chr2:98279004..98283186,3	MCF-7	breast:
2	chr2:98205832..98206585-chr20:2450969..2451709,2	NB4	blood:
3	chr2:98206110..98207769-chr2:98279652..98281540,2	K562	blood:
4	chr2:98204043..98208769-chr2:98260858..98263741,4	MCF-7	breast:

Variant related genes	Relation type
ANKRD36B	TF binding region
ANKRD36B	CpG island
ENSG00000201806	chromatin interactions
ENSG00000125835	chromatin interactions
ENSG00000228486	chromatin interactions
ENSG00000115073	chromatin interactions
ENSG00000135940	chromatin interactions

Extended variants
information (count: 38 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:38 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3866780	chr2:98205416-98205417	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs1809113	chr2:98205724-98205725	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs1814508	chr2:98205744-98205745	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs563999457	chr2:98205799-98205800	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs2924068	chr2:98205859-98205860	Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs144857350	chr2:98205882-98205883	Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
7	rs528964047	chr2:98205887-98205888	Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs74177639	chr2:98205924-98205925	Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
9	rs542767678	chr2:98205925-98205926	Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs185401750	chr2:98206012-98206013	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs188661236	chr2:98206013-98206014	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs367931009	chr2:98206050-98206051	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs2309264	chr2:98206060-98206061	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs4069655	chr2:98206105-98206106	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs2309265	chr2:98206106-98206107	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs2309266	chr2:98206110-98206111	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs551779525	chr2:98206158-98206159	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs2871168	chr2:98206172-98206173	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs571958025	chr2:98206176-98206177	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs2309267	chr2:98206183-98206184	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs1868445	chr2:98206188-98206189	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs117911431	chr2:98206189-98206190	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs181403494	chr2:98206193-98206194	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs553051845	chr2:98206216-98206217	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs565696308	chr2:98206220-98206221	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs537026595	chr2:98206243-98206244	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs28415903	chr2:98206282-98206283	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs185739345	chr2:98206283-98206284	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs375849557	chr2:98206284-98206285	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs1814506	chr2:98206289-98206290	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs76987115	chr2:98206291-98206292	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs1814505	chr2:98206293-98206294	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs3896685	chr2:98206320-98206321	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs368969039	chr2:98206355-98206356	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs573684603	chr2:98206381-98206382	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs370546211	chr2:98206408-98206409	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs3866776	chr2:98206429-98206430	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs573357099	chr2:98206459-98206460	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
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
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	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
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:181 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:98143600-98205600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:98156200-98205600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr2:98160200-98205800	Weak transcription	K562	blood
4	chr2:98166400-98205600	Weak transcription	Brain Germinal Matrix	brain
5	chr2:98168400-98205800	Weak transcription	Fetal Lung	lung
6	chr2:98168400-98205800	Weak transcription	Fetal Muscle Trunk	muscle
7	chr2:98168600-98206000	Weak transcription	NHDF-Ad	bronchial
8	chr2:98169600-98205800	Weak transcription	Fetal Intestine Large	intestine
9	chr2:98171600-98205800	Weak transcription	Primary B cells from peripheral blood	blood
10	chr2:98172200-98205600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr2:98172200-98205800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr2:98172200-98205800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr2:98172200-98205800	Weak transcription	Duodenum Mucosa	Duodenum
14	chr2:98172200-98206000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr2:98172400-98206000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr2:98173400-98205600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr2:98173400-98205800	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr2:98173400-98206000	Weak transcription	Primary T cells from cord blood	blood
19	chr2:98175000-98205800	Weak transcription	Adipose Nuclei	Adipose
20	chr2:98175200-98205600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr2:98175200-98205600	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr2:98175200-98206000	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr2:98176200-98205800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr2:98176400-98205600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr2:98177000-98205800	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr2:98177000-98205800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr2:98177200-98205800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr2:98187400-98206000	Weak transcription	Brain Anterior Caudate	brain
29	chr2:98188600-98205600	Weak transcription	Fetal Stomach	stomach
30	chr2:98193800-98205800	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr2:98193800-98205800	Weak transcription	Stomach Smooth Muscle	stomach
32	chr2:98193800-98205800	Weak transcription	NH-A	brain
33	chr2:98194000-98205800	Weak transcription	HSMM	muscle
34	chr2:98194800-98205800	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr2:98195000-98205800	Weak transcription	HepG2	liver
36	chr2:98196600-98205800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr2:98196800-98205600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:98196800-98205800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr2:98197000-98205800	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr2:98197000-98205800	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr2:98199800-98205800	Weak transcription	NHEK	skin
42	chr2:98204800-98205600	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr2:98204800-98205600	Weak transcription	Fetal Brain Female	brain
44	chr2:98204800-98205800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr2:98204800-98205800	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr2:98204800-98206000	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr2:98204800-98206000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr2:98204800-98207000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr2:98205000-98205600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr2:98205000-98205800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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