Variant report

Variant	esv19383
Chromosome Location	chr21:45326239-45334057
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	ARID3A	chr21:45331214-45331604	HepG2	liver:	n/a	n/a
2	ATF1	chr21:45333799-45334132	K562	blood:	n/a	n/a
3	BHLHE40	chr21:45331208-45331755	HepG2	liver:	n/a	n/a
4	CBX3	chr21:45332580-45333244	K562	blood:	n/a	n/a
5	CBX3	chr21:45332852-45333191	K562	blood:	n/a	n/a
6	CBX3	chr21:45333340-45334152	K562	blood:	n/a	n/a
7	CEBPB	chr21:45331278-45331466	H1-hESC	embryonic stem cell:	n/a	chr21:45331345-45331356 chr21:45331345-45331358
8	CEBPB	chr21:45331155-45331561	HepG2	liver:	n/a	chr21:45331345-45331356 chr21:45331345-45331358
9	CEBPB	chr21:45331346-45331357	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr21:45331095-45331577	HepG2	liver:	n/a	chr21:45331345-45331356 chr21:45331345-45331358
11	CEBPB	chr21:45326006-45326276	IMR90	lung:	n/a	chr21:45326170-45326183 chr21:45326172-45326183
12	CEBPB	chr21:45331212-45331468	IMR90	lung:	n/a	chr21:45331345-45331356 chr21:45331345-45331358
13	CEBPB	chr21:45331153-45331508	K562	blood:	n/a	chr21:45331345-45331356 chr21:45331345-45331358
14	CEBPB	chr21:45331209-45331459	HepG2	liver:	n/a	chr21:45331345-45331356 chr21:45331345-45331358
15	CEBPB	chr21:45331158-45331547	HepG2	liver:	n/a	chr21:45331345-45331356 chr21:45331345-45331358
16	CEBPB	chr21:45333959-45334275	K562	blood:	n/a	n/a
17	CEBPB	chr21:45332854-45333162	K562	blood:	n/a	n/a
18	CEBPB	chr21:45331154-45331530	K562	blood:	n/a	chr21:45331345-45331356 chr21:45331345-45331358
19	CEBPD	chr21:45331160-45331500	HepG2	liver:	n/a	n/a
20	CEBPD	chr21:45331212-45331547	HepG2	liver:	n/a	n/a
21	CREB1	chr21:45333739-45334116	GM12878	blood:	n/a	n/a
22	CREB1	chr21:45333732-45334238	K562	blood:	n/a	n/a
23	CTCF	chr21:45331280-45331430	RPTEC	kidney:	n/a	n/a
24	CTCF	chr21:45331230-45331505	HepG2	liver:	n/a	n/a
25	CTCF	chr21:45331394-45331410	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr21:45331280-45331430	HepG2	liver:	n/a	n/a
27	CTCF	chr21:45331340-45331490	AG09319	gingival:	n/a	n/a
28	CTCF	chr21:45331320-45331470	Caco-2	colon:	n/a	n/a
29	CTCF	chr21:45331277-45331496	HepG2	liver:	n/a	n/a
30	CTCF	chr21:45331180-45331330	HMEC	breast:	n/a	n/a
31	CTCF	chr21:45331350-45331413	K562	blood:	n/a	n/a
32	CTCF	chr21:45331320-45331470	AG09319	gingival:	n/a	n/a
33	CTCF	chr21:45331300-45331450	HepG2	liver:	n/a	n/a
34	CTCF	chr21:45331180-45331330	HVMF	connective:	n/a	n/a
35	CTCF	chr21:45331411-45331414	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr21:45331340-45331490	HCPEpiC	choroid plexus:	n/a	n/a
37	EGR1	chr21:45330371-45330689	K562	blood:	n/a	n/a
38	EGR1	chr21:45330449-45330631	K562	blood:	n/a	n/a
39	EP300	chr21:45331218-45331569	HepG2	liver:	n/a	n/a
40	EP300	chr21:45333942-45334008	GM12878	blood:	n/a	n/a
41	EP300	chr21:45333962-45333971	GM12878	blood:	n/a	n/a
42	FOS	chr21:45328163-45328444	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr21:45328281-45328450	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr21:45328004-45328381	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr21:45326008-45326243	MCF10A-Er-Src	breast:	n/a	chr21:45326208-45326217 chr21:45326222-45326230
46	FOS	chr21:45328224-45328425	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr21:45326006-45326287	MCF10A-Er-Src	breast:	n/a	chr21:45326208-45326217 chr21:45326222-45326230
48	FOXA2	chr21:45332615-45332832	HepG2	liver:	n/a	n/a
49	HDAC2	chr21:45331158-45331554	HepG2	liver:	n/a	n/a
50	HMGN3	chr21:45326584-45326694	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr21:45288583..45290615-chr21:45331081..45332792,2	K562	blood:
2	chr21:45322017..45325690-chr21:45333512..45336768,4	MCF-7	breast:
3	chr21:45284170..45285770-chr21:45332539..45334040,2	K562	blood:
4	chr21:45330659..45332526-chr21:45353655..45356430,2	K562	blood:
5	chr21:45328806..45331467-chr21:45333310..45336234,3	MCF-7	breast:
6	chr21:45326835..45328852-chr21:45330580..45332384,2	MCF-7	breast:
7	chr21:45317953..45320008-chr21:45333800..45335769,2	K562	blood:
8	chr21:45230328..45230908-chr21:45327950..45328510,2	MCF-7	breast:
9	chr21:45328589..45330821-chr21:45430342..45432197,2	K562	blood:
10	chr21:45306480..45309508-chr21:45330034..45333269,3	K562	blood:
11	chr21:45309208..45311155-chr21:45330121..45331958,2	K562	blood:
12	chr21:45317264..45322147-chr21:45323792..45330212,11	K562	blood:
13	chr21:45278596..45280417-chr21:45324857..45327468,2	K562	blood:
14	chr21:45305766..45308236-chr21:45323857..45326352,2	K562	blood:
15	chr21:45326835..45328852-chr21:45330580..45332384,2	MCF-7	breast:
16	chr21:45319240..45321879-chr21:45325042..45326833,2	MCF-7	breast:
17	chr21:45284135..45286457-chr21:45327856..45332723,5	MCF-7	breast:
18	chr21:45324387..45327703-chr21:45346695..45349157,3	MCF-7	breast:
19	chr21:45311265..45313637-chr21:45328494..45330243,2	K562	blood:

Variant related genes	Relation type
AGPAT3	TF binding region
ENSG00000160216	chromatin interactions

Extended variants
information (count: 322 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571074411	chr21:45326249-45326250	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs538513346	chr21:45326272-45326273	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs117497369	chr21:45326286-45326287	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35572047	chr21:45326304-45326305	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568697090	chr21:45326335-45326336	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535835757	chr21:45326337-45326338	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553905275	chr21:45326353-45326354	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs62228754	chr21:45326398-45326399	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs139540498	chr21:45326408-45326409	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs374805629	chr21:45326412-45326413	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558301650	chr21:45326413-45326414	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191201301	chr21:45326441-45326442	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544138440	chr21:45326452-45326453	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576364829	chr21:45326458-45326459	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530522695	chr21:45326464-45326465	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541790192	chr21:45326532-45326533	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs75677426	chr21:45326534-45326535	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560228117	chr21:45326578-45326579	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527348874	chr21:45326583-45326584	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552325507	chr21:45326587-45326588	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs117184761	chr21:45326609-45326610	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574213396	chr21:45326635-45326636	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149294906	chr21:45326636-45326637	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2838430	chr21:45326665-45326666	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs113666889	chr21:45326682-45326683	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535806009	chr21:45326719-45326720	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553716343	chr21:45326723-45326724	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547454915	chr21:45326731-45326732	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565757959	chr21:45326732-45326733	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539499658	chr21:45326759-45326760	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557841113	chr21:45326760-45326761	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs371640546	chr21:45326789-45326790	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544393226	chr21:45326825-45326826	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556113292	chr21:45326841-45326842	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574663707	chr21:45326866-45326867	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541777002	chr21:45326889-45326890	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560164824	chr21:45326893-45326894	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75267823	chr21:45326928-45326929	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4819341	chr21:45326939-45326940	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs375084020	chr21:45326949-45326950	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs116291303	chr21:45326975-45326976	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369574888	chr21:45326976-45326977	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550456670	chr21:45327017-45327018	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550333065	chr21:45327034-45327035	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs8128394	chr21:45327035-45327036	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs371438957	chr21:45327040-45327041	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529563419	chr21:45327059-45327060	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547687716	chr21:45327063-45327064	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565696998	chr21:45327075-45327076	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539438327	chr21:45327077-45327078	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Ewing''s sarcoma	21437220	CNVD
Lung adenocarcinoma	17086460	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute myeloid leukemia	21358987	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	23341502	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Cholangiocarcinoma	16830362	CNVD
Down syndrome	17334655	CNVD
Neuroticism	17667963	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Autoimmune polyendocrine syndrome	18200029	CNVD
Prostate cancer	19363497	CNVD
Lung cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	19805367	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45287400-45330200	Weak transcription	Fetal Kidney	kidney
2	chr21:45301000-45328400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr21:45305000-45328000	Weak transcription	NHEK	skin
4	chr21:45305000-45332600	Weak transcription	Colon Smooth Muscle	Colon
5	chr21:45305200-45327600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr21:45309800-45330600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr21:45314000-45330600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr21:45314400-45332000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr21:45314800-45329600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr21:45314800-45336000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr21:45316600-45336000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr21:45319200-45328400	Weak transcription	A549	lung
13	chr21:45319400-45328800	Weak transcription	HepG2	liver
14	chr21:45319600-45331200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr21:45319800-45331000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr21:45319800-45331800	Weak transcription	Brain Germinal Matrix	brain
17	chr21:45320000-45332400	Weak transcription	Primary B cells from peripheral blood	blood
18	chr21:45321000-45327800	Weak transcription	Brain Anterior Caudate	brain
19	chr21:45321000-45331400	Weak transcription	Brain Substantia Nigra	brain
20	chr21:45322600-45328000	Strong transcription	Primary T cells fromperipheralblood	blood
21	chr21:45323000-45331800	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr21:45323200-45328200	Weak transcription	Brain Angular Gyrus	brain
23	chr21:45323200-45332400	Weak transcription	Hela-S3	cervix
24	chr21:45323400-45328400	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr21:45323400-45328800	Strong transcription	Primary T cells from cord blood	blood
26	chr21:45323400-45329200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr21:45323600-45326400	Strong transcription	Fetal Brain Female	brain
28	chr21:45323600-45326800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr21:45323600-45326800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr21:45323600-45327000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr21:45323600-45327800	Strong transcription	Fetal Intestine Small	intestine
32	chr21:45323600-45327800	Weak transcription	Stomach Mucosa	stomach
33	chr21:45323600-45328600	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr21:45323600-45331800	Strong transcription	Fetal Stomach	stomach
35	chr21:45323800-45327000	Strong transcription	Dnd41	blood
36	chr21:45323800-45327400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr21:45323800-45328800	Strong transcription	Thymus	Thymus
38	chr21:45323800-45329600	Weak transcription	Small Intestine	intestine
39	chr21:45323800-45332000	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr21:45323800-45332400	Weak transcription	HUVEC	blood vessel
41	chr21:45324000-45327600	Weak transcription	Adipose Nuclei	Adipose
42	chr21:45324000-45327800	Weak transcription	Fetal Heart	heart
43	chr21:45324000-45327800	Weak transcription	Gastric	stomach
44	chr21:45324000-45328400	Weak transcription	Fetal Lung	lung
45	chr21:45324000-45336000	Weak transcription	Brain Cingulate Gyrus	brain
46	chr21:45324200-45328000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr21:45324200-45328000	Strong transcription	Esophagus	oesophagus
48	chr21:45324200-45328800	Strong transcription	Rectal Smooth Muscle	rectum
49	chr21:45324200-45332400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr21:45324400-45326800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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