Variant report

Variant	nsv2598
Chromosome Location	chr2:7088737-7133415
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	chr2:7126726-7126909	K562	blood:	n/a	n/a
2	ARID3A	chr2:7119452-7119468	K562	blood:	n/a	n/a
3	BACH1	chr2:7132244-7132559	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:7100500-7100504	K562	blood:	n/a	n/a
5	BHLHE40	chr2:7119276-7119379	K562	blood:	n/a	n/a
6	BHLHE40	chr2:7097203-7097634	HepG2	liver:	n/a	n/a
7	CBX3	chr2:7120785-7121381	K562	blood:	n/a	n/a
8	CBX3	chr2:7116156-7116556	HCT-116	colon:	n/a	n/a
9	CEBPB	chr2:7115943-7116704	HCT-116	colon:	n/a	chr2:7116620-7116633 chr2:7116620-7116633
10	CEBPB	chr2:7116188-7116527	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr2:7116006-7116692	HCT-116	colon:	n/a	chr2:7116620-7116633 chr2:7116620-7116633
12	CEBPB	chr2:7116210-7116565	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:7126697-7126981	K562	blood:	n/a	chr2:7126870-7126881
14	CEBPB	chr2:7116273-7116501	K562	blood:	n/a	n/a
15	CEBPB	chr2:7116222-7116648	MCF-7	breast:	n/a	chr2:7116620-7116633 chr2:7116620-7116633
16	CEBPB	chr2:7116200-7116510	MCF-7	breast:	n/a	n/a
17	CEBPB	chr2:7089319-7089337	K562	blood:	n/a	n/a
18	CEBPB	chr2:7116134-7116588	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr2:7090383-7090701	HepG2	liver:	n/a	chr2:7090514-7090525
20	CEBPB	chr2:7126695-7127294	HepG2	liver:	n/a	chr2:7126870-7126881
21	CEBPB	chr2:7126815-7127051	IMR90	lung:	n/a	chr2:7126870-7126881
22	CEBPB	chr2:7126798-7126998	K562	blood:	n/a	chr2:7126870-7126881
23	CEBPB	chr2:7122256-7122567	HepG2	liver:	n/a	chr2:7122398-7122415 chr2:7122399-7122412
24	CEBPB	chr2:7119589-7119719	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:7116074-7116696	A549	lung:	n/a	chr2:7116620-7116633 chr2:7116620-7116633
26	CEBPB	chr2:7090352-7090683	A549	lung:	n/a	chr2:7090514-7090525
27	CEBPB	chr2:7116183-7116501	A549	lung:	n/a	n/a
28	CEBPB	chr2:7122396-7122489	K562	blood:	n/a	chr2:7122398-7122415 chr2:7122399-7122412
29	CEBPB	chr2:7126695-7127043	K562	blood:	n/a	chr2:7126870-7126881
30	CEBPB	chr2:7116211-7116540	A549	lung:	n/a	n/a
31	CEBPB	chr2:7115880-7116007	K562	blood:	n/a	n/a
32	CHD2	chr2:7126297-7126299	HepG2	liver:	n/a	n/a
33	CTCF	chr2:7108560-7108710	AG09309	skin:	n/a	n/a
34	CTCF	chr2:7108615-7108749	MCF-7	breast:	n/a	chr2:7108711-7108729 chr2:7108713-7108726 chr2:7108712-7108728
35	CTCF	chr2:7108880-7109030	GM12873	blood:	n/a	n/a
36	CTCF	chr2:7108682-7108744	GM13977	blood:	n/a	chr2:7108711-7108729 chr2:7108713-7108726 chr2:7108712-7108728
37	CTCF	chr2:7108644-7108762	MCF-7	breast:	n/a	chr2:7108711-7108729 chr2:7108713-7108726 chr2:7108712-7108728
38	CTCF	chr2:7108613-7108803	HepG2	liver:	n/a	chr2:7108711-7108729 chr2:7108713-7108726 chr2:7108712-7108728
39	CTCF	chr2:7108607-7108865	K562	blood:	n/a	chr2:7108711-7108729 chr2:7108713-7108726 chr2:7108712-7108728
40	CTCF	chr2:7108720-7108870	K562	blood:	n/a	n/a
41	CTCF	chr2:7108600-7108750	SK-N-SH_RA	brain:	n/a	chr2:7108711-7108729 chr2:7108713-7108726 chr2:7108712-7108728
42	CTCF	chr2:7108620-7108770	HPAF	blood vessel:	n/a	chr2:7108711-7108729 chr2:7108713-7108726 chr2:7108712-7108728
43	CTCF	chr2:7108660-7108810	AG09319	gingival:	n/a	chr2:7108711-7108729 chr2:7108713-7108726 chr2:7108712-7108728
44	CTCF	chr2:7108620-7108770	GM12867	blood:	n/a	chr2:7108711-7108729 chr2:7108713-7108726 chr2:7108712-7108728
45	CTCF	chr2:7108669-7108759	GM10266	blood:	n/a	chr2:7108711-7108729 chr2:7108713-7108726 chr2:7108712-7108728
46	CTCF	chr2:7108640-7108790	HCPEpiC	choroid plexus:	n/a	chr2:7108711-7108729 chr2:7108713-7108726 chr2:7108712-7108728
47	CTCF	chr2:7108600-7108750	HEK293	kidney:	n/a	chr2:7108711-7108729 chr2:7108713-7108726 chr2:7108712-7108728
48	CTCF	chr2:7108620-7108770	HCPEpiC	choroid plexus:	n/a	chr2:7108711-7108729 chr2:7108713-7108726 chr2:7108712-7108728
49	CTCF	chr2:7108680-7108830	HFF-Myc	foreskin:	n/a	chr2:7108711-7108729 chr2:7108713-7108726 chr2:7108712-7108728
50	CTCF	chr2:7108600-7108750	HPAF	blood vessel:	n/a	chr2:7108711-7108729 chr2:7108713-7108726 chr2:7108712-7108728

No.	Distal block	Cell Line	Cell type
1	chr2:7104336..7107302-chr2:7109423..7112409,2	K562	blood:
2	chr2:7082796..7085446-chr2:7087742..7089265,2	K562	blood:
3	chr2:7131290..7134151-chr2:7135559..7137414,2	K562	blood:
4	chr2:7094490..7097337-chr2:7099002..7100919,2	K562	blood:
5	chr2:7126650..7129012-chr2:7161153..7163325,2	K562	blood:
6	chr2:7089064..7092606-chr2:7093987..7098071,5	K562	blood:
7	chr2:7097520..7099257-chr2:7101645..7103417,2	MCF-7	breast:
8	chr2:7099221..7101683-chr2:7105044..7107331,2	K562	blood:
9	chr16:74751556..74754307-chr2:7086271..7088769,2	MCF-7	breast:
10	chr2:7079492..7082070-chr2:7087542..7089279,2	K562	blood:
11	chr2:7104336..7107302-chr2:7109423..7112409,2	K562	blood:
12	chr2:7077733..7080992-chr2:7086392..7089961,3	K562	blood:
13	chr2:7065097..7066741-chr2:7112184..7114861,2	K562	blood:
14	chr2:7097520..7099257-chr2:7101645..7103417,2	MCF-7	breast:
15	chr2:7099221..7101683-chr2:7105044..7107331,2	K562	blood:
16	chr2:7100183..7102854-chr2:7105453..7109313,4	K562	blood:
17	chr2:7113332..7116286-chr2:9136805..9139495,2	MCF-7	breast:
18	chr2:7130628..7133079-chr2:7138526..7140206,2	MCF-7	breast:
19	chr2:7082801..7085400-chr2:7088516..7090192,2	MCF-7	breast:
20	chr2:7005206..7007392-chr2:7127892..7129455,2	K562	blood:
21	chr2:7094490..7097337-chr2:7099002..7100919,2	K562	blood:
22	chr2:7014977..7017559-chr2:7110921..7112588,2	K562	blood:
23	chr2:7097968..7100003-chr2:7109143..7111034,2	K562	blood:
24	chr2:7084388..7085908-chr2:7089261..7091175,2	K562	blood:
25	chr2:7092876..7095990-chr2:7096589..7100919,3	K562	blood:
26	chr2:7071092..7072701-chr2:7129085..7131806,2	MCF-7	breast:
27	chr2:7109657..7111337-chr2:7117211..7119899,2	MCF-7	breast:
28	chr2:7057303..7059038-chr2:7114165..7115903,2	K562	blood:
29	chr2:7097968..7100003-chr2:7109143..7111034,2	K562	blood:
30	chr2:7100183..7102854-chr2:7105453..7109313,4	K562	blood:
31	chr2:7089064..7092606-chr2:7093987..7098071,5	K562	blood:
32	chr2:7092876..7095990-chr2:7096589..7100919,3	K562	blood:

Variant related genes	Relation type
RNF144A	TF binding region
ENSG00000151692	chromatin interactions
ENSG00000228203	chromatin interactions
ENSG00000134321	chromatin interactions
ENSG00000134326	chromatin interactions

Extended variants
information (count: 1821 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1821 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151242144	chr2:7088769-7088770	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs140410932	chr2:7088775-7088776	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs77580854	chr2:7088789-7088790	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147007609	chr2:7088835-7088836	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs76922645	chr2:7088863-7088864	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369020015	chr2:7088879-7088880	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571379708	chr2:7088938-7088939	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371625159	chr2:7088976-7088977	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs180735095	chr2:7089015-7089016	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541944477	chr2:7089056-7089057	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552501212	chr2:7089100-7089101	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538949287	chr2:7089102-7089103	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs3772021	chr2:7089124-7089125	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs534924070	chr2:7089169-7089170	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554756185	chr2:7089181-7089182	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574660560	chr2:7089187-7089188	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs80027966	chr2:7089193-7089194	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532318191	chr2:7089208-7089209	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76287076	chr2:7089229-7089230	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs78169687	chr2:7089259-7089260	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184990191	chr2:7089309-7089310	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs572354617	chr2:7089408-7089409	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs569472368	chr2:7089440-7089441	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190912548	chr2:7089474-7089475	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538397709	chr2:7089505-7089506	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376331126	chr2:7089528-7089529	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547352057	chr2:7089540-7089541	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs373080419	chr2:7089553-7089554	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561067031	chr2:7089601-7089602	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs79479875	chr2:7089653-7089654	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111713116	chr2:7089675-7089676	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs142118838	chr2:7089687-7089688	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs71436167	chr2:7089711-7089712	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532163056	chr2:7089745-7089746	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573743830	chr2:7089746-7089747	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547415322	chr2:7089747-7089748	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565305031	chr2:7089771-7089772	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs184014864	chr2:7089776-7089777	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs565961401	chr2:7089857-7089858	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs7562120	chr2:7089923-7089924	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs537237566	chr2:7090049-7090050	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566474403	chr2:7090072-7090073	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372151380	chr2:7090073-7090074	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533813829	chr2:7090088-7090089	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs188961382	chr2:7090101-7090102	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574892815	chr2:7090115-7090116	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79404601	chr2:7090129-7090130	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs553418159	chr2:7090153-7090154	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145879195	chr2:7090186-7090187	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs74842900	chr2:7090258-7090259	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
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
low-grade B-cell lymphoma tumor	18367492	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
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Neuroblastoma	18923524	CNVD

Chromatin state (count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:7075200-7095600	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr2:7077800-7091200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr2:7078200-7089400	Weak transcription	Fetal Brain Male	brain
4	chr2:7078200-7110800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:7079000-7113400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr2:7080400-7094800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr2:7081200-7089000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:7081400-7089600	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr2:7081400-7112200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr2:7081600-7094600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:7082600-7091800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr2:7082600-7100800	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr2:7082800-7090800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr2:7083800-7129600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr2:7084200-7089200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr2:7084200-7097200	Weak transcription	Fetal Lung	lung
17	chr2:7084200-7122200	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr2:7084400-7100400	Weak transcription	Stomach Smooth Muscle	stomach
19	chr2:7084400-7100600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr2:7084400-7109600	Weak transcription	Fetal Thymus	thymus
21	chr2:7084400-7110800	Weak transcription	Esophagus	oesophagus
22	chr2:7084600-7092000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr2:7084600-7105200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr2:7084600-7112800	Weak transcription	Thymus	Thymus
25	chr2:7084800-7095800	Weak transcription	Fetal Brain Female	brain
26	chr2:7085000-7095600	Weak transcription	Ovary	ovary
27	chr2:7085000-7120200	Weak transcription	Fetal Intestine Small	intestine
28	chr2:7085400-7110400	Weak transcription	Brain Germinal Matrix	brain
29	chr2:7085600-7099600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr2:7085800-7089600	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr2:7085800-7096000	Weak transcription	Primary hematopoietic stem cells	blood
32	chr2:7086000-7088800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr2:7086000-7095200	Weak transcription	Colon Smooth Muscle	Colon
34	chr2:7086200-7088800	Enhancers	GM12878-XiMat	blood
35	chr2:7086200-7089000	Weak transcription	Duodenum Mucosa	Duodenum
36	chr2:7086200-7090600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr2:7086200-7095400	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr2:7086200-7095600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr2:7086200-7095600	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr2:7086200-7098400	Weak transcription	Fetal Muscle Trunk	muscle
41	chr2:7086200-7100600	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr2:7086400-7094600	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr2:7087200-7094600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr2:7087400-7091400	Weak transcription	HUVEC	blood vessel
45	chr2:7087600-7089800	Enhancers	NHDF-Ad	bronchial
46	chr2:7087600-7102800	Strong transcription	Dnd41	blood
47	chr2:7087800-7089200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr2:7087800-7089200	Enhancers	Brain Hippocampus Middle	brain
49	chr2:7087800-7089200	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr2:7087800-7089200	Enhancers	Fetal Muscle Leg	muscle

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