Variant report

Variant	nsv1011400
Chromosome Location	chr2:53899956-53947781
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	chr2:53928413-53928764	K562	blood:	n/a	n/a
2	ARID3A	chr2:53942779-53943047	HepG2	liver:	n/a	n/a
3	BACH1	chr2:53928536-53928700	K562	blood:	n/a	n/a
4	CBX3	chr2:53936100-53936437	K562	blood:	n/a	n/a
5	CBX3	chr2:53936090-53936485	K562	blood:	n/a	n/a
6	CEBPB	chr2:53940521-53940567	K562	blood:	n/a	n/a
7	CEBPB	chr2:53923351-53923501	A549	lung:	n/a	n/a
8	CTCF	chr2:53942748-53943058	IMR90	lung:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
9	CTCF	chr2:53943300-53943450	HEEpiC	esophagus:	n/a	n/a
10	CTCF	chr2:53942820-53942970	HRPEpiC	eye:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
11	CTCF	chr2:53942840-53942990	HPAF	blood vessel:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
12	CTCF	chr2:53942820-53942970	HMEC	breast:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
13	CTCF	chr2:53936065-53936228	K562	blood:	n/a	n/a
14	CTCF	chr2:53942800-53942950	GM12878	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
15	CTCF	chr2:53942800-53942950	NHDF-neo	bronchial:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
16	CTCF	chr2:53942880-53943030	HCM	heart:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
17	CTCF	chr2:53942794-53943046	Medullo	brain:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
18	CTCF	chr2:53943000-53943150	GM12873	blood:	n/a	n/a
19	CTCF	chr2:53942860-53943010	HBMEC	blood vessel:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
20	CTCF	chr2:53942748-53943070	MCF-7	breast:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
21	CTCF	chr2:53942875-53942930	Lung_OC	lung:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
22	CTCF	chr2:53942766-53943147	MCF-7	breast:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
23	CTCF	chr2:53942820-53942970	AG04449	skin:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
24	CTCF	chr2:53942860-53943010	GM12864	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
25	CTCF	chr2:53942880-53943030	MCF-7	breast:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
26	CTCF	chr2:53942871-53942967	Kidney_OC	kidney:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
27	CTCF	chr2:53940956-53940991	Fibrobl	skin:	n/a	n/a
28	CTCF	chr2:53943180-53943330	BJ	skin:	n/a	n/a
29	CTCF	chr2:53942840-53942990	BJ	skin:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
30	CTCF	chr2:53942857-53942999	Pancreas_OC	pancreas:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
31	CTCF	chr2:53942800-53942950	GM12875	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
32	CTCF	chr2:53942840-53942990	HCFaa	heart:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
33	CTCF	chr2:53942800-53942950	AG09319	gingival:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
34	CTCF	chr2:53942840-53942990	HPF	lung:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
35	CTCF	chr2:53942820-53942970	HUVEC	blood vessel:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
36	CTCF	chr2:53942720-53942870	BE2_C	brain:	n/a	n/a
37	CTCF	chr2:53942760-53942910	HFF	foreskin:	n/a	n/a
38	CTCF	chr2:53942820-53942970	GM12870	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
39	CTCF	chr2:53942820-53942970	GM12801	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
40	CTCF	chr2:53942774-53942971	H1-hESC	embryonic stem cell:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
41	CTCF	chr2:53942780-53942930	GM12865	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
42	CTCF	chr2:53942720-53942870	HCT-116	colon:	n/a	n/a
43	CTCF	chr2:53942840-53942990	GM12871	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
44	CTCF	chr2:53942860-53943010	HA-sp	spinal cord:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
45	CTCF	chr2:53942827-53942979	GM13977	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
46	CTCF	chr2:53943180-53943330	GM12878	blood:	n/a	n/a
47	CTCF	chr2:53942807-53942983	HepG2	liver:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
48	CTCF	chr2:53942820-53942970	GM12874	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
49	CTCF	chr2:53942840-53942990	GM12873	blood:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919
50	CTCF	chr2:53942813-53942995	LNCaP	prostate:	n/a	chr2:53942896-53942917 chr2:53942902-53942918 chr2:53942908-53942915 chr2:53942901-53942919

No.	Distal block	Cell Line	Cell type
1	chr1:11966902..11969473-chr2:53944359..53947359,6	MCF-7	breast:
2	chr2:53926842..53929678-chr2:54004293..54006164,2	K562	blood:
3	chr2:53925981..53927589-chr2:53940700..53943084,2	K562	blood:
4	chr2:53920239..53922188-chr2:53922712..53925505,2	K562	blood:
5	chr2:53925981..53927589-chr2:53940700..53943084,2	K562	blood:
6	chr2:53938900..53941731-chr2:54013134..54015288,2	K562	blood:
7	chr17:70758626..70759130-chr2:53924202..53924904,2	MCF-7	breast:
8	chr1:11966927..11968808-chr2:53945839..53947359,4	MCF-7	breast:
9	chr2:53926965..53929338-chr2:53930911..53933227,2	K562	blood:
10	chr1:11967949..11968659-chr2:53945359..53946359,5	MCF-7	breast:
11	chr2:53669933..53670563-chr2:53942920..53943446,2	MCF-7	breast:
12	chr1:11967940..11968599-chr2:53945834..53946359,2	MCF-7	breast:
13	chr2:53927372..53929338-chr2:53931727..53933877,2	K562	blood:
14	chr2:53926965..53929338-chr2:53930911..53933227,2	K562	blood:
15	chr2:53931144..53933214-chr2:53937294..53940246,2	K562	blood:
16	chr2:53687389..53688064-chr2:53942616..53943230,2	MCF-7	breast:
17	chr2:53931144..53933214-chr2:53937294..53940246,2	K562	blood:
18	chr2:53894424..53897447-chr2:53898122..53902216,4	K562	blood:
19	chr2:53901787..53904265-chr2:53994019..53996587,2	K562	blood:
20	chr2:53927372..53929338-chr2:53931727..53933877,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHAC2-5	chr2:53927406-53927679	NONHSAT070694
2	lnc-CHAC2-5	chr2:53941521-53941719	NONHSAT070694

Variant related genes	Relation type
GPR75-ASB3	TF binding region
ENSG00000143942	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000115239	chromatin interactions
ENSG00000068912	chromatin interactions

Extended variants
information (count: 2188 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2188 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139820839	chr2:53899963-53899964	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs188655728	chr2:53899995-53899996	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192406155	chr2:53900097-53900098	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530302139	chr2:53900115-53900116	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553916525	chr2:53900128-53900129	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183351020	chr2:53900129-53900130	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573908782	chr2:53900133-53900134	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542894920	chr2:53900155-53900156	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548476303	chr2:53900207-53900208	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187496364	chr2:53900233-53900234	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139937093	chr2:53900238-53900239	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375217289	chr2:53900268-53900269	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191667868	chr2:53900302-53900303	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs72793627	chr2:53900316-53900317	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs187043954	chr2:53900328-53900329	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145355045	chr2:53900396-53900397	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560374181	chr2:53900405-53900406	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533233228	chr2:53900413-53900414	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191173065	chr2:53900433-53900434	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184598012	chr2:53900468-53900469	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190324609	chr2:53900475-53900476	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs11897630	chr2:53900571-53900572	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569509681	chr2:53900576-53900577	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571174745	chr2:53900616-53900617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147736338	chr2:53900672-53900673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547120694	chr2:53900705-53900706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs567520395	chr2:53900706-53900707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532197439	chr2:53900716-53900717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs371053286	chr2:53900730-53900731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs77798873	chr2:53900731-53900732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556350471	chr2:53900771-53900772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576631234	chr2:53900793-53900794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115819481	chr2:53900801-53900802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs193294207	chr2:53900827-53900828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs149859496	chr2:53900874-53900875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs116266244	chr2:53900880-53900881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541516202	chr2:53900895-53900896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561413306	chr2:53900943-53900944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115547101	chr2:53900952-53900953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559601806	chr2:53900955-53900956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145805841	chr2:53901015-53901016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562543561	chr2:53901024-53901025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531603162	chr2:53901048-53901049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs3770416	chr2:53901053-53901054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185166860	chr2:53901086-53901087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188897654	chr2:53901089-53901090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547083639	chr2:53901131-53901132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181634360	chr2:53901135-53901136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12614169	chr2:53901143-53901144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566984139	chr2:53901147-53901148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	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
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1021 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:53874200-53935000	Weak transcription	Pancreas	Pancrea
2	chr2:53881400-53934400	Weak transcription	Stomach Smooth Muscle	stomach
3	chr2:53885600-53925000	Weak transcription	Fetal Intestine Small	intestine
4	chr2:53885800-53911800	Weak transcription	Adipose Nuclei	Adipose
5	chr2:53888200-53934200	Weak transcription	Lung	lung
6	chr2:53888400-53935200	Weak transcription	Fetal Brain Male	brain
7	chr2:53888600-53935200	Weak transcription	Hela-S3	cervix
8	chr2:53889000-53935800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr2:53891600-53900000	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr2:53892600-53902600	Weak transcription	Rectal Smooth Muscle	rectum
11	chr2:53892600-53918800	Weak transcription	Left Ventricle	heart
12	chr2:53893400-53915200	Weak transcription	Ovary	ovary
13	chr2:53893800-53926800	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr2:53894200-53920800	Weak transcription	Duodenum Mucosa	Duodenum
15	chr2:53894400-53900400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr2:53894400-53912200	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr2:53894400-53914400	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr2:53894400-53925000	Weak transcription	Fetal Muscle Trunk	muscle
19	chr2:53894400-53933800	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr2:53894600-53900000	Weak transcription	Stomach Mucosa	stomach
21	chr2:53894600-53911200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr2:53894800-53900000	Weak transcription	Brain Hippocampus Middle	brain
23	chr2:53895000-53900200	Weak transcription	Brain Substantia Nigra	brain
24	chr2:53895000-53911800	Weak transcription	Primary T cells fromperipheralblood	blood
25	chr2:53895400-53919000	Weak transcription	Fetal Intestine Large	intestine
26	chr2:53895400-53921200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr2:53895400-53925800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr2:53895400-53926200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr2:53895600-53914800	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr2:53895600-53921400	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr2:53895800-53916800	Weak transcription	Brain Anterior Caudate	brain
32	chr2:53895800-53926200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr2:53896000-53900000	Weak transcription	HSMM	muscle
34	chr2:53896000-53913000	Weak transcription	Fetal Muscle Leg	muscle
35	chr2:53896000-53918800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr2:53896200-53911200	Weak transcription	Liver	Liver
37	chr2:53896200-53918400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr2:53896400-53926000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr2:53896600-53900000	Weak transcription	Fetal Heart	heart
40	chr2:53896800-53900200	Weak transcription	NH-A	brain
41	chr2:53896800-53910200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr2:53896800-53910800	Weak transcription	Primary B cells from peripheral blood	blood
43	chr2:53896800-53918800	Weak transcription	Fetal Brain Female	brain
44	chr2:53896800-53924800	Weak transcription	Thymus	Thymus
45	chr2:53896800-53936600	Weak transcription	Aorta	Aorta
46	chr2:53897000-53910400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr2:53897000-53911400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr2:53897400-53900200	Weak transcription	K562	blood
49	chr2:53897400-53910200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr2:53897400-53910200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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