Variant report

Variant	nsv875948
Chromosome Location	chr2:231380697-231420401
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:224)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:224 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:231402056-231402629	GM12878	blood:	n/a	n/a
2	ATF2	chr2:231406476-231407267	GM12878	blood:	n/a	n/a
3	ATF2	chr2:231406622-231407237	GM12878	blood:	n/a	n/a
4	ATF2	chr2:231402096-231402626	GM12878	blood:	n/a	n/a
5	ATF3	chr2:231416932-231417218	K562	blood:	n/a	n/a
6	BATF	chr2:231402126-231402585	GM12878	blood:	n/a	n/a
7	BATF	chr2:231403409-231403676	GM12878	blood:	n/a	n/a
8	BATF	chr2:231403372-231403683	GM12878	blood:	n/a	n/a
9	BATF	chr2:231406513-231407182	GM12878	blood:	n/a	chr2:231406980-231406990
10	BATF	chr2:231401095-231401370	GM12878	blood:	n/a	n/a
11	BATF	chr2:231406610-231407115	GM12878	blood:	n/a	chr2:231406980-231406990
12	BATF	chr2:231401098-231401376	GM12878	blood:	n/a	n/a
13	BATF	chr2:231402155-231402492	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:231402139-231402620	GM12878	blood:	n/a	n/a
15	BCL11A	chr2:231402173-231402516	GM12878	blood:	n/a	n/a
16	BCL3	chr2:231402165-231402627	GM12878	blood:	n/a	n/a
17	BCLAF1	chr2:231402056-231402744	GM12878	blood:	n/a	n/a
18	BCLAF1	chr2:231406327-231407351	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:231406786-231407166	GM12878	blood:	n/a	n/a
20	BHLHE40	chr2:231402827-231402920	GM12878	blood:	n/a	n/a
21	BHLHE40	chr2:231402165-231402596	GM12878	blood:	n/a	n/a
22	CBX3	chr2:231386175-231386409	K562	blood:	n/a	n/a
23	CBX3	chr2:231386169-231386480	K562	blood:	n/a	n/a
24	CEBPB	chr2:231416972-231417256	HepG2	liver:	n/a	chr2:231417071-231417082
25	CEBPB	chr2:231385413-231385778	A549	lung:	n/a	chr2:231385605-231385616
26	CEBPB	chr2:231416966-231417190	IMR90	lung:	n/a	chr2:231417071-231417082
27	CEBPB	chr2:231396319-231396464	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:231416942-231417199	K562	blood:	n/a	chr2:231417071-231417082
29	CEBPB	chr2:231417018-231417127	A549	lung:	n/a	chr2:231417071-231417082
30	CEBPB	chr2:231385445-231385805	A549	lung:	n/a	chr2:231385605-231385616
31	CEBPB	chr2:231416918-231417253	ECC-1	luminal epithelium:	n/a	chr2:231417071-231417082
32	CEBPB	chr2:231385437-231385847	Hela-S3	cervix:	n/a	chr2:231385605-231385616
33	CEBPB	chr2:231385379-231385954	HCT-116	colon:	n/a	chr2:231385605-231385616
34	CEBPB	chr2:231402051-231402801	GM12878	blood:	n/a	n/a
35	CEBPB	chr2:231402222-231402483	GM12878	blood:	n/a	n/a
36	CEBPB	chr2:231407394-231407528	K562	blood:	n/a	chr2:231407508-231407521 chr2:231407508-231407521
37	CEBPB	chr2:231406351-231407313	GM12878	blood:	n/a	n/a
38	CEBPB	chr2:231385453-231385763	HepG2	liver:	n/a	chr2:231385605-231385616
39	CEBPB	chr2:231412431-231412669	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:231416966-231417128	H1-hESC	embryonic stem cell:	n/a	chr2:231417071-231417082
41	CEBPB	chr2:231385424-231385815	IMR90	lung:	n/a	chr2:231385605-231385616
42	CEBPB	chr2:231385366-231385973	A549	lung:	n/a	chr2:231385605-231385616
43	CEBPB	chr2:231396340-231396429	A549	lung:	n/a	n/a
44	CEBPB	chr2:231416862-231417288	HCT-116	colon:	n/a	chr2:231417071-231417082
45	CEBPB	chr2:231417042-231417101	Hela-S3	cervix:	n/a	chr2:231417071-231417082
46	CEBPB	chr2:231385460-231385803	MCF-7	breast:	n/a	chr2:231385605-231385616
47	CHD1	chr2:231406874-231407166	GM12878	blood:	n/a	n/a
48	CHD1	chr2:231399160-231399572	IMR90	lung:	n/a	n/a
49	CHD2	chr2:231402959-231402971	GM12878	blood:	n/a	n/a
50	CHD2	chr2:231404116-231404120	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:231409567-231409617	PANC-1	pancreas:	n/a
2	chr2:231409567-231409617	HCM	heart:	n/a
3	chr2:231409567-231409617	SK-N-MC	brain:	n/a
4	chr2:231409567-231409617	K562	blood:	n/a
5	chr2:231409567-231409617	SK-N-SH	brain:	n/a
6	chr2:231409567-231409617	HRCEpiC	kidney:	n/a
7	chr2:231409567-231409617	HIPEpiC	eye:	n/a
8	chr2:231409567-231409617	HAEpiC	amniotic membrane:	n/a
9	chr2:231409567-231409617	AG04450	lung:	fetal
10	chr2:231409567-231409617	HRE	kidney:	n/a
11	chr2:231409567-231409617	SK-N-SH_RA	brain:	n/a
12	chr2:231409567-231409617	NH-A	brain:	n/a
13	chr2:231409567-231409617	Caco-2	colon:	n/a
14	chr2:231409567-231409617	CMK	blood:	n/a
15	chr2:231409567-231409617	HCPEpiC	choroid plexus:	n/a
16	chr2:231409567-231409617	U87	brain:	n/a
17	chr2:231409567-231409617	NHBE	bronchial:	n/a
18	chr2:231409567-231409617	RPTEC	kidney:	n/a
19	chr2:231409567-231409617	NHDF-neo	bronchial:	n/a
20	chr2:231409567-231409617	HUVEC	blood vessel:	n/a
21	chr2:231409567-231409617	AG09309	skin:	n/a
22	chr2:231409567-231409617	GM12891	blood:	n/a
23	chr2:231409567-231409617	SKMC	muscle:	n/a
24	chr2:231409567-231409617	Hela-S3	cervix:	n/a
25	chr2:231409567-231409617	NB4	blood:	n/a
26	chr2:231409567-231409617	IMR90	lung:	fetal
27	chr2:231409567-231409617	NT2-D1	testis:	n/a
28	chr2:231409567-231409617	GM06990	blood:	n/a
29	chr2:231409567-231409617	PFSK-1	brain:	n/a
30	chr2:231409567-231409617	Jurkat	blood:	n/a
31	chr2:231409567-231409617	HCF	heart:	n/a
32	chr2:231409567-231409617	HCT-116	colon:	n/a
33	chr2:231409567-231409617	HMEC	breast:	n/a
34	chr2:231409567-231409617	ECC-1	luminal epithelium:	n/a
35	chr2:231409567-231409617	HL-60	blood:	n/a
36	chr2:231409567-231409617	HPAEpiC	pulmonary alveolar:	n/a
37	chr2:231409567-231409617	HepG2	liver:	n/a
38	chr2:231409567-231409617	AG10803	skin:	n/a
39	chr2:231409567-231409617	MCF-7	breast:	n/a
40	chr2:231409567-231409617	GM19239	blood:	n/a
41	chr2:231409567-231409617	Hepatocyte	liver:	n/a
42	chr2:231409567-231409617	SAEC	small airway:	n/a
43	chr2:231409567-231409617	HEEpiC	esophagus:	n/a
44	chr2:231409567-231409617	A549	lung:	n/a
45	chr2:231409567-231409617	ProgFib	skin:	n/a
46	chr2:231409567-231409617	GM12878	blood:	n/a
47	chr2:231409567-231409617	AG09319	gingival:	n/a
48	chr2:231409567-231409617	ovcar-3	ovarian:	n/a
49	chr2:231409567-231409617	AG04449	skin:	fetal
50	chr2:231409567-231409617	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:231367823..231370379-chr2:231381226..231383720,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SP110-1	chr2:231403003-231403119	ENSG00000235419.1
2	lnc-SP110-1	chr2:231415763-231415816	ENSG00000235419.1
3	lnc-SP110-1	chr2:231385309-231385388	ENSG00000235419.1
4	lnc-SP100-1	chr2:231412423-231412717	NONHSAT077296
5	lnc-SP110-1	chr2:231415763-231415816	ENSG00000235419.1

No data

Variant related genes	Relation type
SP100	TF binding region
SP100	CpG island
ENSG00000067066	chromatin interactions

Extended variants
information (count: 1702 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1702 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56391445	chr2:231380697-231380698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73097031	chr2:231380714-231380715	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs199911981	chr2:231380735-231380736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs60209140	chr2:231380747-231380748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185884796	chr2:231380763-231380764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192459226	chr2:231380788-231380789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539324335	chr2:231380793-231380794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557934397	chr2:231380795-231380796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575597223	chr2:231380809-231380810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs115288672	chr2:231380840-231380841	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544608334	chr2:231380869-231380870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142102415	chr2:231380969-231380970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183082647	chr2:231381015-231381016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149873999	chr2:231381155-231381156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560082982	chr2:231381165-231381166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372740795	chr2:231381176-231381177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572428941	chr2:231381192-231381193	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546136259	chr2:231381193-231381194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143087542	chr2:231381271-231381272	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs187418336	chr2:231381304-231381305	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs370141923	chr2:231381462-231381463	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs76414439	chr2:231381486-231381487	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs191956388	chr2:231381497-231381498	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs182616425	chr2:231381632-231381633	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs115495277	chr2:231381643-231381644	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs188378507	chr2:231381677-231381678	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs551374081	chr2:231381679-231381680	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs569876042	chr2:231381702-231381703	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs74415594	chr2:231381704-231381705	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs536822089	chr2:231381717-231381718	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs556271141	chr2:231381743-231381744	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs568233266	chr2:231381795-231381796	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs535529922	chr2:231381803-231381804	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs192658131	chr2:231381828-231381829	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs572311922	chr2:231381834-231381835	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546516563	chr2:231381837-231381838	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs76792105	chr2:231381903-231381904	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs35717626	chr2:231381934-231381935	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs184649683	chr2:231381947-231381948	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs113549749	chr2:231382058-231382059	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189164568	chr2:231382060-231382061	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs574815736	chr2:231382077-231382078	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs529000087	chr2:231382168-231382169	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs541086243	chr2:231382230-231382231	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs559431916	chr2:231382237-231382238	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs151157139	chr2:231382239-231382240	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs551680047	chr2:231382261-231382262	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs192525532	chr2:231382293-231382294	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs529355205	chr2:231382341-231382342	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs533937160	chr2:231382381-231382382	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	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
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
prenatal diagnosis	22389664	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231355800-231381400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr2:231361800-231381400	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr2:231364200-231381000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr2:231364600-231385800	Weak transcription	HSMMtube	muscle
5	chr2:231366600-231385200	Weak transcription	HMEC	breast
6	chr2:231370800-231389600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr2:231371000-231409800	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr2:231371200-231384600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr2:231372000-231384600	Weak transcription	Placenta	Placenta
10	chr2:231372400-231386200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr2:231375000-231385600	Weak transcription	HSMM	muscle
12	chr2:231375200-231390200	Weak transcription	Ovary	ovary
13	chr2:231376200-231383400	Weak transcription	GM12878-XiMat	blood
14	chr2:231376400-231381200	Strong transcription	Primary B cells from cord blood	blood
15	chr2:231376400-231381800	Weak transcription	NHEK	skin
16	chr2:231376600-231381200	Strong transcription	Primary B cells from peripheral blood	blood
17	chr2:231376600-231381200	Weak transcription	NHDF-Ad	bronchial
18	chr2:231376600-231383600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr2:231376600-231384000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr2:231376600-231384400	Weak transcription	Primary hematopoietic stem cells	blood
21	chr2:231376600-231384600	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr2:231376600-231384800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr2:231376600-231385000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr2:231376600-231385200	Weak transcription	Right Ventricle	heart
25	chr2:231376600-231385400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr2:231376600-231386000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr2:231376600-231390200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr2:231376600-231390400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr2:231376800-231381800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr2:231377000-231385800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr2:231377800-231382600	Weak transcription	Lung	lung
32	chr2:231377800-231385200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr2:231378000-231384400	Weak transcription	Left Ventricle	heart
34	chr2:231378000-231390800	Weak transcription	Spleen	Spleen
35	chr2:231378200-231381400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr2:231378200-231385200	Weak transcription	NH-A	brain
37	chr2:231378200-231385400	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr2:231378400-231384800	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr2:231378400-231384800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr2:231378400-231385200	Weak transcription	HUVEC	blood vessel
41	chr2:231378400-231385200	Weak transcription	Osteobl	bone
42	chr2:231378400-231386000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr2:231378600-231384000	Weak transcription	Primary T cells from cord blood	blood
44	chr2:231378600-231384400	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr2:231378600-231384400	Weak transcription	Small Intestine	intestine
46	chr2:231378600-231384600	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr2:231378600-231384600	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr2:231378600-231384600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr2:231378600-231385000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr2:231378600-231385000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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