Variant report

Variant	nsv584673
Chromosome Location	chr2:231385231-231433237
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:278)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:278 , 50 per page) page: 1 2 3 4 5 6

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	chr2:231406622-231407237	GM12878	blood:	n/a	n/a
3	ATF2	chr2:231402096-231402626	GM12878	blood:	n/a	n/a
4	ATF2	chr2:231406476-231407267	GM12878	blood:	n/a	n/a
5	ATF3	chr2:231416932-231417218	K562	blood:	n/a	n/a
6	BATF	chr2:231406610-231407115	GM12878	blood:	n/a	chr2:231406980-231406990
7	BATF	chr2:231401095-231401370	GM12878	blood:	n/a	n/a
8	BATF	chr2:231403372-231403683	GM12878	blood:	n/a	n/a
9	BATF	chr2:231403409-231403676	GM12878	blood:	n/a	n/a
10	BATF	chr2:231402155-231402492	GM12878	blood:	n/a	n/a
11	BATF	chr2:231401098-231401376	GM12878	blood:	n/a	n/a
12	BATF	chr2:231429516-231429826	GM12878	blood:	n/a	n/a
13	BATF	chr2:231402126-231402585	GM12878	blood:	n/a	n/a
14	BATF	chr2:231406513-231407182	GM12878	blood:	n/a	chr2:231406980-231406990
15	BCL11A	chr2:231402139-231402620	GM12878	blood:	n/a	n/a
16	BCL11A	chr2:231402173-231402516	GM12878	blood:	n/a	n/a
17	BCL3	chr2:231402165-231402627	GM12878	blood:	n/a	n/a
18	BCLAF1	chr2:231402056-231402744	GM12878	blood:	n/a	n/a
19	BCLAF1	chr2:231406327-231407351	GM12878	blood:	n/a	n/a
20	BCLAF1	chr2:231429404-231429865	GM12878	blood:	n/a	n/a
21	BHLHE40	chr2:231402827-231402920	GM12878	blood:	n/a	n/a
22	BHLHE40	chr2:231402165-231402596	GM12878	blood:	n/a	n/a
23	BHLHE40	chr2:231406786-231407166	GM12878	blood:	n/a	n/a
24	CBX3	chr2:231386169-231386480	K562	blood:	n/a	n/a
25	CBX3	chr2:231386175-231386409	K562	blood:	n/a	n/a
26	CEBPB	chr2:231430617-231430885	IMR90	lung:	n/a	chr2:231430738-231430749 chr2:231430740-231430751
27	CEBPB	chr2:231385424-231385815	IMR90	lung:	n/a	chr2:231385605-231385616
28	CEBPB	chr2:231412431-231412669	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:231402222-231402483	GM12878	blood:	n/a	n/a
30	CEBPB	chr2:231416862-231417288	HCT-116	colon:	n/a	chr2:231417071-231417082
31	CEBPB	chr2:231385460-231385803	MCF-7	breast:	n/a	chr2:231385605-231385616
32	CEBPB	chr2:231416972-231417256	HepG2	liver:	n/a	chr2:231417071-231417082
33	CEBPB	chr2:231385445-231385805	A549	lung:	n/a	chr2:231385605-231385616
34	CEBPB	chr2:231396340-231396429	A549	lung:	n/a	n/a
35	CEBPB	chr2:231430730-231430785	K562	blood:	n/a	chr2:231430738-231430749 chr2:231430740-231430751
36	CEBPB	chr2:231385437-231385847	Hela-S3	cervix:	n/a	chr2:231385605-231385616
37	CEBPB	chr2:231385453-231385763	HepG2	liver:	n/a	chr2:231385605-231385616
38	CEBPB	chr2:231385379-231385954	HCT-116	colon:	n/a	chr2:231385605-231385616
39	CEBPB	chr2:231416966-231417128	H1-hESC	embryonic stem cell:	n/a	chr2:231417071-231417082
40	CEBPB	chr2:231385413-231385778	A549	lung:	n/a	chr2:231385605-231385616
41	CEBPB	chr2:231385366-231385973	A549	lung:	n/a	chr2:231385605-231385616
42	CEBPB	chr2:231430605-231430872	HepG2	liver:	n/a	chr2:231430738-231430749 chr2:231430740-231430751
43	CEBPB	chr2:231407394-231407528	K562	blood:	n/a	chr2:231407508-231407521 chr2:231407508-231407521
44	CEBPB	chr2:231402051-231402801	GM12878	blood:	n/a	n/a
45	CEBPB	chr2:231416918-231417253	ECC-1	luminal epithelium:	n/a	chr2:231417071-231417082
46	CEBPB	chr2:231430624-231430838	A549	lung:	n/a	chr2:231430738-231430749 chr2:231430740-231430751
47	CEBPB	chr2:231406351-231407313	GM12878	blood:	n/a	n/a
48	CEBPB	chr2:231396319-231396464	HepG2	liver:	n/a	n/a
49	CEBPB	chr2:231417042-231417101	Hela-S3	cervix:	n/a	chr2:231417071-231417082
50	CEBPB	chr2:231417018-231417127	A549	lung:	n/a	chr2:231417071-231417082

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:231409567-231409617	Hela-S3	cervix:	n/a
2	chr2:231409567-231409617	A549	lung:	n/a
3	chr2:231409567-231409617	MCF-7	breast:	n/a
4	chr2:231409567-231409617	LNCaP	prostate:	n/a
5	chr2:231409567-231409617	GM19239	blood:	n/a
6	chr2:231409567-231409617	HL-60	blood:	n/a
7	chr2:231409567-231409617	SK-N-MC	brain:	n/a
8	chr2:231409567-231409617	BJ	skin:	n/a
9	chr2:231409567-231409617	Jurkat	blood:	n/a
10	chr2:231409567-231409617	HRPEpiC	eye:	n/a
11	chr2:231409567-231409617	BE2_C	brain:	n/a
12	chr2:231409567-231409617	AG09319	gingival:	n/a
13	chr2:231409567-231409617	PFSK-1	brain:	n/a
14	chr2:231409567-231409617	HCF	heart:	n/a
15	chr2:231409567-231409617	RPTEC	kidney:	n/a
16	chr2:231409567-231409617	HNPCEpiC	eye:	n/a
17	chr2:231409567-231409617	NH-A	brain:	n/a
18	chr2:231409567-231409617	H1-hESC	embryonic stem cell:	embryo
19	chr2:231409567-231409617	HEK293	kidney:	embryo
20	chr2:231409567-231409617	U87	brain:	n/a
21	chr2:231409567-231409617	NHDF-neo	bronchial:	n/a
22	chr2:231409567-231409617	K562	blood:	n/a
23	chr2:231409567-231409617	CMK	blood:	n/a
24	chr2:231409567-231409617	AG10803	skin:	n/a
25	chr2:231409567-231409617	ECC-1	luminal epithelium:	n/a
26	chr2:231409567-231409617	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:231409567-231409617	HepG2	liver:	n/a
28	chr2:231409567-231409617	HMEC	breast:	n/a
29	chr2:231409567-231409617	HUVEC	blood vessel:	n/a
30	chr2:231409567-231409617	NT2-D1	testis:	n/a
31	chr2:231409567-231409617	HRE	kidney:	n/a
32	chr2:231409567-231409617	PANC-1	pancreas:	n/a
33	chr2:231409567-231409617	GM12892	blood:	n/a
34	chr2:231409567-231409617	HIPEpiC	eye:	n/a
35	chr2:231409567-231409617	HCM	heart:	n/a
36	chr2:231409567-231409617	HRCEpiC	kidney:	n/a
37	chr2:231409567-231409617	ovcar-3	ovarian:	n/a
38	chr2:231409567-231409617	SK-N-SH	brain:	n/a
39	chr2:231409567-231409617	SAEC	small airway:	n/a
40	chr2:231409567-231409617	MCF10A-Er-Src	breast:	n/a
41	chr2:231409567-231409617	HCPEpiC	choroid plexus:	n/a
42	chr2:231409567-231409617	Caco-2	colon:	n/a
43	chr2:231409567-231409617	GM12891	blood:	n/a
44	chr2:231409567-231409617	SK-N-SH_RA	brain:	n/a
45	chr2:231409567-231409617	HEEpiC	esophagus:	n/a
46	chr2:231409567-231409617	NHBE	bronchial:	n/a
47	chr2:231409567-231409617	T-47D	breast:	n/a
48	chr2:231409567-231409617	HAEpiC	amniotic membrane:	n/a
49	chr2:231409567-231409617	IMR90	lung:	fetal
50	chr2:231409567-231409617	NB4	blood:	n/a

No data

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

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

No data

Variant related genes	Relation type
SP100	TF binding region
SP100	CpG island

Extended variants
information (count: 2137 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2137 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs890669	chr2:231385231-231385232	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531028195	chr2:231385242-231385243	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs890668	chr2:231385249-231385250	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs1678208	chr2:231385254-231385255	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs528483024	chr2:231385258-231385259	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183803353	chr2:231385277-231385278	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs62193457	chr2:231385285-231385286	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7578340	chr2:231385302-231385303	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs541076545	chr2:231385312-231385313	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs150666475	chr2:231385313-231385314	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs141050082	chr2:231385367-231385368	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs28689992	chr2:231385377-231385378	ZNF genes & repeats Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs535981123	chr2:231385404-231385405	ZNF genes & repeats Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554239081	chr2:231385421-231385422	ZNF genes & repeats Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566157089	chr2:231385546-231385547	ZNF genes & repeats Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533764311	chr2:231385567-231385568	ZNF genes & repeats Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558232849	chr2:231385621-231385622	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532924320	chr2:231385622-231385623	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550134544	chr2:231385651-231385652	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577088311	chr2:231385659-231385660	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs372762801	chr2:231385680-231385681	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs115326805	chr2:231385693-231385694	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556401644	chr2:231385695-231385696	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574677125	chr2:231385696-231385697	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs193008031	chr2:231385706-231385707	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529148802	chr2:231385728-231385729	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs561346445	chr2:231385737-231385738	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144912351	chr2:231385769-231385770	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs548896223	chr2:231385779-231385780	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565827194	chr2:231385781-231385782	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576853958	chr2:231385795-231385796	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565108786	chr2:231385797-231385798	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534036517	chr2:231385840-231385841	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs55759935	chr2:231385845-231385846	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs550824487	chr2:231385849-231385850	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs1479178	chr2:231385874-231385875	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs530208778	chr2:231385897-231385898	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs147527448	chr2:231385922-231385923	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs182790552	chr2:231385926-231385927	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs533623396	chr2:231385934-231385935	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs552152005	chr2:231385998-231385999	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs570310267	chr2:231386004-231386005	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs538185041	chr2:231386026-231386027	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556464783	chr2:231386027-231386028	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs369699031	chr2:231386047-231386048	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375390158	chr2:231386069-231386070	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs574714277	chr2:231386084-231386085	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs187899753	chr2:231386129-231386130	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553977214	chr2:231386148-231386149	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs140300165	chr2:231386164-231386165	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers	n/a	n/a	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:407 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231364600-231385800	Weak transcription	HSMMtube	muscle
2	chr2:231370800-231389600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr2:231371000-231409800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr2:231372400-231386200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr2:231375000-231385600	Weak transcription	HSMM	muscle
6	chr2:231375200-231390200	Weak transcription	Ovary	ovary
7	chr2:231376600-231385400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr2:231376600-231386000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr2:231376600-231390200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr2:231376600-231390400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr2:231377000-231385800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr2:231378000-231390800	Weak transcription	Spleen	Spleen
13	chr2:231378200-231385400	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr2:231378400-231386000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr2:231383600-231385400	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
16	chr2:231383800-231386800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr2:231383800-231387200	ZNF genes & repeats	Primary B cells from cord blood	blood
18	chr2:231384000-231386600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr2:231384200-231386800	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
20	chr2:231384200-231387200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
21	chr2:231384400-231385600	Strong transcription	Primary neutrophils fromperipheralblood	blood
22	chr2:231384400-231386200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
23	chr2:231384600-231385800	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
24	chr2:231384600-231386600	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
25	chr2:231384600-231386800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
26	chr2:231384600-231386800	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
27	chr2:231384800-231386000	Enhancers	Muscle Satellite Cultured Cells	--
28	chr2:231384800-231386200	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
29	chr2:231384800-231386400	ZNF genes & repeats	Primary T cells from cord blood	blood
30	chr2:231384800-231386800	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
31	chr2:231385000-231385400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr2:231385000-231385600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr2:231385000-231385600	Enhancers	Hela-S3	cervix
34	chr2:231385000-231385800	Enhancers	Liver	Liver
35	chr2:231385000-231386400	ZNF genes & repeats	GM12878-XiMat	blood
36	chr2:231385000-231386600	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
37	chr2:231385000-231386800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr2:231385000-231387000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
39	chr2:231385200-231385400	ZNF genes & repeats	HUVEC	blood vessel
40	chr2:231385200-231385400	Enhancers	NH-A	brain
41	chr2:231385200-231385400	Enhancers	Osteobl	bone
42	chr2:231385200-231385600	Enhancers	HMEC	breast
43	chr2:231385200-231386600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr2:231385200-231386600	ZNF genes & repeats	Adipose Nuclei	Adipose
45	chr2:231385200-231386600	ZNF genes & repeats	Left Ventricle	heart
46	chr2:231385200-231387000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr2:231385200-231390400	Weak transcription	Small Intestine	intestine
48	chr2:231385400-231385600	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr2:231385400-231385800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
50	chr2:231385400-231385800	Weak transcription	Osteobl	bone

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links