Variant report

Variant	nsv1008675
Chromosome Location	chr2:235002241-235021724
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:227)
CpG islands
(count:122)
Chromatin interactive
region (count:4)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:227 , 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	ATF3	chr2:235020069-235020735	HCT-116	colon:	n/a	n/a
2	ATF3	chr2:235020109-235020686	HCT-116	colon:	n/a	n/a
3	BACH1	chr2:235016572-235016629	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr2:235004531-235005272	GM12878	blood:	n/a	n/a
5	BCL3	chr2:235004571-235005325	GM12878	blood:	n/a	n/a
6	CBX3	chr2:235019872-235020744	HCT-116	colon:	n/a	n/a
7	CBX3	chr2:235020000-235020787	HCT-116	colon:	n/a	n/a
8	CEBPB	chr2:235008678-235008734	HepG2	liver:	n/a	chr2:235008689-235008700
9	CEBPB	chr2:235010836-235011070	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:235020260-235020437	A549	lung:	n/a	n/a
11	CEBPB	chr2:235020040-235020743	HCT-116	colon:	n/a	n/a
12	CEBPB	chr2:235019960-235020892	HCT-116	colon:	n/a	n/a
13	CTCF	chr2:235010840-235010990	WERI-Rb-1	eye:	n/a	n/a
14	CTCF	chr2:235018960-235019110	HMEC	breast:	n/a	n/a
15	CTCF	chr2:235010894-235011004	Spleen_OC	spleen:	n/a	n/a
16	CTCF	chr2:235010840-235010990	HMEC	breast:	n/a	n/a
17	CTCF	chr2:235010880-235011030	HEK293	kidney:	n/a	n/a
18	CTCF	chr2:235010810-235011051	MCF-7	breast:	n/a	n/a
19	CTCF	chr2:235010819-235011104	GM12878	blood:	n/a	n/a
20	CTCF	chr2:235010880-235011030	HMEC	breast:	n/a	n/a
21	CTCF	chr2:235010800-235010950	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr2:235010860-235011010	SAEC	small airway:	n/a	n/a
23	CTCF	chr2:235019052-235019064	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr2:235010860-235011010	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr2:235018980-235019130	HCFaa	heart:	n/a	n/a
26	CTCF	chr2:235010860-235011010	NHEK	skin:	n/a	n/a
27	CTCF	chr2:235003780-235003930	GM12871	blood:	n/a	chr2:235003800-235003809
28	CTCF	chr2:235018960-235019110	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr2:235010900-235011050	RPTEC	kidney:	n/a	n/a
30	CTCF	chr2:235006909-235007029	MCF-7	breast:	n/a	n/a
31	CTCF	chr2:235010800-235010950	SAEC	small airway:	n/a	n/a
32	CTCF	chr2:235010848-235010962	MCF-7	breast:	n/a	n/a
33	CTCF	chr2:235010891-235010985	HepG2	liver:	n/a	n/a
34	CTCF	chr2:235010831-235011035	MCF-7	breast:	n/a	n/a
35	CTCF	chr2:235010839-235010966	MCF-7	breast:	n/a	n/a
36	CTCF	chr2:235010839-235010945	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:235010840-235010990	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr2:235004640-235004753	GM19239	blood:	n/a	n/a
39	CTCF	chr2:235010880-235011030	Caco-2	colon:	n/a	n/a
40	CTCF	chr2:235010880-235011030	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:235010808-235011020	NHEK	skin:	n/a	n/a
42	CTCF	chr2:235010738-235011176	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:235010900-235011050	HRE	kidney:	n/a	n/a
44	CTCF	chr2:235010866-235010998	LNCaP	prostate:	n/a	n/a
45	CTCF	chr2:235010860-235011010	RPTEC	kidney:	n/a	n/a
46	CTCF	chr2:235013720-235013870	Caco-2	colon:	n/a	n/a
47	CTCF	chr2:235010807-235011163	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:235010908-235011018	LNCaP	prostate:	n/a	n/a
49	CTCF	chr2:235010860-235011010	Caco-2	colon:	n/a	n/a
50	CTCF	chr2:235010766-235011004	T-47D	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:235004843-235004893	SKMC	muscle:	n/a
2	chr2:235004843-235004893	HIPEpiC	eye:	n/a
3	chr2:235004843-235004893	H1-hESC	embryonic stem cell:	embryo
4	chr2:235005011-235005061	HEEpiC	esophagus:	n/a
5	chr2:235005011-235005061	MCF10A-Er-Src	breast:	n/a
6	chr2:235005011-235005061	AG09319	gingival:	n/a
7	chr2:235004843-235004893	NT2-D1	testis:	n/a
8	chr2:235004843-235004893	AG10803	skin:	n/a
9	chr2:235005011-235005061	Caco-2	colon:	n/a
10	chr2:235005011-235005061	HepG2	liver:	n/a
11	chr2:235005011-235005061	AG10803	skin:	n/a
12	chr2:235005011-235005061	ProgFib	skin:	n/a
13	chr2:235005011-235005061	HNPCEpiC	eye:	n/a
14	chr2:235004843-235004893	HUVEC	blood vessel:	n/a
15	chr2:235004843-235004893	AG04449	skin:	fetal
16	chr2:235004843-235004893	HCPEpiC	choroid plexus:	n/a
17	chr2:235004843-235004893	GM12891	blood:	n/a
18	chr2:235004843-235004893	ECC-1	luminal epithelium:	n/a
19	chr2:235004843-235004893	GM19239	blood:	n/a
20	chr2:235004843-235004893	HRE	kidney:	n/a
21	chr2:235004843-235004893	U87	brain:	n/a
22	chr2:235004843-235004893	PFSK-1	brain:	n/a
23	chr2:235004843-235004893	SAEC	small airway:	n/a
24	chr2:235005011-235005061	IMR90	lung:	fetal
25	chr2:235004843-235004893	BE2_C	brain:	n/a
26	chr2:235005011-235005061	GM19239	blood:	n/a
27	chr2:235004843-235004893	Hela-S3	cervix:	n/a
28	chr2:235004843-235004893	T-47D	breast:	n/a
29	chr2:235005011-235005061	NH-A	brain:	n/a
30	chr2:235004843-235004893	Jurkat	blood:	n/a
31	chr2:235005011-235005061	SK-N-SH_RA	brain:	n/a
32	chr2:235005011-235005061	H1-hESC	embryonic stem cell:	embryo
33	chr2:235005011-235005061	Hela-S3	cervix:	n/a
34	chr2:235005011-235005061	AG04450	lung:	fetal
35	chr2:235005011-235005061	HCPEpiC	choroid plexus:	n/a
36	chr2:235005011-235005061	NHBE	bronchial:	n/a
37	chr2:235005011-235005061	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:235004843-235004893	AG09319	gingival:	n/a
39	chr2:235005011-235005061	AG09309	skin:	n/a
40	chr2:235005011-235005061	RPTEC	kidney:	n/a
41	chr2:235004843-235004893	HCT-116	colon:	n/a
42	chr2:235005011-235005061	HIPEpiC	eye:	n/a
43	chr2:235004843-235004893	AG04450	lung:	fetal
44	chr2:235004843-235004893	PANC-1	pancreas:	n/a
45	chr2:235005011-235005061	HCF	heart:	n/a
46	chr2:235005011-235005061	MCF-7	breast:	n/a
47	chr2:235004843-235004893	GM12878	blood:	n/a
48	chr2:235005011-235005061	PANC-1	pancreas:	n/a
49	chr2:235004843-235004893	Hepatocyte	liver:	n/a
50	chr2:235004843-235004893	RPTEC	kidney:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:234837551..234838340-chr2:235010553..235011295,2	MCF-7	breast:
2	chr2:235010202..235011716-chr2:235012741..235015207,2	K562	blood:
3	chr2:234917584..234918293-chr2:235010462..235011245,3	MCF-7	breast:
4	chr2:235010202..235011716-chr2:235012741..235015207,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPP2-1	chr2:235017724-235017853	NONHSAT077526
2	lnc-SPP2-1	chr2:235017967-235018125	NONHSAT077526
3	lnc-SPP2-1	chr2:235017360-235017670	XLOC_001901
4	lnc-SPP2-1	chr2:235017359-235017670	NONHSAT077526
5	lnc-SPP2-1	chr2:235017968-235018125	XLOC_001901
6	lnc-SPP2-1	chr2:235017725-235017853	XLOC_001901
7	lnc-SPP2-1	chr2:235017725-235017853	ENSG00000226442.2
8	lnc-SPP2-1	chr2:235017968-235018125	ENSG00000226442.2

No data

Variant related genes	Relation type
ENSG00000226442	TF binding region
ENSG00000226442	CpG island

Extended variants
information (count: 937 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:937 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16850380	chr2:235002241-235002242	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576446486	chr2:235002276-235002277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145176835	chr2:235002287-235002288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561115206	chr2:235002289-235002290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529880148	chr2:235002349-235002350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374103613	chr2:235002358-235002359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560060533	chr2:235002380-235002381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532275810	chr2:235002388-235002389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34888834	chr2:235002431-235002432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147588080	chr2:235002465-235002466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568536978	chr2:235002491-235002492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34024796	chr2:235002505-235002506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562822939	chr2:235002523-235002524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs34022695	chr2:235002562-235002563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs59187200	chr2:235002577-235002578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568630829	chr2:235002612-235002613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376801043	chr2:235002624-235002625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554411773	chr2:235002647-235002648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs16850383	chr2:235002665-235002666	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs75901430	chr2:235002674-235002675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142053848	chr2:235002694-235002695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs576386508	chr2:235002742-235002743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115230508	chr2:235002801-235002802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs250938	chr2:235002822-235002823	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs151226410	chr2:235002834-235002835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187611791	chr2:235002869-235002870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs140371805	chr2:235002878-235002879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532247583	chr2:235002927-235002928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545723285	chr2:235002932-235002933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs57795197	chr2:235002956-235002957	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs531248866	chr2:235003007-235003008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548265089	chr2:235003101-235003102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192863019	chr2:235003143-235003144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs16850388	chr2:235003219-235003220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547077139	chr2:235003366-235003367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs532068488	chr2:235003368-235003369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527392213	chr2:235003394-235003395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs11888017	chr2:235003408-235003409	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs570526637	chr2:235003417-235003418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11901675	chr2:235003459-235003460	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs373928242	chr2:235003470-235003471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540113986	chr2:235003556-235003557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs115395808	chr2:235003583-235003584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374933185	chr2:235003584-235003585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35939146	chr2:235003624-235003625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184827206	chr2:235003630-235003631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs535525640	chr2:235003637-235003638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370529665	chr2:235003678-235003679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs113114713	chr2:235003695-235003696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs34674380	chr2:235003704-235003705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Esophageal adenocarcinoma	18519675	CNVD
Wilms tumour	21544195	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
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234999000-235002600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr2:235000000-235002400	Enhancers	Pancreas	Pancrea
3	chr2:235000800-235003800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:235000800-235004800	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr2:235001400-235002400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr2:235001400-235004600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr2:235001400-235005800	Weak transcription	Liver	Liver
8	chr2:235001600-235004600	Weak transcription	Fetal Brain Male	brain
9	chr2:235001600-235006800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr2:235002200-235002800	Weak transcription	Brain Germinal Matrix	brain
11	chr2:235002400-235004800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr2:235002400-235010000	Weak transcription	Pancreas	Pancrea
13	chr2:235002600-235006600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr2:235002800-235003000	Enhancers	Brain Germinal Matrix	brain
15	chr2:235003000-235004000	Weak transcription	Brain Germinal Matrix	brain
16	chr2:235003800-235004600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr2:235004000-235004200	Enhancers	Brain Germinal Matrix	brain
18	chr2:235004600-235004800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr2:235004600-235005200	Enhancers	Fetal Brain Male	brain
20	chr2:235004800-235005000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr2:235005000-235005200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr2:235005200-235006600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr2:235005800-235007400	Strong transcription	Liver	Liver
24	chr2:235006600-235007000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr2:235006600-235007200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr2:235006600-235008400	Enhancers	Primary B cells from peripheral blood	blood
27	chr2:235006800-235011600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr2:235007000-235007400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr2:235007000-235010800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr2:235007200-235008200	Enhancers	GM12878-XiMat	blood
31	chr2:235007200-235008600	Enhancers	Primary B cells from cord blood	blood
32	chr2:235007400-235008400	Enhancers	Fetal Kidney	kidney
33	chr2:235007400-235009200	Weak transcription	Liver	Liver
34	chr2:235007600-235011400	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr2:235007600-235011400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr2:235007800-235008000	Enhancers	Fetal Thymus	thymus
37	chr2:235007800-235008200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
38	chr2:235007800-235009400	Enhancers	Primary T cells from cord blood	blood
39	chr2:235007800-235009600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr2:235007800-235010000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr2:235007800-235010200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr2:235007800-235011200	Enhancers	Primary T helper cells PMA-I stimulated	--
43	chr2:235007800-235011400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr2:235007800-235011400	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr2:235007800-235011400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr2:235007800-235011600	Enhancers	Primary T cells fromperipheralblood	blood
47	chr2:235008000-235009600	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr2:235008000-235009600	Enhancers	Dnd41	blood
49	chr2:235008000-235009800	Weak transcription	Fetal Thymus	thymus
50	chr2:235008200-235008600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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