Variant report

Variant	nsv874234
Chromosome Location	chr2:63606001-63666590
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:454)
CpG islands
(count:244)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:454 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:63605820-63606016	K562	blood:	n/a	n/a
2	ATF3	chr2:63651975-63652239	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:63661567-63661570	K562	blood:	n/a	n/a
4	BACH1	chr2:63651998-63652341	K562	blood:	n/a	n/a
5	BACH1	chr2:63635782-63635980	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:63659498-63659825	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr2:63659689-63659772	K562	blood:	n/a	n/a
8	BACH1	chr2:63651760-63652326	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:63605900-63606036	K562	blood:	n/a	chr2:63605922-63605936
10	BHLHE40	chr2:63651894-63652271	K562	blood:	n/a	n/a
11	CBX3	chr2:63651895-63652291	K562	blood:	n/a	n/a
12	CCNT2	chr2:63651735-63652265	K562	blood:	n/a	n/a
13	CCNT2	chr2:63645901-63646101	K562	blood:	n/a	n/a
14	CEBPB	chr2:63652009-63652358	K562	blood:	n/a	n/a
15	CEBPB	chr2:63651996-63652336	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr2:63625354-63625626	A549	lung:	n/a	n/a
17	CEBPB	chr2:63651995-63652326	A549	lung:	n/a	n/a
18	CEBPB	chr2:63657962-63658025	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr2:63652023-63652296	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:63625474-63625513	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr2:63651976-63652328	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr2:63651954-63652320	K562	blood:	n/a	n/a
23	CEBPB	chr2:63625411-63625650	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:63621990-63622190	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:63652005-63652330	IMR90	lung:	n/a	n/a
26	CEBPB	chr2:63612350-63612611	HepG2	liver:	n/a	n/a
27	CTCF	chr2:63651899-63652320	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr2:63652040-63652190	GM12867	blood:	n/a	n/a
29	CTCF	chr2:63652033-63652259	MCF-7	breast:	n/a	n/a
30	CTCF	chr2:63652100-63652250	GM12864	blood:	n/a	n/a
31	CTCF	chr2:63652100-63652250	NB4	blood:	n/a	n/a
32	CTCF	chr2:63651660-63651810	GM12864	blood:	n/a	n/a
33	CTCF	chr2:63652034-63652142	GM12891	blood:	n/a	n/a
34	CTCF	chr2:63652080-63652230	HVMF	connective:	n/a	n/a
35	CTCF	chr2:63652062-63652236	A549	lung:	n/a	n/a
36	CTCF	chr2:63652020-63652170	HAc	cerebellar:	n/a	n/a
37	CTCF	chr2:63652000-63652150	AG04450	lung:	n/a	n/a
38	CTCF	chr2:63655631-63655661	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr2:63652040-63652190	GM12878	blood:	n/a	n/a
40	CTCF	chr2:63652080-63652230	GM12866	blood:	n/a	n/a
41	CTCF	chr2:63652060-63652210	GM12868	blood:	n/a	n/a
42	CTCF	chr2:63652085-63652236	LNCaP	prostate:	n/a	n/a
43	CTCF	chr2:63652009-63652289	Gliobla	brain:	n/a	n/a
44	CTCF	chr2:63652029-63652152	GM19238	blood:	n/a	n/a
45	CTCF	chr2:63652015-63652256	K562	blood:	n/a	n/a
46	CTCF	chr2:63652080-63652230	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr2:63652022-63652287	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr2:63652040-63652190	GM12870	blood:	n/a	n/a
49	CTCF	chr2:63652100-63652250	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr2:63652080-63652230	GM12869	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:63662027-63662077	NHDF-neo	bronchial:	n/a
2	chr2:63662027-63662077	ovcar-3	ovarian:	n/a
3	chr2:63665072-63665122	HepG2	liver:	n/a
4	chr2:63661375-63661425	GM19239	blood:	n/a
5	chr2:63606136-63606186	HCPEpiC	choroid plexus:	n/a
6	chr2:63665072-63665122	HUVEC	blood vessel:	n/a
7	chr2:63665072-63665122	HRE	kidney:	n/a
8	chr2:63665072-63665122	HNPCEpiC	eye:	n/a
9	chr2:63606136-63606186	HL-60	blood:	n/a
10	chr2:63661375-63661425	HUVEC	blood vessel:	n/a
11	chr2:63662027-63662077	PFSK-1	brain:	n/a
12	chr2:63661375-63661425	LNCaP	prostate:	n/a
13	chr2:63662027-63662077	BE2_C	brain:	n/a
14	chr2:63665072-63665122	U87	brain:	n/a
15	chr2:63661375-63661425	PFSK-1	brain:	n/a
16	chr2:63661375-63661425	AG04450	lung:	fetal
17	chr2:63665072-63665122	GM06990	blood:	n/a
18	chr2:63661375-63661425	HepG2	liver:	n/a
19	chr2:63606136-63606186	A549	lung:	n/a
20	chr2:63661375-63661425	NB4	blood:	n/a
21	chr2:63606136-63606186	RPTEC	kidney:	n/a
22	chr2:63606136-63606186	GM12878	blood:	n/a
23	chr2:63606136-63606186	HEEpiC	esophagus:	n/a
24	chr2:63661375-63661425	HEK293	kidney:	embryo
25	chr2:63661375-63661425	ovcar-3	ovarian:	n/a
26	chr2:63661375-63661425	AoSMC	blood vessel:	n/a
27	chr2:63662027-63662077	Jurkat	blood:	n/a
28	chr2:63606136-63606186	BJ	skin:	n/a
29	chr2:63661375-63661425	HL-60	blood:	n/a
30	chr2:63606136-63606186	Jurkat	blood:	n/a
31	chr2:63606136-63606186	AG09319	gingival:	n/a
32	chr2:63665072-63665122	Caco-2	colon:	n/a
33	chr2:63661375-63661425	HRE	kidney:	n/a
34	chr2:63665072-63665122	AG04449	skin:	fetal
35	chr2:63662027-63662077	T-47D	breast:	n/a
36	chr2:63661375-63661425	Hepatocyte	liver:	n/a
37	chr2:63606136-63606186	IMR90	lung:	fetal
38	chr2:63665072-63665122	SK-N-SH	brain:	n/a
39	chr2:63661375-63661425	BE2_C	brain:	n/a
40	chr2:63661375-63661425	SK-N-SH	brain:	n/a
41	chr2:63661375-63661425	ECC-1	luminal epithelium:	n/a
42	chr2:63606136-63606186	NH-A	brain:	n/a
43	chr2:63665072-63665122	AoSMC	blood vessel:	n/a
44	chr2:63606136-63606186	HepG2	liver:	n/a
45	chr2:63661375-63661425	MCF-7	breast:	n/a
46	chr2:63661375-63661425	HEEpiC	esophagus:	n/a
47	chr2:63661375-63661425	PANC-1	pancreas:	n/a
48	chr2:63606136-63606186	SAEC	small airway:	n/a
49	chr2:63662027-63662077	AG10803	skin:	n/a
50	chr2:63606136-63606186	HRCEpiC	kidney:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:86367748..86369747-chr2:63664289..63665809,2	MCF-7	breast:
2	chr2:63603673..63606325-chr2:63611148..63612797,2	K562	blood:
3	chr2:63574920..63576944-chr2:63604308..63606529,2	K562	blood:
4	chr2:63603673..63606325-chr2:63611148..63612797,2	K562	blood:
5	chr2:63648880..63650710-chr2:63662533..63665016,2	K562	blood:
6	chr2:63662111..63664772-chr2:63666351..63669219,2	K562	blood:
7	chr2:63604162..63606247-chr2:63607052..63609917,2	K562	blood:
8	chr2:63415883..63416512-chr2:63651703..63652517,3	MCF-7	breast:
9	chr2:63648880..63650710-chr2:63662533..63665016,2	K562	blood:

No data

Variant related genes	Relation type
WDPCP	TF binding region
WDPCP	CpG island
ENSG00000264406	chromatin interactions
ENSG00000143951	chromatin interactions

Extended variants
information (count: 1996 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1996 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17616913	chr2:63606001-63606002	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs908621	chr2:63606042-63606043	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs184311561	chr2:63606095-63606096	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs150626196	chr2:63606149-63606150	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs2421887	chr2:63606219-63606220	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs2901580	chr2:63606274-63606275	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs74987254	chr2:63606277-63606278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113217225	chr2:63606327-63606328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545238282	chr2:63606337-63606338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563538050	chr2:63606379-63606380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539618732	chr2:63606399-63606400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553051284	chr2:63606418-63606419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549398416	chr2:63606458-63606459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561595295	chr2:63606482-63606483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549245134	chr2:63606536-63606537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187848644	chr2:63606561-63606562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546930323	chr2:63606617-63606618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114639357	chr2:63606656-63606657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577794515	chr2:63606660-63606661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550820966	chr2:63606662-63606663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569054910	chr2:63606715-63606716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192311695	chr2:63606733-63606734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531612095	chr2:63606757-63606758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184377605	chr2:63606770-63606771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189107386	chr2:63606796-63606797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566711360	chr2:63606856-63606857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs551616762	chr2:63606903-63606904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571609926	chr2:63606983-63606984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533563155	chr2:63607027-63607028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558514937	chr2:63607118-63607119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545273508	chr2:63607183-63607184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560343839	chr2:63607203-63607204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576577717	chr2:63607215-63607216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528023720	chr2:63607262-63607263	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34610776	chr2:63607295-63607296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35561305	chr2:63607311-63607312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543882437	chr2:63607353-63607354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557168841	chr2:63607362-63607363	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574035054	chr2:63607375-63607376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs74931719	chr2:63607384-63607385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12618974	chr2:63607443-63607444	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs139199582	chr2:63607462-63607463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs78008791	chr2:63607472-63607473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528770874	chr2:63607525-63607526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181875548	chr2:63607526-63607527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565256327	chr2:63607535-63607536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12615652	chr2:63607538-63607539	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs551109470	chr2:63607598-63607599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113704554	chr2:63607695-63607696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184895001	chr2:63607705-63607706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Follicular lymphoma	17699855	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:392 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:63572000-63624000	Weak transcription	Left Ventricle	heart
2	chr2:63581400-63622000	Weak transcription	Ovary	ovary
3	chr2:63584200-63621800	Weak transcription	Primary B cells from cord blood	blood
4	chr2:63595000-63612200	Weak transcription	HSMM	muscle
5	chr2:63595200-63631200	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr2:63597800-63649200	Weak transcription	Fetal Lung	lung
7	chr2:63598000-63611000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr2:63598800-63631200	Weak transcription	Dnd41	blood
9	chr2:63599000-63631000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr2:63599200-63621800	Weak transcription	Adipose Nuclei	Adipose
11	chr2:63599400-63607000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr2:63599400-63609000	Weak transcription	Gastric	stomach
13	chr2:63599400-63631200	Weak transcription	Aorta	Aorta
14	chr2:63599400-63631600	Weak transcription	Pancreas	Pancrea
15	chr2:63599800-63631200	Weak transcription	Thymus	Thymus
16	chr2:63600600-63608200	Weak transcription	Primary hematopoietic stem cells	blood
17	chr2:63600800-63614800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr2:63602400-63610400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr2:63603600-63611200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr2:63603800-63606600	Weak transcription	Liver	Liver
21	chr2:63604000-63613600	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr2:63604200-63617600	Weak transcription	Fetal Heart	heart
23	chr2:63605000-63642400	Weak transcription	HSMMtube	muscle
24	chr2:63605400-63606800	Enhancers	NHEK	skin
25	chr2:63605400-63609200	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr2:63605600-63606800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr2:63605600-63606800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr2:63605600-63606800	Enhancers	K562	blood
29	chr2:63605600-63607000	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr2:63605600-63607000	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr2:63605600-63607000	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr2:63605600-63631200	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr2:63605800-63606400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr2:63605800-63606800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr2:63605800-63606800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr2:63605800-63608400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr2:63605800-63624800	Weak transcription	Primary T cells from cord blood	blood
38	chr2:63605800-63631200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr2:63606000-63606400	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr2:63606000-63606800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr2:63606000-63610400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr2:63606000-63632800	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr2:63606200-63606800	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr2:63606400-63609400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr2:63606600-63606800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr2:63606800-63608000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr2:63607000-63609200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr2:63607600-63610000	Weak transcription	Primary B cells from peripheral blood	blood
49	chr2:63607600-63631200	Weak transcription	Right Ventricle	heart
50	chr2:63607800-63610800	Weak transcription	Rectal Smooth Muscle	rectum

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