Variant report

Variant	nsv591358
Chromosome Location	chr3:118734271-118809508
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:517)
CpG islands
(count:918)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:517 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:118753735-118753935	K562	blood:	n/a	n/a
2	ATF1	chr3:118739149-118739350	K562	blood:	n/a	n/a
3	BACH1	chr3:118753370-118754199	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr3:118753664-118753967	GM12878	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
5	BHLHE40	chr3:118753613-118754025	K562	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
6	CCNT2	chr3:118753087-118754043	K562	blood:	n/a	n/a
7	CEBPB	chr3:118740984-118741309	IMR90	lung:	n/a	chr3:118741136-118741147
8	CEBPB	chr3:118745368-118745633	HepG2	liver:	n/a	chr3:118745489-118745500
9	CEBPB	chr3:118778947-118779140	HepG2	liver:	n/a	chr3:118779069-118779080
10	CEBPB	chr3:118741064-118741238	H1-hESC	embryonic stem cell:	n/a	chr3:118741136-118741147
11	CEBPB	chr3:118741045-118741288	HepG2	liver:	n/a	chr3:118741136-118741147
12	CEBPB	chr3:118741024-118741203	K562	blood:	n/a	chr3:118741136-118741147
13	CEBPB	chr3:118741075-118741275	A549	lung:	n/a	chr3:118741136-118741147
14	CEBPB	chr3:118737472-118737647	A549	lung:	n/a	n/a
15	CHD1	chr3:118753827-118753996	GM12878	blood:	n/a	n/a
16	CHD1	chr3:118752910-118753656	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr3:118753548-118753681	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr3:118753607-118753878	GM12878	blood:	n/a	chr3:118753765-118753775
19	CHD2	chr3:118753658-118753827	HepG2	liver:	n/a	chr3:118753765-118753775
20	CREB1	chr3:118753090-118753994	A549	lung:	n/a	n/a
21	CTBP2	chr3:118753482-118754214	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr3:118753720-118753870	HL-60	blood:	n/a	n/a
23	CTCF	chr3:118753380-118753530	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr3:118753740-118753890	GM12871	blood:	n/a	n/a
25	CTCF	chr3:118754080-118754230	AG04450	lung:	n/a	n/a
26	CTCF	chr3:118753565-118754007	GM12891	blood:	n/a	n/a
27	CTCF	chr3:118804040-118804190	GM12869	blood:	n/a	n/a
28	CTCF	chr3:118753480-118753630	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr3:118753740-118753890	GM06990	blood:	n/a	n/a
30	CTCF	chr3:118753672-118753959	K562	blood:	n/a	n/a
31	CTCF	chr3:118803940-118804090	GM12873	blood:	n/a	n/a
32	CTCF	chr3:118753720-118753870	GM12864	blood:	n/a	n/a
33	CTCF	chr3:118741946-118741964	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr3:118753649-118753976	K562	blood:	n/a	n/a
35	CTCF	chr3:118753740-118753890	HCT-116	colon:	n/a	n/a
36	CTCF	chr3:118753760-118753910	HEK293	kidney:	n/a	n/a
37	CTCF	chr3:118753740-118753890	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr3:118753520-118753670	HCM	heart:	n/a	n/a
39	CTCF	chr3:118753750-118753927	HepG2	liver:	n/a	n/a
40	CTCF	chr3:118753720-118753870	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr3:118753700-118753850	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr3:118753740-118753890	AG10803	skin:	n/a	n/a
43	CTCF	chr3:118753521-118753966	HepG2	liver:	n/a	n/a
44	CTCF	chr3:118753315-118754013	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr3:118753720-118753870	GM12865	blood:	n/a	n/a
46	CTCF	chr3:118804080-118804230	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:118753740-118753890	GM12865	blood:	n/a	n/a
48	CTCF	chr3:118753439-118754040	ProgFib	skin:	n/a	n/a
49	CTCF	chr3:118753543-118754092	A549	lung:	n/a	n/a
50	CTCF	chr3:118754020-118754170	GM12866	blood:	n/a	n/a

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:118753871-118753921	ECC-1	luminal epithelium:	n/a
2	chr3:118753093-118753143	H1-hESC	embryonic stem cell:	embryo
3	chr3:118757898-118757948	Jurkat	blood:	n/a
4	chr3:118753871-118753921	ECC-1	luminal epithelium:	n/a
5	chr3:118753093-118753143	H1-hESC	embryonic stem cell:	embryo
6	chr3:118757898-118757948	Jurkat	blood:	n/a
7	chr3:118757898-118757948	SAEC	small airway:	n/a
8	chr3:118754376-118754426	AG09309	skin:	n/a
9	chr3:118753714-118753764	HCPEpiC	choroid plexus:	n/a
10	chr3:118753093-118753143	K562	blood:	n/a
11	chr3:118754376-118754426	AG04449	skin:	fetal
12	chr3:118753610-118753660	GM19239	blood:	n/a
13	chr3:118753005-118753055	MCF10A-Er-Src	breast:	n/a
14	chr3:118734756-118734806	HRPEpiC	eye:	n/a
15	chr3:118754376-118754426	NHBE	bronchial:	n/a
16	chr3:118754097-118754147	AoSMC	blood vessel:	n/a
17	chr3:118750463-118750513	NB4	blood:	n/a
18	chr3:118753871-118753921	PANC-1	pancreas:	n/a
19	chr3:118753714-118753764	HRCEpiC	kidney:	n/a
20	chr3:118792317-118792367	A549	lung:	n/a
21	chr3:118753610-118753660	GM12892	blood:	n/a
22	chr3:118753871-118753921	SK-N-SH	brain:	n/a
23	chr3:118754376-118754426	U87	brain:	n/a
24	chr3:118753610-118753660	HPAEpiC	pulmonary alveolar:	n/a
25	chr3:118753871-118753921	GM06990	blood:	n/a
26	chr3:118753005-118753055	HIPEpiC	eye:	n/a
27	chr3:118753871-118753921	NHBE	bronchial:	n/a
28	chr3:118754376-118754426	NH-A	brain:	n/a
29	chr3:118757898-118757948	NHDF-neo	bronchial:	n/a
30	chr3:118753610-118753660	AG09309	skin:	n/a
31	chr3:118750463-118750513	CMK	blood:	n/a
32	chr3:118753705-118753755	HPAEpiC	pulmonary alveolar:	n/a
33	chr3:118753660-118753710	Hepatocyte	liver:	n/a
34	chr3:118750463-118750513	HL-60	blood:	n/a
35	chr3:118753738-118753788	HCF	heart:	n/a
36	chr3:118753660-118753710	Jurkat	blood:	n/a
37	chr3:118753707-118753757	SAEC	small airway:	n/a
38	chr3:118753093-118753143	ovcar-3	ovarian:	n/a
39	chr3:118753714-118753764	Hela-S3	cervix:	n/a
40	chr3:118734756-118734806	AG10803	skin:	n/a
41	chr3:118753610-118753660	PrEC	prostate:	n/a
42	chr3:118753714-118753764	AoSMC	blood vessel:	n/a
43	chr3:118753705-118753755	Jurkat	blood:	n/a
44	chr3:118753093-118753143	GM06990	blood:	n/a
45	chr3:118753738-118753788	ovcar-3	ovarian:	n/a
46	chr3:118754097-118754147	PFSK-1	brain:	n/a
47	chr3:118753705-118753755	NHDF-neo	bronchial:	n/a
48	chr3:118753610-118753660	HCF	heart:	n/a
49	chr3:118750463-118750513	AG04449	skin:	fetal
50	chr3:118753610-118753660	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
2	chr3:118600892..118601643-chr3:118803705..118804296,2	K562	blood:
3	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
4	chr19:34079834..34082285-chr3:118740671..118743263,2	MCF-7	breast:
5	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
6	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
7	chr3:118603583..118604395-chr3:118755020..118755749,3	MCF-7	breast:
8	chr3:118604102..118604821-chr3:118803607..118804317,2	MCF-7	breast:

No data

Variant related genes	Relation type
IGSF11	TF binding region
IGSF11	CpG island
ENSG00000232429	chromatin interactions

Extended variants
information (count: 1295 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1295 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35872	chr3:118734271-118734272	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189253393	chr3:118734284-118734285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577420812	chr3:118734288-118734289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560470846	chr3:118734294-118734295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs146955572	chr3:118734302-118734303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529822265	chr3:118734345-118734346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560128119	chr3:118734360-118734361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556388020	chr3:118734417-118734418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376434507	chr3:118734421-118734422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140606816	chr3:118734549-118734550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs76530299	chr3:118734577-118734578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112588333	chr3:118734595-118734596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs58073296	chr3:118734596-118734597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563503523	chr3:118734597-118734598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560171521	chr3:118734607-118734608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs397963392	chr3:118734608-118734609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548816196	chr3:118734617-118734618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527322198	chr3:118734682-118734683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551751628	chr3:118734731-118734732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148020512	chr3:118734821-118734822	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs964493	chr3:118734825-118734826	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs549428173	chr3:118734830-118734831	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs181736272	chr3:118734837-118734838	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs72970450	chr3:118734868-118734869	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs185688945	chr3:118734947-118734948	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs12053925	chr3:118735022-118735023	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs141685433	chr3:118735026-118735027	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs150499880	chr3:118735027-118735028	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs386665087	chr3:118735031-118735032	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs544740874	chr3:118735032-118735033	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs114215046	chr3:118735056-118735057	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs76964840	chr3:118735076-118735077	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs139473176	chr3:118735117-118735118	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs560444645	chr3:118735130-118735131	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs41497149	chr3:118735159-118735160	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs371473258	chr3:118735177-118735178	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs563752343	chr3:118735202-118735203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531177923	chr3:118735222-118735223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549873444	chr3:118735226-118735227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142220311	chr3:118735235-118735236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373029931	chr3:118735253-118735254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530367773	chr3:118735268-118735269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548502936	chr3:118735326-118735327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567017093	chr3:118735367-118735368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534513918	chr3:118735378-118735379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552876694	chr3:118735407-118735408	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs10934472	chr3:118735409-118735410	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs71325355	chr3:118735416-118735417	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs556658113	chr3:118735423-118735424	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs574832937	chr3:118735519-118735520	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Myelofibrosis	22110671	CNVD
Characteristic facial feature	22180640	CNVD
hypoplastic male genitals	22180640	CNVD
postnatal overgrowth	22180640	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:540 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118725200-118737600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:118727800-118734400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr3:118730000-118742000	Enhancers	Brain Angular Gyrus	brain
4	chr3:118730800-118736400	Enhancers	Fetal Brain Male	brain
5	chr3:118730800-118738600	Enhancers	Brain Anterior Caudate	brain
6	chr3:118730800-118741800	Enhancers	Brain Substantia Nigra	brain
7	chr3:118731400-118737000	Weak transcription	Stomach Smooth Muscle	stomach
8	chr3:118731400-118738000	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr3:118731800-118736200	Enhancers	Brain Cingulate Gyrus	brain
10	chr3:118732000-118737600	Weak transcription	Psoas Muscle	Psoas
11	chr3:118732600-118735200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
12	chr3:118733000-118734600	Weak transcription	Ovary	ovary
13	chr3:118733000-118740000	Enhancers	Brain Hippocampus Middle	brain
14	chr3:118733200-118734600	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr3:118733200-118735200	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr3:118733400-118734600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr3:118733600-118734800	Weak transcription	Fetal Brain Female	brain
18	chr3:118733800-118734800	Weak transcription	Brain Germinal Matrix	brain
19	chr3:118734200-118735000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr3:118734400-118735000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr3:118734600-118735000	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr3:118734600-118735000	Enhancers	Ovary	ovary
23	chr3:118734600-118735200	Enhancers	H1 Cell Line	embryonic stem cell
24	chr3:118734600-118735200	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr3:118734600-118736000	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr3:118734800-118735000	Enhancers	Brain Germinal Matrix	brain
27	chr3:118734800-118735200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:118734800-118735200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr3:118734800-118735200	Enhancers	Pancreas	Pancrea
30	chr3:118734800-118736000	Enhancers	Fetal Brain Female	brain
31	chr3:118735000-118735200	Flanking Active TSS	Brain Germinal Matrix	brain
32	chr3:118735000-118736200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr3:118735000-118737400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr3:118735000-118737600	Weak transcription	Ovary	ovary
35	chr3:118735200-118735400	Enhancers	Brain Germinal Matrix	brain
36	chr3:118735200-118735600	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr3:118735200-118738000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr3:118735200-118738200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr3:118735200-118738400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr3:118735200-118739000	Weak transcription	Pancreas	Pancrea
41	chr3:118735400-118735800	Flanking Active TSS	Brain Germinal Matrix	brain
42	chr3:118735600-118735800	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr3:118735800-118738800	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr3:118735800-118739600	Enhancers	Brain Germinal Matrix	brain
45	chr3:118736000-118737000	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr3:118736000-118737600	Weak transcription	Fetal Brain Female	brain
47	chr3:118736200-118736600	Weak transcription	Brain Cingulate Gyrus	brain
48	chr3:118736200-118738200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr3:118736400-118736800	Weak transcription	Fetal Brain Male	brain
50	chr3:118736600-118744400	Enhancers	Brain Cingulate Gyrus	brain

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