Variant report

Variant	nsv1003674
Chromosome Location	chr3:118733110-118834142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:754)
CpG islands
(count:916)
Chromatin interactive
region (count:18)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:754 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:118734227-118734231	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:118753735-118753935	K562	blood:	n/a	n/a
3	ATF1	chr3:118739149-118739350	K562	blood:	n/a	n/a
4	ATF1	chr3:118817076-118817276	K562	blood:	n/a	n/a
5	BACH1	chr3:118753370-118754199	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr3:118753664-118753967	GM12878	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
7	BHLHE40	chr3:118753613-118754025	K562	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
8	CCNT2	chr3:118753087-118754043	K562	blood:	n/a	n/a
9	CEBPB	chr3:118817555-118817690	K562	blood:	n/a	n/a
10	CEBPB	chr3:118741024-118741203	K562	blood:	n/a	chr3:118741136-118741147
11	CEBPB	chr3:118741045-118741288	HepG2	liver:	n/a	chr3:118741136-118741147
12	CEBPB	chr3:118745368-118745633	HepG2	liver:	n/a	chr3:118745489-118745500
13	CEBPB	chr3:118737472-118737647	A549	lung:	n/a	n/a
14	CEBPB	chr3:118741064-118741238	H1-hESC	embryonic stem cell:	n/a	chr3:118741136-118741147
15	CEBPB	chr3:118741075-118741275	A549	lung:	n/a	chr3:118741136-118741147
16	CEBPB	chr3:118778947-118779140	HepG2	liver:	n/a	chr3:118779069-118779080
17	CEBPB	chr3:118740984-118741309	IMR90	lung:	n/a	chr3:118741136-118741147
18	CHD1	chr3:118752910-118753656	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD1	chr3:118753827-118753996	GM12878	blood:	n/a	n/a
20	CHD2	chr3:118753607-118753878	GM12878	blood:	n/a	chr3:118753765-118753775
21	CHD2	chr3:118753658-118753827	HepG2	liver:	n/a	chr3:118753765-118753775
22	CHD2	chr3:118753548-118753681	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr3:118753090-118753994	A549	lung:	n/a	n/a
24	CTBP2	chr3:118753482-118754214	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr3:118753315-118754013	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr3:118817514-118817805	HUVEC	blood vessel:	n/a	chr3:118817652-118817670
27	CTCF	chr3:118753720-118753870	GM12875	blood:	n/a	n/a
28	CTCF	chr3:118754020-118754170	GM12866	blood:	n/a	n/a
29	CTCF	chr3:118819634-118819725	GM12878	blood:	n/a	n/a
30	CTCF	chr3:118753780-118753930	GM12873	blood:	n/a	n/a
31	CTCF	chr3:118817560-118817710	SAEC	small airway:	n/a	chr3:118817652-118817670
32	CTCF	chr3:118753672-118753959	K562	blood:	n/a	n/a
33	CTCF	chr3:118753700-118753850	HMF	breast:	n/a	n/a
34	CTCF	chr3:118817580-118817730	AG10803	skin:	n/a	chr3:118817652-118817670
35	CTCF	chr3:118753720-118753870	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr3:118817460-118817750	GM12878	blood:	n/a	chr3:118817652-118817670
37	CTCF	chr3:118817600-118817750	HPAF	blood vessel:	n/a	chr3:118817652-118817670
38	CTCF	chr3:118817580-118817730	GM12868	blood:	n/a	chr3:118817652-118817670
39	CTCF	chr3:118753440-118753590	BJ	skin:	n/a	n/a
40	CTCF	chr3:118770467-118770489	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr3:118753740-118753890	A549	lung:	n/a	n/a
42	CTCF	chr3:118817560-118817710	GM12870	blood:	n/a	chr3:118817652-118817670
43	CTCF	chr3:118753704-118753965	GM13976	blood:	n/a	n/a
44	CTCF	chr3:118817580-118817730	HL-60	blood:	n/a	chr3:118817652-118817670
45	CTCF	chr3:118817540-118817690	NHEK	skin:	n/a	chr3:118817652-118817670
46	CTCF	chr3:118753480-118753630	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr3:118817570-118817740	H1-hESC	embryonic stem cell:	n/a	chr3:118817652-118817670
48	CTCF	chr3:118753740-118753890	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr3:118804020-118804170	GM12873	blood:	n/a	n/a
50	CTCF	chr3:118817560-118817710	GM12801	blood:	n/a	chr3:118817652-118817670

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:118734756-118734806	H1-hESC	embryonic stem cell:	embryo
2	chr3:118734756-118734806	H1-hESC	embryonic stem cell:	embryo
3	chr3:118753738-118753788	HL-60	blood:	n/a
4	chr3:118753610-118753660	SK-N-SH	brain:	n/a
5	chr3:118753714-118753764	SK-N-SH_RA	brain:	n/a
6	chr3:118753871-118753921	HRPEpiC	eye:	n/a
7	chr3:118754097-118754147	NHDF-neo	bronchial:	n/a
8	chr3:118734756-118734806	K562	blood:	n/a
9	chr3:118753714-118753764	IMR90	lung:	fetal
10	chr3:118753660-118753710	HCPEpiC	choroid plexus:	n/a
11	chr3:118753738-118753788	ECC-1	luminal epithelium:	n/a
12	chr3:118750463-118750513	Hepatocyte	liver:	n/a
13	chr3:118750463-118750513	Caco-2	colon:	n/a
14	chr3:118753738-118753788	AG04450	lung:	fetal
15	chr3:118753005-118753055	CMK	blood:	n/a
16	chr3:118757898-118757948	ECC-1	luminal epithelium:	n/a
17	chr3:118753705-118753755	PFSK-1	brain:	n/a
18	chr3:118754376-118754426	HUVEC	blood vessel:	n/a
19	chr3:118792317-118792367	Hepatocyte	liver:	n/a
20	chr3:118753660-118753710	K562	blood:	n/a
21	chr3:118753705-118753755	HepG2	liver:	n/a
22	chr3:118753705-118753755	HUVEC	blood vessel:	n/a
23	chr3:118753610-118753660	SK-N-SH_RA	brain:	n/a
24	chr3:118753005-118753055	NHDF-neo	bronchial:	n/a
25	chr3:118754376-118754426	A549	lung:	n/a
26	chr3:118754376-118754426	SK-N-SH_RA	brain:	n/a
27	chr3:118757898-118757948	LNCaP	prostate:	n/a
28	chr3:118754097-118754147	AG04449	skin:	fetal
29	chr3:118753005-118753055	HL-60	blood:	n/a
30	chr3:118757898-118757948	MCF-7	breast:	n/a
31	chr3:118753707-118753757	LNCaP	prostate:	n/a
32	chr3:118753660-118753710	BJ	skin:	n/a
33	chr3:118734756-118734806	AG10803	skin:	n/a
34	chr3:118754376-118754426	RPTEC	kidney:	n/a
35	chr3:118753707-118753757	PrEC	prostate:	n/a
36	chr3:118753610-118753660	HRCEpiC	kidney:	n/a
37	chr3:118753705-118753755	HCM	heart:	n/a
38	chr3:118753738-118753788	U87	brain:	n/a
39	chr3:118753705-118753755	NH-A	brain:	n/a
40	chr3:118753707-118753757	GM12892	blood:	n/a
41	chr3:118753005-118753055	HAEpiC	amniotic membrane:	n/a
42	chr3:118750463-118750513	SK-N-MC	brain:	n/a
43	chr3:118753005-118753055	BJ	skin:	n/a
44	chr3:118792317-118792367	HRE	kidney:	n/a
45	chr3:118754376-118754426	Caco-2	colon:	n/a
46	chr3:118753610-118753660	HCF	heart:	n/a
47	chr3:118754376-118754426	U87	brain:	n/a
48	chr3:118753714-118753764	HCF	heart:	n/a
49	chr3:118734756-118734806	HIPEpiC	eye:	n/a
50	chr3:118753714-118753764	SK-N-SH	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:118601857..118602685-chr3:118817256..118818095,2	MCF-7	breast:
2	chr20:55795723..55796346-chr3:118817504..118818179,2	MCF-7	breast:
3	chr3:118603151..118604416-chr3:118816830..118818388,23	MCF-7	breast:
4	chr3:116489803..116490556-chr3:118816385..118817077,2	K562	blood:
5	chr3:118753444..118753993-chr3:118815481..118816221,2	MCF-7	breast:
6	chr3:118603511..118604421-chr3:118817152..118818248,5	MCF-7	breast:
7	chr3:118600892..118601643-chr3:118803705..118804296,2	K562	blood:
8	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
9	chr3:118601491..118603517-chr3:118818904..118820959,2	MCF-7	breast:
10	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
11	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
12	chr3:118603251..118604473-chr3:118817204..118818111,6	K562	blood:
13	chr3:118600900..118602263-chr3:118817111..118818102,7	MCF-7	breast:
14	chr19:34079834..34082285-chr3:118740671..118743263,2	MCF-7	breast:
15	chr3:118600918..118601876-chr3:118816856..118817797,3	K562	blood:
16	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
17	chr3:118603583..118604395-chr3:118755020..118755749,3	MCF-7	breast:
18	chr3:118604102..118604821-chr3:118803607..118804317,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-B4GALT4-2	chr3:118823991-118824052	NONHSAT091373
2	lnc-B4GALT4-2	chr3:118831521-118831625	NONHSAT091373

No data

Variant related genes	Relation type
IGSF11	TF binding region
IGSF11	CpG island
ENSG00000144847	chromatin interactions
ENSG00000232429	chromatin interactions

Extended variants
information (count: 1821 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1821 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12054067	chr3:118733110-118733111	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs139719282	chr3:118733122-118733123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546735064	chr3:118733127-118733128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558451739	chr3:118733144-118733145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565089341	chr3:118733148-118733149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550931521	chr3:118733200-118733201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569166460	chr3:118733259-118733260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs151073997	chr3:118733265-118733266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548171842	chr3:118733272-118733273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577747544	chr3:118733282-118733283	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs369582811	chr3:118733324-118733325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566304670	chr3:118733332-118733333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs58950736	chr3:118733335-118733336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140933484	chr3:118733343-118733344	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558203421	chr3:118733346-118733347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375215811	chr3:118733384-118733385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538830723	chr3:118733396-118733397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536624759	chr3:118733409-118733410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557271061	chr3:118733458-118733459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187254520	chr3:118733476-118733477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150180683	chr3:118733529-118733530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561340698	chr3:118733539-118733540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551729737	chr3:118733548-118733549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371884577	chr3:118733549-118733550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573118545	chr3:118733594-118733595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs145714834	chr3:118733600-118733601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs76209382	chr3:118733650-118733651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191629280	chr3:118733682-118733683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146207393	chr3:118733759-118733760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562626416	chr3:118733764-118733765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530013070	chr3:118733773-118733774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540211755	chr3:118733781-118733782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144310062	chr3:118733867-118733868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs3049115	chr3:118733868-118733869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs397710479	chr3:118733870-118733871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566485367	chr3:118733932-118733933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138806566	chr3:118734009-118734010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554671453	chr3:118734010-118734011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184134649	chr3:118734051-118734052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142829008	chr3:118734061-118734062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs116194959	chr3:118734144-118734145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs373557727	chr3:118734148-118734149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs557134021	chr3:118734167-118734168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs543570231	chr3:118734179-118734180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs61387366	chr3:118734237-118734238	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs563757985	chr3:118734263-118734264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573226063	chr3:118734264-118734265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs35872	chr3:118734271-118734272	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs189253393	chr3:118734284-118734285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs577420812	chr3:118734288-118734289	Weak transcription Enhancers	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:563 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	chr3:118731400-118734200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr3:118731400-118737000	Weak transcription	Stomach Smooth Muscle	stomach
9	chr3:118731400-118738000	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr3:118731600-118733600	Enhancers	Fetal Brain Female	brain
11	chr3:118731800-118736200	Enhancers	Brain Cingulate Gyrus	brain
12	chr3:118732000-118737600	Weak transcription	Psoas Muscle	Psoas
13	chr3:118732600-118733400	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr3:118732600-118735200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
15	chr3:118732800-118733200	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr3:118733000-118734600	Weak transcription	Ovary	ovary
17	chr3:118733000-118740000	Enhancers	Brain Hippocampus Middle	brain
18	chr3:118733200-118734600	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr3:118733200-118735200	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr3:118733400-118734600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr3:118733600-118733800	Enhancers	Brain Germinal Matrix	brain
22	chr3:118733600-118734800	Weak transcription	Fetal Brain Female	brain
23	chr3:118733800-118734800	Weak transcription	Brain Germinal Matrix	brain
24	chr3:118734200-118735000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr3:118734400-118735000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr3:118734600-118735000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr3:118734600-118735000	Enhancers	Ovary	ovary
28	chr3:118734600-118735200	Enhancers	H1 Cell Line	embryonic stem cell
29	chr3:118734600-118735200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr3:118734600-118736000	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr3:118734800-118735000	Enhancers	Brain Germinal Matrix	brain
32	chr3:118734800-118735200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr3:118734800-118735200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr3:118734800-118735200	Enhancers	Pancreas	Pancrea
35	chr3:118734800-118736000	Enhancers	Fetal Brain Female	brain
36	chr3:118735000-118735200	Flanking Active TSS	Brain Germinal Matrix	brain
37	chr3:118735000-118736200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr3:118735000-118737400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr3:118735000-118737600	Weak transcription	Ovary	ovary
40	chr3:118735200-118735400	Enhancers	Brain Germinal Matrix	brain
41	chr3:118735200-118735600	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr3:118735200-118738000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr3:118735200-118738200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr3:118735200-118738400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr3:118735200-118739000	Weak transcription	Pancreas	Pancrea
46	chr3:118735400-118735800	Flanking Active TSS	Brain Germinal Matrix	brain
47	chr3:118735600-118735800	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr3:118735800-118738800	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr3:118735800-118739600	Enhancers	Brain Germinal Matrix	brain
50	chr3:118736000-118737000	Weak transcription	Cortex derived primary cultured neurospheres	brain

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