Variant report

Variant	nsv870438
Chromosome Location	chr3:118732054-118824020
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:746)
CpG islands
(count:916)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:746 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

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	chr3:118817076-118817276	K562	blood:	n/a	n/a
4	ATF1	chr3:118739149-118739350	K562	blood:	n/a	n/a
5	BACH1	chr3:118753370-118754199	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr3:118753613-118754025	K562	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
7	BHLHE40	chr3:118753664-118753967	GM12878	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	chr3:118741075-118741275	A549	lung:	n/a	chr3:118741136-118741147
10	CEBPB	chr3:118741045-118741288	HepG2	liver:	n/a	chr3:118741136-118741147
11	CEBPB	chr3:118740984-118741309	IMR90	lung:	n/a	chr3:118741136-118741147
12	CEBPB	chr3:118741064-118741238	H1-hESC	embryonic stem cell:	n/a	chr3:118741136-118741147
13	CEBPB	chr3:118737472-118737647	A549	lung:	n/a	n/a
14	CEBPB	chr3:118741024-118741203	K562	blood:	n/a	chr3:118741136-118741147
15	CEBPB	chr3:118778947-118779140	HepG2	liver:	n/a	chr3:118779069-118779080
16	CEBPB	chr3:118745368-118745633	HepG2	liver:	n/a	chr3:118745489-118745500
17	CEBPB	chr3:118817555-118817690	K562	blood:	n/a	n/a
18	CHD1	chr3:118753827-118753996	GM12878	blood:	n/a	n/a
19	CHD1	chr3:118752910-118753656	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr3:118753658-118753827	HepG2	liver:	n/a	chr3:118753765-118753775
21	CHD2	chr3:118753548-118753681	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr3:118753607-118753878	GM12878	blood:	n/a	chr3:118753765-118753775
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	chr3:118817580-118817730	GM12872	blood:	n/a	chr3:118817652-118817670
26	CTCF	chr3:118817443-118817882	GM12878	blood:	n/a	chr3:118817652-118817670
27	CTCF	chr3:118804017-118804168	MCF-7	breast:	n/a	n/a
28	CTCF	chr3:118817655-118817686	NHEK	skin:	n/a	n/a
29	CTCF	chr3:118753592-118753971	GM12878	blood:	n/a	n/a
30	CTCF	chr3:118753260-118753410	SAEC	small airway:	n/a	n/a
31	CTCF	chr3:118817580-118817730	AoAF	blood vessel:	n/a	chr3:118817652-118817670
32	CTCF	chr3:118753480-118753630	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr3:118753740-118753890	GM12872	blood:	n/a	n/a
34	CTCF	chr3:118753500-118753650	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr3:118817580-118817730	NHDF-neo	bronchial:	n/a	chr3:118817652-118817670
36	CTCF	chr3:118817540-118817690	GM12875	blood:	n/a	chr3:118817652-118817670
37	CTCF	chr3:118817620-118817770	HUVEC	blood vessel:	n/a	chr3:118817652-118817670
38	CTCF	chr3:118817561-118817807	LNCaP	prostate:	n/a	chr3:118817652-118817670
39	CTCF	chr3:118817540-118817690	GM12872	blood:	n/a	chr3:118817652-118817670
40	CTCF	chr3:118753680-118753830	AG09309	skin:	n/a	n/a
41	CTCF	chr3:118753125-118753227	MCF-7	breast:	n/a	n/a
42	CTCF	chr3:118753649-118753976	K562	blood:	n/a	n/a
43	CTCF	chr3:118753380-118753530	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr3:118753494-118753981	MCF-7	breast:	n/a	n/a
45	CTCF	chr3:118817560-118817710	HFF	foreskin:	n/a	chr3:118817652-118817670
46	CTCF	chr3:118817600-118817750	Caco-2	colon:	n/a	chr3:118817652-118817670
47	CTCF	chr3:118804000-118804150	HCT-116	colon:	n/a	n/a
48	CTCF	chr3:118753740-118753890	SAEC	small airway:	n/a	n/a
49	CTCF	chr3:118804114-118804120	HepG2	liver:	n/a	n/a
50	CTCF	chr3:118795861-118795898	Spleen_OC	spleen:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:118754376-118754426	NHDF-neo	bronchial:	n/a
2	chr3:118754376-118754426	NHDF-neo	bronchial:	n/a
3	chr3:118754376-118754426	T-47D	breast:	n/a
4	chr3:118753714-118753764	NH-A	brain:	n/a
5	chr3:118753714-118753764	ovcar-3	ovarian:	n/a
6	chr3:118753714-118753764	HEK293	kidney:	embryo
7	chr3:118754097-118754147	HRPEpiC	eye:	n/a
8	chr3:118753714-118753764	ECC-1	luminal epithelium:	n/a
9	chr3:118753707-118753757	HEEpiC	esophagus:	n/a
10	chr3:118757898-118757948	HCT-116	colon:	n/a
11	chr3:118753871-118753921	SKMC	muscle:	n/a
12	chr3:118753705-118753755	NHDF-neo	bronchial:	n/a
13	chr3:118754097-118754147	MCF10A-Er-Src	breast:	n/a
14	chr3:118734756-118734806	BE2_C	brain:	n/a
15	chr3:118753871-118753921	GM12878	blood:	n/a
16	chr3:118754097-118754147	GM19239	blood:	n/a
17	chr3:118754097-118754147	HCM	heart:	n/a
18	chr3:118750463-118750513	HAEpiC	amniotic membrane:	n/a
19	chr3:118753660-118753710	PANC-1	pancreas:	n/a
20	chr3:118753705-118753755	T-47D	breast:	n/a
21	chr3:118753660-118753710	PrEC	prostate:	n/a
22	chr3:118753610-118753660	NH-A	brain:	n/a
23	chr3:118750463-118750513	AG10803	skin:	n/a
24	chr3:118753093-118753143	NB4	blood:	n/a
25	chr3:118753660-118753710	ovcar-3	ovarian:	n/a
26	chr3:118757898-118757948	AG09309	skin:	n/a
27	chr3:118753738-118753788	HCT-116	colon:	n/a
28	chr3:118753871-118753921	HCPEpiC	choroid plexus:	n/a
29	chr3:118753705-118753755	PANC-1	pancreas:	n/a
30	chr3:118792317-118792367	NHDF-neo	bronchial:	n/a
31	chr3:118754376-118754426	HEEpiC	esophagus:	n/a
32	chr3:118734756-118734806	NHDF-neo	bronchial:	n/a
33	chr3:118753610-118753660	GM12891	blood:	n/a
34	chr3:118753871-118753921	HNPCEpiC	eye:	n/a
35	chr3:118753610-118753660	ovcar-3	ovarian:	n/a
36	chr3:118757898-118757948	ECC-1	luminal epithelium:	n/a
37	chr3:118753738-118753788	T-47D	breast:	n/a
38	chr3:118792317-118792367	Jurkat	blood:	n/a
39	chr3:118753871-118753921	HCM	heart:	n/a
40	chr3:118753707-118753757	HUVEC	blood vessel:	n/a
41	chr3:118753660-118753710	HRE	kidney:	n/a
42	chr3:118753705-118753755	SK-N-MC	brain:	n/a
43	chr3:118753714-118753764	HCPEpiC	choroid plexus:	n/a
44	chr3:118750463-118750513	PANC-1	pancreas:	n/a
45	chr3:118753871-118753921	AG04450	lung:	fetal
46	chr3:118750463-118750513	AG09309	skin:	n/a
47	chr3:118792317-118792367	HUVEC	blood vessel:	n/a
48	chr3:118753005-118753055	HCF	heart:	n/a
49	chr3:118757898-118757948	GM12892	blood:	n/a
50	chr3:118792317-118792367	HAEpiC	amniotic membrane:	n/a

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-B4GALT4-2	chr3:118823991-118824052	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: 1670 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1670 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55685141	chr3:118732057-118732058	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs138845905	chr3:118732110-118732111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs56327977	chr3:118732118-118732119	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs142737187	chr3:118732131-118732132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs34441373	chr3:118732143-118732144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs75953193	chr3:118732161-118732162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575298738	chr3:118732214-118732215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs75139020	chr3:118732217-118732218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188977498	chr3:118732227-118732228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147386581	chr3:118732264-118732265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs139024174	chr3:118732267-118732268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149468883	chr3:118732347-118732348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs9872674	chr3:118732356-118732357	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs144390613	chr3:118732375-118732376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs56053606	chr3:118732413-118732414	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs148785766	chr3:118732414-118732415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567731831	chr3:118732435-118732436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs79392456	chr3:118732528-118732529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546768924	chr3:118732611-118732612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375510785	chr3:118732641-118732642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544021118	chr3:118732644-118732645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79923298	chr3:118732707-118732708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568902083	chr3:118732742-118732743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536230592	chr3:118732750-118732751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143914732	chr3:118732761-118732762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146837963	chr3:118732764-118732765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533607065	chr3:118732875-118732876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs28410549	chr3:118732882-118732883	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs577782450	chr3:118732902-118732903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564160232	chr3:118732904-118732905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192469289	chr3:118732954-118732955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564835195	chr3:118732961-118732962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563618041	chr3:118733012-118733013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184309069	chr3:118733042-118733043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542997714	chr3:118733048-118733049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12054067	chr3:118733110-118733111	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs139719282	chr3:118733122-118733123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546735064	chr3:118733127-118733128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558451739	chr3:118733144-118733145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565089341	chr3:118733148-118733149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550931521	chr3:118733200-118733201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569166460	chr3:118733259-118733260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs151073997	chr3:118733265-118733266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548171842	chr3:118733272-118733273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577747544	chr3:118733282-118733283	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs369582811	chr3:118733324-118733325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566304670	chr3:118733332-118733333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs58950736	chr3:118733335-118733336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140933484	chr3:118733343-118733344	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558203421	chr3:118733346-118733347	Enhancers Weak transcription	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:559 , 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	chr3:118729600-118732800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr3:118730000-118742000	Enhancers	Brain Angular Gyrus	brain
5	chr3:118730800-118736400	Enhancers	Fetal Brain Male	brain
6	chr3:118730800-118738600	Enhancers	Brain Anterior Caudate	brain
7	chr3:118730800-118741800	Enhancers	Brain Substantia Nigra	brain
8	chr3:118731400-118732200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
9	chr3:118731400-118734200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr3:118731400-118737000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr3:118731400-118738000	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr3:118731600-118732400	Enhancers	Ovary	ovary
13	chr3:118731600-118733600	Enhancers	Fetal Brain Female	brain
14	chr3:118731800-118736200	Enhancers	Brain Cingulate Gyrus	brain
15	chr3:118732000-118733000	Weak transcription	Brain Hippocampus Middle	brain
16	chr3:118732000-118737600	Weak transcription	Psoas Muscle	Psoas
17	chr3:118732200-118732600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr3:118732400-118732800	Weak transcription	Ovary	ovary
19	chr3:118732600-118733400	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr3:118732600-118735200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
21	chr3:118732800-118733000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr3:118732800-118733000	Enhancers	Ovary	ovary
23	chr3:118732800-118733200	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr3:118733000-118734600	Weak transcription	Ovary	ovary
25	chr3:118733000-118740000	Enhancers	Brain Hippocampus Middle	brain
26	chr3:118733200-118734600	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr3:118733200-118735200	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr3:118733400-118734600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr3:118733600-118733800	Enhancers	Brain Germinal Matrix	brain
30	chr3:118733600-118734800	Weak transcription	Fetal Brain Female	brain
31	chr3:118733800-118734800	Weak transcription	Brain Germinal Matrix	brain
32	chr3:118734200-118735000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr3:118734400-118735000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr3:118734600-118735000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr3:118734600-118735000	Enhancers	Ovary	ovary
36	chr3:118734600-118735200	Enhancers	H1 Cell Line	embryonic stem cell
37	chr3:118734600-118735200	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr3:118734600-118736000	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr3:118734800-118735000	Enhancers	Brain Germinal Matrix	brain
40	chr3:118734800-118735200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr3:118734800-118735200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr3:118734800-118735200	Enhancers	Pancreas	Pancrea
43	chr3:118734800-118736000	Enhancers	Fetal Brain Female	brain
44	chr3:118735000-118735200	Flanking Active TSS	Brain Germinal Matrix	brain
45	chr3:118735000-118736200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr3:118735000-118737400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr3:118735000-118737600	Weak transcription	Ovary	ovary
48	chr3:118735200-118735400	Enhancers	Brain Germinal Matrix	brain
49	chr3:118735200-118735600	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr3:118735200-118738000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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