Variant report

Variant	esv2756586
Chromosome Location	chr3:118688611-118863998
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:953)
CpG islands
(count:1039)
Chromatin interactive
region (count:24)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:953 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

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	ARID3A	chr3:118703634-118704104	K562	blood:	n/a	n/a
3	ARID3A	chr3:118734227-118734231	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:118851202-118851284	HepG2	liver:	n/a	n/a
5	ATF1	chr3:118739149-118739350	K562	blood:	n/a	n/a
6	ATF1	chr3:118817076-118817276	K562	blood:	n/a	n/a
7	ATF1	chr3:118703609-118703888	K562	blood:	n/a	n/a
8	ATF1	chr3:118705608-118705894	K562	blood:	n/a	n/a
9	ATF3	chr3:118703574-118703992	K562	blood:	n/a	n/a
10	BACH1	chr3:118753370-118754199	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr3:118703611-118703902	K562	blood:	n/a	chr3:118703784-118703805
12	BHLHE40	chr3:118753664-118753967	GM12878	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
13	BHLHE40	chr3:118753613-118754025	K562	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
14	CCNT2	chr3:118703639-118703962	K562	blood:	n/a	n/a
15	CCNT2	chr3:118753087-118754043	K562	blood:	n/a	n/a
16	CEBPB	chr3:118851187-118851503	H1-hESC	embryonic stem cell:	n/a	chr3:118851326-118851337
17	CEBPB	chr3:118851161-118851499	Hela-S3	cervix:	n/a	chr3:118851326-118851337
18	CEBPB	chr3:118817555-118817690	K562	blood:	n/a	n/a
19	CEBPB	chr3:118708183-118708258	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr3:118741024-118741203	K562	blood:	n/a	chr3:118741136-118741147
21	CEBPB	chr3:118741064-118741238	H1-hESC	embryonic stem cell:	n/a	chr3:118741136-118741147
22	CEBPB	chr3:118745368-118745633	HepG2	liver:	n/a	chr3:118745489-118745500
23	CEBPB	chr3:118741075-118741275	A549	lung:	n/a	chr3:118741136-118741147
24	CEBPB	chr3:118778947-118779140	HepG2	liver:	n/a	chr3:118779069-118779080
25	CEBPB	chr3:118851148-118851507	A549	lung:	n/a	chr3:118851326-118851337
26	CEBPB	chr3:118851145-118851519	HepG2	liver:	n/a	chr3:118851326-118851337
27	CEBPB	chr3:118740984-118741309	IMR90	lung:	n/a	chr3:118741136-118741147
28	CEBPB	chr3:118851168-118851498	K562	blood:	n/a	chr3:118851326-118851337
29	CEBPB	chr3:118741045-118741288	HepG2	liver:	n/a	chr3:118741136-118741147
30	CEBPB	chr3:118851143-118851518	IMR90	lung:	n/a	chr3:118851326-118851337
31	CEBPB	chr3:118737472-118737647	A549	lung:	n/a	n/a
32	CEBPD	chr3:118703581-118703942	K562	blood:	n/a	n/a
33	CHD1	chr3:118753827-118753996	GM12878	blood:	n/a	n/a
34	CHD1	chr3:118752910-118753656	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr3:118753658-118753827	HepG2	liver:	n/a	chr3:118753765-118753775
36	CHD2	chr3:118753548-118753681	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr3:118753607-118753878	GM12878	blood:	n/a	chr3:118753765-118753775
38	CREB1	chr3:118753090-118753994	A549	lung:	n/a	n/a
39	CTBP2	chr3:118753482-118754214	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr3:118753620-118753770	GM12872	blood:	n/a	n/a
41	CTCF	chr3:118753740-118753890	A549	lung:	n/a	n/a
42	CTCF	chr3:118753780-118753930	HCT-116	colon:	n/a	n/a
43	CTCF	chr3:118753691-118753967	A549	lung:	n/a	n/a
44	CTCF	chr3:118751280-118751430	GM12871	blood:	n/a	n/a
45	CTCF	chr3:118753740-118753890	MCF-7	breast:	n/a	n/a
46	CTCF	chr3:118841100-118841250	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr3:118817580-118817730	GM12873	blood:	n/a	chr3:118817652-118817670
48	CTCF	chr3:118804320-118804400	GM10248	blood:	n/a	n/a
49	CTCF	chr3:118817560-118817710	GM12867	blood:	n/a	chr3:118817652-118817670
50	CTCF	chr3:118804020-118804170	GM12873	blood:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:118753705-118753755	GM12878	blood:	n/a
2	chr3:118792317-118792367	AG04450	lung:	fetal
3	chr3:118753705-118753755	GM12878	blood:	n/a
4	chr3:118792317-118792367	AG04450	lung:	fetal
5	chr3:118706648-118706698	NB4	blood:	n/a
6	chr3:118753093-118753143	HEK293	kidney:	embryo
7	chr3:118750463-118750513	SKMC	muscle:	n/a
8	chr3:118754097-118754147	AG04449	skin:	fetal
9	chr3:118753714-118753764	SK-N-MC	brain:	n/a
10	chr3:118753093-118753143	GM12878	blood:	n/a
11	chr3:118753871-118753921	PFSK-1	brain:	n/a
12	chr3:118753005-118753055	HNPCEpiC	eye:	n/a
13	chr3:118753093-118753143	SK-N-SH_RA	brain:	n/a
14	chr3:118753610-118753660	NT2-D1	testis:	n/a
15	chr3:118792317-118792367	HUVEC	blood vessel:	n/a
16	chr3:118757898-118757948	NT2-D1	testis:	n/a
17	chr3:118753738-118753788	ProgFib	skin:	n/a
18	chr3:118753714-118753764	H1-hESC	embryonic stem cell:	embryo
19	chr3:118753610-118753660	HEEpiC	esophagus:	n/a
20	chr3:118754376-118754426	ECC-1	luminal epithelium:	n/a
21	chr3:118753005-118753055	AG10803	skin:	n/a
22	chr3:118753705-118753755	GM19239	blood:	n/a
23	chr3:118792317-118792367	SKMC	muscle:	n/a
24	chr3:118734756-118734806	Jurkat	blood:	n/a
25	chr3:118792317-118792367	H1-hESC	embryonic stem cell:	embryo
26	chr3:118753093-118753143	ECC-1	luminal epithelium:	n/a
27	chr3:118753707-118753757	SK-N-MC	brain:	n/a
28	chr3:118734756-118734806	HMEC	breast:	n/a
29	chr3:118753660-118753710	AG04450	lung:	fetal
30	chr3:118753610-118753660	HRPEpiC	eye:	n/a
31	chr3:118753610-118753660	H1-hESC	embryonic stem cell:	embryo
32	chr3:118753738-118753788	HL-60	blood:	n/a
33	chr3:118753738-118753788	HepG2	liver:	n/a
34	chr3:118753610-118753660	T-47D	breast:	n/a
35	chr3:118757898-118757948	U87	brain:	n/a
36	chr3:118705126-118705176	HRCEpiC	kidney:	n/a
37	chr3:118750463-118750513	GM19239	blood:	n/a
38	chr3:118753707-118753757	U87	brain:	n/a
39	chr3:118753871-118753921	HepG2	liver:	n/a
40	chr3:118753707-118753757	NHDF-neo	bronchial:	n/a
41	chr3:118753093-118753143	NB4	blood:	n/a
42	chr3:118753093-118753143	T-47D	breast:	n/a
43	chr3:118753871-118753921	NHBE	bronchial:	n/a
44	chr3:118750463-118750513	GM12892	blood:	n/a
45	chr3:118753093-118753143	H1-hESC	embryonic stem cell:	embryo
46	chr3:118734756-118734806	NT2-D1	testis:	n/a
47	chr3:118734756-118734806	GM19239	blood:	n/a
48	chr3:118734756-118734806	CMK	blood:	n/a
49	chr3:118753705-118753755	HepG2	liver:	n/a
50	chr3:118750463-118750513	ECC-1	luminal epithelium:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:118603251..118604473-chr3:118817204..118818111,6	K562	blood:
2	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
3	chr3:118863850..118864593-chr3:118925031..118926020,4	MCF-7	breast:
4	chr3:118601491..118603517-chr3:118818904..118820959,2	MCF-7	breast:
5	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
6	chr3:118604102..118604821-chr3:118803607..118804317,2	MCF-7	breast:
7	chr3:118601857..118602685-chr3:118817256..118818095,2	MCF-7	breast:
8	chr3:118600918..118601876-chr3:118816856..118817797,3	K562	blood:
9	chr3:116489803..116490556-chr3:118816385..118817077,2	K562	blood:
10	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
11	chr3:118588536..118591419-chr3:118859926..118861811,2	K562	blood:
12	chr3:118603511..118604421-chr3:118817152..118818248,5	MCF-7	breast:
13	chr3:118860786..118863641-chr3:119040567..119042267,2	MCF-7	breast:
14	chr3:118863219..118864917-chr3:118959824..118960983,11	MCF-7	breast:
15	chr3:118603151..118604416-chr3:118816830..118818388,23	MCF-7	breast:
16	chr3:118753444..118753993-chr3:118815481..118816221,2	MCF-7	breast:
17	chr20:55795723..55796346-chr3:118817504..118818179,2	MCF-7	breast:
18	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
19	chr3:118863177..118864705-chr3:118958357..118960193,2	K562	blood:
20	chr3:118600900..118602263-chr3:118817111..118818102,7	MCF-7	breast:
21	chr3:118600892..118601643-chr3:118803705..118804296,2	K562	blood:
22	chr19:34079834..34082285-chr3:118740671..118743263,2	MCF-7	breast:
23	chr3:118863527..118866220-chr3:118958408..118962544,4	MCF-7	breast:
24	chr3:118603583..118604395-chr3:118755020..118755749,3	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
IGSF11	TF binding region
ENSG00000251012	TF binding region
C3orf30	TF binding region
IGSF11	CpG island
ENSG00000251012	CpG island
C3orf30	CpG island
ENSG00000144847	chromatin interactions
ENSG00000232429	chromatin interactions
ENSG00000241155	chromatin interactions
ENSG00000121578	chromatin interactions

Extended variants
information (count: 4201 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4201 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6795721	chr3:118688611-118688612	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569159103	chr3:118688662-118688663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551439390	chr3:118688663-118688664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563825266	chr3:118688695-118688696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538198271	chr3:118688740-118688741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549190404	chr3:118688808-118688809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187247098	chr3:118688824-118688825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375266135	chr3:118688829-118688830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555331393	chr3:118688847-118688848	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376823268	chr3:118688851-118688852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534641006	chr3:118688885-118688886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546498799	chr3:118688930-118688931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571165430	chr3:118688944-118688945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538653501	chr3:118689045-118689046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376185450	chr3:118689079-118689080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575333418	chr3:118689090-118689091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535943681	chr3:118689091-118689092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555972337	chr3:118689092-118689093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371390782	chr3:118689095-118689096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs191622368	chr3:118689096-118689097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs578047328	chr3:118689195-118689196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541594240	chr3:118689202-118689203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560091440	chr3:118689221-118689222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs578242860	chr3:118689265-118689266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184561189	chr3:118689295-118689296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563516854	chr3:118689300-118689301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190144131	chr3:118689304-118689305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs181837954	chr3:118689310-118689311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561007414	chr3:118689316-118689317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs116559344	chr3:118689357-118689358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546363938	chr3:118689390-118689391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573863020	chr3:118689454-118689455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571226187	chr3:118689480-118689481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554763312	chr3:118689492-118689493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542937792	chr3:118689511-118689512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149676972	chr3:118689517-118689518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs568755308	chr3:118689549-118689550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs536384438	chr3:118689592-118689593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs377136370	chr3:118689597-118689598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs369202993	chr3:118689598-118689599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs397965478	chr3:118689613-118689614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs79806441	chr3:118689615-118689616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs12487299	chr3:118689618-118689619	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs16829196	chr3:118689692-118689693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535253609	chr3:118689704-118689705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575142422	chr3:118689716-118689717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553569211	chr3:118689769-118689770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77879838	chr3:118689789-118689790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs11716016	chr3:118689796-118689797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112689392	chr3:118689841-118689842	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:1044 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118681200-118694000	Enhancers	Brain Substantia Nigra	brain
2	chr3:118681400-118690000	Enhancers	Brain Hippocampus Middle	brain
3	chr3:118681800-118692800	Enhancers	Brain Anterior Caudate	brain
4	chr3:118683400-118696200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr3:118683800-118689000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr3:118684400-118690000	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr3:118684600-118690200	Enhancers	Brain Cingulate Gyrus	brain
8	chr3:118684800-118690200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr3:118684800-118694000	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr3:118685000-118688800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr3:118685000-118690000	Enhancers	Brain Angular Gyrus	brain
12	chr3:118685400-118689400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
13	chr3:118686200-118689000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr3:118686600-118690200	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr3:118687000-118690000	Enhancers	Stomach Smooth Muscle	stomach
16	chr3:118687200-118690200	Enhancers	Fetal Heart	heart
17	chr3:118687400-118691800	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr3:118687400-118691800	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr3:118687600-118689000	Enhancers	H1 Cell Line	embryonic stem cell
20	chr3:118687800-118688800	Enhancers	Right Atrium	heart
21	chr3:118687800-118690400	Enhancers	Brain Germinal Matrix	brain
22	chr3:118688200-118689000	Enhancers	Ovary	ovary
23	chr3:118688200-118689000	Enhancers	Psoas Muscle	Psoas
24	chr3:118688200-118689200	Enhancers	Left Ventricle	heart
25	chr3:118688200-118689400	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr3:118688400-118689000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr3:118688600-118691200	Weak transcription	Rectal Smooth Muscle	rectum
28	chr3:118688800-118689000	Enhancers	Pancreas	Pancrea
29	chr3:118688800-118706000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr3:118689000-118689400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr3:118689000-118691600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr3:118689000-118703600	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr3:118689200-118689800	Weak transcription	Left Ventricle	heart
34	chr3:118689400-118689800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr3:118689400-118690200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr3:118689800-118690000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr3:118689800-118690000	Enhancers	Left Ventricle	heart
38	chr3:118690000-118691000	Weak transcription	Brain Angular Gyrus	brain
39	chr3:118690000-118691000	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr3:118690000-118691200	Weak transcription	Brain Hippocampus Middle	brain
41	chr3:118690000-118691400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr3:118690000-118691400	Weak transcription	Stomach Smooth Muscle	stomach
43	chr3:118690200-118691200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr3:118690200-118691200	Weak transcription	Brain Cingulate Gyrus	brain
45	chr3:118690200-118691400	Weak transcription	Fetal Heart	heart
46	chr3:118690200-118691600	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr3:118690200-118691800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr3:118690400-118690800	Weak transcription	Brain Germinal Matrix	brain
49	chr3:118690800-118692400	Enhancers	Brain Germinal Matrix	brain
50	chr3:118691000-118692200	Enhancers	Brain Angular Gyrus	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links