Variant report

Variant	nsv877372
Chromosome Location	chr3:118729114-118824418
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:747)
CpG islands
(count:916)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:747 , 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	chr3:118753735-118753935	K562	blood:	n/a	n/a
2	ARID3A	chr3:118734227-118734231	HepG2	liver:	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	chr3:118753664-118753967	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	chr3:118741024-118741203	K562	blood:	n/a	chr3:118741136-118741147
10	CEBPB	chr3:118741045-118741288	HepG2	liver:	n/a	chr3:118741136-118741147
11	CEBPB	chr3:118778947-118779140	HepG2	liver:	n/a	chr3:118779069-118779080
12	CEBPB	chr3:118817555-118817690	K562	blood:	n/a	n/a
13	CEBPB	chr3:118741075-118741275	A549	lung:	n/a	chr3:118741136-118741147
14	CEBPB	chr3:118745368-118745633	HepG2	liver:	n/a	chr3:118745489-118745500
15	CEBPB	chr3:118740984-118741309	IMR90	lung:	n/a	chr3:118741136-118741147
16	CEBPB	chr3:118741064-118741238	H1-hESC	embryonic stem cell:	n/a	chr3:118741136-118741147
17	CEBPB	chr3:118737472-118737647	A549	lung:	n/a	n/a
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	chr3:118753691-118753967	A549	lung:	n/a	n/a
26	CTCF	chr3:118754081-118754169	GM13977	blood:	n/a	n/a
27	CTCF	chr3:118753368-118754014	MCF-7	breast:	n/a	n/a
28	CTCF	chr3:118817580-118817730	NHDF-neo	bronchial:	n/a	chr3:118817652-118817670
29	CTCF	chr3:118753580-118753870	NHEK	skin:	n/a	n/a
30	CTCF	chr3:118753750-118753927	HepG2	liver:	n/a	n/a
31	CTCF	chr3:118753460-118753610	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr3:118753440-118753590	BJ	skin:	n/a	n/a
33	CTCF	chr3:118753592-118753971	GM12878	blood:	n/a	n/a
34	CTCF	chr3:118753720-118753870	GM12865	blood:	n/a	n/a
35	CTCF	chr3:118817620-118817770	HUVEC	blood vessel:	n/a	chr3:118817652-118817670
36	CTCF	chr3:118817420-118817821	H1-hESC	embryonic stem cell:	n/a	chr3:118817652-118817670
37	CTCF	chr3:118753729-118754017	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr3:118817514-118817805	HUVEC	blood vessel:	n/a	chr3:118817652-118817670
39	CTCF	chr3:118817580-118817730	HRPEpiC	eye:	n/a	chr3:118817652-118817670
40	CTCF	chr3:118817540-118817690	BE2_C	brain:	n/a	chr3:118817652-118817670
41	CTCF	chr3:118804092-118804100	GM12878	blood:	n/a	n/a
42	CTCF	chr3:118753200-118753350	HRE	kidney:	n/a	n/a
43	CTCF	chr3:118753720-118753870	GM12874	blood:	n/a	n/a
44	CTCF	chr3:118817501-118817854	MCF-7	breast:	n/a	chr3:118817652-118817670
45	CTCF	chr3:118753491-118754113	K562	blood:	n/a	n/a
46	CTCF	chr3:118817435-118817868	K562	blood:	n/a	chr3:118817652-118817670
47	CTCF	chr3:118753439-118754040	ProgFib	skin:	n/a	n/a
48	CTCF	chr3:118817534-118817780	Lung_OC	lung:	n/a	chr3:118817652-118817670
49	CTCF	chr3:118817580-118817730	HCT-116	colon:	n/a	chr3:118817652-118817670
50	CTCF	chr3:118753518-118753521	GM19240	blood:	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	chr3:118757898-118757948	ProgFib	skin:	n/a
2	chr3:118757898-118757948	ProgFib	skin:	n/a
3	chr3:118750463-118750513	HepG2	liver:	n/a
4	chr3:118753093-118753143	U87	brain:	n/a
5	chr3:118750463-118750513	A549	lung:	n/a
6	chr3:118754376-118754426	NHBE	bronchial:	n/a
7	chr3:118754376-118754426	GM19239	blood:	n/a
8	chr3:118792317-118792367	U87	brain:	n/a
9	chr3:118750463-118750513	SK-N-MC	brain:	n/a
10	chr3:118753705-118753755	PANC-1	pancreas:	n/a
11	chr3:118753705-118753755	MCF-7	breast:	n/a
12	chr3:118792317-118792367	ECC-1	luminal epithelium:	n/a
13	chr3:118792317-118792367	AG04450	lung:	fetal
14	chr3:118753871-118753921	HepG2	liver:	n/a
15	chr3:118792317-118792367	PFSK-1	brain:	n/a
16	chr3:118750463-118750513	HNPCEpiC	eye:	n/a
17	chr3:118753093-118753143	SK-N-SH	brain:	n/a
18	chr3:118757898-118757948	AG09309	skin:	n/a
19	chr3:118750463-118750513	HCT-116	colon:	n/a
20	chr3:118754097-118754147	HPAEpiC	pulmonary alveolar:	n/a
21	chr3:118753610-118753660	HUVEC	blood vessel:	n/a
22	chr3:118753005-118753055	Hepatocyte	liver:	n/a
23	chr3:118753705-118753755	HCT-116	colon:	n/a
24	chr3:118753610-118753660	GM12891	blood:	n/a
25	chr3:118754097-118754147	HNPCEpiC	eye:	n/a
26	chr3:118753093-118753143	AG09319	gingival:	n/a
27	chr3:118750463-118750513	AG04450	lung:	fetal
28	chr3:118734756-118734806	HepG2	liver:	n/a
29	chr3:118753738-118753788	HRE	kidney:	n/a
30	chr3:118753093-118753143	AG04450	lung:	fetal
31	chr3:118753871-118753921	HRCEpiC	kidney:	n/a
32	chr3:118753005-118753055	U87	brain:	n/a
33	chr3:118753610-118753660	HCPEpiC	choroid plexus:	n/a
34	chr3:118757898-118757948	RPTEC	kidney:	n/a
35	chr3:118750463-118750513	SK-N-SH	brain:	n/a
36	chr3:118753660-118753710	HRPEpiC	eye:	n/a
37	chr3:118754097-118754147	GM12891	blood:	n/a
38	chr3:118757898-118757948	HL-60	blood:	n/a
39	chr3:118753714-118753764	HIPEpiC	eye:	n/a
40	chr3:118734756-118734806	NHBE	bronchial:	n/a
41	chr3:118754097-118754147	GM12878	blood:	n/a
42	chr3:118753714-118753764	SK-N-SH_RA	brain:	n/a
43	chr3:118753660-118753710	HAEpiC	amniotic membrane:	n/a
44	chr3:118792317-118792367	GM12891	blood:	n/a
45	chr3:118734756-118734806	HAEpiC	amniotic membrane:	n/a
46	chr3:118753707-118753757	GM19239	blood:	n/a
47	chr3:118753714-118753764	PFSK-1	brain:	n/a
48	chr3:118753610-118753660	NHBE	bronchial:	n/a
49	chr3:118754097-118754147	SKMC	muscle:	n/a
50	chr3:118753707-118753757	Jurkat	blood:	n/a

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

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

(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: 1766 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1766 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1369582	chr3:118729114-118729115	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs527926542	chr3:118729133-118729134	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552492752	chr3:118729208-118729209	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536485657	chr3:118729211-118729212	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556094529	chr3:118729235-118729236	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76234110	chr3:118729253-118729254	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538546992	chr3:118729254-118729255	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs140577413	chr3:118729339-118729340	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs114595580	chr3:118729370-118729371	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145711400	chr3:118729405-118729406	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536060256	chr3:118729468-118729469	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572436339	chr3:118729522-118729523	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539664267	chr3:118729553-118729554	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557545158	chr3:118729561-118729562	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs79845523	chr3:118729598-118729599	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551523381	chr3:118729612-118729613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185521825	chr3:118729616-118729617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561628032	chr3:118729659-118729660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189987335	chr3:118729660-118729661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372067294	chr3:118729776-118729777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564800529	chr3:118729803-118729804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540660998	chr3:118729807-118729808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375146795	chr3:118729839-118729840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532888365	chr3:118729843-118729844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369388142	chr3:118729926-118729927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182889012	chr3:118729929-118729930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572140430	chr3:118730026-118730027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376244155	chr3:118730079-118730080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564684958	chr3:118730132-118730133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551227836	chr3:118730171-118730172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531911290	chr3:118730185-118730186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550521311	chr3:118730187-118730188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568641895	chr3:118730236-118730237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs146539759	chr3:118730268-118730269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547468226	chr3:118730278-118730279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566027411	chr3:118730297-118730298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539567113	chr3:118730321-118730322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9882006	chr3:118730404-118730405	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs575862154	chr3:118730420-118730421	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536834591	chr3:118730494-118730495	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs527437925	chr3:118730496-118730497	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555284034	chr3:118730517-118730518	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149147252	chr3:118730534-118730535	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547617578	chr3:118730535-118730536	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs9862556	chr3:118730537-118730538	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs75741434	chr3:118730567-118730568	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577531184	chr3:118730726-118730727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545145199	chr3:118730761-118730762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563349725	chr3:118730784-118730785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531974964	chr3:118730785-118730786	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:578 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118715400-118731800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr3:118725200-118737600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr3:118727000-118729600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
4	chr3:118727000-118729600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:118727200-118731600	Weak transcription	Psoas Muscle	Psoas
6	chr3:118727400-118730800	Weak transcription	Brain Substantia Nigra	brain
7	chr3:118727400-118731600	Weak transcription	Ovary	ovary
8	chr3:118727800-118734400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr3:118729000-118729600	Enhancers	Brain Anterior Caudate	brain
10	chr3:118729000-118729600	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr3:118729600-118730400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr3:118729600-118730800	Weak transcription	Brain Anterior Caudate	brain
13	chr3:118729600-118730800	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr3:118729600-118732800	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr3:118730000-118742000	Enhancers	Brain Angular Gyrus	brain
16	chr3:118730400-118730600	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr3:118730600-118731200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr3:118730800-118731000	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr3:118730800-118731400	Active TSS	Stomach Smooth Muscle	stomach
20	chr3:118730800-118732000	Enhancers	Brain Hippocampus Middle	brain
21	chr3:118730800-118736400	Enhancers	Fetal Brain Male	brain
22	chr3:118730800-118738600	Enhancers	Brain Anterior Caudate	brain
23	chr3:118730800-118741800	Enhancers	Brain Substantia Nigra	brain
24	chr3:118731000-118731400	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr3:118731200-118731400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr3:118731400-118732200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr3:118731400-118734200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr3:118731400-118737000	Weak transcription	Stomach Smooth Muscle	stomach
29	chr3:118731400-118738000	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr3:118731600-118732000	Enhancers	Psoas Muscle	Psoas
31	chr3:118731600-118732400	Enhancers	Ovary	ovary
32	chr3:118731600-118733600	Enhancers	Fetal Brain Female	brain
33	chr3:118731800-118736200	Enhancers	Brain Cingulate Gyrus	brain
34	chr3:118732000-118733000	Weak transcription	Brain Hippocampus Middle	brain
35	chr3:118732000-118737600	Weak transcription	Psoas Muscle	Psoas
36	chr3:118732200-118732600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr3:118732400-118732800	Weak transcription	Ovary	ovary
38	chr3:118732600-118733400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr3:118732600-118735200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr3:118732800-118733000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr3:118732800-118733000	Enhancers	Ovary	ovary
42	chr3:118732800-118733200	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr3:118733000-118734600	Weak transcription	Ovary	ovary
44	chr3:118733000-118740000	Enhancers	Brain Hippocampus Middle	brain
45	chr3:118733200-118734600	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr3:118733200-118735200	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr3:118733400-118734600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr3:118733600-118733800	Enhancers	Brain Germinal Matrix	brain
49	chr3:118733600-118734800	Weak transcription	Fetal Brain Female	brain
50	chr3:118733800-118734800	Weak transcription	Brain Germinal Matrix	brain

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