Variant report

Variant	nsv536702
Chromosome Location	chr3:118747219-118817507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:559)
CpG islands
(count:854)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:559 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	chr3:118817076-118817276	K562	blood:	n/a	n/a
3	BACH1	chr3:118753370-118754199	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr3:118753613-118754025	K562	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
5	BHLHE40	chr3:118753664-118753967	GM12878	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	chr3:118778947-118779140	HepG2	liver:	n/a	chr3:118779069-118779080
8	CHD1	chr3:118753827-118753996	GM12878	blood:	n/a	n/a
9	CHD1	chr3:118752910-118753656	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr3:118753658-118753827	HepG2	liver:	n/a	chr3:118753765-118753775
11	CHD2	chr3:118753548-118753681	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr3:118753607-118753878	GM12878	blood:	n/a	chr3:118753765-118753775
13	CREB1	chr3:118753090-118753994	A549	lung:	n/a	n/a
14	CTBP2	chr3:118753482-118754214	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr3:118753760-118753910	GM12873	blood:	n/a	n/a
16	CTCF	chr3:118753740-118753890	AoAF	blood vessel:	n/a	n/a
17	CTCF	chr3:118754060-118754210	HRPEpiC	eye:	n/a	n/a
18	CTCF	chr3:118753720-118753870	K562	blood:	n/a	n/a
19	CTCF	chr3:118753491-118754018	K562	blood:	n/a	n/a
20	CTCF	chr3:118817443-118817882	GM12878	blood:	n/a	chr3:118817652-118817670
21	CTCF	chr3:118753760-118753910	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr3:118753648-118753921	HepG2	liver:	n/a	n/a
23	CTCF	chr3:118804017-118804168	MCF-7	breast:	n/a	n/a
24	CTCF	chr3:118795861-118795898	Spleen_OC	spleen:	n/a	n/a
25	CTCF	chr3:118753547-118753633	LNCaP	prostate:	n/a	n/a
26	CTCF	chr3:118753707-118753971	Pancreas_OC	pancreas:	n/a	n/a
27	CTCF	chr3:118753700-118753850	AG09309	skin:	n/a	n/a
28	CTCF	chr3:118753690-118753932	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr3:118817432-118817821	A549	lung:	n/a	chr3:118817652-118817670
30	CTCF	chr3:118791905-118791974	GM10248	blood:	n/a	n/a
31	CTCF	chr3:118753584-118753947	T-47D	breast:	n/a	n/a
32	CTCF	chr3:118753740-118753890	GM12872	blood:	n/a	n/a
33	CTCF	chr3:118753740-118753890	GM12871	blood:	n/a	n/a
34	CTCF	chr3:118753460-118753610	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr3:118817433-118817908	MCF-7	breast:	n/a	chr3:118817652-118817670
36	CTCF	chr3:118753689-118753969	GM10248	blood:	n/a	n/a
37	CTCF	chr3:118753540-118753996	Gliobla	brain:	n/a	n/a
38	CTCF	chr3:118753720-118753870	AG04450	lung:	n/a	n/a
39	CTCF	chr3:118753720-118753870	GM12865	blood:	n/a	n/a
40	CTCF	chr3:118753672-118753959	K562	blood:	n/a	n/a
41	CTCF	chr3:118753750-118753927	HepG2	liver:	n/a	n/a
42	CTCF	chr3:118753740-118753890	GM12866	blood:	n/a	n/a
43	CTCF	chr3:118753558-118754052	GM12878	blood:	n/a	n/a
44	CTCF	chr3:118753760-118753910	GM12867	blood:	n/a	n/a
45	CTCF	chr3:118753393-118754053	K562	blood:	n/a	n/a
46	CTCF	chr3:118753720-118753870	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr3:118753780-118753930	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr3:118752952-118754403	A549	lung:	n/a	n/a
49	CTCF	chr3:118753760-118753910	RPTEC	kidney:	n/a	n/a
50	CTCF	chr3:118753480-118753630	HA-sp	spinal cord:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:118754097-118754147	HCF	heart:	n/a
2	chr3:118753610-118753660	SK-N-MC	brain:	n/a
3	chr3:118753707-118753757	Hela-S3	cervix:	n/a
4	chr3:118754097-118754147	BE2_C	brain:	n/a
5	chr3:118757898-118757948	NB4	blood:	n/a
6	chr3:118750463-118750513	PANC-1	pancreas:	n/a
7	chr3:118753705-118753755	ECC-1	luminal epithelium:	n/a
8	chr3:118754097-118754147	AG04449	skin:	fetal
9	chr3:118753005-118753055	SK-N-SH	brain:	n/a
10	chr3:118757898-118757948	HPAEpiC	pulmonary alveolar:	n/a
11	chr3:118753005-118753055	NHBE	bronchial:	n/a
12	chr3:118753714-118753764	GM12891	blood:	n/a
13	chr3:118754376-118754426	GM12878	blood:	n/a
14	chr3:118753738-118753788	ovcar-3	ovarian:	n/a
15	chr3:118753707-118753757	Jurkat	blood:	n/a
16	chr3:118750463-118750513	HPAEpiC	pulmonary alveolar:	n/a
17	chr3:118754376-118754426	AG04449	skin:	fetal
18	chr3:118754097-118754147	SK-N-MC	brain:	n/a
19	chr3:118753707-118753757	SKMC	muscle:	n/a
20	chr3:118753705-118753755	SK-N-SH_RA	brain:	n/a
21	chr3:118753093-118753143	PrEC	prostate:	n/a
22	chr3:118792317-118792367	HUVEC	blood vessel:	n/a
23	chr3:118753707-118753757	AoSMC	blood vessel:	n/a
24	chr3:118753093-118753143	HUVEC	blood vessel:	n/a
25	chr3:118753093-118753143	GM12878	blood:	n/a
26	chr3:118753871-118753921	GM12891	blood:	n/a
27	chr3:118757898-118757948	AG10803	skin:	n/a
28	chr3:118750463-118750513	AG04450	lung:	fetal
29	chr3:118753707-118753757	HNPCEpiC	eye:	n/a
30	chr3:118754097-118754147	HCPEpiC	choroid plexus:	n/a
31	chr3:118753005-118753055	ECC-1	luminal epithelium:	n/a
32	chr3:118753707-118753757	U87	brain:	n/a
33	chr3:118753714-118753764	GM12892	blood:	n/a
34	chr3:118753610-118753660	NB4	blood:	n/a
35	chr3:118753714-118753764	AG09319	gingival:	n/a
36	chr3:118754097-118754147	HRE	kidney:	n/a
37	chr3:118750463-118750513	HNPCEpiC	eye:	n/a
38	chr3:118753714-118753764	SK-N-SH_RA	brain:	n/a
39	chr3:118753660-118753710	HL-60	blood:	n/a
40	chr3:118750463-118750513	SK-N-SH_RA	brain:	n/a
41	chr3:118754097-118754147	T-47D	breast:	n/a
42	chr3:118792317-118792367	HRCEpiC	kidney:	n/a
43	chr3:118753005-118753055	SK-N-SH_RA	brain:	n/a
44	chr3:118750463-118750513	NHBE	bronchial:	n/a
45	chr3:118753093-118753143	GM12892	blood:	n/a
46	chr3:118754097-118754147	AG10803	skin:	n/a
47	chr3:118753738-118753788	ProgFib	skin:	n/a
48	chr3:118754376-118754426	PrEC	prostate:	n/a
49	chr3:118753660-118753710	HMEC	breast:	n/a
50	chr3:118754376-118754426	K562	blood:	n/a

(count:16 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 1008 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1008 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555146713	chr3:118747233-118747234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573384973	chr3:118747241-118747242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs112426308	chr3:118747290-118747291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs140742595	chr3:118747294-118747295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs72970472	chr3:118747308-118747309	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs576947564	chr3:118747347-118747348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150268925	chr3:118747396-118747397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138983369	chr3:118747426-118747427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs202111054	chr3:118747443-118747444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541430802	chr3:118747449-118747450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs149432215	chr3:118747461-118747462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570598678	chr3:118747477-118747478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs35719654	chr3:118747492-118747493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188036213	chr3:118747538-118747539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs200104261	chr3:118747549-118747550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200862721	chr3:118747550-118747551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs397990918	chr3:118747559-118747560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192229412	chr3:118747563-118747564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147078549	chr3:118747583-118747584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551436155	chr3:118747590-118747591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185013381	chr3:118747598-118747599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539479044	chr3:118747609-118747610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112253231	chr3:118747611-118747612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189424301	chr3:118747619-118747620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551030424	chr3:118747640-118747641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116668385	chr3:118747661-118747662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112483632	chr3:118747670-118747671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113082553	chr3:118747671-118747672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138488861	chr3:118747785-118747786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546564036	chr3:118747821-118747822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184357592	chr3:118747823-118747824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs859018	chr3:118747851-118747852	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs570598216	chr3:118747864-118747865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141453817	chr3:118747893-118747894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs202235604	chr3:118748021-118748022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs71719785	chr3:118748046-118748047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs66598029	chr3:118748056-118748057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs144425931	chr3:118748085-118748086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs79516305	chr3:118748119-118748120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs140515077	chr3:118748121-118748122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10662902	chr3:118748122-118748123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs62273460	chr3:118748123-118748124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs150533649	chr3:118748124-118748125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs72251348	chr3:118748125-118748126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541683606	chr3:118748163-118748164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189501159	chr3:118748192-118748193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147280870	chr3:118748228-118748229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs113632966	chr3:118748238-118748239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs545614398	chr3:118748243-118748244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs375312430	chr3:118748299-118748300	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:407 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118739400-118753000	Weak transcription	Pancreas	Pancrea
2	chr3:118739600-118750400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr3:118740000-118750400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr3:118742000-118751200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr3:118743200-118751000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr3:118743400-118749400	Weak transcription	Ovary	ovary
7	chr3:118743600-118749400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr3:118744400-118747800	Weak transcription	Brain Cingulate Gyrus	brain
9	chr3:118744400-118751400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr3:118745600-118747400	Enhancers	Brain Hippocampus Middle	brain
11	chr3:118745600-118748000	Weak transcription	Brain Substantia Nigra	brain
12	chr3:118745600-118748200	Weak transcription	Brain Angular Gyrus	brain
13	chr3:118746000-118747600	Enhancers	Brain Anterior Caudate	brain
14	chr3:118746400-118751000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:118747000-118748000	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr3:118747400-118747800	Weak transcription	Brain Hippocampus Middle	brain
17	chr3:118747600-118748000	Weak transcription	Brain Anterior Caudate	brain
18	chr3:118747800-118748400	Enhancers	Brain Cingulate Gyrus	brain
19	chr3:118747800-118749800	Enhancers	Brain Hippocampus Middle	brain
20	chr3:118748000-118748200	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr3:118748000-118750800	Enhancers	Brain Anterior Caudate	brain
22	chr3:118748000-118750800	Enhancers	Brain Substantia Nigra	brain
23	chr3:118748200-118749000	Enhancers	Brain Angular Gyrus	brain
24	chr3:118748200-118749600	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr3:118748400-118750600	Weak transcription	Brain Cingulate Gyrus	brain
26	chr3:118749000-118751000	Weak transcription	Brain Angular Gyrus	brain
27	chr3:118749400-118749600	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr3:118749400-118750000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr3:118749400-118750000	Enhancers	Ovary	ovary
30	chr3:118749600-118750000	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr3:118749600-118751000	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr3:118749800-118750200	Weak transcription	Brain Hippocampus Middle	brain
33	chr3:118750000-118751000	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr3:118750000-118751000	Weak transcription	Ovary	ovary
35	chr3:118750200-118750400	Enhancers	Brain Hippocampus Middle	brain
36	chr3:118750400-118750600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr3:118750400-118751000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr3:118750400-118751000	Enhancers	Brain Germinal Matrix	brain
39	chr3:118750400-118751000	Weak transcription	Brain Hippocampus Middle	brain
40	chr3:118750600-118751000	Enhancers	Brain Cingulate Gyrus	brain
41	chr3:118750600-118751200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr3:118750800-118751000	Weak transcription	Brain Anterior Caudate	brain
43	chr3:118750800-118751000	Weak transcription	Brain Substantia Nigra	brain
44	chr3:118751000-118751200	Active TSS	Brain Germinal Matrix	brain
45	chr3:118751000-118751200	Weak transcription	Fetal Brain Female	brain
46	chr3:118751000-118751400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
47	chr3:118751000-118751400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr3:118751000-118751400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
49	chr3:118751000-118751400	Flanking Active TSS	Ovary	ovary
50	chr3:118751000-118753200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links