Variant report

Variant	nsv877375
Chromosome Location	chr3:118747851-118824418
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:704)
CpG islands
(count:856)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:704 , 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	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	chr3:118817555-118817690	K562	blood:	n/a	n/a
8	CEBPB	chr3:118778947-118779140	HepG2	liver:	n/a	chr3:118779069-118779080
9	CHD1	chr3:118752910-118753656	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD1	chr3:118753827-118753996	GM12878	blood:	n/a	n/a
11	CHD2	chr3:118753607-118753878	GM12878	blood:	n/a	chr3:118753765-118753775
12	CHD2	chr3:118753548-118753681	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr3:118753658-118753827	HepG2	liver:	n/a	chr3:118753765-118753775
14	CREB1	chr3:118753090-118753994	A549	lung:	n/a	n/a
15	CTBP2	chr3:118753482-118754214	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr3:118753584-118753947	T-47D	breast:	n/a	n/a
17	CTCF	chr3:118804320-118804400	GM10248	blood:	n/a	n/a
18	CTCF	chr3:118753671-118753970	GM10266	blood:	n/a	n/a
19	CTCF	chr3:118753720-118753870	MCF-7	breast:	n/a	n/a
20	CTCF	chr3:118753740-118753890	HepG2	liver:	n/a	n/a
21	CTCF	chr3:118817580-118817730	MCF-7	breast:	n/a	chr3:118817652-118817670
22	CTCF	chr3:118753780-118753930	HRPEpiC	eye:	n/a	n/a
23	CTCF	chr3:118819634-118819725	GM12878	blood:	n/a	n/a
24	CTCF	chr3:118754260-118754410	HRE	kidney:	n/a	n/a
25	CTCF	chr3:118753491-118754018	K562	blood:	n/a	n/a
26	CTCF	chr3:118817600-118817750	HRE	kidney:	n/a	chr3:118817652-118817670
27	CTCF	chr3:118753689-118753969	GM10248	blood:	n/a	n/a
28	CTCF	chr3:118817600-118817750	BE2_C	brain:	n/a	chr3:118817652-118817670
29	CTCF	chr3:118753547-118753633	LNCaP	prostate:	n/a	n/a
30	CTCF	chr3:118753780-118753930	GM12873	blood:	n/a	n/a
31	CTCF	chr3:118753720-118753870	GM12873	blood:	n/a	n/a
32	CTCF	chr3:118753440-118753590	BJ	skin:	n/a	n/a
33	CTCF	chr3:118753690-118753932	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr3:118803991-118804179	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:118817540-118817690	GM12871	blood:	n/a	chr3:118817652-118817670
36	CTCF	chr3:118753658-118753667	K562	blood:	n/a	n/a
37	CTCF	chr3:118754080-118754230	RPTEC	kidney:	n/a	n/a
38	CTCF	chr3:118753691-118753995	GM13977	blood:	n/a	n/a
39	CTCF	chr3:118817500-118817650	WI-38	lung:	n/a	n/a
40	CTCF	chr3:118817576-118817753	ProgFib	skin:	n/a	chr3:118817652-118817670
41	CTCF	chr3:118817540-118817690	WERI-Rb-1	eye:	n/a	chr3:118817652-118817670
42	CTCF	chr3:118817567-118817753	Gliobla	brain:	n/a	chr3:118817652-118817670
43	CTCF	chr3:118817546-118817774	K562	blood:	n/a	chr3:118817652-118817670
44	CTCF	chr3:118753720-118753870	GM12865	blood:	n/a	n/a
45	CTCF	chr3:118817463-118817853	ECC-1	luminal epithelium:	n/a	chr3:118817652-118817670
46	CTCF	chr3:118817600-118817750	GM12866	blood:	n/a	chr3:118817652-118817670
47	CTCF	chr3:118817600-118817750	HPAF	blood vessel:	n/a	chr3:118817652-118817670
48	CTCF	chr3:118753740-118753890	GM12866	blood:	n/a	n/a
49	CTCF	chr3:118753527-118753956	LNCaP	prostate:	n/a	n/a
50	CTCF	chr3:118753700-118753850	HPAF	blood vessel:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:118753714-118753764	AG10803	skin:	n/a
2	chr3:118753871-118753921	MCF10A-Er-Src	breast:	n/a
3	chr3:118753714-118753764	AG10803	skin:	n/a
4	chr3:118753871-118753921	MCF10A-Er-Src	breast:	n/a
5	chr3:118753660-118753710	K562	blood:	n/a
6	chr3:118757898-118757948	H1-hESC	embryonic stem cell:	embryo
7	chr3:118754097-118754147	IMR90	lung:	fetal
8	chr3:118753660-118753710	HMEC	breast:	n/a
9	chr3:118792317-118792367	RPTEC	kidney:	n/a
10	chr3:118757898-118757948	SKMC	muscle:	n/a
11	chr3:118753093-118753143	SAEC	small airway:	n/a
12	chr3:118753871-118753921	GM12891	blood:	n/a
13	chr3:118753660-118753710	MCF-7	breast:	n/a
14	chr3:118753610-118753660	BE2_C	brain:	n/a
15	chr3:118753005-118753055	GM06990	blood:	n/a
16	chr3:118750463-118750513	Hepatocyte	liver:	n/a
17	chr3:118753005-118753055	T-47D	breast:	n/a
18	chr3:118757898-118757948	SAEC	small airway:	n/a
19	chr3:118792317-118792367	HMEC	breast:	n/a
20	chr3:118753738-118753788	HNPCEpiC	eye:	n/a
21	chr3:118753660-118753710	PFSK-1	brain:	n/a
22	chr3:118757898-118757948	SK-N-MC	brain:	n/a
23	chr3:118753705-118753755	HMEC	breast:	n/a
24	chr3:118753705-118753755	HAEpiC	amniotic membrane:	n/a
25	chr3:118753093-118753143	SK-N-MC	brain:	n/a
26	chr3:118753093-118753143	PrEC	prostate:	n/a
27	chr3:118753660-118753710	ProgFib	skin:	n/a
28	chr3:118753610-118753660	T-47D	breast:	n/a
29	chr3:118754376-118754426	GM12891	blood:	n/a
30	chr3:118753705-118753755	GM12891	blood:	n/a
31	chr3:118753714-118753764	MCF10A-Er-Src	breast:	n/a
32	chr3:118753610-118753660	HCPEpiC	choroid plexus:	n/a
33	chr3:118754097-118754147	SAEC	small airway:	n/a
34	chr3:118753660-118753710	MCF10A-Er-Src	breast:	n/a
35	chr3:118753660-118753710	HCPEpiC	choroid plexus:	n/a
36	chr3:118753705-118753755	GM12878	blood:	n/a
37	chr3:118754376-118754426	SK-N-SH_RA	brain:	n/a
38	chr3:118753705-118753755	A549	lung:	n/a
39	chr3:118753610-118753660	Hepatocyte	liver:	n/a
40	chr3:118754097-118754147	HAEpiC	amniotic membrane:	n/a
41	chr3:118757898-118757948	NHDF-neo	bronchial:	n/a
42	chr3:118753093-118753143	NB4	blood:	n/a
43	chr3:118753707-118753757	PANC-1	pancreas:	n/a
44	chr3:118753707-118753757	Caco-2	colon:	n/a
45	chr3:118757898-118757948	HPAEpiC	pulmonary alveolar:	n/a
46	chr3:118753707-118753757	Hepatocyte	liver:	n/a
47	chr3:118792317-118792367	HEK293	kidney:	embryo
48	chr3:118757898-118757948	MCF-7	breast:	n/a
49	chr3:118750463-118750513	NB4	blood:	n/a
50	chr3:118753660-118753710	RPTEC	kidney:	n/a

(count:17 , 50 per page) page: 1

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

Extended variants
information (count: 1085 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1085 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs859018	chr3:118747851-118747852	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs570598216	chr3:118747864-118747865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141453817	chr3:118747893-118747894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs202235604	chr3:118748021-118748022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs71719785	chr3:118748046-118748047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs66598029	chr3:118748056-118748057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs144425931	chr3:118748085-118748086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs79516305	chr3:118748119-118748120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs140515077	chr3:118748121-118748122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs10662902	chr3:118748122-118748123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs62273460	chr3:118748123-118748124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs150533649	chr3:118748124-118748125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs72251348	chr3:118748125-118748126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541683606	chr3:118748163-118748164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189501159	chr3:118748192-118748193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs147280870	chr3:118748228-118748229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs113632966	chr3:118748238-118748239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545614398	chr3:118748243-118748244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375312430	chr3:118748299-118748300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564197318	chr3:118748325-118748326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532643216	chr3:118748340-118748341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544822073	chr3:118748341-118748342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs57906926	chr3:118748380-118748381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182050314	chr3:118748440-118748441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567857397	chr3:118748520-118748521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530439409	chr3:118748603-118748604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548879069	chr3:118748652-118748653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187168595	chr3:118748710-118748711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567160070	chr3:118748728-118748729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527678074	chr3:118748836-118748837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs62273461	chr3:118748845-118748846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570930140	chr3:118748882-118748883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191144505	chr3:118748897-118748898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555952816	chr3:118749001-118749002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567882619	chr3:118749036-118749037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150825236	chr3:118749148-118749149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553632672	chr3:118749222-118749223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571985415	chr3:118749223-118749224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539414145	chr3:118749336-118749337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555410584	chr3:118749417-118749418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576096598	chr3:118749445-118749446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534735338	chr3:118749466-118749467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs180808393	chr3:118749484-118749485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs16829287	chr3:118749554-118749555	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs139599921	chr3:118749571-118749572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76781519	chr3:118749580-118749581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149749424	chr3:118749593-118749594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186622051	chr3:118749596-118749597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527934138	chr3:118749623-118749624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552553492	chr3:118749631-118749632	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:405 , 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	chr3:118744400-118751400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr3:118745600-118748000	Weak transcription	Brain Substantia Nigra	brain
10	chr3:118745600-118748200	Weak transcription	Brain Angular Gyrus	brain
11	chr3:118746400-118751000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr3:118747000-118748000	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr3:118747600-118748000	Weak transcription	Brain Anterior Caudate	brain
14	chr3:118747800-118748400	Enhancers	Brain Cingulate Gyrus	brain
15	chr3:118747800-118749800	Enhancers	Brain Hippocampus Middle	brain
16	chr3:118748000-118748200	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr3:118748000-118750800	Enhancers	Brain Anterior Caudate	brain
18	chr3:118748000-118750800	Enhancers	Brain Substantia Nigra	brain
19	chr3:118748200-118749000	Enhancers	Brain Angular Gyrus	brain
20	chr3:118748200-118749600	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr3:118748400-118750600	Weak transcription	Brain Cingulate Gyrus	brain
22	chr3:118749000-118751000	Weak transcription	Brain Angular Gyrus	brain
23	chr3:118749400-118749600	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr3:118749400-118750000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr3:118749400-118750000	Enhancers	Ovary	ovary
26	chr3:118749600-118750000	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr3:118749600-118751000	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr3:118749800-118750200	Weak transcription	Brain Hippocampus Middle	brain
29	chr3:118750000-118751000	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr3:118750000-118751000	Weak transcription	Ovary	ovary
31	chr3:118750200-118750400	Enhancers	Brain Hippocampus Middle	brain
32	chr3:118750400-118750600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr3:118750400-118751000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr3:118750400-118751000	Enhancers	Brain Germinal Matrix	brain
35	chr3:118750400-118751000	Weak transcription	Brain Hippocampus Middle	brain
36	chr3:118750600-118751000	Enhancers	Brain Cingulate Gyrus	brain
37	chr3:118750600-118751200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr3:118750800-118751000	Weak transcription	Brain Anterior Caudate	brain
39	chr3:118750800-118751000	Weak transcription	Brain Substantia Nigra	brain
40	chr3:118751000-118751200	Active TSS	Brain Germinal Matrix	brain
41	chr3:118751000-118751200	Weak transcription	Fetal Brain Female	brain
42	chr3:118751000-118751400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
43	chr3:118751000-118751400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr3:118751000-118751400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
45	chr3:118751000-118751400	Flanking Active TSS	Ovary	ovary
46	chr3:118751000-118753200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr3:118751000-118754000	Active TSS	Brain Hippocampus Middle	brain
48	chr3:118751000-118754200	Active TSS	Brain Anterior Caudate	brain
49	chr3:118751000-118754200	Active TSS	Brain Cingulate Gyrus	brain
50	chr3:118751000-118754200	Active TSS	Brain Substantia Nigra	brain

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