Variant report

Variant	nsv965553
Chromosome Location	chr5:80360468-80369049
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr5:80362950-80363274	IMR90	lung:	n/a	chr5:80363100-80363113 chr5:80363097-80363114 chr5:80363116-80363127
2	CEBPB	chr5:80363026-80363204	A549	lung:	n/a	chr5:80363100-80363113 chr5:80363097-80363114 chr5:80363116-80363127
3	CEBPB	chr5:80366769-80367077	HepG2	liver:	n/a	chr5:80366900-80366913 chr5:80366891-80366902 chr5:80366893-80366902 chr5:80366893-80366904 chr5:80366891-80366904 chr5:80366900-80366911
4	CEBPB	chr5:80366806-80367007	A549	lung:	n/a	chr5:80366900-80366913 chr5:80366891-80366902 chr5:80366893-80366902 chr5:80366893-80366904 chr5:80366891-80366904 chr5:80366900-80366911
5	CEBPB	chr5:80362961-80363200	HepG2	liver:	n/a	chr5:80363100-80363113 chr5:80363097-80363114 chr5:80363116-80363127
6	CEBPB	chr5:80366756-80367054	IMR90	lung:	n/a	chr5:80366900-80366913 chr5:80366891-80366902 chr5:80366893-80366902 chr5:80366893-80366904 chr5:80366891-80366904 chr5:80366900-80366911
7	CEBPB	chr5:80362948-80363228	Hela-S3	cervix:	n/a	chr5:80363100-80363113 chr5:80363097-80363114 chr5:80363116-80363127
8	CEBPB	chr5:80366771-80367041	K562	blood:	n/a	chr5:80366900-80366913 chr5:80366891-80366902 chr5:80366893-80366902 chr5:80366893-80366904 chr5:80366891-80366904 chr5:80366900-80366911
9	CTCF	chr5:80362260-80362410	HPF	lung:	n/a	n/a
10	FOXA1	chr5:80361371-80361586	T-47D	breast:	n/a	n/a
11	JUN	chr5:80363105-80363122	HepG2	liver:	n/a	n/a
12	JUN	chr5:80363871-80364218	HUVEC	blood vessel:	n/a	n/a
13	JUND	chr5:80363081-80363218	HepG2	liver:	n/a	n/a
14	MAFF	chr5:80361927-80362300	HepG2	liver:	n/a	chr5:80362115-80362133
15	MAFF	chr5:80366848-80366884	HepG2	liver:	n/a	chr5:80366853-80366871
16	MAFK	chr5:80366836-80366970	HepG2	liver:	n/a	chr5:80366859-80366870 chr5:80366854-80366869 chr5:80366857-80366871
17	MAFK	chr5:80366748-80366957	HepG2	liver:	n/a	chr5:80366859-80366870 chr5:80366854-80366869 chr5:80366857-80366871
18	MAFK	chr5:80361829-80362305	HepG2	liver:	n/a	chr5:80362117-80362133 chr5:80362117-80362128 chr5:80362117-80362132
19	MAFK	chr5:80361840-80362286	HepG2	liver:	n/a	chr5:80362117-80362133 chr5:80362117-80362128 chr5:80362117-80362132
20	MAFK	chr5:80361944-80362313	IMR90	lung:	n/a	chr5:80362117-80362133 chr5:80362117-80362128 chr5:80362117-80362132
21	MAFK	chr5:80362046-80362257	H1-hESC	embryonic stem cell:	n/a	chr5:80362117-80362133 chr5:80362117-80362128 chr5:80362117-80362132
22	POLR2A	chr5:80368756-80368847	MCF10A-Er-Src	breast:	n/a	n/a
23	POLR2A	chr5:80362447-80362527	MCF10A-Er-Src	breast:	n/a	n/a
24	POLR2A	chr5:80365954-80365971	MCF-7	breast:	n/a	n/a
25	SMC3	chr5:80366885-80366937	HepG2	liver:	n/a	n/a
26	TEAD4	chr5:80364501-80364933	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:80362130-80362180	GM12892	blood:	n/a
2	chr5:80362130-80362180	AG04449	skin:	fetal
3	chr5:80362130-80362180	A549	lung:	n/a
4	chr5:80362130-80362180	Hepatocyte	liver:	n/a
5	chr5:80364036-80364086	NB4	blood:	n/a
6	chr5:80362130-80362180	SKMC	muscle:	n/a
7	chr5:80362130-80362180	HRE	kidney:	n/a
8	chr5:80364036-80364086	MCF-7	breast:	n/a
9	chr5:80364036-80364086	ProgFib	skin:	n/a
10	chr5:80362130-80362180	AG10803	skin:	n/a
11	chr5:80364036-80364086	NHBE	bronchial:	n/a
12	chr5:80362130-80362180	MCF10A-Er-Src	breast:	n/a
13	chr5:80362130-80362180	Jurkat	blood:	n/a
14	chr5:80362130-80362180	U87	brain:	n/a
15	chr5:80362130-80362180	HCT-116	colon:	n/a
16	chr5:80362130-80362180	HCM	heart:	n/a
17	chr5:80364036-80364086	AG09309	skin:	n/a
18	chr5:80362130-80362180	NH-A	brain:	n/a
19	chr5:80364036-80364086	AG04450	lung:	fetal
20	chr5:80362130-80362180	HIPEpiC	eye:	n/a
21	chr5:80364036-80364086	SK-N-MC	brain:	n/a
22	chr5:80362130-80362180	HCPEpiC	choroid plexus:	n/a
23	chr5:80364036-80364086	GM12892	blood:	n/a
24	chr5:80362130-80362180	K562	blood:	n/a
25	chr5:80364036-80364086	GM06990	blood:	n/a
26	chr5:80364036-80364086	PFSK-1	brain:	n/a
27	chr5:80364036-80364086	Hepatocyte	liver:	n/a
28	chr5:80362130-80362180	H1-hESC	embryonic stem cell:	embryo
29	chr5:80362130-80362180	SK-N-SH	brain:	n/a
30	chr5:80364036-80364086	BE2_C	brain:	n/a
31	chr5:80362130-80362180	AG09309	skin:	n/a
32	chr5:80362130-80362180	ECC-1	luminal epithelium:	n/a
33	chr5:80364036-80364086	MCF10A-Er-Src	breast:	n/a
34	chr5:80364036-80364086	SAEC	small airway:	n/a
35	chr5:80364036-80364086	HMEC	breast:	n/a
36	chr5:80362130-80362180	Caco-2	colon:	n/a
37	chr5:80364036-80364086	Jurkat	blood:	n/a
38	chr5:80364036-80364086	HIPEpiC	eye:	n/a
39	chr5:80364036-80364086	SKMC	muscle:	n/a
40	chr5:80362130-80362180	NHBE	bronchial:	n/a
41	chr5:80362130-80362180	AoSMC	blood vessel:	n/a
42	chr5:80364036-80364086	AG04449	skin:	fetal
43	chr5:80364036-80364086	HEEpiC	esophagus:	n/a
44	chr5:80362130-80362180	PrEC	prostate:	n/a
45	chr5:80362130-80362180	HL-60	blood:	n/a
46	chr5:80364036-80364086	RPTEC	kidney:	n/a
47	chr5:80362130-80362180	RPTEC	kidney:	n/a
48	chr5:80362130-80362180	PANC-1	pancreas:	n/a
49	chr5:80364036-80364086	GM12878	blood:	n/a
50	chr5:80362130-80362180	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:80359519..80361336-chr5:80366163..80368065,2	K562	blood:
2	chr5:80359519..80361336-chr5:80366163..80368065,2	K562	blood:

Variant related genes	Relation type
RASGRF2	TF binding region
RASGRF2	CpG island

Extended variants
information (count: 298 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:298 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538049359	chr5:80360478-80360479	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs72769292	chr5:80360495-80360496	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs574472017	chr5:80360511-80360512	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188138641	chr5:80360540-80360541	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545181905	chr5:80360578-80360579	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559927715	chr5:80360580-80360581	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs26899	chr5:80360612-80360613	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs192665273	chr5:80360616-80360617	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565126263	chr5:80360617-80360618	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551914577	chr5:80360619-80360620	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs77998540	chr5:80360644-80360645	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561019450	chr5:80360654-80360655	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530150075	chr5:80360680-80360681	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183709804	chr5:80360691-80360692	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs28736706	chr5:80360703-80360704	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs141987921	chr5:80360720-80360721	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs72635624	chr5:80360751-80360752	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs116282025	chr5:80360752-80360753	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146296058	chr5:80360757-80360758	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529777151	chr5:80360759-80360760	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538014258	chr5:80360781-80360782	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554819381	chr5:80360839-80360840	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574458664	chr5:80360858-80360859	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533679641	chr5:80360915-80360916	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs26900	chr5:80360921-80360922	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs115358021	chr5:80360923-80360924	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138244614	chr5:80360927-80360928	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149585737	chr5:80360959-80360960	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28625589	chr5:80361010-80361011	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs536223376	chr5:80361014-80361015	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544362622	chr5:80361035-80361036	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375503531	chr5:80361045-80361046	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs75225895	chr5:80361102-80361103	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368545893	chr5:80361106-80361107	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112815023	chr5:80361202-80361203	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530186002	chr5:80361213-80361214	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569258023	chr5:80361215-80361216	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs374809303	chr5:80361224-80361225	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560647087	chr5:80361266-80361267	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186720563	chr5:80361277-80361278	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs56129907	chr5:80361287-80361288	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538142047	chr5:80361300-80361301	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554700242	chr5:80361447-80361448	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs26901	chr5:80361462-80361463	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs148664581	chr5:80361488-80361489	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs548383344	chr5:80361505-80361506	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs55769439	chr5:80361518-80361519	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs568211641	chr5:80361589-80361590	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533879250	chr5:80361635-80361636	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372993894	chr5:80361649-80361650	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:80319600-80374200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr5:80337200-80368600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr5:80338200-80370600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:80338200-80376200	Weak transcription	NHLF	lung
5	chr5:80339200-80368600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr5:80339800-80374200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr5:80343200-80366000	Weak transcription	Adipose Nuclei	Adipose
8	chr5:80343200-80394400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr5:80344400-80368800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr5:80344800-80382600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr5:80346400-80364800	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr5:80346400-80365800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr5:80346600-80367000	Weak transcription	Brain Angular Gyrus	brain
14	chr5:80353600-80375400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr5:80354200-80382400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr5:80354400-80367800	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr5:80356200-80370400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr5:80356600-80374600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr5:80357800-80365800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr5:80359200-80361200	Strong transcription	HepG2	liver
21	chr5:80359800-80360800	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr5:80359800-80361400	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr5:80360000-80361400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
24	chr5:80360000-80361600	Enhancers	Brain Substantia Nigra	brain
25	chr5:80360000-80362600	Weak transcription	Left Ventricle	heart
26	chr5:80360200-80360600	Weak transcription	Primary T cells from cord blood	blood
27	chr5:80360200-80360800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr5:80360400-80360800	Enhancers	Colon Smooth Muscle	Colon
29	chr5:80360400-80361600	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr5:80360400-80364400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr5:80360600-80361000	Strong transcription	Primary T cells from cord blood	blood
32	chr5:80360600-80361800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr5:80360800-80361200	Weak transcription	Colon Smooth Muscle	Colon
34	chr5:80360800-80361400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr5:80360800-80361600	Enhancers	Brain Cingulate Gyrus	brain
36	chr5:80360800-80361600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr5:80360800-80361800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr5:80360800-80364000	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr5:80361000-80363800	Weak transcription	Primary T cells from cord blood	blood
40	chr5:80361200-80361600	Enhancers	Colon Smooth Muscle	Colon
41	chr5:80361200-80361600	Genic enhancers	HepG2	liver
42	chr5:80361400-80364000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr5:80361400-80374200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr5:80361400-80374600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr5:80361400-80374600	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr5:80361600-80362800	Strong transcription	Primary T helper cells PMA-I stimulated	--
47	chr5:80361600-80363800	Weak transcription	HepG2	liver
48	chr5:80361600-80374200	Weak transcription	Brain Cingulate Gyrus	brain
49	chr5:80361600-80374200	Weak transcription	Brain Substantia Nigra	brain
50	chr5:80361600-80374600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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