Variant report

Variant	nsv1010116
Chromosome Location	chr2:78399683-78660165
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	ARID3A	chr2:78532952-78532953	K562	blood:	n/a	n/a
2	ARID3A	chr2:78413821-78414186	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:78578391-78578636	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:78487915-78488675	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:78578413-78578720	K562	blood:	n/a	n/a
6	ARID3A	chr2:78643666-78644757	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:78653375-78653864	HepG2	liver:	n/a	n/a
8	ATF1	chr2:78408127-78408325	K562	blood:	n/a	n/a
9	BACH1	chr2:78477710-78477711	K562	blood:	n/a	n/a
10	BATF	chr2:78508305-78508535	GM12878	blood:	n/a	n/a
11	BATF	chr2:78508306-78508624	GM12878	blood:	n/a	n/a
12	BATF	chr2:78428253-78428380	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:78508311-78508495	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:78508455-78508636	GM12878	blood:	n/a	n/a
15	BHLHE40	chr2:78490807-78490864	GM12878	blood:	n/a	n/a
16	BHLHE40	chr2:78487986-78488343	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:78645132-78645485	ECC-1	luminal epithelium:	n/a	chr2:78645291-78645302
18	CEBPB	chr2:78589546-78589687	H1-hESC	embryonic stem cell:	n/a	chr2:78589637-78589648
19	CEBPB	chr2:78645108-78645536	Hela-S3	cervix:	n/a	chr2:78645291-78645302
20	CEBPB	chr2:78518569-78518898	K562	blood:	n/a	chr2:78518707-78518718
21	CEBPB	chr2:78445231-78445562	IMR90	lung:	n/a	chr2:78445380-78445391
22	CEBPB	chr2:78420652-78420781	K562	blood:	n/a	n/a
23	CEBPB	chr2:78577085-78577438	A549	lung:	n/a	chr2:78577256-78577265 chr2:78577254-78577265 chr2:78577256-78577267 chr2:78577256-78577265 chr2:78577256-78577265 chr2:78577256-78577265
24	CEBPB	chr2:78589510-78589810	Hela-S3	cervix:	n/a	chr2:78589637-78589648
25	CEBPB	chr2:78445211-78445551	A549	lung:	n/a	chr2:78445380-78445391
26	CEBPB	chr2:78590365-78590520	A549	lung:	n/a	n/a
27	CEBPB	chr2:78645169-78645536	ECC-1	luminal epithelium:	n/a	chr2:78645291-78645302
28	CEBPB	chr2:78445215-78445558	K562	blood:	n/a	chr2:78445380-78445391
29	CEBPB	chr2:78643741-78644061	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:78445242-78445505	Hela-S3	cervix:	n/a	chr2:78445380-78445391
31	CEBPB	chr2:78560444-78560597	HepG2	liver:	n/a	chr2:78560467-78560478
32	CEBPB	chr2:78633266-78633466	HepG2	liver:	n/a	chr2:78633403-78633416 chr2:78633404-78633415
33	CEBPB	chr2:78537183-78537401	K562	blood:	n/a	n/a
34	CEBPB	chr2:78420619-78420902	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:78420675-78420797	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr2:78400416-78400616	HepG2	liver:	n/a	chr2:78400485-78400496
37	CEBPB	chr2:78642053-78642249	K562	blood:	n/a	n/a
38	CEBPB	chr2:78518603-78518888	A549	lung:	n/a	chr2:78518707-78518718
39	CEBPB	chr2:78560369-78560622	A549	lung:	n/a	chr2:78560467-78560478
40	CEBPB	chr2:78531972-78532139	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr2:78640682-78640882	A549	lung:	n/a	chr2:78640779-78640790 chr2:78640781-78640790
42	CEBPB	chr2:78589457-78589745	A549	lung:	n/a	chr2:78589637-78589648
43	CEBPB	chr2:78577094-78577436	HepG2	liver:	n/a	chr2:78577256-78577265 chr2:78577254-78577265 chr2:78577256-78577267 chr2:78577256-78577265 chr2:78577256-78577265 chr2:78577256-78577265
44	CEBPB	chr2:78589467-78589821	K562	blood:	n/a	chr2:78589637-78589648
45	CEBPB	chr2:78641675-78642156	A549	lung:	n/a	chr2:78641752-78641763
46	CEBPB	chr2:78583349-78583384	K562	blood:	n/a	n/a
47	CEBPB	chr2:78580776-78580817	A549	lung:	n/a	n/a
48	CEBPB	chr2:78577077-78577375	IMR90	lung:	n/a	chr2:78577256-78577265 chr2:78577254-78577265 chr2:78577256-78577267 chr2:78577256-78577265 chr2:78577256-78577265 chr2:78577256-78577265
49	CEBPB	chr2:78606574-78606774	A549	lung:	n/a	n/a
50	CEBPB	chr2:78641606-78642279	HepG2	liver:	n/a	chr2:78641752-78641763

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:78545567-78545617	MCF-7	breast:	n/a
2	chr2:78545567-78545617	NB4	blood:	n/a
3	chr2:78545567-78545617	PrEC	prostate:	n/a
4	chr2:78545567-78545617	GM12892	blood:	n/a
5	chr2:78545567-78545617	Hepatocyte	liver:	n/a
6	chr2:78545567-78545617	Caco-2	colon:	n/a
7	chr2:78545567-78545617	AG04449	skin:	fetal
8	chr2:78545567-78545617	PANC-1	pancreas:	n/a
9	chr2:78545567-78545617	AG10803	skin:	n/a
10	chr2:78545567-78545617	HAEpiC	amniotic membrane:	n/a
11	chr2:78545567-78545617	HCM	heart:	n/a
12	chr2:78545567-78545617	HPAEpiC	pulmonary alveolar:	n/a
13	chr2:78545567-78545617	HUVEC	blood vessel:	n/a
14	chr2:78545567-78545617	Jurkat	blood:	n/a
15	chr2:78545567-78545617	Hela-S3	cervix:	n/a
16	chr2:78545567-78545617	AG09319	gingival:	n/a
17	chr2:78545567-78545617	ProgFib	skin:	n/a
18	chr2:78545567-78545617	BE2_C	brain:	n/a
19	chr2:78545567-78545617	GM06990	blood:	n/a
20	chr2:78545567-78545617	SK-N-MC	brain:	n/a
21	chr2:78545567-78545617	CMK	blood:	n/a
22	chr2:78545567-78545617	PFSK-1	brain:	n/a
23	chr2:78545567-78545617	NHBE	bronchial:	n/a
24	chr2:78545567-78545617	ECC-1	luminal epithelium:	n/a
25	chr2:78545567-78545617	HMEC	breast:	n/a
26	chr2:78545567-78545617	SK-N-SH_RA	brain:	n/a
27	chr2:78545567-78545617	HRCEpiC	kidney:	n/a
28	chr2:78545567-78545617	T-47D	breast:	n/a
29	chr2:78545567-78545617	SAEC	small airway:	n/a
30	chr2:78545567-78545617	HCPEpiC	choroid plexus:	n/a
31	chr2:78545567-78545617	ovcar-3	ovarian:	n/a
32	chr2:78545567-78545617	H1-hESC	embryonic stem cell:	embryo
33	chr2:78545567-78545617	HCT-116	colon:	n/a
34	chr2:78545567-78545617	GM12878	blood:	n/a
35	chr2:78545567-78545617	HIPEpiC	eye:	n/a
36	chr2:78545567-78545617	SK-N-SH	brain:	n/a
37	chr2:78545567-78545617	SKMC	muscle:	n/a
38	chr2:78545567-78545617	HNPCEpiC	eye:	n/a
39	chr2:78545567-78545617	K562	blood:	n/a
40	chr2:78545567-78545617	NH-A	brain:	n/a
41	chr2:78545567-78545617	AoSMC	blood vessel:	n/a
42	chr2:78545567-78545617	NT2-D1	testis:	n/a
43	chr2:78545567-78545617	AG04450	lung:	fetal
44	chr2:78545567-78545617	HEK293	kidney:	embryo
45	chr2:78545567-78545617	BJ	skin:	n/a
46	chr2:78545567-78545617	HRE	kidney:	n/a
47	chr2:78545567-78545617	HEEpiC	esophagus:	n/a
48	chr2:78545567-78545617	NHDF-neo	bronchial:	n/a
49	chr2:78545567-78545617	U87	brain:	n/a
50	chr2:78545567-78545617	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:78538765..78541253-chr2:78550718..78553114,2	K562	blood:
2	chr2:78578454..78579130-chr2:79226516..79227199,2	MCF-7	breast:
3	chr2:78578903..78584135-chr2:78585848..78590226,6	K562	blood:
4	chr2:78519747..78522682-chr2:78785137..78786876,2	K562	blood:
5	chr2:78658362..78658925-chr2:79089675..79090181,2	MCF-7	breast:
6	chr2:78658404..78659062-chr2:79206498..79207224,3	MCF-7	breast:
7	chr2:78637554..78639977-chr2:78766787..78768860,2	K562	blood:
8	chr2:78552005..78554249-chr2:78556086..78558009,2	K562	blood:
9	chr2:78607954..78609567-chr2:78764622..78766807,2	K562	blood:
10	chr2:78577613..78578539-chr2:79206466..79207847,3	MCF-7	breast:
11	chr2:78577011..78577791-chr8:96157456..96158424,2	MCF-7	breast:
12	chr2:78578903..78584135-chr2:78585848..78590226,6	K562	blood:
13	chr2:78552005..78554249-chr2:78556086..78558009,2	K562	blood:
14	chr2:78578299..78578916-chr2:79206809..79207351,2	MCF-7	breast:
15	chr2:78538765..78541253-chr2:78550718..78553114,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRTM4-3	chr2:78639919-78640220	NONHSAT071847
2	lnc-LRRTM4-3	chr2:78517514-78517857	NR_110288
3	lnc-LRRTM4-3	chr2:78637204-78640302	NONHSAT071835
4	lnc-LRRTM4-3	chr2:78639673-78640302	NONHSAT071846

Variant related genes	Relation type
CYCSP6	TF binding region
ENSG00000270470	TF binding region
CYCSP6	CpG island
ENSG00000270470	CpG island

Extended variants
information (count: 4856 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:4856 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539294985	chr2:78402625-78402626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs7568442	chr2:78402637-78402638	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs573266408	chr2:78402679-78402680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542162105	chr2:78402710-78402711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs116307924	chr2:78402842-78402843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575977561	chr2:78402937-78402938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552604089	chr2:78402941-78402942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7581193	chr2:78402942-78402943	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs564801590	chr2:78402961-78402962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555483930	chr2:78402989-78402990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533564937	chr2:78403013-78403014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540477848	chr2:78403014-78403015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559349960	chr2:78403023-78403024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528194147	chr2:78403052-78403053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76086421	chr2:78403061-78403062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs181323158	chr2:78403101-78403102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs149275798	chr2:78403137-78403138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530450995	chr2:78403152-78403153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550458694	chr2:78403182-78403183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573717574	chr2:78403184-78403185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs143490567	chr2:78403197-78403198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539206373	chr2:78403204-78403205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528723692	chr2:78403239-78403240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115138262	chr2:78403264-78403265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76149684	chr2:78403265-78403266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555866242	chr2:78403291-78403292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs77471151	chr2:78403318-78403319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544667186	chr2:78403447-78403448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116167398	chr2:78403463-78403464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs578250225	chr2:78403470-78403471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375255700	chr2:78403540-78403541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540790261	chr2:78403552-78403553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560533908	chr2:78403664-78403665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554127960	chr2:78403669-78403670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529523629	chr2:78403722-78403723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6706359	chr2:78403733-78403734	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs72819056	chr2:78403750-78403751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201051992	chr2:78403828-78403829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs199497901	chr2:78403837-78403838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375263095	chr2:78403897-78403898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550170392	chr2:78403930-78403931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570367307	chr2:78403979-78403980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74752102	chr2:78403999-78404000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546740833	chr2:78404001-78404002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190235295	chr2:78404050-78404051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561897502	chr2:78404145-78404146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535669661	chr2:78404193-78404194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114024484	chr2:78404196-78404197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs58843972	chr2:78404209-78404210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569417136	chr2:78404222-78404223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:272 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:78402600-78403400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:78402800-78403200	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr2:78402800-78403200	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr2:78403200-78408200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr2:78405000-78405200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:78408000-78408600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr2:78408000-78408600	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr2:78408200-78408600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr2:78408200-78408600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr2:78408200-78408600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr2:78408200-78408600	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr2:78413600-78414600	Enhancers	HepG2	liver
13	chr2:78414600-78418600	Weak transcription	HepG2	liver
14	chr2:78418600-78418800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr2:78418600-78419000	Enhancers	HepG2	liver
16	chr2:78418800-78428000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr2:78419000-78432400	Weak transcription	HepG2	liver
18	chr2:78428000-78431200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr2:78428200-78428600	Active TSS	Brain Anterior Caudate	brain
20	chr2:78428400-78428800	Active TSS	Brain Angular Gyrus	brain
21	chr2:78428400-78428800	Active TSS	Brain Cingulate Gyrus	brain
22	chr2:78428400-78428800	Active TSS	Brain Inferior Temporal Lobe	brain
23	chr2:78428400-78428800	Active TSS	Brain Substantia Nigra	brain
24	chr2:78428400-78430000	Active TSS	Brain Hippocampus Middle	brain
25	chr2:78428800-78429600	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr2:78428800-78429600	Weak transcription	Brain Substantia Nigra	brain
27	chr2:78428800-78430400	Weak transcription	Brain Cingulate Gyrus	brain
28	chr2:78429600-78430000	Active TSS	Brain Inferior Temporal Lobe	brain
29	chr2:78429600-78430000	Active TSS	Brain Substantia Nigra	brain
30	chr2:78430000-78430400	Flanking Active TSS	Brain Hippocampus Middle	brain
31	chr2:78430000-78430600	Weak transcription	Brain Substantia Nigra	brain
32	chr2:78430200-78430800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr2:78430400-78430800	Enhancers	Brain Cingulate Gyrus	brain
34	chr2:78430400-78430800	Enhancers	Brain Hippocampus Middle	brain
35	chr2:78430600-78430800	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr2:78430600-78431200	Enhancers	Brain Substantia Nigra	brain
37	chr2:78445400-78445800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr2:78445600-78446200	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr2:78445800-78446200	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr2:78447400-78448200	Enhancers	Brain Hippocampus Middle	brain
41	chr2:78447600-78448400	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr2:78448200-78453200	Weak transcription	Brain Hippocampus Middle	brain
43	chr2:78448400-78448800	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr2:78448800-78449400	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr2:78453200-78454000	ZNF genes & repeats	Brain Hippocampus Middle	brain
46	chr2:78454000-78454400	Weak transcription	Brain Hippocampus Middle	brain
47	chr2:78459800-78472400	Weak transcription	HepG2	liver
48	chr2:78460800-78462000	Enhancers	Brain Substantia Nigra	brain
49	chr2:78467000-78467200	Enhancers	Brain Hippocampus Middle	brain
50	chr2:78467000-78468000	Weak transcription	Brain Substantia Nigra	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links