Variant report

Variant	nsv592207
Chromosome Location	chr3:162310379-162391801
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	ATF1	chr3:162387319-162387469	K562	blood:	n/a	n/a
2	BRCA1	chr3:162343607-162343624	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr3:162375910-162376151	ECC-1	luminal epithelium:	n/a	chr3:162375998-162376009 chr3:162375998-162376011 chr3:162375960-162375971 chr3:162375999-162376010 chr3:162375998-162376011 chr3:162375998-162376009
4	CEBPB	chr3:162375820-162376163	HepG2	liver:	n/a	chr3:162375998-162376009 chr3:162375998-162376011 chr3:162375960-162375971 chr3:162375999-162376010 chr3:162375998-162376011 chr3:162375998-162376009
5	CEBPB	chr3:162375840-162376163	A549	lung:	n/a	chr3:162375998-162376009 chr3:162375998-162376011 chr3:162375960-162375971 chr3:162375999-162376010 chr3:162375998-162376011 chr3:162375998-162376009
6	CEBPB	chr3:162328054-162328397	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr3:162375773-162376159	MCF-7	breast:	n/a	chr3:162375998-162376009 chr3:162375998-162376011 chr3:162375960-162375971 chr3:162375999-162376010 chr3:162375998-162376011 chr3:162375998-162376009
8	CEBPB	chr3:162363990-162364207	A549	lung:	n/a	chr3:162364112-162364123 chr3:162364019-162364030
9	CEBPB	chr3:162318673-162319181	HepG2	liver:	n/a	chr3:162318771-162318782 chr3:162318770-162318783 chr3:162318770-162318783 chr3:162318770-162318781 chr3:162318772-162318781
10	CEBPB	chr3:162318597-162318906	IMR90	lung:	n/a	chr3:162318771-162318782 chr3:162318770-162318783 chr3:162318770-162318783 chr3:162318770-162318781 chr3:162318772-162318781
11	CEBPB	chr3:162318973-162319104	HepG2	liver:	n/a	n/a
12	CEBPB	chr3:162375834-162376167	IMR90	lung:	n/a	chr3:162375998-162376009 chr3:162375998-162376011 chr3:162375960-162375971 chr3:162375999-162376010 chr3:162375998-162376011 chr3:162375998-162376009
13	CEBPB	chr3:162364026-162364261	Hela-S3	cervix:	n/a	chr3:162364112-162364123
14	CEBPB	chr3:162375783-162376266	MCF-7	breast:	n/a	chr3:162375998-162376009 chr3:162375998-162376011 chr3:162375960-162375971 chr3:162375999-162376010 chr3:162375998-162376011 chr3:162375998-162376009
15	CEBPB	chr3:162363967-162364264	HepG2	liver:	n/a	chr3:162364112-162364123 chr3:162364019-162364030
16	CEBPB	chr3:162323772-162323878	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr3:162375805-162376171	Hela-S3	cervix:	n/a	chr3:162375998-162376009 chr3:162375998-162376011 chr3:162375960-162375971 chr3:162375999-162376010 chr3:162375998-162376011 chr3:162375998-162376009
18	CTCF	chr3:162383040-162383190	GM12872	blood:	n/a	n/a
19	CTCF	chr3:162383140-162383290	HCT-116	colon:	n/a	n/a
20	CTCF	chr3:162383174-162383196	HepG2	liver:	n/a	n/a
21	CTCF	chr3:162361320-162361351	GM13976	blood:	n/a	n/a
22	CTCF	chr3:162383160-162383310	HEK293	kidney:	n/a	n/a
23	CTCF	chr3:162383138-162383251	MCF-7	breast:	n/a	n/a
24	CTCF	chr3:162314580-162314730	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr3:162383060-162383210	HRE	kidney:	n/a	n/a
26	CTCF	chr3:162383180-162383330	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr3:162377841-162377879	MCF-7	breast:	n/a	n/a
28	CTCF	chr3:162383100-162383250	HRE	kidney:	n/a	n/a
29	CTCF	chr3:162361763-162361785	MCF-7	breast:	n/a	n/a
30	CTCF	chr3:162383160-162383310	GM12871	blood:	n/a	n/a
31	CTCF	chr3:162383040-162383190	A549	lung:	n/a	n/a
32	CTCF	chr3:162383060-162383210	BE2_C	brain:	n/a	n/a
33	CTCF	chr3:162383175-162383238	MCF-7	breast:	n/a	n/a
34	CTCF	chr3:162383116-162383273	HepG2	liver:	n/a	n/a
35	CTCF	chr3:162383140-162383290	BE2_C	brain:	n/a	n/a
36	CTCF	chr3:162383149-162383254	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr3:162383100-162383250	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr3:162377836-162377844	MCF-7	breast:	n/a	n/a
39	CTCF	chr3:162338003-162338037	GM20000	blood:	n/a	n/a
40	CTCF	chr3:162357965-162358027	GM20000	blood:	n/a	n/a
41	CTCF	chr3:162383143-162383258	A549	lung:	n/a	n/a
42	CTCF	chr3:162383200-162383350	HMF	breast:	n/a	n/a
43	CTCF	chr3:162383059-162383215	GM12878	blood:	n/a	n/a
44	CTCF	chr3:162383120-162383270	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr3:162323516-162323574	GM10248	blood:	n/a	n/a
46	CTCF	chr3:162361738-162361757	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:162323510-162323512	GM10248	blood:	n/a	n/a
48	CTCF	chr3:162383167-162383228	MCF-7	breast:	n/a	n/a
49	CUX1	chr3:162317068-162317249	GM12878	blood:	n/a	n/a
50	E2F6	chr3:162382963-162383353	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:162317560-162317610	Caco-2	colon:	n/a
2	chr3:162317560-162317610	IMR90	lung:	fetal
3	chr3:162317560-162317610	HCM	heart:	n/a
4	chr3:162317560-162317610	HEEpiC	esophagus:	n/a
5	chr3:162317560-162317610	PFSK-1	brain:	n/a
6	chr3:162317560-162317610	A549	lung:	n/a
7	chr3:162317560-162317610	Jurkat	blood:	n/a
8	chr3:162317560-162317610	H1-hESC	embryonic stem cell:	embryo
9	chr3:162317560-162317610	HNPCEpiC	eye:	n/a
10	chr3:162317560-162317610	GM12878	blood:	n/a
11	chr3:162317560-162317610	GM19239	blood:	n/a
12	chr3:162317560-162317610	NB4	blood:	n/a
13	chr3:162317560-162317610	HCF	heart:	n/a
14	chr3:162317560-162317610	MCF10A-Er-Src	breast:	n/a
15	chr3:162317560-162317610	AG09309	skin:	n/a
16	chr3:162317560-162317610	SK-N-SH	brain:	n/a
17	chr3:162317560-162317610	NHDF-neo	bronchial:	n/a
18	chr3:162317560-162317610	HRPEpiC	eye:	n/a
19	chr3:162317560-162317610	HEK293	kidney:	embryo
20	chr3:162317560-162317610	AG04449	skin:	fetal
21	chr3:162317560-162317610	SK-N-MC	brain:	n/a
22	chr3:162317560-162317610	Hepatocyte	liver:	n/a
23	chr3:162317560-162317610	HepG2	liver:	n/a
24	chr3:162317560-162317610	GM12891	blood:	n/a
25	chr3:162317560-162317610	AG10803	skin:	n/a
26	chr3:162317560-162317610	ovcar-3	ovarian:	n/a
27	chr3:162317560-162317610	HAEpiC	amniotic membrane:	n/a
28	chr3:162317560-162317610	NT2-D1	testis:	n/a
29	chr3:162317560-162317610	HL-60	blood:	n/a
30	chr3:162317560-162317610	HCPEpiC	choroid plexus:	n/a
31	chr3:162317560-162317610	GM06990	blood:	n/a
32	chr3:162317560-162317610	SK-N-SH_RA	brain:	n/a
33	chr3:162317560-162317610	U87	brain:	n/a
34	chr3:162317560-162317610	CMK	blood:	n/a
35	chr3:162317560-162317610	PrEC	prostate:	n/a
36	chr3:162317560-162317610	MCF-7	breast:	n/a
37	chr3:162317560-162317610	SAEC	small airway:	n/a
38	chr3:162317560-162317610	LNCaP	prostate:	n/a
39	chr3:162317560-162317610	PANC-1	pancreas:	n/a
40	chr3:162317560-162317610	T-47D	breast:	n/a
41	chr3:162317560-162317610	AG09319	gingival:	n/a
42	chr3:162317560-162317610	SKMC	muscle:	n/a
43	chr3:162317560-162317610	NH-A	brain:	n/a
44	chr3:162317560-162317610	GM12892	blood:	n/a
45	chr3:162317560-162317610	HUVEC	blood vessel:	n/a
46	chr3:162317560-162317610	BJ	skin:	n/a
47	chr3:162317560-162317610	HMEC	breast:	n/a
48	chr3:162317560-162317610	Hela-S3	cervix:	n/a
49	chr3:162317560-162317610	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:162317560-162317610	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:162367684..162370185-chr3:162370811..162372665,2	MCF-7	breast:
2	chr3:162367684..162370185-chr3:162370811..162372665,2	MCF-7	breast:
3	chr3:162307801..162310469-chr3:162314134..162316904,3	MCF-7	breast:
4	chr3:162307801..162310469-chr3:162314134..162316904,3	MCF-7	breast:
5	chr3:162268890..162270552-chr3:162314764..162316650,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000243044	TF binding region
ENSG00000243044	CpG island

Extended variants
information (count: 2382 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2382 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9290128	chr3:162310379-162310380	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566606039	chr3:162310412-162310413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186448323	chr3:162310433-162310434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554461335	chr3:162310482-162310483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574624696	chr3:162310521-162310522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs9290129	chr3:162310571-162310572	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs558864132	chr3:162310786-162310787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs9860466	chr3:162310848-162310849	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs9822369	chr3:162310862-162310863	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs189735069	chr3:162310867-162310868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144981118	chr3:162310870-162310871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572835457	chr3:162310874-162310875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs59391629	chr3:162310893-162310894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs61045464	chr3:162310986-162310987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562948260	chr3:162310998-162310999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79583016	chr3:162311032-162311033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182630839	chr3:162311041-162311042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542771318	chr3:162311072-162311073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376513267	chr3:162311079-162311080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550771397	chr3:162311134-162311135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182894957	chr3:162311236-162311237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373462686	chr3:162311238-162311239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs397793840	chr3:162311246-162311247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533465700	chr3:162311247-162311248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs9823059	chr3:162311248-162311249	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs566898927	chr3:162311316-162311317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535575027	chr3:162311347-162311348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549411233	chr3:162311360-162311361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79489357	chr3:162311395-162311396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537218270	chr3:162311418-162311419	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557216552	chr3:162311447-162311448	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs188196441	chr3:162311466-162311467	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs721762	chr3:162311498-162311499	Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs192763799	chr3:162311500-162311501	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552993261	chr3:162311547-162311548	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531717713	chr3:162311564-162311565	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572839333	chr3:162311612-162311613	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183665337	chr3:162311650-162311651	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549910009	chr3:162311687-162311688	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541464540	chr3:162311727-162311728	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187514555	chr3:162311734-162311735	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561781638	chr3:162311780-162311781	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs562942999	chr3:162311811-162311812	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs557331178	chr3:162311842-162311843	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs149080923	chr3:162311853-162311854	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs17757426	chr3:162311903-162311904	Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs192134620	chr3:162311911-162311912	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs113872402	chr3:162311941-162311942	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs547741999	chr3:162311942-162311943	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565665067	chr3:162311958-162311959	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Sudden cardiac death	19188705	CNVD
Mantle cell lymphoma	19029149	CNVD
Malformation	19546859	CNVD
Schizophrenia	19546859	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:160 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:162308800-162310400	Enhancers	Dnd41	blood
2	chr3:162310400-162311400	Weak transcription	Dnd41	blood
3	chr3:162311400-162312800	Genic enhancers	Dnd41	blood
4	chr3:162312800-162314400	Enhancers	Dnd41	blood
5	chr3:162313800-162317200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr3:162314200-162316400	Enhancers	Brain Substantia Nigra	brain
7	chr3:162314200-162317200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr3:162314400-162315200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr3:162314400-162315800	Flanking Active TSS	Dnd41	blood
10	chr3:162314400-162316400	Enhancers	Brain Hippocampus Middle	brain
11	chr3:162314400-162318800	Weak transcription	HSMM	muscle
12	chr3:162314800-162315200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr3:162314800-162315600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr3:162314800-162315600	Enhancers	Brain Angular Gyrus	brain
15	chr3:162314800-162316200	Enhancers	Brain Cingulate Gyrus	brain
16	chr3:162314800-162316600	Enhancers	Brain Anterior Caudate	brain
17	chr3:162314800-162316800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr3:162315000-162315200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:162315000-162315600	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr3:162315000-162315800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr3:162315000-162315800	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr3:162315000-162316200	Enhancers	GM12878-XiMat	blood
23	chr3:162315200-162315600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:162315200-162316000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr3:162315200-162316000	Enhancers	Brain Germinal Matrix	brain
26	chr3:162315200-162316600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:162315600-162316000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr3:162315600-162317400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr3:162315800-162316200	Enhancers	Dnd41	blood
30	chr3:162316000-162316200	Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr3:162316000-162316400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr3:162316200-162316400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr3:162316200-162316400	Flanking Active TSS	GM12878-XiMat	blood
34	chr3:162316200-162316800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr3:162316200-162316800	Enhancers	Fetal Muscle Leg	muscle
36	chr3:162316200-162317000	Enhancers	Fetal Heart	heart
37	chr3:162316200-162317400	Flanking Active TSS	Dnd41	blood
38	chr3:162316400-162317000	Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr3:162316400-162317000	Active TSS	GM12878-XiMat	blood
40	chr3:162316600-162317000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:162317000-162317200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr3:162317000-162317200	Enhancers	GM12878-XiMat	blood
43	chr3:162317000-162318400	Weak transcription	Fetal Heart	heart
44	chr3:162317400-162317600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr3:162317400-162318000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
46	chr3:162317400-162318200	Transcr. at gene 5' and 3'	Dnd41	blood
47	chr3:162317600-162319000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr3:162317800-162332400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr3:162318000-162323800	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr3:162318200-162318400	Flanking Active TSS	Dnd41	blood

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