Variant report

Variant	nsv437338
Chromosome Location	chr3:116076289-116110635
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	CHD2	chr3:116086850-116087132	GM12878	blood:	n/a	n/a
2	CTCF	chr3:116084851-116084891	Kidney_OC	kidney:	n/a	n/a
3	CTCF	chr3:116105081-116105411	GM12878	blood:	n/a	n/a
4	CTCF	chr3:116086968-116087199	GM12878	blood:	n/a	n/a
5	CTCF	chr3:116105194-116105292	K562	blood:	n/a	n/a
6	CTCF	chr3:116105120-116105270	GM12865	blood:	n/a	n/a
7	CTCF	chr3:116105128-116105292	K562	blood:	n/a	n/a
8	CTCF	chr3:116087000-116087150	GM12873	blood:	n/a	n/a
9	CTCF	chr3:116105160-116105310	GM06990	blood:	n/a	n/a
10	CTCF	chr3:116086960-116087110	MCF-7	breast:	n/a	n/a
11	CTCF	chr3:116105208-116105268	GM12878	blood:	n/a	n/a
12	E2F4	chr3:116092825-116093012	MCF10A-Er-Src	breast:	n/a	n/a
13	EP300	chr3:116086819-116087072	GM12878	blood:	n/a	n/a
14	FOXA2	chr3:116079181-116079422	A549	lung:	n/a	n/a
15	FOXA2	chr3:116079017-116079667	A549	lung:	n/a	n/a
16	GATA3	chr3:116104285-116104440	SH-SY5Y	brain:	n/a	n/a
17	GATA3	chr3:116099350-116099395	SH-SY5Y	brain:	n/a	n/a
18	GATA3	chr3:116092447-116092527	SH-SY5Y	brain:	n/a	n/a
19	GTF2F1	chr3:116091473-116091478	H1-hESC	embryonic stem cell:	n/a	n/a
20	JUN	chr3:116109239-116109415	H1-hESC	embryonic stem cell:	n/a	n/a
21	JUND	chr3:116109212-116109412	H1-hESC	embryonic stem cell:	n/a	n/a
22	MAFF	chr3:116077457-116077716	HepG2	liver:	n/a	chr3:116077550-116077568
23	MAFF	chr3:116093921-116094121	HepG2	liver:	n/a	chr3:116094018-116094036
24	MAFK	chr3:116077388-116077741	HepG2	liver:	n/a	chr3:116077551-116077565 chr3:116077552-116077568 chr3:116077553-116077564 chr3:116077552-116077567 chr3:116077552-116077563 chr3:116077553-116077564 chr3:116077552-116077563
25	MAFK	chr3:116077475-116077699	HepG2	liver:	n/a	chr3:116077551-116077565 chr3:116077552-116077568 chr3:116077553-116077564 chr3:116077552-116077567 chr3:116077552-116077563 chr3:116077553-116077564 chr3:116077552-116077563
26	MAFK	chr3:116093901-116094140	IMR90	lung:	n/a	chr3:116094020-116094035 chr3:116094019-116094033 chr3:116094020-116094031 chr3:116094021-116094032 chr3:116094020-116094031 chr3:116094020-116094036
27	MAFK	chr3:116093941-116094089	HepG2	liver:	n/a	chr3:116094020-116094035 chr3:116094019-116094033 chr3:116094020-116094031 chr3:116094021-116094032 chr3:116094020-116094031 chr3:116094020-116094036
28	MAFK	chr3:116093910-116094146	HepG2	liver:	n/a	chr3:116094020-116094035 chr3:116094019-116094033 chr3:116094020-116094031 chr3:116094021-116094032 chr3:116094020-116094031 chr3:116094020-116094036
29	MAFK	chr3:116077412-116077697	IMR90	lung:	n/a	chr3:116077551-116077565 chr3:116077552-116077568 chr3:116077553-116077564 chr3:116077552-116077567 chr3:116077552-116077563 chr3:116077553-116077564 chr3:116077552-116077563
30	MAFK	chr3:116077372-116077547	H1-hESC	embryonic stem cell:	n/a	n/a
31	MAX	chr3:116107726-116107867	H1-hESC	embryonic stem cell:	n/a	n/a
32	MXI1	chr3:116099752-116099808	GM12878	blood:	n/a	n/a
33	MYC	chr3:116110516-116110601	H1-hESC	embryonic stem cell:	n/a	n/a
34	NANOG	chr3:116109215-116109418	H1-hESC	embryonic stem cell:	n/a	n/a
35	NFIC	chr3:116106279-116106780	GM12878	blood:	n/a	n/a
36	NFYA	chr3:116098662-116098840	GM12878	blood:	n/a	n/a
37	POLR2A	chr3:116089479-116089649	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr3:116097576-116097650	GM12878	blood:	n/a	n/a
39	POLR2A	chr3:116096619-116096795	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr3:116094070-116094270	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr3:116086844-116086845	MCF10A-Er-Src	breast:	n/a	n/a
42	RAD21	chr3:116086897-116087162	H1-hESC	embryonic stem cell:	n/a	n/a
43	RAD21	chr3:116104976-116105375	H1-hESC	embryonic stem cell:	n/a	n/a
44	RAD21	chr3:116105092-116105300	H1-hESC	embryonic stem cell:	n/a	n/a
45	RAD21	chr3:116105117-116105313	GM12878	blood:	n/a	n/a
46	RAD21	chr3:116086925-116087175	H1-hESC	embryonic stem cell:	n/a	n/a
47	RCOR1	chr3:116093772-116093856	GM12878	blood:	n/a	n/a
48	RUNX3	chr3:116086745-116087034	GM12878	blood:	n/a	chr3:116086903-116086920
49	RUNX3	chr3:116096807-116097191	GM12878	blood:	n/a	n/a
50	RUNX3	chr3:116106374-116106654	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:116108178-116108228	T-47D	breast:	n/a
2	chr3:116108178-116108228	T-47D	breast:	n/a
3	chr3:116079127-116079177	AG04449	skin:	fetal
4	chr3:116079112-116079162	AG09309	skin:	n/a
5	chr3:116079127-116079177	NB4	blood:	n/a
6	chr3:116108178-116108228	AoSMC	blood vessel:	n/a
7	chr3:116079127-116079177	AG04450	lung:	fetal
8	chr3:116079112-116079162	PFSK-1	brain:	n/a
9	chr3:116079112-116079162	U87	brain:	n/a
10	chr3:116079127-116079177	HL-60	blood:	n/a
11	chr3:116079112-116079162	GM12891	blood:	n/a
12	chr3:116108178-116108228	NB4	blood:	n/a
13	chr3:116079112-116079162	H1-hESC	embryonic stem cell:	embryo
14	chr3:116079127-116079177	LNCaP	prostate:	n/a
15	chr3:116079127-116079177	AG10803	skin:	n/a
16	chr3:116079112-116079162	NT2-D1	testis:	n/a
17	chr3:116079112-116079162	HCM	heart:	n/a
18	chr3:116108178-116108228	HRCEpiC	kidney:	n/a
19	chr3:116108178-116108228	AG04449	skin:	fetal
20	chr3:116079112-116079162	AG10803	skin:	n/a
21	chr3:116079112-116079162	NHDF-neo	bronchial:	n/a
22	chr3:116108178-116108228	SAEC	small airway:	n/a
23	chr3:116079127-116079177	Hela-S3	cervix:	n/a
24	chr3:116079112-116079162	GM06990	blood:	n/a
25	chr3:116079112-116079162	Hepatocyte	liver:	n/a
26	chr3:116079127-116079177	H1-hESC	embryonic stem cell:	embryo
27	chr3:116079112-116079162	K562	blood:	n/a
28	chr3:116079112-116079162	SK-N-MC	brain:	n/a
29	chr3:116108178-116108228	GM06990	blood:	n/a
30	chr3:116079127-116079177	BE2_C	brain:	n/a
31	chr3:116079112-116079162	Caco-2	colon:	n/a
32	chr3:116108178-116108228	GM19239	blood:	n/a
33	chr3:116108178-116108228	GM12891	blood:	n/a
34	chr3:116079112-116079162	IMR90	lung:	fetal
35	chr3:116079112-116079162	NH-A	brain:	n/a
36	chr3:116079127-116079177	RPTEC	kidney:	n/a
37	chr3:116079127-116079177	ECC-1	luminal epithelium:	n/a
38	chr3:116079112-116079162	GM12892	blood:	n/a
39	chr3:116079112-116079162	HEEpiC	esophagus:	n/a
40	chr3:116079127-116079177	HRCEpiC	kidney:	n/a
41	chr3:116079127-116079177	HCF	heart:	n/a
42	chr3:116108178-116108228	Caco-2	colon:	n/a
43	chr3:116079127-116079177	Caco-2	colon:	n/a
44	chr3:116079127-116079177	HepG2	liver:	n/a
45	chr3:116108178-116108228	HepG2	liver:	n/a
46	chr3:116079127-116079177	HMEC	breast:	n/a
47	chr3:116079127-116079177	HCM	heart:	n/a
48	chr3:116079127-116079177	SK-N-SH_RA	brain:	n/a
49	chr3:116079112-116079162	HCT-116	colon:	n/a
50	chr3:116079127-116079177	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:115858694..115859203-chr3:116105156..116105712,2	MCF-7	breast:
2	chr3:116068430..116070631-chr3:116074599..116076825,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GAP43-4	chr3:116086789-116086882	NR_109998
2	lnc-GAP43-4	chr3:116088678-116088937	ENSG00000240922.1
3	lnc-GAP43-4	chr3:116078871-116078940	NR_109998
4	lnc-GAP43-4	chr3:116086990-116087118	ENSG00000240922.1
5	lnc-GAP43-15	chr3:116094581-116094795	uc_122_+
6	lnc-GAP43-4	chr3:116088678-116088932	NR_109998
7	lnc-GAP43-4	chr3:116086789-116086882	ENSG00000240922.1
8	lnc-GAP43-4	chr3:116078871-116078940	ENSG00000240922.1
9	lnc-GAP43-4	chr3:116086990-116087118	NR_109998
10	lnc-ZBTB20-6	chr3:116094581-116094795	uc_122_-

Variant related genes	Relation type
LSAMP-AS1	TF binding region
LSAMP-AS1	CpG island

Extended variants
information (count: 935 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:935 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375834258	chr3:116076450-116076451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563958130	chr3:116076459-116076460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531165895	chr3:116076477-116076478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549308518	chr3:116076489-116076490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78070974	chr3:116076492-116076493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12488477	chr3:116076496-116076497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143737277	chr3:116076512-116076513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs546592887	chr3:116076515-116076516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs76741326	chr3:116076524-116076525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs367656796	chr3:116076574-116076575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538631647	chr3:116076593-116076594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs114796184	chr3:116076602-116076603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs569847987	chr3:116076608-116076609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537289367	chr3:116076627-116076628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374368960	chr3:116076641-116076642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142602368	chr3:116076642-116076643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs116584066	chr3:116076675-116076676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567036939	chr3:116076701-116076702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs80294375	chr3:116076764-116076765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79411508	chr3:116076765-116076766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs201324262	chr3:116076772-116076773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs146405574	chr3:116076780-116076781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs77833751	chr3:116076794-116076795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537741289	chr3:116076839-116076840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73149192	chr3:116076845-116076846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs141487532	chr3:116076852-116076853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs369148478	chr3:116076861-116076862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150849485	chr3:116076881-116076882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138617092	chr3:116076954-116076955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs199866909	chr3:116076960-116076961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs190300107	chr3:116076961-116076962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577948546	chr3:116077009-116077010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376083281	chr3:116077013-116077014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540360207	chr3:116077021-116077022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113158585	chr3:116077061-116077062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs533962789	chr3:116077119-116077120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565016177	chr3:116077176-116077177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs34642483	chr3:116077197-116077198	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs149298666	chr3:116077231-116077232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569940162	chr3:116077257-116077258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144526554	chr3:116077280-116077281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs111787923	chr3:116077308-116077309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549180423	chr3:116077375-116077376	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs139428474	chr3:116077388-116077389	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs116474113	chr3:116077418-116077419	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs553134538	chr3:116077424-116077425	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs571364998	chr3:116077465-116077466	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs543195823	chr3:116077467-116077468	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs142639436	chr3:116077468-116077469	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs375153234	chr3:116077472-116077473	Weak transcription Enhancers	TF binding region	1 gene(s)	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
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Ovarian cancer	22174824	CNVD
Myelofibrosis	22110671	CNVD
Characteristic facial feature	22180640	CNVD
hypoplastic male genitals	22180640	CNVD
postnatal overgrowth	22180640	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:116076400-116077200	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr3:116076600-116077400	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr3:116076800-116077200	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr3:116076800-116077200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr3:116076800-116077200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr3:116076800-116077200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr3:116076800-116077400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr3:116076800-116077400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr3:116076800-116077600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr3:116076800-116077600	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr3:116077200-116077400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr3:116077200-116078200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr3:116077200-116078400	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr3:116077400-116079600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr3:116077600-116078000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr3:116078000-116078600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr3:116078200-116078400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr3:116078400-116078800	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr3:116078400-116079400	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr3:116078400-116079400	Active TSS	HUES6 Cell Line	embryonic stem cell
21	chr3:116078600-116079400	Active TSS	iPS-15b Cell Line	embryonic stem cell
22	chr3:116078800-116079400	Active TSS	H9 Cell Line	embryonic stem cell
23	chr3:116085000-116085600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:116086800-116087200	Active TSS	Pancreatic Islets	Pancreatic Islet
25	chr3:116087000-116087200	Enhancers	Brain Anterior Caudate	brain
26	chr3:116087200-116088000	Weak transcription	Brain Anterior Caudate	brain
27	chr3:116087400-116088800	Enhancers	Colon Smooth Muscle	Colon
28	chr3:116087800-116088400	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr3:116088000-116088200	Enhancers	Brain Anterior Caudate	brain
30	chr3:116088000-116088400	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr3:116088200-116088800	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr3:116088200-116089000	Weak transcription	Brain Anterior Caudate	brain
33	chr3:116088600-116089600	Enhancers	Brain Hippocampus Middle	brain
34	chr3:116088800-116093400	Weak transcription	Colon Smooth Muscle	Colon
35	chr3:116089000-116089600	Enhancers	Brain Anterior Caudate	brain
36	chr3:116089400-116089600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:116089600-116093400	Weak transcription	Brain Hippocampus Middle	brain
38	chr3:116089600-116093600	Weak transcription	Brain Anterior Caudate	brain
39	chr3:116093200-116095800	Enhancers	Fetal Lung	lung
40	chr3:116093400-116094000	Enhancers	Brain Hippocampus Middle	brain
41	chr3:116093400-116094000	Enhancers	Colon Smooth Muscle	Colon
42	chr3:116093600-116093800	Enhancers	Fetal Kidney	kidney
43	chr3:116093600-116094000	Enhancers	Brain Anterior Caudate	brain
44	chr3:116093600-116094000	Enhancers	Ovary	ovary
45	chr3:116093600-116094000	Enhancers	Rectal Smooth Muscle	rectum
46	chr3:116093600-116095000	Enhancers	Brain Substantia Nigra	brain
47	chr3:116094000-116095000	Weak transcription	Colon Smooth Muscle	Colon
48	chr3:116094000-116095200	Weak transcription	Brain Hippocampus Middle	brain
49	chr3:116095000-116095400	Enhancers	Colon Smooth Muscle	Colon
50	chr3:116095200-116095400	Enhancers	Brain Hippocampus Middle	brain

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