Variant report

Variant	nsv471254
Chromosome Location	chr15:76811390-76978139
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:678)
CpG islands
(count:122)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:678 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:76865111-76865365	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:76935433-76935442	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:76825612-76826689	HepG2	liver:	n/a	n/a
4	ATF2	chr15:76867574-76868256	GM12878	blood:	n/a	n/a
5	ATF2	chr15:76867545-76868188	GM12878	blood:	n/a	n/a
6	BATF	chr15:76907137-76907384	GM12878	blood:	n/a	n/a
7	BATF	chr15:76867629-76868083	GM12878	blood:	n/a	n/a
8	BATF	chr15:76907151-76907359	GM12878	blood:	n/a	n/a
9	BATF	chr15:76946672-76946896	GM12878	blood:	n/a	n/a
10	BATF	chr15:76868780-76869125	GM12878	blood:	n/a	n/a
11	BATF	chr15:76946679-76946925	GM12878	blood:	n/a	n/a
12	BATF	chr15:76867553-76868299	GM12878	blood:	n/a	n/a
13	BCL11A	chr15:76867646-76868017	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:76946684-76946864	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:76867571-76868071	GM12878	blood:	n/a	n/a
16	BCL3	chr15:76825735-76826094	GM12878	blood:	n/a	n/a
17	BCL3	chr15:76825763-76826141	GM12878	blood:	n/a	n/a
18	BCL3	chr15:76867594-76868106	GM12878	blood:	n/a	n/a
19	BCL3	chr15:76867671-76868118	GM12878	blood:	n/a	n/a
20	BCLAF1	chr15:76867603-76868092	GM12878	blood:	n/a	n/a
21	BCLAF1	chr15:76867350-76868205	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:76946680-76946809	GM12878	blood:	n/a	n/a
23	BHLHE40	chr15:76867676-76868010	GM12878	blood:	n/a	n/a
24	BRCA1	chr15:76969668-76969722	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr15:76928439-76928711	K562	blood:	n/a	n/a
26	CBX3	chr15:76928484-76928676	K562	blood:	n/a	n/a
27	CEBPB	chr15:76857118-76857460	HepG2	liver:	n/a	chr15:76857283-76857294
28	CEBPB	chr15:76867691-76868041	GM12878	blood:	n/a	n/a
29	CEBPB	chr15:76865274-76865637	IMR90	lung:	n/a	chr15:76865442-76865453
30	CEBPB	chr15:76857146-76857335	Hela-S3	cervix:	n/a	chr15:76857283-76857294
31	CEBPB	chr15:76825694-76826267	MCF-7	breast:	n/a	chr15:76825991-76826004 chr15:76825947-76825958
32	CEBPB	chr15:76825775-76826096	IMR90	lung:	n/a	chr15:76825991-76826004 chr15:76825947-76825958
33	CEBPB	chr15:76825743-76826204	HepG2	liver:	n/a	chr15:76825991-76826004 chr15:76825947-76825958
34	CEBPB	chr15:76857150-76857393	K562	blood:	n/a	chr15:76857283-76857294
35	CEBPB	chr15:76865082-76865698	A549	lung:	n/a	chr15:76865442-76865453
36	CEBPB	chr15:76825720-76826202	A549	lung:	n/a	chr15:76825991-76826004 chr15:76825947-76825958
37	CEBPB	chr15:76825764-76826110	HepG2	liver:	n/a	chr15:76825991-76826004 chr15:76825947-76825958
38	CEBPB	chr15:76825807-76825998	HepG2	liver:	n/a	chr15:76825947-76825958
39	CEBPB	chr15:76869227-76869506	HepG2	liver:	n/a	n/a
40	CEBPB	chr15:76865304-76865598	K562	blood:	n/a	chr15:76865442-76865453
41	CEBPB	chr15:76857129-76857461	A549	lung:	n/a	chr15:76857283-76857294
42	CEBPB	chr15:76839190-76839507	HepG2	liver:	n/a	chr15:76839336-76839347
43	CEBPB	chr15:76825760-76826178	A549	lung:	n/a	chr15:76825991-76826004 chr15:76825947-76825958
44	CEBPB	chr15:76960844-76961108	A549	lung:	n/a	n/a
45	CEBPB	chr15:76865289-76865622	HepG2	liver:	n/a	chr15:76865442-76865453
46	CEBPB	chr15:76865196-76865634	A549	lung:	n/a	chr15:76865442-76865453
47	CEBPB	chr15:76825727-76826237	MCF-7	breast:	n/a	chr15:76825991-76826004 chr15:76825947-76825958
48	CEBPB	chr15:76839201-76839452	A549	lung:	n/a	chr15:76839336-76839347
49	CEBPB	chr15:76960889-76961156	HepG2	liver:	n/a	n/a
50	CEBPB	chr15:76865278-76865665	Hela-S3	cervix:	n/a	chr15:76865442-76865453

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76868964-76869014	ovcar-3	ovarian:	n/a
2	chr15:76868964-76869014	ECC-1	luminal epithelium:	n/a
3	chr15:76901065-76901115	AG10803	skin:	n/a
4	chr15:76868964-76869014	HCPEpiC	choroid plexus:	n/a
5	chr15:76901065-76901115	HPAEpiC	pulmonary alveolar:	n/a
6	chr15:76901065-76901115	HUVEC	blood vessel:	n/a
7	chr15:76868964-76869014	MCF10A-Er-Src	breast:	n/a
8	chr15:76901065-76901115	AoSMC	blood vessel:	n/a
9	chr15:76868964-76869014	AG04450	lung:	fetal
10	chr15:76868964-76869014	HRPEpiC	eye:	n/a
11	chr15:76901065-76901115	HEEpiC	esophagus:	n/a
12	chr15:76868964-76869014	NH-A	brain:	n/a
13	chr15:76868964-76869014	NHDF-neo	bronchial:	n/a
14	chr15:76901065-76901115	AG09319	gingival:	n/a
15	chr15:76868964-76869014	BJ	skin:	n/a
16	chr15:76901065-76901115	BE2_C	brain:	n/a
17	chr15:76901065-76901115	SK-N-SH_RA	brain:	n/a
18	chr15:76901065-76901115	BJ	skin:	n/a
19	chr15:76868964-76869014	SKMC	muscle:	n/a
20	chr15:76901065-76901115	T-47D	breast:	n/a
21	chr15:76868964-76869014	HCM	heart:	n/a
22	chr15:76868964-76869014	T-47D	breast:	n/a
23	chr15:76901065-76901115	Jurkat	blood:	n/a
24	chr15:76901065-76901115	HCPEpiC	choroid plexus:	n/a
25	chr15:76901065-76901115	HL-60	blood:	n/a
26	chr15:76901065-76901115	Hepatocyte	liver:	n/a
27	chr15:76868964-76869014	NT2-D1	testis:	n/a
28	chr15:76901065-76901115	GM12878	blood:	n/a
29	chr15:76901065-76901115	HCT-116	colon:	n/a
30	chr15:76901065-76901115	NT2-D1	testis:	n/a
31	chr15:76901065-76901115	HCF	heart:	n/a
32	chr15:76868964-76869014	HIPEpiC	eye:	n/a
33	chr15:76901065-76901115	AG09309	skin:	n/a
34	chr15:76901065-76901115	AG04449	skin:	fetal
35	chr15:76901065-76901115	NH-A	brain:	n/a
36	chr15:76901065-76901115	HRPEpiC	eye:	n/a
37	chr15:76901065-76901115	ovcar-3	ovarian:	n/a
38	chr15:76901065-76901115	MCF10A-Er-Src	breast:	n/a
39	chr15:76901065-76901115	HRE	kidney:	n/a
40	chr15:76868964-76869014	H1-hESC	embryonic stem cell:	embryo
41	chr15:76868964-76869014	Hepatocyte	liver:	n/a
42	chr15:76868964-76869014	HUVEC	blood vessel:	n/a
43	chr15:76901065-76901115	SK-N-SH	brain:	n/a
44	chr15:76901065-76901115	NHDF-neo	bronchial:	n/a
45	chr15:76901065-76901115	MCF-7	breast:	n/a
46	chr15:76868964-76869014	BE2_C	brain:	n/a
47	chr15:76868964-76869014	HepG2	liver:	n/a
48	chr15:76901065-76901115	SK-N-MC	brain:	n/a
49	chr15:76868964-76869014	HEK293	kidney:	embryo
50	chr15:76868964-76869014	CMK	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:76812872..76815537-chr15:76817323..76820278,2	MCF-7	breast:
2	chr15:76934226..76937075-chr15:76948287..76950112,2	MCF-7	breast:
3	chr15:76810534..76813037-chr15:76815373..76817326,2	MCF-7	breast:
4	chr15:76493051..76495991-chr15:76813493..76815400,2	MCF-7	breast:
5	chr15:76959064..76961382-chr15:76964223..76965946,2	MCF-7	breast:
6	chr15:76967596..76970375-chr15:76976896..76979262,2	K562	blood:
7	chr15:76934897..76935640-chr15:77158999..77159764,3	MCF-7	breast:
8	chr15:76964455..76968844-chr15:76969640..76972722,4	K562	blood:
9	chr15:76934226..76937075-chr15:76948287..76950112,2	MCF-7	breast:
10	chr15:76959064..76961382-chr15:76964223..76965946,2	MCF-7	breast:
11	chr15:76967596..76970375-chr15:76976896..76979262,2	K562	blood:
12	chr15:76969596..76972550-chr15:76979737..76981959,2	MCF-7	breast:
13	chr15:76964455..76968844-chr15:76969640..76972722,4	K562	blood:
14	chr15:76877558..76879609-chr15:76881319..76882907,2	K562	blood:
15	chr15:76821101..76824629-chr15:76825214..76826999,4	K562	blood:
16	chr15:76810534..76813037-chr15:76815373..76817326,2	MCF-7	breast:
17	chr15:76855877..76857707-chr15:76866696..76869240,2	MCF-7	breast:
18	chr15:76812872..76815537-chr15:76817323..76820278,2	MCF-7	breast:
19	chr15:76934737..76935336-chr15:77133237..77133799,2	MCF-7	breast:
20	chr15:76855877..76857707-chr15:76866696..76869240,2	MCF-7	breast:
21	chr15:76821101..76824629-chr15:76825214..76826999,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ETFA-5	chr15:76833537-76833934	NONHSAT047406

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3713	chr15:76878988-76879007	MIMAT0018164

No data

Variant related genes	Relation type
SCAPER	TF binding region
MIR3713	TF binding region
SCAPER	CpG island
MIR3713	CpG island
ENSG00000266449	chromatin interactions

Extended variants
information (count: 5661 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:5661 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1603856	chr15:76811390-76811391	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370585979	chr15:76811399-76811400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148022944	chr15:76811433-76811434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141741826	chr15:76811488-76811489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs369306901	chr15:76811498-76811499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570380861	chr15:76811616-76811617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543292370	chr15:76811622-76811623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375195943	chr15:76811691-76811692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35983091	chr15:76811711-76811712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs367818165	chr15:76811757-76811758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371623031	chr15:76811778-76811779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568209762	chr15:76811796-76811797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535273620	chr15:76811829-76811830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs75409140	chr15:76811845-76811846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536286228	chr15:76811898-76811899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186482721	chr15:76812029-76812030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576110496	chr15:76812030-76812031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114183548	chr15:76812040-76812041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558904772	chr15:76812109-76812110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576855789	chr15:76812112-76812113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577208187	chr15:76812113-76812114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541670471	chr15:76812118-76812119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150580890	chr15:76812172-76812173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138665137	chr15:76812215-76812216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73444294	chr15:76812305-76812306	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs12441247	chr15:76812316-76812317	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs530599971	chr15:76812323-76812324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552034131	chr15:76812385-76812386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559667610	chr15:76812405-76812406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565097974	chr15:76812414-76812415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573268562	chr15:76812425-76812426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116129424	chr15:76812515-76812516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369578014	chr15:76812553-76812554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368533308	chr15:76812591-76812592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374046566	chr15:76812669-76812670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568037497	chr15:76812683-76812684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143822210	chr15:76812744-76812745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556714896	chr15:76812777-76812778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190522099	chr15:76812781-76812782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537136936	chr15:76812821-76812822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558792547	chr15:76812861-76812862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577122668	chr15:76812862-76812863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183050816	chr15:76812888-76812889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs1074793	chr15:76812901-76812902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553594978	chr15:76812950-76812951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372484661	chr15:76813028-76813029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575172128	chr15:76813070-76813071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532161800	chr15:76813103-76813104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185549298	chr15:76813113-76813114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563869903	chr15:76813184-76813185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:998 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76725800-76812600	Weak transcription	Left Ventricle	heart
2	chr15:76788400-76813600	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr15:76797400-76825000	Weak transcription	Primary B cells from cord blood	blood
4	chr15:76805600-76845800	Weak transcription	Primary T cells from cord blood	blood
5	chr15:76807600-76817800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr15:76808000-76816200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr15:76808400-76825000	Weak transcription	Fetal Intestine Small	intestine
8	chr15:76808400-76825600	Weak transcription	Fetal Intestine Large	intestine
9	chr15:76810600-76811800	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr15:76811200-76813000	Weak transcription	Fetal Heart	heart
11	chr15:76811200-76825400	Weak transcription	Fetal Stomach	stomach
12	chr15:76812600-76813000	Enhancers	Esophagus	oesophagus
13	chr15:76812600-76813000	Enhancers	Left Ventricle	heart
14	chr15:76813000-76813600	Enhancers	Fetal Heart	heart
15	chr15:76813000-76821600	Weak transcription	Left Ventricle	heart
16	chr15:76816200-76816800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr15:76816200-76819400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr15:76817200-76818400	Weak transcription	Fetal Brain Male	brain
19	chr15:76817800-76818000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr15:76818000-76819800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr15:76818400-76818600	Enhancers	Fetal Brain Male	brain
22	chr15:76819400-76828400	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr15:76819800-76820000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr15:76822400-76822800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr15:76823600-76823800	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr15:76823800-76825200	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr15:76825000-76825400	Enhancers	Primary B cells from cord blood	blood
28	chr15:76825000-76826800	Enhancers	Fetal Intestine Small	intestine
29	chr15:76825000-76826800	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr15:76825000-76826800	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr15:76825200-76825800	Enhancers	Duodenum Mucosa	Duodenum
32	chr15:76825200-76826800	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr15:76825200-76826800	Enhancers	Stomach Mucosa	stomach
34	chr15:76825200-76826800	Enhancers	A549	lung
35	chr15:76825200-76826800	Enhancers	HepG2	liver
36	chr15:76825400-76826600	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr15:76825400-76827600	Enhancers	Fetal Stomach	stomach
38	chr15:76825600-76826800	Enhancers	Fetal Intestine Large	intestine
39	chr15:76825800-76826200	Enhancers	Fetal Brain Male	brain
40	chr15:76826000-76826800	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr15:76826000-76826800	Enhancers	Fetal Lung	lung
42	chr15:76826000-76826800	Enhancers	Rectal Mucosa Donor 29	rectum
43	chr15:76826000-76826800	Enhancers	Small Intestine	intestine
44	chr15:76826400-76826800	Enhancers	Colon Smooth Muscle	Colon
45	chr15:76826400-76827000	Enhancers	NHLF	lung
46	chr15:76835800-76836200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr15:76837600-76838200	Enhancers	Fetal Heart	heart
48	chr15:76842000-76844200	Weak transcription	Fetal Stomach	stomach
49	chr15:76842200-76845400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr15:76842400-76845600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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