Variant report

Variant	nsv1046271
Chromosome Location	chr15:31741255-31795961
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1489)
CpG islands
(count:1282)
Chromatin interactive
region (count:32)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1489 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:31780793-31781117	K562	blood:	n/a	n/a
2	ARID3A	chr15:31780846-31781135	HepG2	liver:	n/a	n/a
3	ATF2	chr15:31751192-31751725	GM12878	blood:	n/a	n/a
4	ATF2	chr15:31780255-31781128	GM12878	blood:	n/a	n/a
5	ATF2	chr15:31780042-31780621	GM12878	blood:	n/a	n/a
6	ATF2	chr15:31751038-31751815	GM12878	blood:	n/a	n/a
7	BACH1	chr15:31747847-31747986	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr15:31775531-31776385	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr15:31751257-31751640	GM12878	blood:	n/a	n/a
10	BATF	chr15:31783524-31783756	GM12878	blood:	n/a	n/a
11	BATF	chr15:31783531-31783735	GM12878	blood:	n/a	n/a
12	BATF	chr15:31780127-31781131	GM12878	blood:	n/a	chr15:31780490-31780500
13	BATF	chr15:31780250-31780659	GM12878	blood:	n/a	chr15:31780490-31780500
14	BCL11A	chr15:31751147-31751700	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:31780285-31780642	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:31780237-31780696	GM12878	blood:	n/a	n/a
17	BCL3	chr15:31749134-31749475	GM12878	blood:	n/a	n/a
18	BCL3	chr15:31759025-31759318	GM12878	blood:	n/a	n/a
19	BCL3	chr15:31780314-31780731	GM12878	blood:	n/a	n/a
20	BCL3	chr15:31749116-31749537	GM12878	blood:	n/a	n/a
21	BCLAF1	chr15:31751116-31751769	GM12878	blood:	n/a	n/a
22	BCLAF1	chr15:31765120-31765606	GM12878	blood:	n/a	n/a
23	BHLHE40	chr15:31765070-31765532	GM12878	blood:	n/a	n/a
24	BHLHE40	chr15:31751153-31751981	GM12878	blood:	n/a	n/a
25	BHLHE40	chr15:31780166-31781139	GM12878	blood:	n/a	n/a
26	BRCA1	chr15:31780865-31781329	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr15:31775170-31775650	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr15:31764050-31764472	IMR90	lung:	n/a	n/a
29	CEBPB	chr15:31780347-31781396	IMR90	lung:	n/a	n/a
30	CEBPB	chr15:31780797-31781118	K562	blood:	n/a	n/a
31	CEBPB	chr15:31744337-31744446	HepG2	liver:	n/a	n/a
32	CEBPB	chr15:31780806-31781068	HepG2	liver:	n/a	n/a
33	CEBPB	chr15:31780805-31781109	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr15:31780589-31781407	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr15:31744179-31744562	A549	lung:	n/a	n/a
36	CEBPB	chr15:31744226-31744567	IMR90	lung:	n/a	n/a
37	CEBPB	chr15:31780796-31781145	A549	lung:	n/a	n/a
38	CHD1	chr15:31780006-31782011	IMR90	lung:	n/a	n/a
39	CHD1	chr15:31782059-31782809	IMR90	lung:	n/a	n/a
40	CHD1	chr15:31751187-31751648	GM12878	blood:	n/a	n/a
41	CHD1	chr15:31780100-31780215	GM12878	blood:	n/a	n/a
42	CHD2	chr15:31780002-31781149	GM12878	blood:	n/a	n/a
43	CHD2	chr15:31775207-31775735	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr15:31780901-31781458	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr15:31751202-31751893	GM12878	blood:	n/a	n/a
46	CREB1	chr15:31780957-31781492	A549	lung:	n/a	n/a
47	CREB1	chr15:31749858-31750147	A549	lung:	n/a	n/a
48	CTCF	chr15:31782253-31782564	GM12878	blood:	n/a	chr15:31782425-31782434 chr15:31782422-31782432 chr15:31782420-31782436 chr15:31782419-31782437
49	CTCF	chr15:31780120-31780270	GM12864	blood:	n/a	chr15:31780193-31780214 chr15:31780198-31780216
50	CTCF	chr15:31780140-31780253	HUVEC	blood vessel:	n/a	chr15:31780193-31780214 chr15:31780198-31780216

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31749573-31749623	NB4	blood:	n/a
2	chr15:31749573-31749623	NB4	blood:	n/a
3	chr15:31745916-31745966	AG04450	lung:	fetal
4	chr15:31773057-31773107	PFSK-1	brain:	n/a
5	chr15:31745519-31745569	HCM	heart:	n/a
6	chr15:31749573-31749623	NHDF-neo	bronchial:	n/a
7	chr15:31775406-31775456	HMEC	breast:	n/a
8	chr15:31776741-31776791	ProgFib	skin:	n/a
9	chr15:31745648-31745698	IMR90	lung:	fetal
10	chr15:31781955-31782005	PFSK-1	brain:	n/a
11	chr15:31774773-31774823	AG04450	lung:	fetal
12	chr15:31774773-31774823	NHDF-neo	bronchial:	n/a
13	chr15:31744207-31744257	RPTEC	kidney:	n/a
14	chr15:31745519-31745569	NT2-D1	testis:	n/a
15	chr15:31777358-31777408	CMK	blood:	n/a
16	chr15:31749573-31749623	HCM	heart:	n/a
17	chr15:31744207-31744257	SK-N-SH	brain:	n/a
18	chr15:31774976-31775026	HAEpiC	amniotic membrane:	n/a
19	chr15:31780722-31780772	AG04450	lung:	fetal
20	chr15:31744207-31744257	NHBE	bronchial:	n/a
21	chr15:31742799-31742849	PFSK-1	brain:	n/a
22	chr15:31774773-31774823	GM19239	blood:	n/a
23	chr15:31764211-31764261	NT2-D1	testis:	n/a
24	chr15:31745648-31745698	Caco-2	colon:	n/a
25	chr15:31775895-31775945	AG04449	skin:	fetal
26	chr15:31742799-31742849	A549	lung:	n/a
27	chr15:31745519-31745569	Caco-2	colon:	n/a
28	chr15:31777358-31777408	NHBE	bronchial:	n/a
29	chr15:31749573-31749623	BE2_C	brain:	n/a
30	chr15:31745729-31745779	HCT-116	colon:	n/a
31	chr15:31781955-31782005	MCF10A-Er-Src	breast:	n/a
32	chr15:31775049-31775099	HEK293	kidney:	embryo
33	chr15:31777358-31777408	PrEC	prostate:	n/a
34	chr15:31749573-31749623	NT2-D1	testis:	n/a
35	chr15:31774976-31775026	AG10803	skin:	n/a
36	chr15:31746330-31746380	AoSMC	blood vessel:	n/a
37	chr15:31781955-31782005	HCPEpiC	choroid plexus:	n/a
38	chr15:31780722-31780772	AG09319	gingival:	n/a
39	chr15:31775049-31775099	GM06990	blood:	n/a
40	chr15:31775049-31775099	ECC-1	luminal epithelium:	n/a
41	chr15:31776741-31776791	SKMC	muscle:	n/a
42	chr15:31775895-31775945	MCF-7	breast:	n/a
43	chr15:31774773-31774823	SK-N-SH_RA	brain:	n/a
44	chr15:31776450-31776500	HRE	kidney:	n/a
45	chr15:31745894-31745944	HCF	heart:	n/a
46	chr15:31742799-31742849	HCPEpiC	choroid plexus:	n/a
47	chr15:31749573-31749623	SAEC	small airway:	n/a
48	chr15:31780722-31780772	K562	blood:	n/a
49	chr15:31764211-31764261	Caco-2	colon:	n/a
50	chr15:31780722-31780772	HIPEpiC	eye:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:31729614..31735490-chr15:31778794..31782835,6	MCF-7	breast:
2	chr15:31730666..31732248-chr15:31779741..31781482,12	MCF-7	breast:
3	chr15:31492707..31493313-chr15:31780465..31781069,2	MCF-7	breast:
4	chr15:31731428..31732434-chr15:31780398..31781184,5	K562	blood:
5	chr15:31748477..31753108-chr15:31776889..31783172,7	MCF-7	breast:
6	chr15:31747904..31750478-chr15:31754531..31757245,2	MCF-7	breast:
7	chr15:31753960..31755078-chr15:31780591..31781425,3	MCF-7	breast:
8	chr15:31753960..31755078-chr15:31780591..31781425,3	MCF-7	breast:
9	chr15:31768996..31771688-chr15:31773371..31775681,2	MCF-7	breast:
10	chr15:31507500..31508054-chr15:31782035..31782545,2	K562	blood:
11	chr15:31753115..31755985-chr15:31766097..31768042,2	MCF-7	breast:
12	chr15:31728928..31731704-chr15:31776995..31778781,2	MCF-7	breast:
13	chr15:31748477..31753108-chr15:31776889..31783172,7	MCF-7	breast:
14	chr15:31492924..31493816-chr15:31781800..31782800,3	K562	blood:
15	chr15:31775112..31777688-chr15:31780214..31782887,2	K562	blood:
16	chr15:31775112..31777688-chr15:31780214..31782887,2	K562	blood:
17	chr15:31753115..31755985-chr15:31766097..31768042,2	MCF-7	breast:
18	chr15:31780894..31782465-chr15:31785232..31787543,2	MCF-7	breast:
19	chr15:31747904..31750478-chr15:31754531..31757245,2	MCF-7	breast:
20	chr15:31780894..31782465-chr15:31785232..31787543,2	MCF-7	breast:
21	chr15:31789301..31792220-chr15:31792871..31795372,2	K562	blood:
22	chr15:31489768..31490355-chr15:31780489..31781405,2	K562	blood:
23	chr15:31731222..31732109-chr15:31780643..31781604,3	MCF-7	breast:
24	chr15:31507301..31508500-chr15:31780431..31781449,6	K562	blood:
25	chr15:31507689..31508257-chr15:31779754..31780346,2	K562	blood:
26	chr15:31492529..31493483-chr15:31780441..31781476,6	MCF-7	breast:
27	chr15:31789301..31792220-chr15:31792871..31795372,2	K562	blood:
28	chr15:31753081..31754904-chr15:31769113..31772729,3	MCF-7	breast:
29	chr15:31727262..31728165-chr15:31780632..31781327,2	MCF-7	breast:
30	chr15:31731861..31735385-chr15:31748681..31751856,6	MCF-7	breast:
31	chr15:31753081..31754904-chr15:31769113..31772729,3	MCF-7	breast:
32	chr15:31768996..31771688-chr15:31773371..31775681,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OTUD7A-1	chr15:31767607-31770705	NONHSAT041463

No data

Variant related genes	Relation type
ENSG00000259696	TF binding region
ENSG00000259696	CpG island
ENSG00000259448	chromatin interactions

Extended variants
information (count: 2219 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2219 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143879027	chr15:31741283-31741284	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs146890596	chr15:31741325-31741326	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs191769778	chr15:31741336-31741337	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs527993597	chr15:31741371-31741372	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs183504590	chr15:31741384-31741385	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs368346416	chr15:31741406-31741407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542490545	chr15:31741464-31741465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188186844	chr15:31741538-31741539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs111834793	chr15:31741548-31741549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs544490565	chr15:31741649-31741650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181735112	chr15:31741677-31741678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577714973	chr15:31741693-31741694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185548126	chr15:31741705-31741706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs150036291	chr15:31741708-31741709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs117259424	chr15:31741738-31741739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549231610	chr15:31741748-31741749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145232306	chr15:31741777-31741778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190800939	chr15:31741779-31741780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546160323	chr15:31741811-31741812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571512599	chr15:31741898-31741899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533862429	chr15:31741907-31741908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs551403131	chr15:31741916-31741917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541732058	chr15:31742039-31742040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547547280	chr15:31742080-31742081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567247147	chr15:31742100-31742101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535887881	chr15:31742149-31742150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181677409	chr15:31742162-31742163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149168438	chr15:31742163-31742164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546324391	chr15:31742196-31742197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538578710	chr15:31742213-31742214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564243920	chr15:31742217-31742218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557923044	chr15:31742219-31742220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs72724946	chr15:31742301-31742302	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs143306902	chr15:31742302-31742303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560235905	chr15:31742305-31742306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs139010440	chr15:31742342-31742343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141590715	chr15:31742368-31742369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs562754882	chr15:31742381-31742382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs77026083	chr15:31742416-31742417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs551738812	chr15:31742428-31742429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565056143	chr15:31742450-31742451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs527507772	chr15:31742464-31742465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs187098800	chr15:31742474-31742475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567262348	chr15:31742498-31742499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536200576	chr15:31742521-31742522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150334086	chr15:31742583-31742584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549510374	chr15:31742584-31742585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs71110880	chr15:31742605-31742606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546802820	chr15:31742626-31742627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561916053	chr15:31742649-31742650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	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
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	CNVD
Colorectal cancer	16774939	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
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Epilepsy	20502679	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Pancreatic cancer	17952125	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31733800-31741800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr15:31734400-31750000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:31740000-31741400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr15:31740000-31741400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr15:31740000-31742000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr15:31740200-31741400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr15:31740200-31741400	Enhancers	GM12878-XiMat	blood
8	chr15:31740200-31742000	Enhancers	Primary hematopoietic stem cells	blood
9	chr15:31740200-31742000	Enhancers	HUVEC	blood vessel
10	chr15:31740600-31741400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr15:31740600-31741400	Enhancers	NHEK	skin
12	chr15:31740600-31741600	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr15:31740600-31741800	Enhancers	K562	blood
14	chr15:31740800-31741400	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr15:31740800-31741400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr15:31740800-31741400	Enhancers	Esophagus	oesophagus
17	chr15:31740800-31741400	Enhancers	Fetal Thymus	thymus
18	chr15:31740800-31741400	Enhancers	Stomach Mucosa	stomach
19	chr15:31740800-31741800	Enhancers	Placenta	Placenta
20	chr15:31741000-31741400	Enhancers	Primary T cells fromperipheralblood	blood
21	chr15:31741000-31741400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr15:31741000-31741400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr15:31741000-31741400	Enhancers	Fetal Muscle Leg	muscle
24	chr15:31741000-31741600	Enhancers	HSMMtube	muscle
25	chr15:31741000-31742000	Enhancers	Spleen	Spleen
26	chr15:31741200-31741400	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr15:31741200-31741800	Enhancers	Gastric	stomach
28	chr15:31741200-31743600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr15:31741400-31741800	Enhancers	Liver	Liver
30	chr15:31741400-31742000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr15:31741400-31742000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr15:31741400-31743800	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr15:31741400-31744200	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr15:31741400-31747800	Weak transcription	GM12878-XiMat	blood
35	chr15:31741400-31749400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr15:31741800-31742200	Weak transcription	K562	blood
37	chr15:31741800-31744800	Weak transcription	Liver	Liver
38	chr15:31742200-31742600	Enhancers	K562	blood
39	chr15:31743600-31743800	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr15:31743800-31744800	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr15:31744200-31744800	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr15:31744800-31745400	Enhancers	Liver	Liver
43	chr15:31745000-31745400	Enhancers	Psoas Muscle	Psoas
44	chr15:31745000-31745800	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr15:31745400-31745800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr15:31745600-31746000	Bivalent Enhancer	K562	blood
47	chr15:31745600-31748800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr15:31745800-31748800	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr15:31745800-31750000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr15:31747000-31750800	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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