Variant report

Variant	nsv569209
Chromosome Location	chr15:39188421-39385921
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	chr15:39377574-39377770	HepG2	liver:	n/a	n/a
2	ATF1	chr15:39377608-39377721	K562	blood:	n/a	n/a
3	BCL3	chr15:39371583-39372097	A549	lung:	n/a	chr15:39371878-39371887
4	BRCA1	chr15:39288214-39288368	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr15:39213774-39213778	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr15:39233535-39233870	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr15:39306970-39307129	A549	lung:	n/a	n/a
8	CEBPB	chr15:39340675-39340848	HepG2	liver:	n/a	chr15:39340732-39340743 chr15:39340731-39340744 chr15:39340731-39340744
9	CEBPB	chr15:39234765-39234969	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr15:39286689-39286798	HepG2	liver:	n/a	chr15:39286754-39286765
11	CEBPB	chr15:39288227-39288799	IMR90	lung:	n/a	n/a
12	CEBPB	chr15:39242700-39242901	HepG2	liver:	n/a	chr15:39242757-39242768
13	CEBPB	chr15:39223230-39223702	IMR90	lung:	n/a	n/a
14	CEBPB	chr15:39212792-39213107	IMR90	lung:	n/a	chr15:39212940-39212953 chr15:39212942-39212953 chr15:39212942-39212951 chr15:39212942-39212951 chr15:39212940-39212951 chr15:39212942-39212951 chr15:39212942-39212951
15	CEBPB	chr15:39302492-39302600	Hela-S3	cervix:	n/a	chr15:39302535-39302546
16	CEBPB	chr15:39345311-39345521	HepG2	liver:	n/a	chr15:39345414-39345425
17	CEBPB	chr15:39214313-39214490	Hela-S3	cervix:	n/a	chr15:39214358-39214367 chr15:39214358-39214367 chr15:39214358-39214367 chr15:39214358-39214367
18	CEBPB	chr15:39214273-39214499	A549	lung:	n/a	chr15:39214358-39214367 chr15:39214358-39214367 chr15:39214358-39214367 chr15:39214358-39214367
19	CEBPB	chr15:39331154-39331162	K562	blood:	n/a	n/a
20	CEBPB	chr15:39317527-39317741	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr15:39204770-39204897	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr15:39371495-39371993	IMR90	lung:	n/a	n/a
23	CEBPB	chr15:39242636-39242880	IMR90	lung:	n/a	chr15:39242757-39242768
24	CEBPB	chr15:39204523-39204622	IMR90	lung:	n/a	n/a
25	CEBPB	chr15:39375432-39375699	IMR90	lung:	n/a	n/a
26	CEBPB	chr15:39276466-39276656	IMR90	lung:	n/a	chr15:39276496-39276507
27	CEBPB	chr15:39306922-39307127	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr15:39352187-39352497	IMR90	lung:	n/a	n/a
29	CEBPB	chr15:39214214-39214522	HepG2	liver:	n/a	chr15:39214358-39214367 chr15:39214502-39214515 chr15:39214358-39214367 chr15:39214358-39214367 chr15:39214358-39214367
30	CEBPB	chr15:39233482-39234033	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr15:39242711-39242902	K562	blood:	n/a	chr15:39242757-39242768
32	CEBPB	chr15:39377471-39377801	A549	lung:	n/a	chr15:39377653-39377666
33	CEBPB	chr15:39371689-39372041	A549	lung:	n/a	n/a
34	CEBPB	chr15:39377532-39377768	A549	lung:	n/a	chr15:39377653-39377666
35	CEBPB	chr15:39212798-39213103	Hela-S3	cervix:	n/a	chr15:39212940-39212953 chr15:39212942-39212953 chr15:39212942-39212951 chr15:39212942-39212951 chr15:39212940-39212951 chr15:39212942-39212951 chr15:39212942-39212951
36	CEBPB	chr15:39376834-39377267	Hela-S3	cervix:	n/a	chr15:39377000-39377013 chr15:39377000-39377011 chr15:39377000-39377011 chr15:39377000-39377013 chr15:39377018-39377031 chr15:39377000-39377013
37	CEBPB	chr15:39380476-39380692	Hela-S3	cervix:	n/a	chr15:39380589-39380600 chr15:39380541-39380554
38	CEBPB	chr15:39371416-39371997	A549	lung:	n/a	chr15:39371442-39371454
39	CEBPB	chr15:39226080-39226258	HepG2	liver:	n/a	chr15:39226190-39226199 chr15:39226188-39226201 chr15:39226188-39226199 chr15:39226189-39226200
40	CEBPB	chr15:39315553-39315610	HepG2	liver:	n/a	n/a
41	CEBPB	chr15:39212811-39213096	A549	lung:	n/a	chr15:39212940-39212953 chr15:39212942-39212953 chr15:39212942-39212951 chr15:39212942-39212951 chr15:39212940-39212951 chr15:39212942-39212951 chr15:39212942-39212951
42	CEBPB	chr15:39345258-39345532	Hela-S3	cervix:	n/a	chr15:39345414-39345425
43	CEBPB	chr15:39267620-39268344	A549	lung:	n/a	n/a
44	CEBPB	chr15:39376948-39377172	A549	lung:	n/a	chr15:39377000-39377013 chr15:39377000-39377011 chr15:39377000-39377011 chr15:39377000-39377013 chr15:39377018-39377031 chr15:39377000-39377013
45	CEBPB	chr15:39288287-39288676	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr15:39276368-39276579	HepG2	liver:	n/a	chr15:39276496-39276507
47	CEBPB	chr15:39331190-39331297	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr15:39284837-39285052	IMR90	lung:	n/a	n/a
49	CEBPB	chr15:39331117-39331299	HepG2	liver:	n/a	n/a
50	CEBPB	chr15:39226177-39226178	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:39205040-39205090	NT2-D1	testis:	n/a
2	chr15:39371335-39371385	NHDF-neo	bronchial:	n/a
3	chr15:39354532-39354582	GM06990	blood:	n/a
4	chr15:39205040-39205090	NT2-D1	testis:	n/a
5	chr15:39371335-39371385	NHDF-neo	bronchial:	n/a
6	chr15:39354532-39354582	GM06990	blood:	n/a
7	chr15:39287147-39287197	IMR90	lung:	fetal
8	chr15:39354532-39354582	A549	lung:	n/a
9	chr15:39205040-39205090	Hepatocyte	liver:	n/a
10	chr15:39354532-39354582	HRPEpiC	eye:	n/a
11	chr15:39317391-39317441	Hepatocyte	liver:	n/a
12	chr15:39205040-39205090	RPTEC	kidney:	n/a
13	chr15:39317391-39317441	NH-A	brain:	n/a
14	chr15:39354532-39354582	HepG2	liver:	n/a
15	chr15:39371335-39371385	HEK293	kidney:	embryo
16	chr15:39317391-39317441	AG09319	gingival:	n/a
17	chr15:39287147-39287197	PANC-1	pancreas:	n/a
18	chr15:39354532-39354582	HUVEC	blood vessel:	n/a
19	chr15:39283510-39283560	Jurkat	blood:	n/a
20	chr15:39371335-39371385	GM06990	blood:	n/a
21	chr15:39287147-39287197	GM06990	blood:	n/a
22	chr15:39310779-39310829	BJ	skin:	n/a
23	chr15:39371335-39371385	ECC-1	luminal epithelium:	n/a
24	chr15:39205040-39205090	SK-N-SH_RA	brain:	n/a
25	chr15:39354532-39354582	Hela-S3	cervix:	n/a
26	chr15:39317391-39317441	HNPCEpiC	eye:	n/a
27	chr15:39371335-39371385	HepG2	liver:	n/a
28	chr15:39371335-39371385	HAEpiC	amniotic membrane:	n/a
29	chr15:39287147-39287197	SK-N-SH_RA	brain:	n/a
30	chr15:39317391-39317441	HRCEpiC	kidney:	n/a
31	chr15:39205040-39205090	HEEpiC	esophagus:	n/a
32	chr15:39354532-39354582	GM19239	blood:	n/a
33	chr15:39377571-39377621	ProgFib	skin:	n/a
34	chr15:39283510-39283560	BE2_C	brain:	n/a
35	chr15:39283510-39283560	HEK293	kidney:	embryo
36	chr15:39317391-39317441	SK-N-SH_RA	brain:	n/a
37	chr15:39317391-39317441	BJ	skin:	n/a
38	chr15:39287147-39287197	H1-hESC	embryonic stem cell:	embryo
39	chr15:39377571-39377621	NT2-D1	testis:	n/a
40	chr15:39205040-39205090	SK-N-MC	brain:	n/a
41	chr15:39354532-39354582	HEK293	kidney:	embryo
42	chr15:39283510-39283560	NB4	blood:	n/a
43	chr15:39354532-39354582	H1-hESC	embryonic stem cell:	embryo
44	chr15:39287147-39287197	HRPEpiC	eye:	n/a
45	chr15:39317391-39317441	LNCaP	prostate:	n/a
46	chr15:39317391-39317441	PFSK-1	brain:	n/a
47	chr15:39283510-39283560	HepG2	liver:	n/a
48	chr15:39205040-39205090	HCT-116	colon:	n/a
49	chr15:39377571-39377621	GM12891	blood:	n/a
50	chr15:39283510-39283560	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:39380963..39383121-chr15:39384281..39386524,3	K562	blood:
2	chr15:39320004..39322270-chr15:39324093..39326152,2	MCF-7	breast:
3	chr15:39187046..39189183-chr15:39189684..39192597,2	K562	blood:
4	chr15:39109610..39110793-chr15:39283014..39284012,10	MCF-7	breast:
5	chr15:39321444..39323682-chr15:39326429..39329006,2	K562	blood:
6	chr15:39361028..39363675-chr15:39364810..39366784,2	MCF-7	breast:
7	chr15:39202180..39205083-chr15:39208531..39210971,2	MCF-7	breast:
8	chr15:39380963..39383121-chr15:39384281..39386524,3	K562	blood:
9	chr15:39321444..39323682-chr15:39326429..39329006,2	K562	blood:
10	chr15:39166239..39168554-chr15:39281502..39284029,2	MCF-7	breast:
11	chr15:39193427..39196259-chr15:39198844..39201559,2	K562	blood:
12	chr15:39109626..39110574-chr15:39283075..39284008,7	MCF-7	breast:
13	chr15:39202180..39205083-chr15:39208531..39210971,2	MCF-7	breast:
14	chr15:39193427..39196259-chr15:39198844..39201559,2	K562	blood:
15	chr15:39252222..39253818-chr15:39254086..39255839,2	MCF-7	breast:
16	chr15:39361028..39363675-chr15:39364810..39366784,2	MCF-7	breast:
17	chr15:39085713..39088566-chr15:39372910..39375619,2	MCF-7	breast:
18	chr15:39252222..39253818-chr15:39254086..39255839,2	MCF-7	breast:
19	chr15:39187046..39189183-chr15:39189684..39192597,2	K562	blood:
20	chr15:39149816..39152151-chr15:39367805..39370175,2	K562	blood:
21	chr15:39275466..39278159-chr15:39872431..39874155,2	MCF-7	breast:
22	chr15:39320004..39322270-chr15:39324093..39326152,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSIP1-5	chr15:39363704-39363809	ENSG00000259345.1
2	lnc-FSIP1-5	chr15:39310703-39310782	ENSG00000259345.1
3	lnc-FSIP1-5	chr15:39363704-39363809	ENSG00000259345.1
4	lnc-FSIP1-9	chr15:39384973-39386019	l_1147_chr15:39377529-39386019_breast
5	lnc-FSIP1-9	chr15:39377530-39381679	l_1147_chr15:39377529-39386019_breast
6	lnc-FSIP1-5	chr15:39266356-39266436	ENSG00000259345.1
7	lnc-C15orf54-3	chr15:39311434-39311525	ENSG00000259278.1
8	lnc-C15orf54-3	chr15:39316355-39316560	ENSG00000259278.1
9	lnc-FSIP1-5	chr15:39363772-39363809	ENSG00000259345.1
10	lnc-FSIP1-5	chr15:39363704-39363809	ENSG00000259345.1
11	lnc-FSIP1-4	chr15:39266356-39266439	NONHSAT041726
12	lnc-FSIP1-5	chr15:39266356-39266436	ENSG00000259345.1
13	lnc-FSIP1-5	chr15:39266356-39266436	ENSG00000259345.1
14	lnc-C15orf54-3	chr15:39316844-39317119	ENSG00000259278.1

Variant related genes	Relation type
ENSG00000259278	TF binding region
ENSG00000259278	CpG island
ENSG00000137801	chromatin interactions

Extended variants
information (count: 6665 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:6665 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11852946	chr15:39188421-39188422	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182382832	chr15:39188455-39188456	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs372007062	chr15:39188483-39188484	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs79340828	chr15:39188510-39188511	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs144897258	chr15:39188521-39188522	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs75741312	chr15:39188529-39188530	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs148265150	chr15:39188538-39188539	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs140376062	chr15:39188539-39188540	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs374820784	chr15:39188607-39188608	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs75072142	chr15:39188609-39188610	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs115878158	chr15:39188625-39188626	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs374758574	chr15:39188649-39188650	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs550540768	chr15:39188654-39188655	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs568858240	chr15:39188662-39188663	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs150201407	chr15:39188694-39188695	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs547989026	chr15:39188723-39188724	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs576162721	chr15:39188736-39188737	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs187097473	chr15:39188748-39188749	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs114553509	chr15:39188761-39188762	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs59259932	chr15:39188766-39188767	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs79818199	chr15:39188787-39188788	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs556186406	chr15:39188831-39188832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138721373	chr15:39188856-39188857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183806264	chr15:39188869-39188870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143115655	chr15:39188878-39188879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573354664	chr15:39188906-39188907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561040129	chr15:39188919-39188920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115305853	chr15:39188925-39188926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147473194	chr15:39188937-39188938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77558024	chr15:39188965-39188966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2411220	chr15:39189053-39189054	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs188691624	chr15:39189174-39189175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562499273	chr15:39189185-39189186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs193300285	chr15:39189224-39189225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548049968	chr15:39189243-39189244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112215461	chr15:39189339-39189340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560104537	chr15:39189382-39189383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527515261	chr15:39189383-39189384	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552063049	chr15:39189443-39189444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532408931	chr15:39189462-39189463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570568475	chr15:39189474-39189475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77455143	chr15:39189478-39189479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138488743	chr15:39189525-39189526	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549806328	chr15:39189539-39189540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143964589	chr15:39189540-39189541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183749017	chr15:39189600-39189601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186632911	chr15:39189618-39189619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144327323	chr15:39189620-39189621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534452509	chr15:39189623-39189624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558873143	chr15:39189632-39189633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Melanoma	18172304	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
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21129771	CNVD
Breast cancer	21045282	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	22032731	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Colorectal cancer	21645411	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:864 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:39176200-39197600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr15:39185000-39189200	Enhancers	HSMM	muscle
3	chr15:39185000-39189800	Enhancers	HUVEC	blood vessel
4	chr15:39185000-39189800	Enhancers	NHDF-Ad	bronchial
5	chr15:39185000-39192000	Enhancers	Muscle Satellite Cultured Cells	--
6	chr15:39185200-39189600	Enhancers	Osteobl	bone
7	chr15:39185200-39192800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr15:39185400-39188800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr15:39185400-39190000	Enhancers	HSMMtube	muscle
10	chr15:39185400-39190200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr15:39185400-39191200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr15:39185800-39188800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr15:39185800-39188800	Enhancers	Fetal Heart	heart
14	chr15:39185800-39188800	Enhancers	HMEC	breast
15	chr15:39186200-39188800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr15:39186400-39188600	Enhancers	NHEK	skin
17	chr15:39186600-39189200	Enhancers	Hela-S3	cervix
18	chr15:39186600-39189200	Enhancers	NH-A	brain
19	chr15:39186800-39188800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr15:39187000-39189000	Enhancers	NHLF	lung
21	chr15:39187200-39189000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr15:39187400-39189800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr15:39187400-39191600	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr15:39187800-39189600	Enhancers	Ovary	ovary
25	chr15:39188000-39189000	Weak transcription	Fetal Lung	lung
26	chr15:39188000-39189800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr15:39188200-39188600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr15:39188200-39188600	Weak transcription	Fetal Kidney	kidney
29	chr15:39188400-39188800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr15:39188400-39188800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr15:39188400-39188800	Enhancers	Placenta	Placenta
32	chr15:39188400-39197000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr15:39188600-39188800	Enhancers	Fetal Kidney	kidney
34	chr15:39188800-39189200	Weak transcription	Fetal Heart	heart
35	chr15:39188800-39189600	Weak transcription	Fetal Kidney	kidney
36	chr15:39188800-39190200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr15:39188800-39191200	Weak transcription	HMEC	breast
38	chr15:39188800-39192000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr15:39189000-39189400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr15:39189000-39189800	Enhancers	Fetal Lung	lung
41	chr15:39189000-39189800	Weak transcription	NHLF	lung
42	chr15:39189200-39190200	Weak transcription	HSMM	muscle
43	chr15:39189200-39190800	Enhancers	Fetal Heart	heart
44	chr15:39189400-39189600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr15:39189400-39189600	Enhancers	Right Ventricle	heart
46	chr15:39189600-39189800	Enhancers	Fetal Kidney	kidney
47	chr15:39189600-39189800	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr15:39189600-39190000	Weak transcription	Osteobl	bone
49	chr15:39189600-39190400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr15:39189600-39190400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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