Variant report

Variant	nsv904268
Chromosome Location	chr15:58763678-58803225
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:548)
CpG islands
(count:306)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:548 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:58785240-58785433	K562	blood:	n/a	n/a
2	ARID3A	chr15:58767778-58769308	HepG2	liver:	n/a	n/a
3	ATF1	chr15:58763625-58763852	K562	blood:	n/a	n/a
4	ATF2	chr15:58765953-58766459	GM12878	blood:	n/a	n/a
5	ATF2	chr15:58765955-58766385	GM12878	blood:	n/a	n/a
6	BACH1	chr15:58785153-58785591	K562	blood:	n/a	n/a
7	BACH1	chr15:58785186-58785562	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr15:58765883-58766370	GM12878	blood:	n/a	n/a
9	BATF	chr15:58765966-58766352	GM12878	blood:	n/a	n/a
10	BATF	chr15:58778294-58778642	GM12878	blood:	n/a	n/a
11	BCLAF1	chr15:58765870-58766475	GM12878	blood:	n/a	chr15:58766176-58766185 chr15:58766177-58766186
12	BCLAF1	chr15:58766975-58767520	GM12878	blood:	n/a	n/a
13	BHLHE40	chr15:58778283-58778640	K562	blood:	n/a	n/a
14	BHLHE40	chr15:58763674-58763876	K562	blood:	n/a	n/a
15	BHLHE40	chr15:58785276-58785597	K562	blood:	n/a	n/a
16	BHLHE40	chr15:58789487-58789598	K562	blood:	n/a	n/a
17	BHLHE40	chr15:58803043-58803273	K562	blood:	n/a	n/a
18	BHLHE40	chr15:58766003-58766342	GM12878	blood:	n/a	n/a
19	BRCA1	chr15:58767486-58767613	GM12878	blood:	n/a	n/a
20	CBX3	chr15:58781477-58781856	K562	blood:	n/a	n/a
21	CBX3	chr15:58778224-58778695	K562	blood:	n/a	n/a
22	CBX3	chr15:58781484-58781792	K562	blood:	n/a	n/a
23	CEBPB	chr15:58779439-58780009	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr15:58799361-58799994	A549	lung:	n/a	n/a
25	CEBPB	chr15:58767682-58768654	HepG2	liver:	n/a	n/a
26	CEBPB	chr15:58799491-58799840	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr15:58767768-58768010	HepG2	liver:	n/a	n/a
28	CEBPB	chr15:58782548-58783441	ECC-1	luminal epithelium:	n/a	chr15:58782871-58782884
29	CEBPB	chr15:58767788-58768086	K562	blood:	n/a	n/a
30	CEBPB	chr15:58763567-58763902	Hela-S3	cervix:	n/a	chr15:58763742-58763759
31	CEBPB	chr15:58786364-58786481	K562	blood:	n/a	chr15:58786415-58786426
32	CEBPB	chr15:58767695-58768638	HepG2	liver:	n/a	n/a
33	CEBPB	chr15:58799477-58799850	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr15:58799484-58799792	K562	blood:	n/a	n/a
35	CEBPB	chr15:58799486-58799846	HepG2	liver:	n/a	n/a
36	CEBPB	chr15:58767743-58768085	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr15:58799481-58799851	A549	lung:	n/a	n/a
38	CEBPB	chr15:58767627-58768142	HepG2	liver:	n/a	n/a
39	CEBPB	chr15:58787873-58788106	IMR90	lung:	n/a	n/a
40	CEBPB	chr15:58799476-58799866	K562	blood:	n/a	n/a
41	CEBPB	chr15:58799539-58799823	MCF-7	breast:	n/a	n/a
42	CEBPB	chr15:58799477-58799851	IMR90	lung:	n/a	n/a
43	CEBPB	chr15:58765969-58766352	IMR90	lung:	n/a	n/a
44	CEBPB	chr15:58782594-58783016	ECC-1	luminal epithelium:	n/a	chr15:58782871-58782884
45	CEBPB	chr15:58767725-58768071	A549	lung:	n/a	n/a
46	CEBPB	chr15:58766598-58766763	HepG2	liver:	n/a	chr15:58766660-58766671
47	CEBPB	chr15:58786272-58786518	HepG2	liver:	n/a	chr15:58786415-58786426
48	CEBPB	chr15:58767644-58768219	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPB	chr15:58766002-58766324	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr15:58768982-58769377	HepG2	liver:	n/a	chr15:58769189-58769200

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:58766885-58766935	HAEpiC	amniotic membrane:	n/a
2	chr15:58766885-58766935	HAEpiC	amniotic membrane:	n/a
3	chr15:58782685-58782735	PANC-1	pancreas:	n/a
4	chr15:58791257-58791307	PFSK-1	brain:	n/a
5	chr15:58791257-58791307	HUVEC	blood vessel:	n/a
6	chr15:58797839-58797889	HEK293	kidney:	embryo
7	chr15:58782685-58782735	HEEpiC	esophagus:	n/a
8	chr15:58766885-58766935	PrEC	prostate:	n/a
9	chr15:58782685-58782735	RPTEC	kidney:	n/a
10	chr15:58766885-58766935	AG09319	gingival:	n/a
11	chr15:58766885-58766935	T-47D	breast:	n/a
12	chr15:58797839-58797889	AG10803	skin:	n/a
13	chr15:58782685-58782735	PrEC	prostate:	n/a
14	chr15:58782685-58782735	HNPCEpiC	eye:	n/a
15	chr15:58782685-58782735	AG10803	skin:	n/a
16	chr15:58782685-58782735	NT2-D1	testis:	n/a
17	chr15:58797839-58797889	HRE	kidney:	n/a
18	chr15:58791257-58791307	HCF	heart:	n/a
19	chr15:58782685-58782735	HCT-116	colon:	n/a
20	chr15:58782685-58782735	K562	blood:	n/a
21	chr15:58782685-58782735	HRE	kidney:	n/a
22	chr15:58766885-58766935	SK-N-SH	brain:	n/a
23	chr15:58782688-58782738	GM12878	blood:	n/a
24	chr15:58782688-58782738	GM19239	blood:	n/a
25	chr15:58782685-58782735	HepG2	liver:	n/a
26	chr15:58782685-58782735	NB4	blood:	n/a
27	chr15:58791257-58791307	GM12878	blood:	n/a
28	chr15:58766885-58766935	GM12878	blood:	n/a
29	chr15:58791257-58791307	HRE	kidney:	n/a
30	chr15:58766885-58766935	SK-N-MC	brain:	n/a
31	chr15:58782685-58782735	GM12891	blood:	n/a
32	chr15:58797839-58797889	Caco-2	colon:	n/a
33	chr15:58797839-58797889	HCM	heart:	n/a
34	chr15:58791257-58791307	SK-N-MC	brain:	n/a
35	chr15:58766885-58766935	HNPCEpiC	eye:	n/a
36	chr15:58766885-58766935	MCF-7	breast:	n/a
37	chr15:58791257-58791307	GM19239	blood:	n/a
38	chr15:58782688-58782738	RPTEC	kidney:	n/a
39	chr15:58791257-58791307	GM12891	blood:	n/a
40	chr15:58797839-58797889	AG04450	lung:	fetal
41	chr15:58791257-58791307	NHDF-neo	bronchial:	n/a
42	chr15:58782685-58782735	ECC-1	luminal epithelium:	n/a
43	chr15:58791257-58791307	Hepatocyte	liver:	n/a
44	chr15:58782688-58782738	NB4	blood:	n/a
45	chr15:58791257-58791307	HL-60	blood:	n/a
46	chr15:58782685-58782735	AoSMC	blood vessel:	n/a
47	chr15:58797839-58797889	HepG2	liver:	n/a
48	chr15:58766885-58766935	LNCaP	prostate:	n/a
49	chr15:58766885-58766935	Caco-2	colon:	n/a
50	chr15:58782685-58782735	SK-N-SH_RA	brain:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:58623181..58625459-chr15:58764481..58766715,2	MCF-7	breast:
2	chr15:58767751..58769658-chr15:58771265..58773299,2	MCF-7	breast:
3	chr15:58758547..58760128-chr15:58777523..58780209,2	MCF-7	breast:
4	chr15:58787065..58789640-chr15:58800910..58803456,2	MCF-7	breast:
5	chr15:58767751..58769658-chr15:58771265..58773299,2	MCF-7	breast:
6	chr15:58801519..58805506-chr15:58811166..58813986,3	K562	blood:
7	chr15:58791633..58793802-chr15:58794935..58797234,3	K562	blood:
8	chr15:58786761..58788774-chr15:59039911..59042146,2	K562	blood:
9	chr15:58767133..58770014-chr15:58770584..58772843,2	MCF-7	breast:
10	chr15:58762574..58764554-chr15:58812167..58813777,2	K562	blood:
11	chr15:58790757..58793256-chr15:58794935..58797026,2	K562	blood:
12	chr15:58767133..58770014-chr15:58770584..58772843,2	MCF-7	breast:
13	chr15:58787065..58789640-chr15:58800910..58803456,2	MCF-7	breast:
14	chr15:58800980..58802725-chr15:58817478..58819244,2	K562	blood:
15	chr15:58778802..58780678-chr15:58783257..58786951,3	K562	blood:
16	chr15:58778802..58780678-chr15:58783257..58786951,3	K562	blood:
17	chr15:58769989..58771899-chr15:58773674..58776005,2	K562	blood:
18	chr15:58769989..58771899-chr15:58773674..58776005,2	K562	blood:
19	chr15:58800669..58805424-chr15:58807712..58810883,4	K562	blood:
20	chr15:58783009..58786824-chr15:58787772..58790243,5	K562	blood:
21	chr15:58797035..58800948-chr15:58803702..58808140,4	K562	blood:
22	chr15:58797460..58800451-chr15:58803881..58805523,2	K562	blood:
23	chr15:58765282..58766825-chr15:58783128..58785341,2	K562	blood:
24	chr15:58762234..58763977-chr15:59040711..59042531,2	K562	blood:
25	chr15:58791633..58793802-chr15:58794935..58797234,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM10-9	chr15:58789916-58790065	NONHSAT044093
2	lnc-ADAM10-9	chr15:58765830-58765959	NONHSAT044093
3	lnc-ALDH1A2-1	chr15:58790838-58790934	ENSG00000259293.1
4	lnc-ALDH1A2-1	chr15:58786972-58787082	ENSG00000259293.1

No data

Variant related genes	Relation type
ENSG00000259293	TF binding region
ALDH1A2	TF binding region
ENSG00000259293	CpG island
ALDH1A2	CpG island
ENSG00000128918	chromatin interactions
ENSG00000137845	chromatin interactions
ENSG00000259476	chromatin interactions
ENSG00000259293	chromatin interactions

Extended variants
information (count: 1833 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1833 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17190580	chr15:58763678-58763679	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs542818455	chr15:58763698-58763699	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs563007614	chr15:58763758-58763759	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs531660216	chr15:58763788-58763789	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs533739711	chr15:58763798-58763799	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs545093565	chr15:58763869-58763870	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs564976764	chr15:58763876-58763877	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs527660599	chr15:58763912-58763913	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs180913373	chr15:58763917-58763918	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs547319600	chr15:58763925-58763926	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs567423399	chr15:58763938-58763939	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs529918060	chr15:58764017-58764018	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs549671733	chr15:58764076-58764077	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs12911658	chr15:58764088-58764089	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs558677266	chr15:58764090-58764091	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs115364213	chr15:58764114-58764115	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs142898685	chr15:58764134-58764135	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs375774642	chr15:58764147-58764148	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs536124978	chr15:58764275-58764276	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs554462647	chr15:58764306-58764307	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs574209763	chr15:58764314-58764315	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs185477035	chr15:58764330-58764331	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs556524915	chr15:58764340-58764341	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs190233231	chr15:58764347-58764348	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs28478642	chr15:58764362-58764363	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs373168210	chr15:58764376-58764377	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs181369394	chr15:58764397-58764398	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs572132428	chr15:58764406-58764407	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs150254622	chr15:58764467-58764468	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs145932002	chr15:58764470-58764471	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs35901617	chr15:58764491-58764492	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs58968414	chr15:58764492-58764493	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs28713618	chr15:58764523-58764524	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs537058744	chr15:58764539-58764540	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs555401159	chr15:58764571-58764572	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs369073478	chr15:58764601-58764602	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs529902643	chr15:58764604-58764605	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs550047923	chr15:58764624-58764625	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs563378850	chr15:58764670-58764671	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs561658243	chr15:58764682-58764683	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs530409696	chr15:58764698-58764699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs532331541	chr15:58764712-58764713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs149561127	chr15:58764737-58764738	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs565746326	chr15:58764750-58764751	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs370323532	chr15:58764776-58764777	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs59071843	chr15:58764793-58764794	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs7180625	chr15:58764798-58764799	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs370655973	chr15:58764821-58764822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs144300074	chr15:58764854-58764855	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs568043342	chr15:58764954-58764955	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:996 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58743800-58770400	Enhancers	Fetal Thymus	thymus
2	chr15:58752800-58765000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:58755400-58765000	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr15:58755400-58765000	Weak transcription	Fetal Muscle Trunk	muscle
5	chr15:58755800-58765800	Weak transcription	Gastric	stomach
6	chr15:58758600-58764000	Weak transcription	Thymus	Thymus
7	chr15:58759400-58768400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr15:58759400-58770400	Enhancers	Placenta	Placenta
9	chr15:58759600-58765200	Weak transcription	Fetal Lung	lung
10	chr15:58759600-58765200	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr15:58759800-58763800	Weak transcription	GM12878-XiMat	blood
12	chr15:58759800-58765000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr15:58759800-58765000	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr15:58760400-58764400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr15:58760400-58770200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr15:58760600-58764600	Weak transcription	Spleen	Spleen
17	chr15:58760600-58765000	Weak transcription	K562	blood
18	chr15:58760600-58767000	Weak transcription	Fetal Intestine Large	intestine
19	chr15:58760800-58765000	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr15:58760800-58765000	Weak transcription	Small Intestine	intestine
21	chr15:58760800-58765200	Enhancers	HMEC	breast
22	chr15:58761000-58767200	Weak transcription	Fetal Intestine Small	intestine
23	chr15:58761400-58763800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr15:58761400-58763800	Enhancers	NH-A	brain
25	chr15:58761400-58764400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr15:58761400-58764400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr15:58761400-58764400	Enhancers	NHDF-Ad	bronchial
28	chr15:58761400-58766600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr15:58761800-58765000	Enhancers	Dnd41	blood
30	chr15:58762000-58763800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr15:58762000-58764000	Enhancers	HepG2	liver
32	chr15:58762000-58764200	Enhancers	HSMMtube	muscle
33	chr15:58762000-58764600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr15:58762000-58765000	Weak transcription	Liver	Liver
35	chr15:58762000-58765000	Weak transcription	Pancreas	Pancrea
36	chr15:58762000-58765000	Weak transcription	NHLF	lung
37	chr15:58762000-58765200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr15:58762000-58766200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr15:58762200-58764400	Enhancers	A549	lung
40	chr15:58762200-58765000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr15:58762200-58765000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr15:58762200-58765000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr15:58762400-58764400	Enhancers	Hela-S3	cervix
44	chr15:58762400-58765000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr15:58762400-58765000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr15:58762400-58765000	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr15:58762400-58765000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr15:58762400-58765000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr15:58762400-58765000	Weak transcription	Fetal Kidney	kidney
50	chr15:58762400-58765000	Weak transcription	Right Atrium	heart

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