Variant report

Variant	nsv903980
Chromosome Location	chr15:33149087-33264201
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1333)
CpG islands
(count:1040)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1333 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:33159576-33159767	K562	blood:	n/a	n/a
2	ATF1	chr15:33218767-33218893	K562	blood:	n/a	n/a
3	ATF1	chr15:33162681-33163010	K562	blood:	n/a	n/a
4	ATF1	chr15:33172177-33172299	K562	blood:	n/a	n/a
5	ATF2	chr15:33191348-33191883	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr15:33191373-33191925	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr15:33200491-33201087	GM12878	blood:	n/a	n/a
8	ATF3	chr15:33162589-33163012	K562	blood:	n/a	n/a
9	BACH1	chr15:33248180-33248533	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr15:33159494-33159789	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr15:33165875-33166293	K562	blood:	n/a	n/a
12	BACH1	chr15:33165863-33166308	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr15:33173812-33174063	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr15:33164881-33164895	K562	blood:	n/a	n/a
15	BACH1	chr15:33221160-33221387	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr15:33175154-33175210	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr15:33175656-33175900	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr15:33162674-33163028	GM12878	blood:	n/a	chr15:33162820-33162831
19	BATF	chr15:33200675-33201039	GM12878	blood:	n/a	n/a
20	BATF	chr15:33216573-33216893	GM12878	blood:	n/a	n/a
21	BATF	chr15:33216580-33216867	GM12878	blood:	n/a	n/a
22	BATF	chr15:33162661-33162960	GM12878	blood:	n/a	chr15:33162820-33162831
23	BCL11A	chr15:33162643-33162955	GM12878	blood:	n/a	n/a
24	BCL11A	chr15:33162608-33162974	GM12878	blood:	n/a	n/a
25	BCL11A	chr15:33200755-33201026	GM12878	blood:	n/a	chr15:33200826-33200835
26	BCL11A	chr15:33191394-33191852	H1-hESC	embryonic stem cell:	n/a	chr15:33191642-33191655
27	BCL11A	chr15:33216557-33216912	GM12878	blood:	n/a	n/a
28	BCL11A	chr15:33200637-33201056	GM12878	blood:	n/a	chr15:33200826-33200835
29	BCL11A	chr15:33191354-33191789	H1-hESC	embryonic stem cell:	n/a	chr15:33191642-33191655
30	BCL3	chr15:33158768-33159753	A549	lung:	n/a	n/a
31	BCL3	chr15:33158650-33159539	A549	lung:	n/a	n/a
32	BCLAF1	chr15:33200479-33201139	GM12878	blood:	n/a	chr15:33200826-33200835
33	BCLAF1	chr15:33216507-33216804	GM12878	blood:	n/a	n/a
34	BHLHE40	chr15:33247941-33248082	K562	blood:	n/a	n/a
35	BHLHE40	chr15:33216326-33216884	GM12878	blood:	n/a	n/a
36	BHLHE40	chr15:33159651-33159697	K562	blood:	n/a	n/a
37	BHLHE40	chr15:33162181-33162900	K562	blood:	n/a	n/a
38	BHLHE40	chr15:33200447-33201288	GM12878	blood:	n/a	n/a
39	BHLHE40	chr15:33191303-33191733	GM12878	blood:	n/a	n/a
40	CCNT2	chr15:33162693-33162976	K562	blood:	n/a	n/a
41	CEBPB	chr15:33215946-33216260	A549	lung:	n/a	chr15:33216107-33216118
42	CEBPB	chr15:33221424-33221778	HepG2	liver:	n/a	n/a
43	CEBPB	chr15:33219349-33219704	IMR90	lung:	n/a	chr15:33219513-33219524
44	CEBPB	chr15:33158767-33159639	A549	lung:	n/a	n/a
45	CEBPB	chr15:33210029-33210280	K562	blood:	n/a	chr15:33210196-33210209 chr15:33210196-33210207
46	CEBPB	chr15:33219343-33219706	A549	lung:	n/a	chr15:33219513-33219524
47	CEBPB	chr15:33219348-33219699	HepG2	liver:	n/a	chr15:33219513-33219524
48	CEBPB	chr15:33258790-33259112	A549	lung:	n/a	chr15:33258951-33258964 chr15:33258952-33258963
49	CEBPB	chr15:33258823-33259097	Hela-S3	cervix:	n/a	chr15:33258951-33258964 chr15:33258952-33258963
50	CEBPB	chr15:33246445-33246700	HepG2	liver:	n/a	chr15:33246558-33246569 chr15:33246558-33246571 chr15:33246558-33246571

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:33165563-33165613	U87	brain:	n/a
2	chr15:33200866-33200916	SK-N-SH	brain:	n/a
3	chr15:33245281-33245331	ovcar-3	ovarian:	n/a
4	chr15:33165563-33165613	U87	brain:	n/a
5	chr15:33200866-33200916	SK-N-SH	brain:	n/a
6	chr15:33245281-33245331	ovcar-3	ovarian:	n/a
7	chr15:33259575-33259625	HEEpiC	esophagus:	n/a
8	chr15:33171339-33171389	BJ	skin:	n/a
9	chr15:33245281-33245331	IMR90	lung:	fetal
10	chr15:33188759-33188809	HEK293	kidney:	embryo
11	chr15:33179514-33179564	A549	lung:	n/a
12	chr15:33251279-33251329	GM06990	blood:	n/a
13	chr15:33220732-33220782	PANC-1	pancreas:	n/a
14	chr15:33171339-33171389	RPTEC	kidney:	n/a
15	chr15:33245281-33245331	K562	blood:	n/a
16	chr15:33259575-33259625	NHDF-neo	bronchial:	n/a
17	chr15:33165563-33165613	MCF-7	breast:	n/a
18	chr15:33171339-33171389	HepG2	liver:	n/a
19	chr15:33179514-33179564	SKMC	muscle:	n/a
20	chr15:33162876-33162926	HMEC	breast:	n/a
21	chr15:33251279-33251329	RPTEC	kidney:	n/a
22	chr15:33177867-33177917	HepG2	liver:	n/a
23	chr15:33191698-33191748	NH-A	brain:	n/a
24	chr15:33162876-33162926	HPAEpiC	pulmonary alveolar:	n/a
25	chr15:33154262-33154312	HepG2	liver:	n/a
26	chr15:33211107-33211157	CMK	blood:	n/a
27	chr15:33188759-33188809	HNPCEpiC	eye:	n/a
28	chr15:33195247-33195297	K562	blood:	n/a
29	chr15:33171339-33171389	PANC-1	pancreas:	n/a
30	chr15:33154262-33154312	Caco-2	colon:	n/a
31	chr15:33188759-33188809	GM19239	blood:	n/a
32	chr15:33162876-33162926	AG04450	lung:	fetal
33	chr15:33162876-33162926	SK-N-SH_RA	brain:	n/a
34	chr15:33245281-33245331	GM12891	blood:	n/a
35	chr15:33154262-33154312	ovcar-3	ovarian:	n/a
36	chr15:33195247-33195297	AG04450	lung:	fetal
37	chr15:33220732-33220782	BJ	skin:	n/a
38	chr15:33211107-33211157	Hepatocyte	liver:	n/a
39	chr15:33179514-33179564	HepG2	liver:	n/a
40	chr15:33154262-33154312	ProgFib	skin:	n/a
41	chr15:33162876-33162926	GM12891	blood:	n/a
42	chr15:33251279-33251329	T-47D	breast:	n/a
43	chr15:33154262-33154312	HRCEpiC	kidney:	n/a
44	chr15:33177867-33177917	RPTEC	kidney:	n/a
45	chr15:33165563-33165613	HCF	heart:	n/a
46	chr15:33165563-33165613	HepG2	liver:	n/a
47	chr15:33191698-33191748	MCF10A-Er-Src	breast:	n/a
48	chr15:33259575-33259625	AoSMC	blood vessel:	n/a
49	chr15:33165563-33165613	T-47D	breast:	n/a
50	chr15:33245281-33245331	NHBE	bronchial:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:33264185..33265845-chr15:33271129..33273337,2	MCF-7	breast:
2	chr15:33232993..33235695-chr15:33238081..33239940,2	K562	blood:
3	chr15:33136574..33137426-chr15:33228228..33228738,2	K562	blood:
4	chr15:33244808..33246374-chr15:33249318..33251534,2	MCF-7	breast:
5	chr15:33177002..33179276-chr15:33196689..33199398,2	K562	blood:
6	chr15:33232993..33235695-chr15:33238081..33239940,2	K562	blood:
7	chr15:33191297..33193263-chr15:33193347..33195988,2	K562	blood:
8	chr15:33245362..33248334-chr15:33358852..33360940,3	MCF-7	breast:
9	chr15:33159839..33162457-chr15:33167259..33169460,2	K562	blood:
10	chr15:33237429..33239397-chr15:33241975..33243636,2	MCF-7	breast:
11	chr15:33159839..33162457-chr15:33167259..33169460,2	K562	blood:
12	chr15:33203701..33205590-chr15:33205602..33207495,2	MCF-7	breast:
13	chr15:33148021..33149698-chr15:33359927..33361500,2	MCF-7	breast:
14	chr15:33191578..33193662-chr15:33205151..33207936,2	MCF-7	breast:
15	chr15:33191578..33193662-chr15:33205151..33207936,2	MCF-7	breast:
16	chr15:33244172..33246376-chr15:33247943..33250082,2	K562	blood:
17	chr15:33203701..33205590-chr15:33205602..33207495,2	MCF-7	breast:
18	chr15:33148879..33150784-chr15:33151258..33154124,2	K562	blood:
19	chr15:33244592..33247228-chr15:33248722..33251718,2	MCF-7	breast:
20	chr15:33152788..33155505-chr15:33160660..33163285,2	K562	blood:
21	chr15:33264165..33266280-chr15:33277864..33279978,2	MCF-7	breast:
22	chr15:33194367..33197072-chr15:33201375..33203984,2	MCF-7	breast:
23	chr15:33244592..33247228-chr15:33248722..33251718,2	MCF-7	breast:
24	chr15:33244808..33246374-chr15:33249318..33251534,2	MCF-7	breast:
25	chr15:33177002..33179276-chr15:33196689..33199398,2	K562	blood:
26	chr15:33244172..33246376-chr15:33247943..33250082,2	K562	blood:
27	chr15:33237429..33239397-chr15:33241975..33243636,2	MCF-7	breast:
28	chr15:33194367..33197072-chr15:33201375..33203984,2	MCF-7	breast:
29	chr15:32954517..32955503-chr15:33228158..33229122,2	MCF-7	breast:
30	chr15:33136039..33136889-chr15:33228248..33228998,3	MCF-7	breast:
31	chr15:32954601..32955459-chr15:33247920..33248524,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000212415	TF binding region
FMN1	TF binding region
ENSG00000238342	TF binding region
ENSG00000212415	CpG island
FMN1	CpG island
ENSG00000238342	CpG island
ENSG00000248905	chromatin interactions

Extended variants
information (count: 5664 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:5664 , 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	rs8032931	chr15:33149087-33149088	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551945721	chr15:33149133-33149134	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs570256276	chr15:33149141-33149142	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs75668978	chr15:33149152-33149153	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs556077850	chr15:33149161-33149162	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs574214730	chr15:33149169-33149170	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs370762225	chr15:33149170-33149171	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs374027347	chr15:33149172-33149173	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs367606290	chr15:33149175-33149176	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs541502365	chr15:33149186-33149187	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs371401743	chr15:33149187-33149188	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs1451888	chr15:33149196-33149197	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs368780529	chr15:33149197-33149198	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs199614323	chr15:33149198-33149199	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs371921827	chr15:33149220-33149221	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs139755114	chr15:33149233-33149234	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs575817325	chr15:33149252-33149253	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs116455579	chr15:33149262-33149263	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs371991451	chr15:33149283-33149284	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs75076908	chr15:33149288-33149289	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs368988373	chr15:33149298-33149299	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs530533964	chr15:33149317-33149318	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529128469	chr15:33149328-33149329	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs371904793	chr15:33149334-33149335	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs372699660	chr15:33149343-33149344	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs547677993	chr15:33149371-33149372	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs559478555	chr15:33149384-33149385	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs545363485	chr15:33149386-33149387	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs533409484	chr15:33149403-33149404	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs563925979	chr15:33149548-33149549	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs551880682	chr15:33149562-33149563	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs181299554	chr15:33149576-33149577	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs537556244	chr15:33149586-33149587	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs528380131	chr15:33149598-33149599	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs12439262	chr15:33149622-33149623	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs376527417	chr15:33149632-33149633	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs558834162	chr15:33149635-33149636	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs149389931	chr15:33149660-33149661	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs535000896	chr15:33149661-33149662	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs553678322	chr15:33149666-33149667	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189933268	chr15:33149687-33149688	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs144674978	chr15:33149751-33149752	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs116208747	chr15:33149807-33149808	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs575705750	chr15:33149814-33149815	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs543115781	chr15:33149817-33149818	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182390224	chr15:33149820-33149821	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs568225903	chr15:33149888-33149889	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs573819418	chr15:33149890-33149891	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs4780048	chr15:33149893-33149894	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs186387296	chr15:33149906-33149907	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	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
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
Abnormal corpus callosum	21572526	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
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
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1594 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33096200-33154000	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr15:33096400-33159000	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr15:33118600-33159000	Weak transcription	Gastric	stomach
4	chr15:33131200-33153800	Weak transcription	Fetal Kidney	kidney
5	chr15:33131800-33164800	Weak transcription	Pancreas	Pancrea
6	chr15:33132400-33154000	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr15:33132800-33154000	Weak transcription	Brain Angular Gyrus	brain
8	chr15:33133000-33150400	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr15:33137800-33153600	Weak transcription	Fetal Thymus	thymus
10	chr15:33138800-33190600	Weak transcription	Thymus	Thymus
11	chr15:33139600-33190600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr15:33142600-33168200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr15:33143400-33150000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr15:33144000-33153600	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr15:33147000-33191400	Weak transcription	Lung	lung
16	chr15:33147200-33149200	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr15:33147200-33150200	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr15:33147400-33149200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr15:33147400-33149400	Enhancers	HUVEC	blood vessel
20	chr15:33147400-33150200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr15:33147400-33150400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr15:33147400-33150400	Enhancers	Osteobl	bone
23	chr15:33147400-33150600	Enhancers	HMEC	breast
24	chr15:33147400-33150800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr15:33147400-33150800	Enhancers	Muscle Satellite Cultured Cells	--
26	chr15:33147400-33150800	Enhancers	NHEK	skin
27	chr15:33147400-33151200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr15:33147400-33152200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr15:33147600-33149400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr15:33147600-33149400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr15:33147600-33149600	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr15:33147600-33150400	Genic enhancers	HSMM	muscle
33	chr15:33147600-33150400	Enhancers	NHLF	lung
34	chr15:33147800-33149200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr15:33147800-33149200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr15:33147800-33149600	Enhancers	Placenta Amnion	Placenta Amnion
37	chr15:33148000-33149400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr15:33148000-33149600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr15:33148000-33150200	Enhancers	Stomach Smooth Muscle	stomach
40	chr15:33148000-33158600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr15:33148200-33149800	Strong transcription	Sigmoid Colon	Sigmoid Colon
42	chr15:33148400-33153800	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr15:33148600-33149200	Strong transcription	Stomach Mucosa	stomach
44	chr15:33148600-33149200	Flanking Active TSS	NH-A	brain
45	chr15:33148600-33149400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr15:33148600-33149400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr15:33148600-33149400	Genic enhancers	Placenta	Placenta
48	chr15:33148600-33149600	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr15:33148600-33153800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr15:33148600-33153800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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