Variant report

Variant	nsv827277
Chromosome Location	chr15:30921917-31089783
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1311)
CpG islands
(count:244)
Chromatin interactive
region (count:4)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1311 , 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	chr15:31058643-31058927	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:30941065-30941323	HepG2	liver:	n/a	chr15:30941184-30941200 chr15:30941198-30941214
3	ATF1	chr15:30942408-30942747	K562	blood:	n/a	n/a
4	ATF2	chr15:30941959-30942874	GM12878	blood:	n/a	n/a
5	BACH1	chr15:31056549-31056561	K562	blood:	n/a	n/a
6	BATF	chr15:30939417-30939718	GM12878	blood:	n/a	n/a
7	BATF	chr15:30939410-30939698	GM12878	blood:	n/a	n/a
8	BATF	chr15:30942101-30942823	GM12878	blood:	n/a	n/a
9	BATF	chr15:30942098-30942760	GM12878	blood:	n/a	n/a
10	BATF	chr15:31078925-31079140	GM12878	blood:	n/a	n/a
11	BATF	chr15:30988651-30989902	GM12878	blood:	n/a	n/a
12	BATF	chr15:31001037-31001298	GM12878	blood:	n/a	chr15:31001194-31001205
13	BATF	chr15:31047306-31047532	GM12878	blood:	n/a	n/a
14	BATF	chr15:30988887-30989837	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:30942112-30942840	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:30988813-30989894	GM12878	blood:	n/a	n/a
17	BCL11A	chr15:31047283-31047543	GM12878	blood:	n/a	n/a
18	BCL11A	chr15:30989215-30989908	GM12878	blood:	n/a	n/a
19	BCL11A	chr15:30988374-30988675	GM12878	blood:	n/a	n/a
20	BCL11A	chr15:30988850-30989149	GM12878	blood:	n/a	n/a
21	BCLAF1	chr15:30942082-30942772	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:30959588-30959606	K562	blood:	n/a	n/a
23	BHLHE40	chr15:30968872-30968884	K562	blood:	n/a	n/a
24	BHLHE40	chr15:30941983-30942693	GM12878	blood:	n/a	n/a
25	BHLHE40	chr15:30989526-30989883	GM12878	blood:	n/a	n/a
26	CEBPB	chr15:30983872-30983981	K562	blood:	n/a	n/a
27	CEBPB	chr15:31058645-31058938	HepG2	liver:	n/a	chr15:31058745-31058756
28	CEBPB	chr15:30953382-30953692	K562	blood:	n/a	chr15:30953517-30953528
29	CEBPB	chr15:30967306-30967676	IMR90	lung:	n/a	chr15:30967474-30967485
30	CEBPB	chr15:30953404-30953637	K562	blood:	n/a	chr15:30953517-30953528
31	CEBPB	chr15:31058558-31059008	IMR90	lung:	n/a	chr15:31058745-31058756
32	CEBPB	chr15:30983768-30983986	A549	lung:	n/a	n/a
33	CEBPB	chr15:30953401-30953667	IMR90	lung:	n/a	chr15:30953517-30953528
34	CEBPB	chr15:30967341-30967670	A549	lung:	n/a	chr15:30967474-30967485
35	CEBPB	chr15:30942518-30943053	IMR90	lung:	n/a	n/a
36	CEBPB	chr15:31084274-31084474	HepG2	liver:	n/a	n/a
37	CEBPB	chr15:30958152-30958542	K562	blood:	n/a	n/a
38	CEBPB	chr15:30983791-30984131	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr15:31058652-31058827	HepG2	liver:	n/a	chr15:31058745-31058756
40	CEBPB	chr15:31058570-31058941	A549	lung:	n/a	chr15:31058745-31058756
41	CEBPB	chr15:30989170-30989954	GM12878	blood:	n/a	n/a
42	CEBPB	chr15:31035071-31035332	IMR90	lung:	n/a	n/a
43	CEBPB	chr15:31058573-31058941	H1-hESC	embryonic stem cell:	n/a	chr15:31058745-31058756
44	CEBPB	chr15:30983881-30984093	HepG2	liver:	n/a	n/a
45	CEBPB	chr15:30958201-30958546	IMR90	lung:	n/a	n/a
46	CEBPB	chr15:31058568-31058944	HepG2	liver:	n/a	chr15:31058745-31058756
47	CEBPB	chr15:30964859-30965084	K562	blood:	n/a	n/a
48	CEBPB	chr15:30953435-30953668	A549	lung:	n/a	chr15:30953517-30953528
49	CEBPB	chr15:31058670-31058834	K562	blood:	n/a	chr15:31058745-31058756
50	CEBPB	chr15:30967310-30967751	A549	lung:	n/a	chr15:30967474-30967485

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31086755-31086805	H1-hESC	embryonic stem cell:	embryo
2	chr15:31086755-31086805	MCF10A-Er-Src	breast:	n/a
3	chr15:30930499-30930549	ECC-1	luminal epithelium:	n/a
4	chr15:31086755-31086805	HL-60	blood:	n/a
5	chr15:30930499-30930549	HIPEpiC	eye:	n/a
6	chr15:31086755-31086805	AG04449	skin:	fetal
7	chr15:31066090-31066140	HCF	heart:	n/a
8	chr15:31088666-31088716	H1-hESC	embryonic stem cell:	embryo
9	chr15:31088666-31088716	HRPEpiC	eye:	n/a
10	chr15:30930499-30930549	RPTEC	kidney:	n/a
11	chr15:31066090-31066140	NB4	blood:	n/a
12	chr15:31088666-31088716	NH-A	brain:	n/a
13	chr15:31086755-31086805	HEK293	kidney:	embryo
14	chr15:31066090-31066140	ovcar-3	ovarian:	n/a
15	chr15:31086755-31086805	BJ	skin:	n/a
16	chr15:31066090-31066140	K562	blood:	n/a
17	chr15:30930499-30930549	HRPEpiC	eye:	n/a
18	chr15:30930499-30930549	AG04450	lung:	fetal
19	chr15:31066090-31066140	SK-N-MC	brain:	n/a
20	chr15:31086755-31086805	HRCEpiC	kidney:	n/a
21	chr15:30930499-30930549	Caco-2	colon:	n/a
22	chr15:31066090-31066140	U87	brain:	n/a
23	chr15:30930499-30930549	AG09319	gingival:	n/a
24	chr15:31088666-31088716	A549	lung:	n/a
25	chr15:30930499-30930549	HAEpiC	amniotic membrane:	n/a
26	chr15:30930499-30930549	PrEC	prostate:	n/a
27	chr15:31066090-31066140	AoSMC	blood vessel:	n/a
28	chr15:31086755-31086805	CMK	blood:	n/a
29	chr15:31088666-31088716	PrEC	prostate:	n/a
30	chr15:31086755-31086805	HCPEpiC	choroid plexus:	n/a
31	chr15:31066090-31066140	BJ	skin:	n/a
32	chr15:30930499-30930549	GM12891	blood:	n/a
33	chr15:31088666-31088716	HPAEpiC	pulmonary alveolar:	n/a
34	chr15:30930499-30930549	NB4	blood:	n/a
35	chr15:31088666-31088716	RPTEC	kidney:	n/a
36	chr15:31086755-31086805	A549	lung:	n/a
37	chr15:31086755-31086805	NHDF-neo	bronchial:	n/a
38	chr15:31066090-31066140	SKMC	muscle:	n/a
39	chr15:31086755-31086805	Jurkat	blood:	n/a
40	chr15:30930499-30930549	CMK	blood:	n/a
41	chr15:31086755-31086805	SK-N-SH	brain:	n/a
42	chr15:30930499-30930549	Jurkat	blood:	n/a
43	chr15:31088666-31088716	HRE	kidney:	n/a
44	chr15:31086755-31086805	SK-N-SH_RA	brain:	n/a
45	chr15:30930499-30930549	HEEpiC	esophagus:	n/a
46	chr15:31086755-31086805	K562	blood:	n/a
47	chr15:31086755-31086805	NH-A	brain:	n/a
48	chr15:31066090-31066140	GM12891	blood:	n/a
49	chr15:30930499-30930549	SK-N-MC	brain:	n/a
50	chr15:31066090-31066140	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:30957691..30960365-chr15:30969306..30971745,2	K562	blood:
2	chr15:30957691..30960365-chr15:30968745..30971745,3	K562	blood:
3	chr15:30957691..30960365-chr15:30969306..30971745,2	K562	blood:
4	chr15:30957691..30960365-chr15:30968745..30971745,3	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP11B-3	chr15:31074599-31075123	NONHSAT041397
2	lnc-ARHGAP11B-1	chr15:31060061-31065209	NONHSAT041384
3	lnc-ARHGAP11B-1	chr15:31008423-31008545	NONHSAT041384
4	lnc-ARHGAP11B-1	chr15:30950920-30951047	NONHSAT041384
5	lnc-ARHGAP11B-1	chr15:30939871-30939917	NONHSAT041382
6	lnc-ARHGAP11B-1	chr15:30938335-30938498	NONHSAT041382
7	lnc-GOLGA8H-2	chr15:30941000-30941732	ENSG00000269974.1
8	lnc-ARHGAP11B-1	chr15:31008423-31008545	NONHSAT041382
9	lnc-ARHGAP11B-1	chr15:31061535-31065196	NONHSAT041388
10	lnc-ARHGAP11B-1	chr15:31015549-31015698	NONHSAT041382
11	lnc-ARHGAP11B-1	chr15:31060916-31061371	NONHSAT041387
12	lnc-ARHGAP11B-1	chr15:31042605-31042759	NONHSAT041384

No data

Variant related genes	Relation type
GOLGA8UP	TF binding region
ARHGAP11B	TF binding region
ENSG00000247728	TF binding region
ENSG00000252602	TF binding region
ENSG00000269974	TF binding region
ENSG00000206846	TF binding region
ENSG00000221379	TF binding region
RN7SL82P	TF binding region
GOLGA8UP	CpG island
ARHGAP11B	CpG island
ENSG00000247728	CpG island
ENSG00000252602	CpG island
ENSG00000269974	CpG island
ENSG00000206846	CpG island
ENSG00000221379	CpG island
RN7SL82P	CpG island

Extended variants
information (count: 6318 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:6318 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570978688	chr15:30921968-30921969	Weak transcription Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs529535708	chr15:30921995-30921996	Weak transcription Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs369131708	chr15:30922001-30922002	Weak transcription Enhancers Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs539989120	chr15:30922007-30922008	Weak transcription Enhancers Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs111261873	chr15:30922021-30922022	Weak transcription Enhancers Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs552829429	chr15:30922040-30922041	Weak transcription Enhancers Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs545628198	chr15:30922082-30922083	Weak transcription Enhancers Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs143164079	chr15:30922124-30922125	Weak transcription Enhancers Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs535126463	chr15:30922130-30922131	Weak transcription Enhancers Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs76266206	chr15:30922155-30922156	Weak transcription Enhancers Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs368697288	chr15:30922164-30922165	Weak transcription Enhancers Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs541569853	chr15:30922214-30922215	Weak transcription Enhancers Active TSS Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs75627387	chr15:30922218-30922219	Weak transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs74881982	chr15:30922222-30922223	Weak transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554936192	chr15:30922346-30922347	Weak transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560618939	chr15:30922348-30922349	Weak transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574845596	chr15:30922384-30922385	Weak transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188590449	chr15:30922433-30922434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564369162	chr15:30922487-30922488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140294567	chr15:30922498-30922499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540399445	chr15:30922532-30922533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559637531	chr15:30922592-30922593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs201243620	chr15:30922605-30922606	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376174652	chr15:30922608-30922609	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528585979	chr15:30922610-30922611	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371290211	chr15:30922689-30922690	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548660702	chr15:30922706-30922707	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs200757156	chr15:30922761-30922762	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201762165	chr15:30922783-30922784	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs193125742	chr15:30922814-30922815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530898515	chr15:30922876-30922877	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372707643	chr15:30922907-30922908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375947784	chr15:30922910-30922911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370160982	chr15:30922911-30922912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371868107	chr15:30922917-30922918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551008146	chr15:30922918-30922919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571110011	chr15:30922972-30922973	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs539675609	chr15:30923005-30923006	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs377099058	chr15:30923015-30923016	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs566274237	chr15:30923043-30923044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185665121	chr15:30923048-30923049	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188431375	chr15:30923051-30923052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375932685	chr15:30923072-30923073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs180908994	chr15:30923091-30923092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557795104	chr15:30923114-30923115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577865165	chr15:30923136-30923137	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs543306526	chr15:30923173-30923174	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs540095569	chr15:30923249-30923250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560398604	chr15:30923321-30923322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369225598	chr15:30923334-30923335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:139)

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
Prader-willi syndrome	21504564	CNVD
The inv dup or idic syndrome	19019226	CNVD
Prader-willi syndrome	21233802	CNVD
Angelman syndrome	16617304	CNVD
Angelman syndrome	20970697	CNVD
Autism	22958593	CNVD
Prader-willi syndrome	16617304	CNVD
Prader-willi syndrome	18923514	CNVD
Prader-willi syndrome	20970697	CNVD
Angelman syndrome	16183798	CNVD
Angelman syndrome	18923514	CNVD
Prader-willi syndrome	22241247	CNVD
Epilepsy	20970697	CNVD
Autism	20970697	CNVD
Autism	19935738	CNVD
Autism	22930557	CNVD
Autism	19966786	CNVD
Autism	18923514	CNVD
Autism	18925931	CNVD
Autism	18835857	CNVD
Prader-willi syndrome	18835857	CNVD
Prader-willi syndrome	22152151	CNVD
Autism	22241247	CNVD
15q-syndrome	21725066	CNVD
Prader-willi syndrome	21503198	CNVD
Autism	21956041	CNVD
Prader-willi syndrome	16760730	CNVD
Prader-willi syndrome	22470819	CNVD
prenatal diagnosis	20453657	CNVD
Prader-willi syndrome	17867985	CNVD
Angelman syndrome	21072004	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
Prader-willi syndrome	18781185	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
Angelman syndrome	18787571	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Abnormal corpus callosum	21572526	CNVD
Neuropsychiatric disorder	20506139	CNVD
Austim spectrum disorder	21302340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Epilepsy	22499536	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Mental retardation	21956041	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Autism	21269290	CNVD
Intellectual disability	21269290	CNVD
Schizophrenia	21269290	CNVD
Colorectal cancer	21128281	CNVD
Epilepsy	19289393	CNVD
Epilepsy	20643615	CNVD
Mental retardation	19289393	CNVD
Mental retardation	20152051	CNVD
Schizophrenia	19289393	CNVD
dysmorphic features	19289393	CNVD
idiopathic epilepsies	19341504	CNVD
idiopathic generalized epilepsy	19592580	CNVD
idiopathic generalized epilepsy	19136953	CNVD
Autism	22094647	CNVD
Developmental delay	19898479	CNVD
Mental retardation	18278044	CNVD
Mental retardation	19898479	CNVD
Prader-willi syndrome	18854863	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Epilepsy	20502679	CNVD
small cell lung cancer	20016488	CNVD
Intellectual disability	21811512	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1298 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30916000-30922400	Active TSS	GM12878-XiMat	blood
2	chr15:30918800-30931200	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr15:30919200-30931000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:30919200-30935400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr15:30919200-30942400	Weak transcription	Primary T cells from cord blood	blood
6	chr15:30919200-30966400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr15:30919400-30924600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr15:30919400-30938400	Weak transcription	Fetal Muscle Trunk	muscle
9	chr15:30919400-30959800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr15:30919400-30969800	Weak transcription	Fetal Lung	lung
11	chr15:30919400-30972800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr15:30919600-30924200	Weak transcription	Fetal Stomach	stomach
13	chr15:30919600-30928800	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr15:30919600-30928800	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr15:30919600-30935200	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr15:30919600-30935400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr15:30919600-30939200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr15:30919600-30948200	Weak transcription	Duodenum Mucosa	Duodenum
19	chr15:30919600-30964000	Weak transcription	Fetal Intestine Large	intestine
20	chr15:30919600-31023200	Weak transcription	Fetal Intestine Small	intestine
21	chr15:30919800-30922000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr15:30919800-30933000	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr15:30919800-30940400	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr15:30919800-30942200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr15:30919800-30961800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr15:30920000-30922400	Weak transcription	Fetal Heart	heart
27	chr15:30920000-30923600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr15:30920000-30923600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr15:30920000-30926600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr15:30920000-30927200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr15:30920000-30928800	Weak transcription	Osteobl	bone
32	chr15:30920000-30938000	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr15:30920000-30938800	Weak transcription	Thymus	Thymus
34	chr15:30920000-30939200	Weak transcription	Fetal Muscle Leg	muscle
35	chr15:30920000-30939800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr15:30920000-30940600	Weak transcription	Primary hematopoietic stem cells	blood
37	chr15:30920000-30955400	Weak transcription	NH-A	brain
38	chr15:30920000-31028200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr15:30920200-30929400	Weak transcription	Fetal Thymus	thymus
40	chr15:30920600-30923600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr15:30920800-30922200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr15:30920800-30922400	Enhancers	Hela-S3	cervix
43	chr15:30920800-30923400	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr15:30920800-30927200	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr15:30920800-30927200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr15:30920800-30928800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr15:30920800-30933800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr15:30920800-30940400	Weak transcription	HSMM	muscle
49	chr15:30920800-30950400	Weak transcription	NHEK	skin
50	chr15:30921000-30922000	Weak transcription	HepG2	liver

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