Variant report

Variant	nsv568771
Chromosome Location	chr15:31357138-31384797
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:276)
CpG islands
(count:976)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:31381129-31381842	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:31361599-31361779	HepG2	liver:	n/a	n/a
3	ATF1	chr15:31371191-31371230	K562	blood:	n/a	n/a
4	ATF1	chr15:31376612-31376664	K562	blood:	n/a	n/a
5	BACH1	chr15:31373087-31373180	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr15:31384773-31385276	A549	lung:	n/a	n/a
7	BCL3	chr15:31369836-31370207	GM12878	blood:	n/a	n/a
8	BHLHE40	chr15:31381061-31382012	HepG2	liver:	n/a	n/a
9	CEBPB	chr15:31381253-31381467	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
10	CEBPB	chr15:31381210-31381539	IMR90	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
11	CEBPB	chr15:31360456-31360715	A549	lung:	n/a	n/a
12	CEBPB	chr15:31360446-31360642	HepG2	liver:	n/a	n/a
13	CEBPB	chr15:31381279-31381497	H1-hESC	embryonic stem cell:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
14	CEBPB	chr15:31381210-31381544	A549	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
15	CEBPB	chr15:31381201-31381538	K562	blood:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
16	CEBPB	chr15:31358174-31358215	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr15:31380951-31381935	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
18	CEBPB	chr15:31358005-31358413	MCF-7	breast:	n/a	n/a
19	CEBPB	chr15:31381101-31381576	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
20	CEBPB	chr15:31371688-31372101	IMR90	lung:	n/a	n/a
21	CEBPB	chr15:31381102-31381941	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
22	CEBPB	chr15:31381146-31381608	A549	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
23	CEBPD	chr15:31380900-31381232	HepG2	liver:	n/a	n/a
24	CEBPD	chr15:31381206-31381450	HepG2	liver:	n/a	n/a
25	CHD2	chr15:31381613-31381922	HepG2	liver:	n/a	n/a
26	CHD2	chr15:31384391-31384410	HepG2	liver:	n/a	n/a
27	CHD2	chr15:31381045-31381371	HepG2	liver:	n/a	n/a
28	CTCF	chr15:31373920-31374070	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr15:31357700-31357850	A549	lung:	n/a	n/a
30	CTCF	chr15:31370019-31370113	GM19239	blood:	n/a	n/a
31	CTCF	chr15:31372940-31373090	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr15:31373160-31373310	GM12875	blood:	n/a	n/a
33	CTCF	chr15:31357640-31357790	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr15:31375940-31376090	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr15:31360130-31360336	HepG2	liver:	n/a	n/a
36	CTCF	chr15:31373980-31374130	SAEC	small airway:	n/a	n/a
37	CTCF	chr15:31357780-31357930	WI-38	lung:	n/a	n/a
38	CTCF	chr15:31360140-31360290	HepG2	liver:	n/a	n/a
39	CTCF	chr15:31358120-31358270	GM12868	blood:	n/a	n/a
40	CTCF	chr15:31373040-31373190	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr15:31357731-31357850	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr15:31381160-31381199	GM10248	blood:	n/a	n/a
43	CTCF	chr15:31373970-31374074	MCF-7	breast:	n/a	n/a
44	CTCF	chr15:31357700-31357850	HEK293	kidney:	n/a	n/a
45	CTCF	chr15:31361820-31361970	BJ	skin:	n/a	n/a
46	CTCF	chr15:31370060-31370134	Fibrobl	skin:	n/a	n/a
47	CTCF	chr15:31373992-31374038	MCF-7	breast:	n/a	n/a
48	CTCF	chr15:31374020-31374170	NHEK	skin:	n/a	n/a
49	CTCF	chr15:31373994-31374013	MCF-7	breast:	n/a	n/a
50	CTCF	chr15:31375620-31375770	SK-N-SH_RA	brain:	n/a	chr15:31375641-31375654 chr15:31375727-31375736

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31358057-31358107	LNCaP	prostate:	n/a
2	chr15:31357238-31357288	SAEC	small airway:	n/a
3	chr15:31379377-31379427	HUVEC	blood vessel:	n/a
4	chr15:31381816-31381866	PrEC	prostate:	n/a
5	chr15:31362182-31362232	NH-A	brain:	n/a
6	chr15:31381015-31381065	CMK	blood:	n/a
7	chr15:31372889-31372939	HEK293	kidney:	embryo
8	chr15:31379377-31379427	NT2-D1	testis:	n/a
9	chr15:31372742-31372792	HPAEpiC	pulmonary alveolar:	n/a
10	chr15:31362182-31362232	HMEC	breast:	n/a
11	chr15:31358323-31358373	AG04450	lung:	fetal
12	chr15:31379377-31379427	PANC-1	pancreas:	n/a
13	chr15:31357535-31357585	RPTEC	kidney:	n/a
14	chr15:31379377-31379427	AG10803	skin:	n/a
15	chr15:31373178-31373228	HRE	kidney:	n/a
16	chr15:31362182-31362232	MCF10A-Er-Src	breast:	n/a
17	chr15:31380908-31380958	CMK	blood:	n/a
18	chr15:31357238-31357288	SK-N-SH	brain:	n/a
19	chr15:31357535-31357585	GM19239	blood:	n/a
20	chr15:31379377-31379427	HCT-116	colon:	n/a
21	chr15:31370762-31370812	AG04450	lung:	fetal
22	chr15:31370762-31370812	U87	brain:	n/a
23	chr15:31357535-31357585	AG10803	skin:	n/a
24	chr15:31357238-31357288	U87	brain:	n/a
25	chr15:31372889-31372939	AG04450	lung:	fetal
26	chr15:31357535-31357585	HEK293	kidney:	embryo
27	chr15:31357535-31357585	HAEpiC	amniotic membrane:	n/a
28	chr15:31383719-31383769	NT2-D1	testis:	n/a
29	chr15:31383719-31383769	CMK	blood:	n/a
30	chr15:31362182-31362232	LNCaP	prostate:	n/a
31	chr15:31372997-31373047	HRCEpiC	kidney:	n/a
32	chr15:31357535-31357585	HRCEpiC	kidney:	n/a
33	chr15:31381816-31381866	NHBE	bronchial:	n/a
34	chr15:31381015-31381065	PANC-1	pancreas:	n/a
35	chr15:31381816-31381866	BE2_C	brain:	n/a
36	chr15:31372889-31372939	LNCaP	prostate:	n/a
37	chr15:31380908-31380958	SKMC	muscle:	n/a
38	chr15:31381816-31381866	AG09309	skin:	n/a
39	chr15:31379377-31379427	RPTEC	kidney:	n/a
40	chr15:31373178-31373228	SKMC	muscle:	n/a
41	chr15:31381015-31381065	HEEpiC	esophagus:	n/a
42	chr15:31380908-31380958	Jurkat	blood:	n/a
43	chr15:31372889-31372939	HCT-116	colon:	n/a
44	chr15:31357238-31357288	AG04450	lung:	fetal
45	chr15:31372742-31372792	NHDF-neo	bronchial:	n/a
46	chr15:31372997-31373047	H1-hESC	embryonic stem cell:	embryo
47	chr15:31380908-31380958	HEK293	kidney:	embryo
48	chr15:31362182-31362232	HL-60	blood:	n/a
49	chr15:31362182-31362232	IMR90	lung:	fetal
50	chr15:31380908-31380958	HMEC	breast:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:31283182..31285507-chr15:31372643..31376293,4	MCF-7	breast:
2	chr15:31282551..31285125-chr15:31384026..31386861,2	MCF-7	breast:
3	chr15:31376554..31379301-chr15:31382366..31384596,2	MCF-7	breast:
4	chr15:31281186..31283904-chr15:31357047..31359370,2	MCF-7	breast:
5	chr15:31376554..31379301-chr15:31382366..31384596,2	MCF-7	breast:
6	chr15:31372825..31374445-chr15:31376180..31377708,2	K562	blood:
7	chr12:30948117..30948824-chr15:31360460..31361082,2	Hela-S3	cervix:
8	chr15:31382233..31384961-chr15:31390192..31392345,2	K562	blood:
9	chr15:31372825..31374445-chr15:31376180..31377708,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTMR10-1	chr15:31383179-31383431	l_1124_chr15:31383178-31385928_brain

miRNA name	Chromosome Location	mirBase accession
hsa-miR-211-3p	chr15:31357262-31357282	MIMAT0022694
hsa-miR-211-5p	chr15:31357298-31357319	MIMAT0000268

No data

Variant related genes	Relation type
TRPM1	TF binding region
MIR211	TF binding region
TRPM1	CpG island
MIR211	CpG island
ENSG00000235884	chromatin interactions
ENSG00000166912	chromatin interactions
RAB22A	Mature miRNA region
IL11	Mature miRNA region
ELOVL6	Mature miRNA region
TCF12	Mature miRNA region
CREB5	Mature miRNA region
KCNMA1	Mature miRNA region
POU3F2	Mature miRNA region
CDH5	Mature miRNA region

Extended variants
information (count: 1227 )
Associated
traits (count: 152 )

Variant overlapped rSNPs/rCNVs (count:1227 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs919001	chr15:31357138-31357139	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs112739225	chr15:31357149-31357150	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs377382359	chr15:31357216-31357217	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs146105159	chr15:31357232-31357233	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs140017415	chr15:31357238-31357239	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs570647489	chr15:31357244-31357245	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs34520022	chr15:31357245-31357246	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs368043674	chr15:31357248-31357249	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs187960998	chr15:31357301-31357302	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region miRNA	9 gene(s)	Overlapped CNVs	n/a
10	rs141424579	chr15:31357325-31357326	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs373848937	chr15:31357328-31357329	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs368632856	chr15:31357331-31357332	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs566338968	chr15:31357354-31357355	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs372885289	chr15:31357363-31357364	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs535707066	chr15:31357382-31357383	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs555394695	chr15:31357402-31357403	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs192817258	chr15:31357414-31357415	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs537475473	chr15:31357415-31357416	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs76580248	chr15:31357430-31357431	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs150581991	chr15:31357431-31357432	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs183457358	chr15:31357445-31357446	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs71474642	chr15:31357447-31357448	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs553567057	chr15:31357456-31357457	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs115184900	chr15:31357471-31357472	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs542482353	chr15:31357491-31357492	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs562274360	chr15:31357534-31357535	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs530920128	chr15:31357536-31357537	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs549511603	chr15:31357563-31357564	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs187408727	chr15:31357568-31357569	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs3825950	chr15:31357591-31357592	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs149708759	chr15:31357616-31357617	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs370067339	chr15:31357673-31357674	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs147402719	chr15:31357695-31357696	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs139712506	chr15:31357729-31357730	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs199500319	chr15:31357767-31357768	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs372716408	chr15:31357851-31357852	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs145109268	chr15:31357879-31357880	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs368529122	chr15:31357933-31357934	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs73374030	chr15:31358001-31358002	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs537842337	chr15:31358029-31358030	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs147597552	chr15:31358039-31358040	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs571274655	chr15:31358049-31358050	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs192595541	chr15:31358058-31358059	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs553932226	chr15:31358123-31358124	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs141925696	chr15:31358134-31358135	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs535704879	chr15:31358137-31358138	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs4779502	chr15:31358138-31358139	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs184833972	chr15:31358194-31358195	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs62038939	chr15:31358218-31358219	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs142072609	chr15:31358219-31358220	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:152)

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
Autism	19521722	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

Chromatin state (count:508 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31351400-31360000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr15:31353200-31363400	Weak transcription	Right Atrium	heart
3	chr15:31353400-31365200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr15:31353600-31360200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr15:31354400-31363200	Weak transcription	Left Ventricle	heart
6	chr15:31355600-31357800	Weak transcription	Esophagus	oesophagus
7	chr15:31355600-31362000	Weak transcription	Spleen	Spleen
8	chr15:31355600-31367800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr15:31357800-31358400	Enhancers	Esophagus	oesophagus
10	chr15:31358200-31358600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr15:31358400-31360200	Weak transcription	Esophagus	oesophagus
12	chr15:31359400-31359600	Enhancers	HepG2	liver
13	chr15:31359600-31360200	Weak transcription	HepG2	liver
14	chr15:31359600-31363400	Enhancers	Ovary	ovary
15	chr15:31360000-31363600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr15:31360000-31363600	Enhancers	Adipose Nuclei	Adipose
17	chr15:31360200-31360400	Enhancers	Esophagus	oesophagus
18	chr15:31360200-31360600	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr15:31360200-31361400	Enhancers	HepG2	liver
20	chr15:31360200-31362600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr15:31360400-31362800	Enhancers	Liver	Liver
22	chr15:31360600-31361400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr15:31361000-31362400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr15:31361200-31361600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr15:31361200-31362400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr15:31361200-31362400	Enhancers	Osteobl	bone
27	chr15:31361400-31361600	Enhancers	Fetal Kidney	kidney
28	chr15:31361400-31362000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr15:31361400-31362000	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr15:31361400-31362000	Flanking Active TSS	HepG2	liver
31	chr15:31361400-31362200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr15:31361400-31362400	Enhancers	Colon Smooth Muscle	Colon
33	chr15:31361400-31362400	Enhancers	HSMMtube	muscle
34	chr15:31361600-31362000	Enhancers	Small Intestine	intestine
35	chr15:31361600-31362200	Weak transcription	Fetal Kidney	kidney
36	chr15:31361800-31362200	Enhancers	Brain Substantia Nigra	brain
37	chr15:31362000-31362600	Enhancers	HepG2	liver
38	chr15:31362000-31363200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr15:31362000-31363400	Weak transcription	Gastric	stomach
40	chr15:31362000-31363600	Enhancers	Spleen	Spleen
41	chr15:31362200-31362400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr15:31362200-31362400	Enhancers	Fetal Kidney	kidney
43	chr15:31362200-31362600	Active TSS	Brain Substantia Nigra	brain
44	chr15:31363200-31363800	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr15:31363400-31363600	Enhancers	Left Ventricle	heart
46	chr15:31363400-31363600	Enhancers	Right Atrium	heart
47	chr15:31363600-31366200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr15:31363600-31372600	Weak transcription	Spleen	Spleen
49	chr15:31363800-31365400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr15:31365000-31369800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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