Variant report

Variant	nsv1040840
Chromosome Location	chr15:31348902-31412706
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:547)
CpG islands
(count:1530)
Chromatin interactive
region (count:15)
LncRNA
region (count:2)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:547 , 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	chr15:31361599-31361779	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:31381129-31381842	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:31384908-31385320	HepG2	liver:	n/a	n/a
4	ATF1	chr15:31376612-31376664	K562	blood:	n/a	n/a
5	ATF1	chr15:31371191-31371230	K562	blood:	n/a	n/a
6	BACH1	chr15:31373087-31373180	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr15:31354380-31354706	GM12878	blood:	n/a	n/a
8	BATF	chr15:31354388-31354668	GM12878	blood:	n/a	n/a
9	BCL3	chr15:31369836-31370207	GM12878	blood:	n/a	n/a
10	BCL3	chr15:31384773-31385276	A549	lung:	n/a	n/a
11	BCL3	chr15:31396399-31396673	GM12878	blood:	n/a	n/a
12	BHLHE40	chr15:31384869-31385246	HepG2	liver:	n/a	n/a
13	BHLHE40	chr15:31381061-31382012	HepG2	liver:	n/a	n/a
14	CEBPB	chr15:31381201-31381538	K562	blood:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
15	CEBPB	chr15:31381102-31381941	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
16	CEBPB	chr15:31380951-31381935	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
17	CEBPB	chr15:31360456-31360715	A549	lung:	n/a	n/a
18	CEBPB	chr15:31381146-31381608	A549	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
19	CEBPB	chr15:31409068-31409078	HepG2	liver:	n/a	n/a
20	CEBPB	chr15:31371688-31372101	IMR90	lung:	n/a	n/a
21	CEBPB	chr15:31381210-31381544	A549	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
22	CEBPB	chr15:31358174-31358215	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr15:31381253-31381467	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
24	CEBPB	chr15:31358005-31358413	MCF-7	breast:	n/a	n/a
25	CEBPB	chr15:31381279-31381497	H1-hESC	embryonic stem cell:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
26	CEBPB	chr15:31360446-31360642	HepG2	liver:	n/a	n/a
27	CEBPB	chr15:31353771-31353804	K562	blood:	n/a	n/a
28	CEBPB	chr15:31381101-31381576	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
29	CEBPB	chr15:31381210-31381539	IMR90	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
30	CEBPD	chr15:31380900-31381232	HepG2	liver:	n/a	n/a
31	CEBPD	chr15:31381206-31381450	HepG2	liver:	n/a	n/a
32	CHD2	chr15:31391094-31391108	HepG2	liver:	n/a	n/a
33	CHD2	chr15:31352970-31353036	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr15:31384828-31385165	HepG2	liver:	n/a	n/a
35	CHD2	chr15:31381045-31381371	HepG2	liver:	n/a	n/a
36	CHD2	chr15:31390949-31391119	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr15:31384391-31384410	HepG2	liver:	n/a	n/a
38	CHD2	chr15:31381613-31381922	HepG2	liver:	n/a	n/a
39	CTCF	chr15:31396299-31396488	HepG2	liver:	n/a	n/a
40	CTCF	chr15:31396323-31396425	GM19239	blood:	n/a	n/a
41	CTCF	chr15:31396300-31396450	HepG2	liver:	n/a	n/a
42	CTCF	chr15:31396275-31396455	GM19238	blood:	n/a	n/a
43	CTCF	chr15:31396255-31396410	GM12878	blood:	n/a	n/a
44	CTCF	chr15:31373980-31374130	SAEC	small airway:	n/a	n/a
45	CTCF	chr15:31396313-31396427	GM12892	blood:	n/a	n/a
46	CTCF	chr15:31391640-31391790	NHEK	skin:	n/a	n/a
47	CTCF	chr15:31402713-31402750	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr15:31391480-31391630	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr15:31391650-31391769	GM10248	blood:	n/a	n/a
50	CTCF	chr15:31391660-31391810	GM12871	blood:	n/a	n/a

(count:1530 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31355304-31355354	AG09319	gingival:	n/a
2	chr15:31355430-31355480	H1-hESC	embryonic stem cell:	embryo
3	chr15:31357238-31357288	NT2-D1	testis:	n/a
4	chr15:31370762-31370812	Jurkat	blood:	n/a
5	chr15:31357535-31357585	AG10803	skin:	n/a
6	chr15:31355304-31355354	AG09319	gingival:	n/a
7	chr15:31355430-31355480	H1-hESC	embryonic stem cell:	embryo
8	chr15:31357238-31357288	NT2-D1	testis:	n/a
9	chr15:31370762-31370812	Jurkat	blood:	n/a
10	chr15:31357535-31357585	AG10803	skin:	n/a
11	chr15:31370762-31370812	PrEC	prostate:	n/a
12	chr15:31358323-31358373	HNPCEpiC	eye:	n/a
13	chr15:31381015-31381065	HRPEpiC	eye:	n/a
14	chr15:31394285-31394335	ProgFib	skin:	n/a
15	chr15:31358323-31358373	SKMC	muscle:	n/a
16	chr15:31357621-31357671	GM12892	blood:	n/a
17	chr15:31357535-31357585	AG04449	skin:	fetal
18	chr15:31358057-31358107	ECC-1	luminal epithelium:	n/a
19	chr15:31380908-31380958	AG10803	skin:	n/a
20	chr15:31394188-31394238	K562	blood:	n/a
21	chr15:31355430-31355480	NH-A	brain:	n/a
22	chr15:31381816-31381866	NHBE	bronchial:	n/a
23	chr15:31395221-31395271	HNPCEpiC	eye:	n/a
24	chr15:31370762-31370812	SK-N-SH_RA	brain:	n/a
25	chr15:31379377-31379427	HepG2	liver:	n/a
26	chr15:31372997-31373047	GM12892	blood:	n/a
27	chr15:31391491-31391541	HRE	kidney:	n/a
28	chr15:31394021-31394071	U87	brain:	n/a
29	chr15:31393845-31393895	HRCEpiC	kidney:	n/a
30	chr15:31373178-31373228	T-47D	breast:	n/a
31	chr15:31379377-31379427	Hela-S3	cervix:	n/a
32	chr15:31394188-31394238	U87	brain:	n/a
33	chr15:31357621-31357671	MCF-7	breast:	n/a
34	chr15:31372997-31373047	AG10803	skin:	n/a
35	chr15:31357238-31357288	AG09309	skin:	n/a
36	chr15:31358057-31358107	BE2_C	brain:	n/a
37	chr15:31395221-31395271	MCF-7	breast:	n/a
38	chr15:31391491-31391541	Hepatocyte	liver:	n/a
39	chr15:31394285-31394335	HCM	heart:	n/a
40	chr15:31394188-31394238	CMK	blood:	n/a
41	chr15:31383719-31383769	HCPEpiC	choroid plexus:	n/a
42	chr15:31393845-31393895	GM12891	blood:	n/a
43	chr15:31373178-31373228	SKMC	muscle:	n/a
44	chr15:31379377-31379427	Caco-2	colon:	n/a
45	chr15:31372997-31373047	IMR90	lung:	fetal
46	chr15:31358057-31358107	GM19239	blood:	n/a
47	chr15:31370762-31370812	A549	lung:	n/a
48	chr15:31358057-31358107	HRE	kidney:	n/a
49	chr15:31355304-31355354	HIPEpiC	eye:	n/a
50	chr15:31394021-31394071	ProgFib	skin:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:31372825..31374445-chr15:31376180..31377708,2	K562	blood:
2	chr15:31282551..31285125-chr15:31384026..31386861,2	MCF-7	breast:
3	chr15:31382233..31384961-chr15:31390192..31392345,2	K562	blood:
4	chr15:31372825..31374445-chr15:31376180..31377708,2	K562	blood:
5	chr12:30948117..30948824-chr15:31360460..31361082,2	Hela-S3	cervix:
6	chr15:31376554..31379301-chr15:31382366..31384596,2	MCF-7	breast:
7	chr15:31382233..31384961-chr15:31390192..31392345,2	K562	blood:
8	chr15:31376554..31379301-chr15:31382366..31384596,2	MCF-7	breast:
9	chr15:31197730..31198708-chr15:31390791..31392081,3	MCF-7	breast:
10	chr15:31197732..31198235-chr15:31391287..31392163,2	MCF-7	breast:
11	chr15:31196058..31198354-chr15:31402829..31405030,2	MCF-7	breast:
12	chr15:31343612..31345849-chr15:31349848..31352849,3	K562	blood:
13	chr15:31349956..31352117-chr15:31353870..31356549,2	K562	blood:
14	chr15:31281186..31283904-chr15:31357047..31359370,2	MCF-7	breast:
15	chr15:31283182..31285507-chr15:31372643..31376293,4	MCF-7	breast:

(count:2 , 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
2	lnc-MTMR10-1	chr15:31385825-31385928	l_1124_chr15:31383178-31385928_brain

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

No data

Variant related genes	Relation type
TRPM1	TF binding region
MIR211	TF binding region
TRPM1	CpG island
MIR211	CpG island
ENSG00000134160	chromatin interactions
ENSG00000235884	chromatin interactions
ENSG00000166912	chromatin interactions
ENSG00000198690	chromatin interactions
POU3F2	Mature miRNA region
CDH5	Mature miRNA region
IL11	Mature miRNA region
ELOVL6	Mature miRNA region
CREB5	Mature miRNA region
KCNMA1	Mature miRNA region
TCF12	Mature miRNA region
RAB22A	Mature miRNA region

Extended variants
information (count: 2453 )
Associated
traits (count: 156 )

Variant overlapped rSNPs/rCNVs (count:2453 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180860975	chr15:31348929-31348930	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs151245828	chr15:31348956-31348957	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185114678	chr15:31348964-31348965	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116136064	chr15:31348966-31348967	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540499071	chr15:31348984-31348985	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs60338503	chr15:31349047-31349048	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs374856556	chr15:31349066-31349067	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs140470421	chr15:31349136-31349137	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557876719	chr15:31349143-31349144	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143459929	chr15:31349268-31349269	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572950478	chr15:31349283-31349284	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs140322649	chr15:31349303-31349304	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530215077	chr15:31349311-31349312	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145474067	chr15:31349312-31349313	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs137957465	chr15:31349332-31349333	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560411279	chr15:31349347-31349348	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538924355	chr15:31349374-31349375	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs74962115	chr15:31349379-31349380	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs377763404	chr15:31349414-31349415	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190292623	chr15:31349415-31349416	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs149060939	chr15:31349438-31349439	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377332981	chr15:31349439-31349440	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143099379	chr15:31349459-31349460	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs117929757	chr15:31349506-31349507	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370702983	chr15:31349512-31349513	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376222226	chr15:31349533-31349534	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556829105	chr15:31349576-31349577	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs148188532	chr15:31349637-31349638	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs62038931	chr15:31349707-31349708	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs73374012	chr15:31349788-31349789	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs527797939	chr15:31349850-31349851	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs11853585	chr15:31349860-31349861	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs75375569	chr15:31349903-31349904	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181149610	chr15:31349914-31349915	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs561438235	chr15:31350032-31350033	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs531831603	chr15:31350063-31350064	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs187062488	chr15:31350073-31350074	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs530565993	chr15:31350091-31350092	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs371842709	chr15:31350093-31350094	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs147527872	chr15:31350106-31350107	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs570116860	chr15:31350113-31350114	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs138567376	chr15:31350117-31350118	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs11070767	chr15:31350121-31350122	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs571969477	chr15:31350129-31350130	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs535008913	chr15:31350130-31350131	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs527991710	chr15:31350164-31350165	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs568470681	chr15:31350172-31350173	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs143944675	chr15:31350197-31350198	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs74478274	chr15:31350208-31350209	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs191500253	chr15:31350209-31350210	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:156)

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
Pancreatic cancer	17952125	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:818 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31343000-31352800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:31343600-31355400	Weak transcription	Spleen	Spleen
3	chr15:31347600-31350200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr15:31348800-31350400	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr15:31350200-31352000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr15:31350400-31351400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr15:31350600-31350800	Enhancers	Hela-S3	cervix
8	chr15:31351400-31360000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr15:31352000-31352200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr15:31352000-31352200	Enhancers	Left Ventricle	heart
11	chr15:31352000-31353600	Enhancers	Pancreas	Pancrea
12	chr15:31352200-31352800	Enhancers	Stomach Mucosa	stomach
13	chr15:31352200-31353000	Weak transcription	Left Ventricle	heart
14	chr15:31352200-31353600	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr15:31352200-31353600	Enhancers	Gastric	stomach
16	chr15:31352400-31352800	Weak transcription	Fetal Kidney	kidney
17	chr15:31352600-31353200	Enhancers	Liver	Liver
18	chr15:31352800-31353200	Enhancers	Esophagus	oesophagus
19	chr15:31352800-31353200	Enhancers	Fetal Kidney	kidney
20	chr15:31352800-31353400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr15:31352800-31353600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr15:31352800-31355600	Enhancers	Fetal Brain Male	brain
23	chr15:31353000-31353200	Enhancers	Right Atrium	heart
24	chr15:31353000-31353600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr15:31353000-31353800	Enhancers	Left Ventricle	heart
26	chr15:31353000-31355600	Enhancers	Brain Germinal Matrix	brain
27	chr15:31353200-31353400	Weak transcription	Fetal Kidney	kidney
28	chr15:31353200-31354400	Weak transcription	Esophagus	oesophagus
29	chr15:31353200-31363400	Weak transcription	Right Atrium	heart
30	chr15:31353400-31355200	Enhancers	Fetal Kidney	kidney
31	chr15:31353400-31355400	Enhancers	Fetal Brain Female	brain
32	chr15:31353400-31365200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr15:31353600-31355200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr15:31353600-31355200	Weak transcription	Pancreas	Pancrea
35	chr15:31353600-31360200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr15:31353800-31354200	Weak transcription	Left Ventricle	heart
37	chr15:31354200-31354400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr15:31354200-31354400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr15:31354200-31354400	Enhancers	Left Ventricle	heart
40	chr15:31354200-31354400	Enhancers	NHDF-Ad	bronchial
41	chr15:31354200-31354600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr15:31354200-31355400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr15:31354200-31355600	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr15:31354400-31354600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr15:31354400-31354600	Enhancers	Esophagus	oesophagus
46	chr15:31354400-31354600	Flanking Active TSS	NHDF-Ad	bronchial
47	chr15:31354400-31355000	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr15:31354400-31355000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr15:31354400-31355200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr15:31354400-31355200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin

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