Variant report

Variant	nsv431372
Chromosome Location	chr15:31341461-31409090
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:573)
CpG islands
(count:1525)
Chromatin interactive
region (count:16)
LncRNA
region (count:2)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	chr15:31384908-31385320	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:31361599-31361779	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	chr15:31354388-31354668	GM12878	blood:	n/a	n/a
8	BATF	chr15:31354380-31354706	GM12878	blood:	n/a	n/a
9	BCL3	chr15:31396399-31396673	GM12878	blood:	n/a	n/a
10	BCL3	chr15:31369836-31370207	GM12878	blood:	n/a	n/a
11	BCL3	chr15:31384773-31385276	A549	lung:	n/a	n/a
12	BHLHE40	chr15:31381061-31382012	HepG2	liver:	n/a	n/a
13	BHLHE40	chr15:31384869-31385246	HepG2	liver:	n/a	n/a
14	BRCA1	chr15:31347397-31347435	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr15:31381101-31381576	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
16	CEBPB	chr15:31381253-31381467	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
17	CEBPB	chr15:31343982-31344206	HepG2	liver:	n/a	n/a
18	CEBPB	chr15:31381279-31381497	H1-hESC	embryonic stem cell:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
19	CEBPB	chr15:31381146-31381608	A549	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
20	CEBPB	chr15:31371688-31372101	IMR90	lung:	n/a	n/a
21	CEBPB	chr15:31381210-31381539	IMR90	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
22	CEBPB	chr15:31381210-31381544	A549	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
23	CEBPB	chr15:31360446-31360642	HepG2	liver:	n/a	n/a
24	CEBPB	chr15:31353771-31353804	K562	blood:	n/a	n/a
25	CEBPB	chr15:31409068-31409078	HepG2	liver:	n/a	n/a
26	CEBPB	chr15:31381201-31381538	K562	blood:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
27	CEBPB	chr15:31380951-31381935	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
28	CEBPB	chr15:31360456-31360715	A549	lung:	n/a	n/a
29	CEBPB	chr15:31381102-31381941	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
30	CEBPB	chr15:31358174-31358215	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr15:31358005-31358413	MCF-7	breast:	n/a	n/a
32	CEBPD	chr15:31380900-31381232	HepG2	liver:	n/a	n/a
33	CEBPD	chr15:31381206-31381450	HepG2	liver:	n/a	n/a
34	CHD2	chr15:31381613-31381922	HepG2	liver:	n/a	n/a
35	CHD2	chr15:31391094-31391108	HepG2	liver:	n/a	n/a
36	CHD2	chr15:31384828-31385165	HepG2	liver:	n/a	n/a
37	CHD2	chr15:31390949-31391119	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr15:31352970-31353036	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr15:31384391-31384410	HepG2	liver:	n/a	n/a
40	CHD2	chr15:31381045-31381371	HepG2	liver:	n/a	n/a
41	CTCF	chr15:31391618-31391772	GM12878	blood:	n/a	n/a
42	CTCF	chr15:31391460-31391610	AG09309	skin:	n/a	n/a
43	CTCF	chr15:31357700-31357850	HepG2	liver:	n/a	n/a
44	CTCF	chr15:31391600-31391750	AG10803	skin:	n/a	n/a
45	CTCF	chr15:31361820-31361970	BJ	skin:	n/a	n/a
46	CTCF	chr15:31391540-31391690	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr15:31396313-31396427	GM12892	blood:	n/a	n/a
48	CTCF	chr15:31396220-31396370	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr15:31357780-31357820	K562	blood:	n/a	n/a
50	CTCF	chr15:31373940-31374035	NHEK	skin:	n/a	n/a

(count:1525 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31355430-31355480	HRE	kidney:	n/a
2	chr15:31372997-31373047	AoSMC	blood vessel:	n/a
3	chr15:31372889-31372939	BJ	skin:	n/a
4	chr15:31358323-31358373	HL-60	blood:	n/a
5	chr15:31357535-31357585	GM12892	blood:	n/a
6	chr15:31357535-31357585	PrEC	prostate:	n/a
7	chr15:31370762-31370812	AG04450	lung:	fetal
8	chr15:31355362-31355412	Hela-S3	cervix:	n/a
9	chr15:31383719-31383769	GM12891	blood:	n/a
10	chr15:31380908-31380958	HCF	heart:	n/a
11	chr15:31394021-31394071	HEK293	kidney:	embryo
12	chr15:31372997-31373047	GM06990	blood:	n/a
13	chr15:31391491-31391541	PrEC	prostate:	n/a
14	chr15:31357621-31357671	HRPEpiC	eye:	n/a
15	chr15:31355362-31355412	T-47D	breast:	n/a
16	chr15:31370762-31370812	RPTEC	kidney:	n/a
17	chr15:31391491-31391541	GM19239	blood:	n/a
18	chr15:31358323-31358373	NT2-D1	testis:	n/a
19	chr15:31391491-31391541	HEEpiC	esophagus:	n/a
20	chr15:31380908-31380958	LNCaP	prostate:	n/a
21	chr15:31358323-31358373	HEEpiC	esophagus:	n/a
22	chr15:31355430-31355480	GM12891	blood:	n/a
23	chr15:31357238-31357288	SK-N-MC	brain:	n/a
24	chr15:31357535-31357585	Caco-2	colon:	n/a
25	chr15:31379377-31379427	GM12892	blood:	n/a
26	chr15:31379377-31379427	HUVEC	blood vessel:	n/a
27	chr15:31381816-31381866	AG04450	lung:	fetal
28	chr15:31355430-31355480	NHDF-neo	bronchial:	n/a
29	chr15:31393845-31393895	GM19239	blood:	n/a
30	chr15:31355304-31355354	HUVEC	blood vessel:	n/a
31	chr15:31357535-31357585	HCM	heart:	n/a
32	chr15:31373178-31373228	AoSMC	blood vessel:	n/a
33	chr15:31373178-31373228	CMK	blood:	n/a
34	chr15:31372997-31373047	MCF-7	breast:	n/a
35	chr15:31393845-31393895	HCT-116	colon:	n/a
36	chr15:31394188-31394238	T-47D	breast:	n/a
37	chr15:31362182-31362232	HMEC	breast:	n/a
38	chr15:31391491-31391541	Jurkat	blood:	n/a
39	chr15:31362182-31362232	Hepatocyte	liver:	n/a
40	chr15:31379377-31379427	HCM	heart:	n/a
41	chr15:31355430-31355480	GM19239	blood:	n/a
42	chr15:31358323-31358373	AG10803	skin:	n/a
43	chr15:31391491-31391541	LNCaP	prostate:	n/a
44	chr15:31357535-31357585	GM12891	blood:	n/a
45	chr15:31394021-31394071	HIPEpiC	eye:	n/a
46	chr15:31380908-31380958	ECC-1	luminal epithelium:	n/a
47	chr15:31370762-31370812	NHBE	bronchial:	n/a
48	chr15:31380908-31380958	HRCEpiC	kidney:	n/a
49	chr15:31357238-31357288	AoSMC	blood vessel:	n/a
50	chr15:31393845-31393895	HCM	heart:	n/a

(count:16 , 50 per page) page: 1

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

(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-211-3p	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
ENSG00000198690	chromatin interactions
ENSG00000235884	chromatin interactions
ENSG00000166912	chromatin interactions
ENSG00000134160	chromatin interactions
CREB5	Mature miRNA region
CDH5	Mature miRNA region
KCNMA1	Mature miRNA region
POU3F2	Mature miRNA region
IL11	Mature miRNA region
TCF12	Mature miRNA region
ELOVL6	Mature miRNA region
RAB22A	Mature miRNA region

Extended variants
information (count: 2746 )
Associated
traits (count: 156 )

Variant overlapped rSNPs/rCNVs (count:2746 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10851487	chr15:31341461-31341462	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539675110	chr15:31341464-31341465	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs202219247	chr15:31341473-31341474	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144371215	chr15:31341485-31341486	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551877477	chr15:31341492-31341493	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2288241	chr15:31341516-31341517	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs73372425	chr15:31341535-31341536	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs376707802	chr15:31341548-31341549	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs17228080	chr15:31341564-31341565	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs373513724	chr15:31341599-31341600	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560504405	chr15:31341602-31341603	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571595564	chr15:31341628-31341629	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377520227	chr15:31341642-31341643	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542831790	chr15:31341651-31341652	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369499909	chr15:31341661-31341662	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373134893	chr15:31341662-31341663	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs148802607	chr15:31341666-31341667	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs370567713	chr15:31341678-31341679	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373717525	chr15:31341705-31341706	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs200170211	chr15:31341712-31341713	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs370458595	chr15:31341728-31341729	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374493963	chr15:31341730-31341731	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535828299	chr15:31341731-31341732	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368852981	chr15:31341751-31341752	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576362110	chr15:31341758-31341759	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs10162957	chr15:31341773-31341774	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs565325974	chr15:31341774-31341775	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576427665	chr15:31341786-31341787	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs527695981	chr15:31341809-31341810	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189031549	chr15:31341816-31341817	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561248913	chr15:31341837-31341838	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529894049	chr15:31341855-31341856	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376023890	chr15:31341861-31341862	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs193013873	chr15:31341879-31341880	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569959919	chr15:31341907-31341908	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528032341	chr15:31341942-31341943	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs58707839	chr15:31341946-31341947	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76783849	chr15:31341961-31341962	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184522441	chr15:31341997-31341998	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs3784594	chr15:31342073-31342074	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs72712230	chr15:31342109-31342110	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs567840154	chr15:31342123-31342124	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs71420544	chr15:31342134-31342135	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536432076	chr15:31342189-31342190	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556379802	chr15:31342192-31342193	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576325025	chr15:31342209-31342210	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs3784595	chr15:31342215-31342216	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs555049282	chr15:31342248-31342249	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145293272	chr15:31342253-31342254	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559003838	chr15:31342263-31342264	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	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:874 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31326800-31342800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:31339400-31342000	Weak transcription	Stomach Mucosa	stomach
3	chr15:31339400-31344600	Enhancers	Primary B cells from peripheral blood	blood
4	chr15:31340000-31341800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr15:31340400-31346400	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr15:31340600-31342800	Enhancers	Primary hematopoietic stem cells	blood
7	chr15:31340800-31343000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr15:31340800-31344000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr15:31341000-31344400	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr15:31341200-31341600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr15:31341200-31341800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr15:31341200-31341800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr15:31341200-31342000	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr15:31341200-31342400	Flanking Active TSS	Primary B cells from cord blood	blood
15	chr15:31341200-31342800	Enhancers	GM12878-XiMat	blood
16	chr15:31341200-31343400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr15:31341200-31343600	Enhancers	Spleen	Spleen
18	chr15:31341200-31344400	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr15:31341600-31342000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr15:31341600-31343000	Enhancers	Lung	lung
21	chr15:31341600-31343600	Enhancers	Esophagus	oesophagus
22	chr15:31341800-31342000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr15:31341800-31343000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr15:31341800-31344200	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr15:31341800-31348800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr15:31342000-31342200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr15:31342000-31342200	Enhancers	NHEK	skin
28	chr15:31342000-31342600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr15:31342000-31342600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr15:31342000-31342600	Enhancers	Stomach Mucosa	stomach
31	chr15:31342000-31342600	Enhancers	HMEC	breast
32	chr15:31342000-31342600	Enhancers	NHDF-Ad	bronchial
33	chr15:31342000-31342800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr15:31342200-31342800	Flanking Active TSS	NHEK	skin
35	chr15:31342200-31343000	Enhancers	Rectal Mucosa Donor 29	rectum
36	chr15:31342400-31342600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr15:31342400-31342600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr15:31342400-31343000	Enhancers	Gastric	stomach
39	chr15:31342400-31343000	Enhancers	Pancreas	Pancrea
40	chr15:31342400-31344200	Enhancers	Primary B cells from cord blood	blood
41	chr15:31342600-31343000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr15:31342800-31343000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr15:31342800-31343200	Weak transcription	Primary hematopoietic stem cells	blood
44	chr15:31342800-31345800	Weak transcription	GM12878-XiMat	blood
45	chr15:31343000-31344000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr15:31343000-31352800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr15:31343200-31343600	Enhancers	Primary hematopoietic stem cells	blood
48	chr15:31343400-31344800	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr15:31343600-31344000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr15:31343600-31355400	Weak transcription	Spleen	Spleen

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