Variant report

Variant	nsv1039726
Chromosome Location	chr15:31355383-31391286
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:334)
CpG islands
(count:1100)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:334 , 50 per page) page: 1 2 3 4 5 6 7

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	ARID3A	chr15:31384908-31385320	HepG2	liver:	n/a	n/a
4	ATF1	chr15:31371191-31371230	K562	blood:	n/a	n/a
5	ATF1	chr15:31376612-31376664	K562	blood:	n/a	n/a
6	BACH1	chr15:31373087-31373180	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr15:31384773-31385276	A549	lung:	n/a	n/a
8	BCL3	chr15:31369836-31370207	GM12878	blood:	n/a	n/a
9	BHLHE40	chr15:31384869-31385246	HepG2	liver:	n/a	n/a
10	BHLHE40	chr15:31381061-31382012	HepG2	liver:	n/a	n/a
11	CEBPB	chr15:31381210-31381544	A549	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
12	CEBPB	chr15:31360456-31360715	A549	lung:	n/a	n/a
13	CEBPB	chr15:31358005-31358413	MCF-7	breast:	n/a	n/a
14	CEBPB	chr15:31381201-31381538	K562	blood:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
15	CEBPB	chr15:31381210-31381539	IMR90	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
16	CEBPB	chr15:31381101-31381576	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
17	CEBPB	chr15:31380951-31381935	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
18	CEBPB	chr15:31381279-31381497	H1-hESC	embryonic stem cell:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
19	CEBPB	chr15:31381253-31381467	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
20	CEBPB	chr15:31381102-31381941	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
21	CEBPB	chr15:31358174-31358215	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr15:31360446-31360642	HepG2	liver:	n/a	n/a
23	CEBPB	chr15:31371688-31372101	IMR90	lung:	n/a	n/a
24	CEBPB	chr15:31381146-31381608	A549	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
25	CEBPD	chr15:31381206-31381450	HepG2	liver:	n/a	n/a
26	CEBPD	chr15:31380900-31381232	HepG2	liver:	n/a	n/a
27	CHD2	chr15:31381045-31381371	HepG2	liver:	n/a	n/a
28	CHD2	chr15:31384828-31385165	HepG2	liver:	n/a	n/a
29	CHD2	chr15:31390949-31391119	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr15:31391094-31391108	HepG2	liver:	n/a	n/a
31	CHD2	chr15:31381613-31381922	HepG2	liver:	n/a	n/a
32	CHD2	chr15:31384391-31384410	HepG2	liver:	n/a	n/a
33	CTCF	chr15:31373994-31374013	MCF-7	breast:	n/a	n/a
34	CTCF	chr15:31357700-31357850	HepG2	liver:	n/a	n/a
35	CTCF	chr15:31361820-31361970	BJ	skin:	n/a	n/a
36	CTCF	chr15:31373940-31374035	NHEK	skin:	n/a	n/a
37	CTCF	chr15:31375620-31375770	SK-N-SH_RA	brain:	n/a	chr15:31375641-31375654 chr15:31375727-31375736
38	CTCF	chr15:31357780-31357930	WI-38	lung:	n/a	n/a
39	CTCF	chr15:31373980-31374130	SAEC	small airway:	n/a	n/a
40	CTCF	chr15:31372980-31373130	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr15:31373940-31374090	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr15:31370012-31370016	GM19239	blood:	n/a	n/a
43	CTCF	chr15:31357680-31357830	GM06990	blood:	n/a	n/a
44	CTCF	chr15:31360187-31360315	HepG2	liver:	n/a	n/a
45	CTCF	chr15:31373060-31373210	BE2_C	brain:	n/a	n/a
46	CTCF	chr15:31370019-31370113	GM19239	blood:	n/a	n/a
47	CTCF	chr15:31388820-31388970	GM12873	blood:	n/a	n/a
48	CTCF	chr15:31357731-31357850	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr15:31381160-31381199	GM10248	blood:	n/a	n/a
50	CTCF	chr15:31373992-31374038	MCF-7	breast:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31370762-31370812	BJ	skin:	n/a
2	chr15:31355362-31355412	AG10803	skin:	n/a
3	chr15:31370762-31370812	BJ	skin:	n/a
4	chr15:31355362-31355412	AG10803	skin:	n/a
5	chr15:31373178-31373228	GM12878	blood:	n/a
6	chr15:31355362-31355412	GM06990	blood:	n/a
7	chr15:31373178-31373228	AG09319	gingival:	n/a
8	chr15:31381816-31381866	AG09309	skin:	n/a
9	chr15:31381816-31381866	HCPEpiC	choroid plexus:	n/a
10	chr15:31355430-31355480	SK-N-MC	brain:	n/a
11	chr15:31358057-31358107	HUVEC	blood vessel:	n/a
12	chr15:31358323-31358373	ECC-1	luminal epithelium:	n/a
13	chr15:31362182-31362232	ovcar-3	ovarian:	n/a
14	chr15:31357535-31357585	HIPEpiC	eye:	n/a
15	chr15:31355362-31355412	SK-N-SH_RA	brain:	n/a
16	chr15:31381816-31381866	HIPEpiC	eye:	n/a
17	chr15:31372997-31373047	AoSMC	blood vessel:	n/a
18	chr15:31357621-31357671	HL-60	blood:	n/a
19	chr15:31362182-31362232	LNCaP	prostate:	n/a
20	chr15:31373178-31373228	HepG2	liver:	n/a
21	chr15:31357238-31357288	PFSK-1	brain:	n/a
22	chr15:31372889-31372939	SK-N-MC	brain:	n/a
23	chr15:31357621-31357671	Hepatocyte	liver:	n/a
24	chr15:31380908-31380958	MCF-7	breast:	n/a
25	chr15:31381015-31381065	GM12891	blood:	n/a
26	chr15:31383719-31383769	HRCEpiC	kidney:	n/a
27	chr15:31358323-31358373	IMR90	lung:	fetal
28	chr15:31357535-31357585	CMK	blood:	n/a
29	chr15:31373178-31373228	HCPEpiC	choroid plexus:	n/a
30	chr15:31373178-31373228	HAEpiC	amniotic membrane:	n/a
31	chr15:31358323-31358373	U87	brain:	n/a
32	chr15:31355362-31355412	NH-A	brain:	n/a
33	chr15:31355430-31355480	SAEC	small airway:	n/a
34	chr15:31370762-31370812	HepG2	liver:	n/a
35	chr15:31383719-31383769	MCF-7	breast:	n/a
36	chr15:31357535-31357585	Hepatocyte	liver:	n/a
37	chr15:31362182-31362232	AG09309	skin:	n/a
38	chr15:31381015-31381065	HRCEpiC	kidney:	n/a
39	chr15:31358323-31358373	HEEpiC	esophagus:	n/a
40	chr15:31383719-31383769	BE2_C	brain:	n/a
41	chr15:31372997-31373047	HepG2	liver:	n/a
42	chr15:31381015-31381065	MCF-7	breast:	n/a
43	chr15:31358057-31358107	NT2-D1	testis:	n/a
44	chr15:31373178-31373228	GM19239	blood:	n/a
45	chr15:31372997-31373047	Jurkat	blood:	n/a
46	chr15:31373178-31373228	HRE	kidney:	n/a
47	chr15:31357238-31357288	GM19239	blood:	n/a
48	chr15:31380908-31380958	HAEpiC	amniotic membrane:	n/a
49	chr15:31373178-31373228	ECC-1	luminal epithelium:	n/a
50	chr15:31370762-31370812	LNCaP	prostate:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:30948117..30948824-chr15:31360460..31361082,2	Hela-S3	cervix:
2	chr15:31372825..31374445-chr15:31376180..31377708,2	K562	blood:
3	chr15:31382233..31384961-chr15:31390192..31392345,2	K562	blood:
4	chr15:31382233..31384961-chr15:31390192..31392345,2	K562	blood:
5	chr15:31372825..31374445-chr15:31376180..31377708,2	K562	blood:
6	chr15:31376554..31379301-chr15:31382366..31384596,2	MCF-7	breast:
7	chr15:31282551..31285125-chr15:31384026..31386861,2	MCF-7	breast:
8	chr15:31376554..31379301-chr15:31382366..31384596,2	MCF-7	breast:
9	chr15:31281186..31283904-chr15:31357047..31359370,2	MCF-7	breast:
10	chr15:31283182..31285507-chr15:31372643..31376293,4	MCF-7	breast:
11	chr15:31197730..31198708-chr15:31390791..31392081,3	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTMR10-1	chr15:31385825-31385928	l_1124_chr15:31383178-31385928_brain
2	lnc-MTMR10-1	chr15:31383179-31383431	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
ENSG00000166912	chromatin interactions
ENSG00000235884	chromatin interactions
POU3F2	Mature miRNA region
CDH5	Mature miRNA region
RAB22A	Mature miRNA region
KCNMA1	Mature miRNA region
CREB5	Mature miRNA region
IL11	Mature miRNA region
ELOVL6	Mature miRNA region
TCF12	Mature miRNA region

Extended variants
information (count: 1580 )
Associated
traits (count: 153 )

Variant overlapped rSNPs/rCNVs (count:1580 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375316696	chr15:31355393-31355394	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs141989605	chr15:31355424-31355425	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs199544597	chr15:31355430-31355431	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs185683952	chr15:31355437-31355438	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs539031474	chr15:31355439-31355440	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs368722464	chr15:31355442-31355443	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs373238282	chr15:31355443-31355444	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs371005282	chr15:31355450-31355451	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs373820045	chr15:31355451-31355452	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs202031791	chr15:31355463-31355464	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs527784977	chr15:31355464-31355465	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs555066398	chr15:31355472-31355473	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs574522837	chr15:31355478-31355479	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs371394864	chr15:31355491-31355492	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs537283316	chr15:31355516-31355517	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs373131413	chr15:31355540-31355541	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs556963833	chr15:31355552-31355553	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs190928801	chr15:31355567-31355568	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs7181532	chr15:31355593-31355594	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs57299770	chr15:31355608-31355609	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs572523229	chr15:31355628-31355629	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374757492	chr15:31355649-31355650	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs28377835	chr15:31355671-31355672	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs28631183	chr15:31355672-31355673	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561399144	chr15:31355690-31355691	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183143616	chr15:31355751-31355752	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530215818	chr15:31355765-31355766	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150266900	chr15:31355773-31355774	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7166431	chr15:31355804-31355805	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs185183460	chr15:31355811-31355812	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs7166442	chr15:31355824-31355825	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs149396075	chr15:31355827-31355828	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535044351	chr15:31355881-31355882	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs143764039	chr15:31355882-31355883	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs372282057	chr15:31355894-31355895	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568578378	chr15:31355928-31355929	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536853086	chr15:31355949-31355950	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532694224	chr15:31356072-31356073	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs28676792	chr15:31356093-31356094	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138274880	chr15:31356116-31356117	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117335839	chr15:31356178-31356179	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552872003	chr15:31356303-31356304	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs115947605	chr15:31356324-31356325	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs553801495	chr15:31356383-31356384	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114468394	chr15:31356397-31356398	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs527343796	chr15:31356403-31356404	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs561618762	chr15:31356423-31356424	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs4779814	chr15:31356425-31356426	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs543980577	chr15:31356456-31356457	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs189649771	chr15:31356495-31356496	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:153)

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

Chromatin state (count:586 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31343600-31355400	Weak transcription	Spleen	Spleen
2	chr15:31351400-31360000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr15:31352800-31355600	Enhancers	Fetal Brain Male	brain
4	chr15:31353000-31355600	Enhancers	Brain Germinal Matrix	brain
5	chr15:31353200-31363400	Weak transcription	Right Atrium	heart
6	chr15:31353400-31355400	Enhancers	Fetal Brain Female	brain
7	chr15:31353400-31365200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr15:31353600-31360200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr15:31354200-31355400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr15:31354200-31355600	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr15:31354400-31355400	Enhancers	Adipose Nuclei	Adipose
12	chr15:31354400-31355600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr15:31354400-31363200	Weak transcription	Left Ventricle	heart
14	chr15:31354600-31355400	Enhancers	H1 Cell Line	embryonic stem cell
15	chr15:31354600-31355400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr15:31354600-31355600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr15:31354800-31355400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr15:31355000-31355400	Enhancers	H9 Cell Line	embryonic stem cell
19	chr15:31355000-31355400	Flanking Active TSS	NHDF-Ad	bronchial
20	chr15:31355000-31355600	Enhancers	Esophagus	oesophagus
21	chr15:31355200-31355400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr15:31355200-31355400	Enhancers	Pancreas	Pancrea
23	chr15:31355200-31355400	Enhancers	HUVEC	blood vessel
24	chr15:31355200-31355600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr15:31355200-31355600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr15:31355200-31355600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
27	chr15:31355400-31355600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr15:31355400-31355600	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
29	chr15:31355400-31355600	Enhancers	Spleen	Spleen
30	chr15:31355400-31355600	Enhancers	NHDF-Ad	bronchial
31	chr15:31355600-31357800	Weak transcription	Esophagus	oesophagus
32	chr15:31355600-31362000	Weak transcription	Spleen	Spleen
33	chr15:31355600-31367800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr15:31357800-31358400	Enhancers	Esophagus	oesophagus
35	chr15:31358200-31358600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr15:31358400-31360200	Weak transcription	Esophagus	oesophagus
37	chr15:31359400-31359600	Enhancers	HepG2	liver
38	chr15:31359600-31360200	Weak transcription	HepG2	liver
39	chr15:31359600-31363400	Enhancers	Ovary	ovary
40	chr15:31360000-31363600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr15:31360000-31363600	Enhancers	Adipose Nuclei	Adipose
42	chr15:31360200-31360400	Enhancers	Esophagus	oesophagus
43	chr15:31360200-31360600	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr15:31360200-31361400	Enhancers	HepG2	liver
45	chr15:31360200-31362600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr15:31360400-31362800	Enhancers	Liver	Liver
47	chr15:31360600-31361400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr15:31361000-31362400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr15:31361200-31361600	Enhancers	Muscle Satellite Cultured Cells	--
50	chr15:31361200-31362400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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