Variant report

Variant	nsv526706
Chromosome Location	chr12:56961932-56988342
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:56984047-56984366	K562	blood:	n/a	n/a
2	ARID3A	chr12:56975587-56975969	K562	blood:	n/a	n/a
3	ATF1	chr12:56975657-56975900	K562	blood:	n/a	n/a
4	ATF1	chr12:56987847-56988223	K562	blood:	n/a	n/a
5	ATF2	chr12:56987749-56988264	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr12:56975614-56976006	GM12878	blood:	n/a	n/a
7	ATF2	chr12:56975552-56976045	GM12878	blood:	n/a	n/a
8	ATF2	chr12:56967220-56967450	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr12:56987939-56988324	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr12:56966496-56967019	GM12878	blood:	n/a	chr12:56966864-56966873
11	BATF	chr12:56963882-56964209	GM12878	blood:	n/a	n/a
12	BATF	chr12:56966704-56967036	GM12878	blood:	n/a	chr12:56966864-56966873
13	BATF	chr12:56975548-56975948	GM12878	blood:	n/a	chr12:56975810-56975820 chr12:56975724-56975735
14	BATF	chr12:56967204-56967467	GM12878	blood:	n/a	n/a
15	BATF	chr12:56975626-56975862	GM12878	blood:	n/a	chr12:56975810-56975820 chr12:56975724-56975735
16	BCL11A	chr12:56975602-56975976	GM12878	blood:	n/a	chr12:56975723-56975732
17	BCL3	chr12:56987594-56989109	A549	lung:	n/a	n/a
18	BCLAF1	chr12:56966648-56966943	GM12878	blood:	n/a	n/a
19	BCLAF1	chr12:56987791-56988313	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:56987906-56988128	K562	blood:	n/a	n/a
21	BHLHE40	chr12:56967225-56967439	GM12878	blood:	n/a	n/a
22	CEBPB	chr12:56967885-56968388	A549	lung:	n/a	chr12:56968106-56968117
23	CEBPB	chr12:56968008-56968212	K562	blood:	n/a	chr12:56968106-56968117
24	CEBPB	chr12:56963867-56964428	ECC-1	luminal epithelium:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
25	CEBPB	chr12:56976387-56976613	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr12:56963938-56964307	IMR90	lung:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
27	CEBPB	chr12:56976391-56976636	A549	lung:	n/a	n/a
28	CEBPB	chr12:56967984-56968230	MCF-7	breast:	n/a	chr12:56968106-56968117
29	CEBPB	chr12:56967859-56968293	K562	blood:	n/a	chr12:56968106-56968117
30	CEBPB	chr12:56967924-56968309	IMR90	lung:	n/a	chr12:56968106-56968117
31	CEBPB	chr12:56963927-56964331	HepG2	liver:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
32	CEBPB	chr12:56963956-56964286	Hela-S3	cervix:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
33	CEBPB	chr12:56967919-56968310	K562	blood:	n/a	chr12:56968106-56968117
34	CEBPB	chr12:56964005-56964245	K562	blood:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
35	CEBPB	chr12:56963879-56964311	HepG2	liver:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
36	CEBPB	chr12:56987822-56988248	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr12:56976395-56976556	HepG2	liver:	n/a	n/a
38	CEBPB	chr12:56976224-56976658	A549	lung:	n/a	n/a
39	CEBPB	chr12:56964018-56964287	A549	lung:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
40	CEBPB	chr12:56964021-56964260	K562	blood:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
41	CEBPB	chr12:56967960-56968297	A549	lung:	n/a	chr12:56968106-56968117
42	CEBPB	chr12:56964028-56964213	HepG2	liver:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
43	CEBPB	chr12:56963939-56964299	HepG2	liver:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
44	CEBPB	chr12:56976360-56976653	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr12:56987782-56988219	IMR90	lung:	n/a	n/a
46	CEBPB	chr12:56963801-56964436	ECC-1	luminal epithelium:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
47	CEBPB	chr12:56968031-56968263	HepG2	liver:	n/a	chr12:56968106-56968117
48	CEBPB	chr12:56987826-56988225	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPD	chr12:56967960-56968335	K562	blood:	n/a	n/a
50	CHD2	chr12:56987940-56988199	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:56981896-56981946	HRCEpiC	kidney:	n/a
2	chr12:56985200-56985250	BE2_C	brain:	n/a
3	chr12:56985200-56985250	AoSMC	blood vessel:	n/a
4	chr12:56985200-56985250	HUVEC	blood vessel:	n/a
5	chr12:56981896-56981946	HAEpiC	amniotic membrane:	n/a
6	chr12:56985200-56985250	AG04450	lung:	fetal
7	chr12:56981896-56981946	HCM	heart:	n/a
8	chr12:56985200-56985250	AG04449	skin:	fetal
9	chr12:56981896-56981946	IMR90	lung:	fetal
10	chr12:56981896-56981946	NHDF-neo	bronchial:	n/a
11	chr12:56981896-56981946	BE2_C	brain:	n/a
12	chr12:56985200-56985250	LNCaP	prostate:	n/a
13	chr12:56985200-56985250	HNPCEpiC	eye:	n/a
14	chr12:56985200-56985250	U87	brain:	n/a
15	chr12:56985200-56985250	SK-N-MC	brain:	n/a
16	chr12:56985200-56985250	PrEC	prostate:	n/a
17	chr12:56981896-56981946	MCF10A-Er-Src	breast:	n/a
18	chr12:56985200-56985250	GM12891	blood:	n/a
19	chr12:56981896-56981946	NH-A	brain:	n/a
20	chr12:56981896-56981946	SK-N-SH	brain:	n/a
21	chr12:56981896-56981946	K562	blood:	n/a
22	chr12:56981896-56981946	MCF-7	breast:	n/a
23	chr12:56985200-56985250	AG09319	gingival:	n/a
24	chr12:56985200-56985250	SK-N-SH_RA	brain:	n/a
25	chr12:56985200-56985250	Caco-2	colon:	n/a
26	chr12:56985200-56985250	K562	blood:	n/a
27	chr12:56981896-56981946	NHBE	bronchial:	n/a
28	chr12:56981896-56981946	HNPCEpiC	eye:	n/a
29	chr12:56985200-56985250	NHBE	bronchial:	n/a
30	chr12:56981896-56981946	AG09309	skin:	n/a
31	chr12:56985200-56985250	RPTEC	kidney:	n/a
32	chr12:56981896-56981946	GM19239	blood:	n/a
33	chr12:56981896-56981946	PANC-1	pancreas:	n/a
34	chr12:56981896-56981946	HEEpiC	esophagus:	n/a
35	chr12:56981896-56981946	SK-N-MC	brain:	n/a
36	chr12:56981896-56981946	BJ	skin:	n/a
37	chr12:56985200-56985250	HPAEpiC	pulmonary alveolar:	n/a
38	chr12:56985200-56985250	PFSK-1	brain:	n/a
39	chr12:56985200-56985250	HCPEpiC	choroid plexus:	n/a
40	chr12:56985200-56985250	HCT-116	colon:	n/a
41	chr12:56981896-56981946	LNCaP	prostate:	n/a
42	chr12:56985200-56985250	HRPEpiC	eye:	n/a
43	chr12:56985200-56985250	HEK293	kidney:	embryo
44	chr12:56981896-56981946	SAEC	small airway:	n/a
45	chr12:56981896-56981946	AoSMC	blood vessel:	n/a
46	chr12:56981896-56981946	Jurkat	blood:	n/a
47	chr12:56981896-56981946	RPTEC	kidney:	n/a
48	chr12:56981896-56981946	PrEC	prostate:	n/a
49	chr12:56985200-56985250	IMR90	lung:	fetal
50	chr12:56981896-56981946	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr12:56880766..56883726-chr12:56966703..56969405,2	MCF-7	breast:
2	chr12:56907179..56908189-chr12:56966615..56967735,8	MCF-7	breast:
3	chr12:56973940..56975962-chr12:57014825..57017431,2	MCF-7	breast:
4	chr12:56979662..56981852-chr12:56983411..56984934,2	K562	blood:
5	chr12:56907064..56908011-chr12:56987808..56988527,2	MCF-7	breast:
6	chr12:56976730..56978679-chr12:56984351..56986438,2	K562	blood:
7	chr12:56984454..56986672-chr12:57038080..57040120,2	K562	blood:
8	chr12:56982987..56986695-chr12:56987397..56990502,5	MCF-7	breast:
9	chr12:56982987..56986695-chr12:56987397..56990502,5	MCF-7	breast:
10	chr12:56966829..56967373-chr12:56983778..56984619,2	MCF-7	breast:
11	chr12:56970739..56972319-chr12:56984927..56986749,2	K562	blood:
12	chr12:56980057..56982231-chr12:56987671..56989333,2	K562	blood:
13	chr12:56979649..56982527-chr12:57037588..57039465,3	K562	blood:
14	chr12:56987624..56988488-chr12:57030233..57030832,2	MCF-7	breast:
15	chr12:56988299..56991768-chr12:57027062..57029523,3	MCF-7	breast:
16	chr12:56972867..56975335-chr12:56976373..56981711,6	K562	blood:
17	chr12:56907111..56908261-chr12:56983746..56984871,6	MCF-7	breast:
18	chr12:56988153..56991262-chr12:57020461..57022957,3	MCF-7	breast:
19	chr12:56976730..56978679-chr12:56984351..56986438,2	K562	blood:
20	chr12:56959480..56961532-chr12:56961606..56964152,2	K562	blood:
21	chr12:56959228..56960829-chr12:56962123..56963896,2	MCF-7	breast:
22	chr12:56980057..56982231-chr12:56987671..56989333,2	K562	blood:
23	chr12:56600398..56603165-chr12:56974127..56977078,2	MCF-7	breast:
24	chr12:56907303..56908109-chr12:56966932..56967838,3	MCF-7	breast:
25	chr12:56907736..56909247-chr12:56979729..56982080,2	K562	blood:
26	chr12:49946981..49947732-chr12:56984035..56984765,2	MCF-7	breast:
27	chr12:56907226..56908165-chr12:56987627..56988474,3	MCF-7	breast:
28	chr12:56977538..56980644-chr12:57023000..57025352,3	MCF-7	breast:
29	chr12:56966829..56967373-chr12:56983778..56984619,2	MCF-7	breast:
30	chr12:56982926..56985609-chr12:56993193..56997020,5	K562	blood:
31	chr12:56582662..56585164-chr12:56962961..56964901,2	K562	blood:
32	chr12:56979662..56981852-chr12:56983411..56984934,2	K562	blood:
33	chr12:56987156..56990068-chr12:56991407..56993523,3	MCF-7	breast:
34	chr12:56988198..56989762-chr12:57027319..57029681,2	MCF-7	breast:
35	chr12:56986611..56988626-chr12:56993679..56996417,2	K562	blood:
36	chr12:56970739..56972319-chr12:56984927..56986749,2	K562	blood:
37	chr12:56984135..56986592-chr12:56989665..56992269,2	MCF-7	breast:
38	chr12:56987817..56988441-chr12:57028533..57029434,2	MCF-7	breast:
39	chr12:56907280..56908193-chr12:56987609..56988520,5	K562	blood:
40	chr12:56982350..56985361-chr12:56995041..56997439,3	MCF-7	breast:
41	chr12:56972867..56975335-chr12:56976373..56981711,6	K562	blood:
42	chr12:56870822..56872349-chr12:56963864..56966406,2	MCF-7	breast:
43	chr12:56907280..56908190-chr12:56983683..56984465,5	K562	blood:
44	chr12:56972892..56975335-chr12:56979018..56981711,3	K562	blood:
45	chr12:56972892..56975335-chr12:56979018..56981711,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBMS2-1	chr12:56984916-56985713	NONHSAT028830

Variant related genes	Relation type
RBMS2	TF binding region
RNU6-343P	TF binding region
RBMS2	CpG island
RNU6-343P	CpG island
ENSG00000135423	chromatin interactions
ENSG00000181852	chromatin interactions
ENSG00000076108	chromatin interactions
ENSG00000110955	chromatin interactions
ENSG00000139613	chromatin interactions
ENSG00000207031	chromatin interactions
ENSG00000258199	chromatin interactions

Extended variants
information (count: 938 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:938 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7305370	chr12:56961932-56961933	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189032972	chr12:56961940-56961941	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs139941491	chr12:56962023-56962024	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145686773	chr12:56962067-56962068	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550631437	chr12:56962077-56962078	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181424289	chr12:56962111-56962112	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530224858	chr12:56962143-56962144	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568981229	chr12:56962271-56962272	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374923687	chr12:56962319-56962320	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs543997084	chr12:56962328-56962329	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs539588319	chr12:56962403-56962404	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112178572	chr12:56962404-56962405	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563892547	chr12:56962470-56962471	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148930217	chr12:56962514-56962515	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532841518	chr12:56962537-56962538	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372329987	chr12:56962610-56962611	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs74091895	chr12:56962625-56962626	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs571425365	chr12:56962639-56962640	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184183952	chr12:56962665-56962666	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574753281	chr12:56962672-56962673	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs370384595	chr12:56962677-56962678	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541979394	chr12:56962688-56962689	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs375958378	chr12:56962690-56962691	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376877413	chr12:56962708-56962709	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376385006	chr12:56962721-56962722	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs199662161	chr12:56962723-56962724	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs368873647	chr12:56962797-56962798	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs202078205	chr12:56962821-56962822	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373002968	chr12:56962862-56962863	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142219464	chr12:56962911-56962912	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75246963	chr12:56962940-56962941	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375627738	chr12:56962942-56962943	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546509140	chr12:56962944-56962945	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs552637381	chr12:56962961-56962962	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs528801122	chr12:56963019-56963020	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs540511543	chr12:56963053-56963054	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs561375988	chr12:56963055-56963056	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs528855000	chr12:56963079-56963080	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs564897071	chr12:56963110-56963111	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs567384573	chr12:56963178-56963179	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs568897163	chr12:56963181-56963182	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs532880107	chr12:56963187-56963188	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs4559722	chr12:56963215-56963216	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs1965584	chr12:56963259-56963260	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs532043866	chr12:56963284-56963285	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs566654338	chr12:56963288-56963289	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs12372083	chr12:56963300-56963301	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs372421570	chr12:56963335-56963336	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs534107009	chr12:56963350-56963351	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs113697707	chr12:56963362-56963363	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	20531469	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	21509527	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glycogen storage disease	18421352	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1109 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56931600-56965000	Weak transcription	Hela-S3	cervix
2	chr12:56948600-56981200	Weak transcription	Brain Cingulate Gyrus	brain
3	chr12:56950800-56975000	Weak transcription	Esophagus	oesophagus
4	chr12:56951400-56963600	Weak transcription	Brain Anterior Caudate	brain
5	chr12:56952600-56966200	Weak transcription	Fetal Brain Female	brain
6	chr12:56952600-56974800	Weak transcription	Pancreas	Pancrea
7	chr12:56953200-56981200	Weak transcription	Brain Substantia Nigra	brain
8	chr12:56954400-56974800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr12:56954600-56993400	Weak transcription	Fetal Brain Male	brain
10	chr12:56956000-56968800	Strong transcription	NHEK	skin
11	chr12:56956200-56970400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
12	chr12:56956600-56975000	Weak transcription	Gastric	stomach
13	chr12:56957400-56962800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr12:56958000-56963000	Weak transcription	Dnd41	blood
15	chr12:56958400-56967400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr12:56959200-56963000	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr12:56959200-56964200	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr12:56959400-56964800	Weak transcription	Brain Hippocampus Middle	brain
19	chr12:56959400-56970000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr12:56959600-56963000	Weak transcription	NH-A	brain
21	chr12:56959600-56963800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr12:56959600-56975000	Weak transcription	Right Ventricle	heart
23	chr12:56959800-56962000	Enhancers	Fetal Intestine Large	intestine
24	chr12:56959800-56962400	Weak transcription	Left Ventricle	heart
25	chr12:56959800-56963000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr12:56959800-56963400	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr12:56959800-56963600	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr12:56959800-56963600	Enhancers	Fetal Intestine Small	intestine
29	chr12:56959800-56970400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:56959800-56971800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr12:56959800-56974800	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr12:56959800-56975000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr12:56959800-56981400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr12:56960000-56962200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr12:56960000-56962400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr12:56960000-56962800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr12:56960000-56962800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr12:56960000-56962800	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr12:56960000-56963000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr12:56960000-56963000	Weak transcription	Thymus	Thymus
41	chr12:56960000-56963200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr12:56960000-56963200	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr12:56960000-56963200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr12:56960000-56963200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr12:56960000-56963400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr12:56960000-56963400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr12:56960000-56963400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr12:56960000-56963400	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr12:56960000-56963600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr12:56960000-56963600	Weak transcription	Muscle Satellite Cultured Cells	--

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