Variant report

Variant	nsv1043992
Chromosome Location	chr12:56976326-57010458
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1067)
CpG islands
(count:428)
Chromatin interactive
region (count:80)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1067 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

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	ATF1	chr12:56987847-56988223	K562	blood:	n/a	n/a
3	ATF2	chr12:56987749-56988264	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr12:56987939-56988324	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:56989645-56989843	K562	blood:	n/a	n/a
6	BCL3	chr12:56987594-56989109	A549	lung:	n/a	n/a
7	BCLAF1	chr12:56987791-56988313	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:56987906-56988128	K562	blood:	n/a	n/a
9	CEBPB	chr12:56996015-56996388	IMR90	lung:	n/a	chr12:56996197-56996208
10	CEBPB	chr12:56996025-56996386	K562	blood:	n/a	chr12:56996197-56996208
11	CEBPB	chr12:56976224-56976658	A549	lung:	n/a	n/a
12	CEBPB	chr12:56996030-56996377	Hela-S3	cervix:	n/a	chr12:56996197-56996208
13	CEBPB	chr12:56976360-56976653	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr12:56976391-56976636	A549	lung:	n/a	n/a
15	CEBPB	chr12:56987822-56988248	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:56996045-56996432	ECC-1	luminal epithelium:	n/a	chr12:56996197-56996208
17	CEBPB	chr12:56996018-56996379	HepG2	liver:	n/a	chr12:56996197-56996208
18	CEBPB	chr12:57007623-57007668	HepG2	liver:	n/a	chr12:57007641-57007652
19	CEBPB	chr12:56996062-56996322	H1-hESC	embryonic stem cell:	n/a	chr12:56996197-56996208
20	CEBPB	chr12:56987826-56988225	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr12:56995954-56996446	A549	lung:	n/a	chr12:56996197-56996208
22	CEBPB	chr12:56996013-56996380	A549	lung:	n/a	chr12:56996197-56996208
23	CEBPB	chr12:56996009-56996355	MCF-7	breast:	n/a	chr12:56996197-56996208
24	CEBPB	chr12:56976395-56976556	HepG2	liver:	n/a	n/a
25	CEBPB	chr12:56976387-56976613	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr12:56987782-56988219	IMR90	lung:	n/a	n/a
27	CEBPB	chr12:56996001-56996392	ECC-1	luminal epithelium:	n/a	chr12:56996197-56996208
28	CEBPB	chr12:56996058-56996342	K562	blood:	n/a	chr12:56996197-56996208
29	CHD2	chr12:56988537-56988558	HepG2	liver:	n/a	n/a
30	CHD2	chr12:56987940-56988199	Hela-S3	cervix:	n/a	n/a
31	CREB1	chr12:56987816-56988174	A549	lung:	n/a	n/a
32	CTBP2	chr12:56987755-56988257	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr12:56995320-56995470	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr12:56988000-56988150	Caco-2	colon:	n/a	n/a
35	CTCF	chr12:56995326-56995478	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr12:56987980-56988130	SAEC	small airway:	n/a	n/a
37	CTCF	chr12:56988000-56988150	AG04450	lung:	n/a	n/a
38	CTCF	chr12:56995293-56995516	HepG2	liver:	n/a	n/a
39	CTCF	chr12:56984180-56984330	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr12:56995240-56995390	HVMF	connective:	n/a	n/a
41	CTCF	chr12:56988240-56988242	GM12878	blood:	n/a	n/a
42	CTCF	chr12:56987824-56988254	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr12:56995350-56995463	Lung_OC	lung:	n/a	n/a
44	CTCF	chr12:56988000-56988150	GM12873	blood:	n/a	n/a
45	CTCF	chr12:56995278-56995480	Gliobla	brain:	n/a	n/a
46	CTCF	chr12:56995340-56995490	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr12:56995200-56995350	WI-38	lung:	n/a	n/a
48	CTCF	chr12:56988000-56988150	GM12875	blood:	n/a	n/a
49	CTCF	chr12:56987948-56988217	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:56988420-56988570	AG04450	lung:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:56989385-56989435	SK-N-MC	brain:	n/a
2	chr12:56989385-56989435	SK-N-MC	brain:	n/a
3	chr12:56981896-56981946	SKMC	muscle:	n/a
4	chr12:56988862-56988912	HCF	heart:	n/a
5	chr12:56985200-56985250	GM12892	blood:	n/a
6	chr12:56981896-56981946	K562	blood:	n/a
7	chr12:56988862-56988912	AG04450	lung:	fetal
8	chr12:56993036-56993086	H1-hESC	embryonic stem cell:	embryo
9	chr12:56989385-56989435	HRPEpiC	eye:	n/a
10	chr12:56981896-56981946	A549	lung:	n/a
11	chr12:56985200-56985250	U87	brain:	n/a
12	chr12:56992994-56993044	NH-A	brain:	n/a
13	chr12:56985200-56985250	PrEC	prostate:	n/a
14	chr12:56985200-56985250	GM19239	blood:	n/a
15	chr12:56992994-56993044	HUVEC	blood vessel:	n/a
16	chr12:56981896-56981946	HRCEpiC	kidney:	n/a
17	chr12:56993036-56993086	ECC-1	luminal epithelium:	n/a
18	chr12:56989385-56989435	HCT-116	colon:	n/a
19	chr12:56985200-56985250	AoSMC	blood vessel:	n/a
20	chr12:56989385-56989435	AG04449	skin:	fetal
21	chr12:56992994-56993044	Hela-S3	cervix:	n/a
22	chr12:56981896-56981946	NH-A	brain:	n/a
23	chr12:56985200-56985250	BE2_C	brain:	n/a
24	chr12:56988862-56988912	U87	brain:	n/a
25	chr12:56992994-56993044	LNCaP	prostate:	n/a
26	chr12:56992994-56993044	AG04449	skin:	fetal
27	chr12:56989385-56989435	SK-N-SH	brain:	n/a
28	chr12:56992955-56993005	BE2_C	brain:	n/a
29	chr12:56988862-56988912	Jurkat	blood:	n/a
30	chr12:56992955-56993005	NB4	blood:	n/a
31	chr12:56993036-56993086	AoSMC	blood vessel:	n/a
32	chr12:56981896-56981946	RPTEC	kidney:	n/a
33	chr12:56988862-56988912	RPTEC	kidney:	n/a
34	chr12:56992994-56993044	NHDF-neo	bronchial:	n/a
35	chr12:56988862-56988912	CMK	blood:	n/a
36	chr12:56989385-56989435	IMR90	lung:	fetal
37	chr12:56989385-56989435	HCPEpiC	choroid plexus:	n/a
38	chr12:56985200-56985250	SK-N-SH	brain:	n/a
39	chr12:56992955-56993005	NHDF-neo	bronchial:	n/a
40	chr12:56988862-56988912	PrEC	prostate:	n/a
41	chr12:56992955-56993005	CMK	blood:	n/a
42	chr12:56989385-56989435	HepG2	liver:	n/a
43	chr12:56981896-56981946	HCF	heart:	n/a
44	chr12:56981896-56981946	HEK293	kidney:	embryo
45	chr12:56992955-56993005	Caco-2	colon:	n/a
46	chr12:56992994-56993044	BE2_C	brain:	n/a
47	chr12:56988862-56988912	Hela-S3	cervix:	n/a
48	chr12:56988862-56988912	HMEC	breast:	n/a
49	chr12:56981896-56981946	ECC-1	luminal epithelium:	n/a
50	chr12:56992994-56993044	SAEC	small airway:	n/a

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:56988887..56992620-chr12:56993590..56996069,4	MCF-7	breast:
2	chr12:56990818..56993211-chr12:57006081..57007735,2	MCF-7	breast:
3	chr12:56997043..57002825-chr12:57025405..57031317,7	MCF-7	breast:
4	chr12:57008148..57010026-chr12:57012306..57015125,2	MCF-7	breast:
5	chr12:56980057..56982231-chr12:56987671..56989333,2	K562	blood:
6	chr12:56984135..56986592-chr12:56989665..56992269,2	MCF-7	breast:
7	chr12:56994821..56997665-chr12:57004443..57006406,2	MCF-7	breast:
8	chr12:56966829..56967373-chr12:56983778..56984619,2	MCF-7	breast:
9	chr12:57000981..57002872-chr12:57003792..57005973,3	MCF-7	breast:
10	chr12:49946981..49947732-chr12:56984035..56984765,2	MCF-7	breast:
11	chr12:57010005..57012841-chr12:57024813..57028519,3	K562	blood:
12	chr12:57005351..57008593-chr12:57022462..57024744,3	MCF-7	breast:
13	chr12:57002618..57004175-chr12:57008066..57010666,2	MCF-7	breast:
14	chr12:56982926..56985609-chr12:56993193..56997020,5	K562	blood:
15	chr12:57006171..57009899-chr12:57021383..57024124,3	K562	blood:
16	chr12:56995143..56995846-chr12:57030393..57030919,3	MCF-7	breast:
17	chr12:56991516..56994347-chr12:57026603..57029452,2	MCF-7	breast:
18	chr12:56907064..56908011-chr12:56987808..56988527,2	MCF-7	breast:
19	chr12:56995113..56995947-chr12:57030215..57031100,3	MCF-7	breast:
20	chr12:56996744..56998793-chr12:57023200..57025186,2	MCF-7	breast:
21	chr12:56984454..56986672-chr12:57038080..57040120,2	K562	blood:
22	chr12:56992957..56994766-chr12:56997474..57000200,2	MCF-7	breast:
23	chr12:56991513..56993644-chr12:56998882..57001815,3	K562	blood:
24	chr12:57002618..57004175-chr12:57008066..57010666,2	MCF-7	breast:
25	chr12:56976730..56978679-chr12:56984351..56986438,2	K562	blood:
26	chr12:56984135..56986592-chr12:56989665..56992269,2	MCF-7	breast:
27	chr12:56907280..56908190-chr12:56983683..56984465,5	K562	blood:
28	chr12:56907280..56908193-chr12:56987609..56988520,5	K562	blood:
29	chr12:56998330..57000367-chr12:57003607..57006426,2	K562	blood:
30	chr12:56989873..56991383-chr15:39992356..39994081,2	K562	blood:
31	chr12:56976730..56978679-chr12:56984351..56986438,2	K562	blood:
32	chr12:56989810..56992363-chr12:57017983..57019817,2	K562	blood:
33	chr12:56982987..56986695-chr12:56987397..56990502,5	MCF-7	breast:
34	chr12:56995376..56997871-chr12:57023394..57025015,2	K562	blood:
35	chr12:56579705..56582945-chr12:57008774..57012343,3	K562	blood:
36	chr12:56994191..56996366-chr12:57144934..57147543,2	K562	blood:
37	chr12:56510786..56513733-chr12:56999811..57001767,2	K562	blood:
38	chr12:56987624..56988488-chr12:57030233..57030832,2	MCF-7	breast:
39	chr12:56907736..56909247-chr12:56979729..56982080,2	K562	blood:
40	chr12:56600398..56603165-chr12:56974127..56977078,2	MCF-7	breast:
41	chr12:56979662..56981852-chr12:56983411..56984934,2	K562	blood:
42	chr12:56988198..56989762-chr12:57027319..57029681,2	MCF-7	breast:
43	chr12:56907111..56908261-chr12:56983746..56984871,6	MCF-7	breast:
44	chr12:57007109..57010688-chr12:57028709..57032558,4	K562	blood:
45	chr12:56987817..56988441-chr12:57028533..57029434,2	MCF-7	breast:
46	chr12:56970739..56972319-chr12:56984927..56986749,2	K562	blood:
47	chr12:56979662..56981852-chr12:56983411..56984934,2	K562	blood:
48	chr12:56992042..56997013-chr12:57005431..57010145,6	K562	blood:
49	chr12:57010005..57012841-chr12:57025383..57028519,3	K562	blood:
50	chr12:56907226..56908165-chr12:56987627..56988474,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP5B-1	chr12:57009305-57009391	NONHSAT028835
2	lnc-RBMS2-1	chr12:56984916-56985713	NONHSAT028830

No data

Variant related genes	Relation type
RNU6-343P	TF binding region
BAZ2A	TF binding region
RNU6-343P	CpG island
BAZ2A	CpG island
ENSG00000257303	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000076108	chromatin interactions
ENSG00000198056	chromatin interactions
ENSG00000062485	chromatin interactions
ENSG00000258345	chromatin interactions
ENSG00000025423	chromatin interactions
ENSG00000207031	chromatin interactions
ENSG00000110955	chromatin interactions
ENSG00000181852	chromatin interactions
ENSG00000139641	chromatin interactions

Extended variants
information (count: 1320 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1320 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565558794	chr12:56976333-56976334	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs536196244	chr12:56976346-56976347	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs556667269	chr12:56976446-56976447	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs373593997	chr12:56976469-56976470	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs531442393	chr12:56976478-56976479	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs180942582	chr12:56976488-56976489	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs536729713	chr12:56976493-56976494	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558367162	chr12:56976516-56976517	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs147550172	chr12:56976522-56976523	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs534634587	chr12:56976525-56976526	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs560414661	chr12:56976602-56976603	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs376995139	chr12:56976609-56976610	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs542896033	chr12:56976625-56976626	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs553186156	chr12:56976638-56976639	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs185220205	chr12:56976643-56976644	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs142007747	chr12:56976652-56976653	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs554997759	chr12:56976654-56976655	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs191159662	chr12:56976696-56976697	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs371809066	chr12:56976700-56976701	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs528036320	chr12:56976701-56976702	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs375186022	chr12:56976706-56976707	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs545485806	chr12:56976724-56976725	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs565495374	chr12:56976737-56976738	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs532709170	chr12:56976754-56976755	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs146902236	chr12:56976874-56976875	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs559953359	chr12:56976877-56976878	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs139387020	chr12:56976895-56976896	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs547812278	chr12:56976896-56976897	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs74095005	chr12:56976984-56976985	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs183328612	chr12:56977036-56977037	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs551831197	chr12:56977122-56977123	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369503850	chr12:56977123-56977124	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs141510866	chr12:56977133-56977134	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188854040	chr12:56977148-56977149	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552884333	chr12:56977165-56977166	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs111288194	chr12:56977169-56977170	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535723283	chr12:56977184-56977185	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373138673	chr12:56977203-56977204	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542019863	chr12:56977253-56977254	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555036336	chr12:56977310-56977311	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576469942	chr12:56977338-56977339	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs61939873	chr12:56977392-56977393	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373087007	chr12:56977394-56977395	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375958429	chr12:56977395-56977396	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541650052	chr12:56977408-56977409	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191603617	chr12:56977428-56977429	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576696172	chr12:56977438-56977439	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs11355412	chr12:56977439-56977440	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs398019725	chr12:56977449-56977450	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs77855187	chr12:56977450-56977451	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:925 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56948600-56981200	Weak transcription	Brain Cingulate Gyrus	brain
2	chr12:56953200-56981200	Weak transcription	Brain Substantia Nigra	brain
3	chr12:56954600-56993400	Weak transcription	Fetal Brain Male	brain
4	chr12:56959800-56981400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr12:56960000-56981000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr12:56960000-56981200	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr12:56960000-56981200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:56960000-56981200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr12:56960000-56981200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:56960000-56987600	Weak transcription	Fetal Heart	heart
11	chr12:56960400-56981000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr12:56961600-56981200	Weak transcription	Brain Angular Gyrus	brain
13	chr12:56964000-56980600	Weak transcription	Brain Anterior Caudate	brain
14	chr12:56964000-56981200	Weak transcription	Liver	Liver
15	chr12:56964000-56987800	Weak transcription	Right Atrium	heart
16	chr12:56964200-56981200	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr12:56964200-56992600	Weak transcription	Stomach Mucosa	stomach
18	chr12:56965200-56981200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr12:56965400-56983600	Strong transcription	Fetal Intestine Small	intestine
20	chr12:56965800-56981200	Weak transcription	Brain Germinal Matrix	brain
21	chr12:56966000-56978200	Strong transcription	Fetal Stomach	stomach
22	chr12:56966800-56976800	Weak transcription	Hela-S3	cervix
23	chr12:56968600-56981400	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr12:56972200-56985000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr12:56972400-56982800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr12:56972800-56978200	Strong transcription	Adipose Nuclei	Adipose
27	chr12:56972800-56985400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr12:56973000-56976600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr12:56973400-56981200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr12:56973600-56977000	Strong transcription	Fetal Intestine Large	intestine
31	chr12:56973800-56990600	Weak transcription	Psoas Muscle	Psoas
32	chr12:56974200-56976400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr12:56974200-56976600	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr12:56974200-56976800	Enhancers	Primary hematopoietic stem cells	blood
35	chr12:56974200-56976800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr12:56974200-56976800	Strong transcription	Spleen	Spleen
37	chr12:56974200-56977200	Strong transcription	NHLF	lung
38	chr12:56974200-56977400	Strong transcription	Fetal Lung	lung
39	chr12:56974200-56977400	Strong transcription	Fetal Muscle Leg	muscle
40	chr12:56974200-56978200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr12:56974200-56978200	Strong transcription	Lung	lung
42	chr12:56974200-56978800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr12:56974400-56976400	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr12:56974400-56976600	Strong transcription	Placenta	Placenta
45	chr12:56974600-56977400	Strong transcription	Primary monocytes fromperipheralblood	blood
46	chr12:56974600-56978000	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr12:56974600-56978600	Strong transcription	Fetal Muscle Trunk	muscle
48	chr12:56974600-56979000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr12:56974800-56976400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr12:56974800-56976400	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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