Variant report

Variant	nsv899163
Chromosome Location	chr12:63288343-63325988
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:435)
CpG islands
(count:244)
Chromatin interactive
region (count:66)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:63294385-63295188	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:63304189-63304733	K562	blood:	n/a	n/a
3	ARID3A	chr12:63293456-63294017	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:63297280-63297288	K562	blood:	n/a	n/a
5	ARID3A	chr12:63289230-63289440	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:63308839-63308845	K562	blood:	n/a	n/a
7	ARID3A	chr12:63307845-63308119	K562	blood:	n/a	n/a
8	ARID3A	chr12:63294910-63295100	K562	blood:	n/a	n/a
9	ATF1	chr12:63325385-63325532	K562	blood:	n/a	n/a
10	ATF1	chr12:63304289-63304687	K562	blood:	n/a	n/a
11	ATF1	chr12:63307746-63308778	K562	blood:	n/a	n/a
12	ATF1	chr12:63294403-63294745	K562	blood:	n/a	n/a
13	ATF3	chr12:63304301-63304734	K562	blood:	n/a	n/a
14	BACH1	chr12:63297268-63297271	K562	blood:	n/a	n/a
15	BHLHE40	chr12:63301421-63301671	K562	blood:	n/a	n/a
16	BHLHE40	chr12:63320021-63320037	K562	blood:	n/a	n/a
17	BHLHE40	chr12:63303003-63303008	K562	blood:	n/a	n/a
18	BHLHE40	chr12:63304340-63304880	K562	blood:	n/a	n/a
19	BHLHE40	chr12:63303244-63303613	K562	blood:	n/a	n/a
20	BHLHE40	chr12:63296971-63297230	K562	blood:	n/a	n/a
21	BHLHE40	chr12:63307785-63308700	K562	blood:	n/a	n/a
22	BHLHE40	chr12:63324861-63325168	K562	blood:	n/a	n/a
23	CCNT2	chr12:63313485-63313712	K562	blood:	n/a	n/a
24	CCNT2	chr12:63304007-63304769	K562	blood:	n/a	chr12:63304531-63304551
25	CCNT2	chr12:63302320-63302820	K562	blood:	n/a	n/a
26	CCNT2	chr12:63305162-63305806	K562	blood:	n/a	n/a
27	CEBPB	chr12:63296735-63296886	A549	lung:	n/a	chr12:63296826-63296839 chr12:63296828-63296839
28	CEBPB	chr12:63307764-63308061	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr12:63322429-63322827	HepG2	liver:	n/a	n/a
30	CEBPB	chr12:63307702-63308471	K562	blood:	n/a	n/a
31	CEBPB	chr12:63294574-63295392	MCF-7	breast:	n/a	chr12:63294954-63294965 chr12:63294956-63294965 chr12:63295009-63295017
32	CEBPB	chr12:63305766-63306046	HepG2	liver:	n/a	chr12:63305867-63305878 chr12:63305864-63305881 chr12:63305867-63305880
33	CEBPB	chr12:63305805-63306043	K562	blood:	n/a	chr12:63305867-63305878 chr12:63305864-63305881 chr12:63305867-63305880
34	CEBPB	chr12:63304241-63304665	K562	blood:	n/a	chr12:63304276-63304289
35	CEBPB	chr12:63293530-63293683	HepG2	liver:	n/a	n/a
36	CEBPB	chr12:63304347-63304705	K562	blood:	n/a	n/a
37	CEBPB	chr12:63312094-63312350	HepG2	liver:	n/a	chr12:63312211-63312222 chr12:63312261-63312273
38	CEBPB	chr12:63322521-63322824	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr12:63294853-63294997	HepG2	liver:	n/a	chr12:63294954-63294965 chr12:63294956-63294965
40	CEBPB	chr12:63325285-63325666	K562	blood:	n/a	n/a
41	CEBPB	chr12:63305746-63306005	A549	lung:	n/a	chr12:63305867-63305878 chr12:63305864-63305881 chr12:63305867-63305880
42	CEBPB	chr12:63325347-63325513	HepG2	liver:	n/a	n/a
43	CEBPB	chr12:63315236-63315267	K562	blood:	n/a	n/a
44	CEBPB	chr12:63296674-63297000	K562	blood:	n/a	chr12:63296826-63296839 chr12:63296828-63296839
45	CEBPB	chr12:63307752-63308480	K562	blood:	n/a	n/a
46	CEBPB	chr12:63293410-63293821	HepG2	liver:	n/a	n/a
47	CEBPB	chr12:63312174-63312289	IMR90	lung:	n/a	chr12:63312211-63312222 chr12:63312261-63312273
48	CEBPB	chr12:63322415-63322784	HepG2	liver:	n/a	n/a
49	CEBPB	chr12:63322480-63322865	HepG2	liver:	n/a	n/a
50	CEBPB	chr12:63293499-63293779	A549	lung:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:63294404-63294454	AG04450	lung:	fetal
2	chr12:63324472-63324522	T-47D	breast:	n/a
3	chr12:63322644-63322694	NH-A	brain:	n/a
4	chr12:63324472-63324522	ECC-1	luminal epithelium:	n/a
5	chr12:63294404-63294454	MCF10A-Er-Src	breast:	n/a
6	chr12:63310660-63310710	AG04450	lung:	fetal
7	chr12:63322644-63322694	IMR90	lung:	fetal
8	chr12:63324472-63324522	HCPEpiC	choroid plexus:	n/a
9	chr12:63294404-63294454	HCF	heart:	n/a
10	chr12:63324472-63324522	HEEpiC	esophagus:	n/a
11	chr12:63310660-63310710	Hepatocyte	liver:	n/a
12	chr12:63322644-63322694	GM12878	blood:	n/a
13	chr12:63322644-63322694	AG04450	lung:	fetal
14	chr12:63322644-63322694	SK-N-SH	brain:	n/a
15	chr12:63324472-63324522	HCM	heart:	n/a
16	chr12:63324472-63324522	GM12892	blood:	n/a
17	chr12:63294404-63294454	HPAEpiC	pulmonary alveolar:	n/a
18	chr12:63294404-63294454	SK-N-SH	brain:	n/a
19	chr12:63294404-63294454	HEK293	kidney:	embryo
20	chr12:63324472-63324522	Caco-2	colon:	n/a
21	chr12:63310660-63310710	MCF-7	breast:	n/a
22	chr12:63324472-63324522	HAEpiC	amniotic membrane:	n/a
23	chr12:63310660-63310710	HCPEpiC	choroid plexus:	n/a
24	chr12:63324472-63324522	PFSK-1	brain:	n/a
25	chr12:63310660-63310710	SAEC	small airway:	n/a
26	chr12:63322644-63322694	U87	brain:	n/a
27	chr12:63322644-63322694	HL-60	blood:	n/a
28	chr12:63310660-63310710	AG09319	gingival:	n/a
29	chr12:63324472-63324522	HEK293	kidney:	embryo
30	chr12:63324472-63324522	GM06990	blood:	n/a
31	chr12:63324472-63324522	H1-hESC	embryonic stem cell:	embryo
32	chr12:63324472-63324522	AG04450	lung:	fetal
33	chr12:63294404-63294454	CMK	blood:	n/a
34	chr12:63310660-63310710	NT2-D1	testis:	n/a
35	chr12:63324472-63324522	SK-N-SH_RA	brain:	n/a
36	chr12:63294404-63294454	SAEC	small airway:	n/a
37	chr12:63324472-63324522	AoSMC	blood vessel:	n/a
38	chr12:63294404-63294454	GM06990	blood:	n/a
39	chr12:63322644-63322694	BE2_C	brain:	n/a
40	chr12:63322644-63322694	GM12892	blood:	n/a
41	chr12:63324472-63324522	HRCEpiC	kidney:	n/a
42	chr12:63322644-63322694	HPAEpiC	pulmonary alveolar:	n/a
43	chr12:63322644-63322694	AG09309	skin:	n/a
44	chr12:63294404-63294454	AoSMC	blood vessel:	n/a
45	chr12:63322644-63322694	HMEC	breast:	n/a
46	chr12:63322644-63322694	NHDF-neo	bronchial:	n/a
47	chr12:63322644-63322694	AG04449	skin:	fetal
48	chr12:63294404-63294454	HL-60	blood:	n/a
49	chr12:63322644-63322694	Jurkat	blood:	n/a
50	chr12:63322644-63322694	AG09319	gingival:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:63297848..63300168-chr12:63310835..63312662,2	MCF-7	breast:
2	chr12:63307556..63310416-chr12:63316957..63319836,2	MCF-7	breast:
3	chr12:63307451..63310079-chr12:63319442..63322699,3	MCF-7	breast:
4	chr12:63284624..63286750-chr12:63293263..63294945,2	MCF-7	breast:
5	chr12:63307556..63310416-chr12:63316957..63319836,2	MCF-7	breast:
6	chr12:63293376..63296810-chr12:63296910..63300842,4	MCF-7	breast:
7	chr12:63322417..63325278-chr12:63327301..63329815,2	K562	blood:
8	chr12:63321809..63323411-chr12:63325612..63327297,2	K562	blood:
9	chr12:63311594..63314180-chr12:63316529..63319500,2	MCF-7	breast:
10	chr12:63292677..63295227-chr12:63307980..63310635,2	MCF-7	breast:
11	chr12:63307451..63310079-chr12:63319442..63322699,3	MCF-7	breast:
12	chr12:63303196..63305906-chr12:63305926..63307721,2	K562	blood:
13	chr12:63298668..63300990-chr12:63326822..63328965,2	MCF-7	breast:
14	chr12:63292677..63295227-chr12:63307980..63310635,2	MCF-7	breast:
15	chr12:63273482..63276105-chr12:63324885..63326810,2	MCF-7	breast:
16	chr12:63320284..63321871-chr12:63327495..63329179,2	K562	blood:
17	chr12:63293103..63295682-chr12:63297040..63300523,3	MCF-7	breast:
18	chr12:63319352..63321356-chr12:63324432..63326785,2	K562	blood:
19	chr12:63291380..63293253-chr12:63327047..63329993,2	MCF-7	breast:
20	chr12:63302887..63305750-chr12:63328233..63330331,2	K562	blood:
21	chr12:63312253..63314057-chr12:63327356..63329169,2	K562	blood:
22	chr12:63300143..63303851-chr12:63306898..63309858,4	MCF-7	breast:
23	chr12:63285182..63289284-chr12:63300308..63304182,3	K562	blood:
24	chr12:63321809..63323411-chr12:63325612..63327297,2	K562	blood:
25	chr12:63298026..63301472-chr12:63301744..63306217,4	K562	blood:
26	chr12:63296377..63298625-chr12:63304984..63307375,2	MCF-7	breast:
27	chr12:63311089..63313901-chr12:63317542..63319982,2	K562	blood:
28	chr12:63285182..63289284-chr12:63300308..63304182,3	K562	blood:
29	chr12:63295243..63298533-chr12:63299392..63301650,3	K562	blood:
30	chr12:63273431..63275241-chr12:63290276..63292669,2	MCF-7	breast:
31	chr12:63311594..63314180-chr12:63316529..63319500,2	MCF-7	breast:
32	chr12:63293103..63295682-chr12:63297040..63300523,3	MCF-7	breast:
33	chr12:63295774..63298533-chr12:63300102..63301857,2	K562	blood:
34	chr12:63284474..63287928-chr12:63291672..63294715,4	MCF-7	breast:
35	chr12:63298722..63300428-chr12:63300794..63302294,2	MCF-7	breast:
36	chr12:63314546..63316947-chr12:63317010..63319516,2	K562	blood:
37	chr12:63275413..63276960-chr12:63307773..63310580,2	K562	blood:
38	chr12:63303143..63306102-chr12:63308178..63311320,4	K562	blood:
39	chr12:63298026..63301472-chr12:63301744..63306217,4	K562	blood:
40	chr12:63312289..63315021-chr12:63318945..63321153,2	MCF-7	breast:
41	chr12:63325863..63329962-chr12:63356030..63360907,6	MCF-7	breast:
42	chr12:63299073..63301932-chr12:63304667..63306675,2	K562	blood:
43	chr12:63296377..63298625-chr12:63304984..63307375,2	MCF-7	breast:
44	chr12:63295243..63298533-chr12:63299392..63301650,3	K562	blood:
45	chr12:63303143..63306102-chr12:63308178..63311320,4	K562	blood:
46	chr12:63312289..63315021-chr12:63318945..63321153,2	MCF-7	breast:
47	chr12:63297848..63300168-chr12:63310835..63312662,2	MCF-7	breast:
48	chr12:63282634..63285463-chr12:63286553..63289663,4	MCF-7	breast:
49	chr12:63324965..63327426-chr12:63334327..63336212,2	K562	blood:
50	chr12:63311089..63313901-chr12:63317542..63319982,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000252660	TF binding region
ENSG00000252660	CpG island
ENSG00000252660	chromatin interactions
ENSG00000111110	chromatin interactions
ENSG00000139239	chromatin interactions
ENSG00000199179	chromatin interactions

Extended variants
information (count: 1352 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1352 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11615624	chr12:63288343-63288344	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537513210	chr12:63288345-63288346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181756092	chr12:63288376-63288377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs373072869	chr12:63288391-63288392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs149426300	chr12:63288409-63288410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185541340	chr12:63288410-63288411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530165635	chr12:63288427-63288428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs624826	chr12:63288437-63288438	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs571047515	chr12:63288502-63288503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542932311	chr12:63288538-63288539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562031342	chr12:63288539-63288540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs625256	chr12:63288541-63288542	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs544671258	chr12:63288576-63288577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs486118	chr12:63288667-63288668	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs56654926	chr12:63288699-63288700	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs546981986	chr12:63288738-63288739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544477712	chr12:63288776-63288777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144456139	chr12:63288906-63288907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148394774	chr12:63288932-63288933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs489033	chr12:63288994-63288995	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs142569789	chr12:63289015-63289016	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs180755672	chr12:63289099-63289100	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551008566	chr12:63289137-63289138	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186143578	chr12:63289221-63289222	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs533917301	chr12:63289278-63289279	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs571271117	chr12:63289289-63289290	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs147577194	chr12:63289294-63289295	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs190907597	chr12:63289300-63289301	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs536116634	chr12:63289304-63289305	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs1545897	chr12:63289345-63289346	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs140401854	chr12:63289350-63289351	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs544610083	chr12:63289397-63289398	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs113762439	chr12:63289410-63289411	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs147820519	chr12:63289451-63289452	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs373717760	chr12:63289458-63289459	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs699569	chr12:63289462-63289463	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs150369159	chr12:63289622-63289623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs112093250	chr12:63289661-63289662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529496209	chr12:63289664-63289665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549218217	chr12:63289704-63289705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562839176	chr12:63289734-63289735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531922128	chr12:63289739-63289740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546779701	chr12:63289817-63289818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183959279	chr12:63289844-63289845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs145717694	chr12:63289853-63289854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533619164	chr12:63289864-63289865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs75356813	chr12:63289880-63289881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376794838	chr12:63289901-63289902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567301657	chr12:63289910-63289911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536449945	chr12:63289974-63289975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
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
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	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
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Man infertility	21397064	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	17426248	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:715 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63271600-63294400	Weak transcription	Ovary	ovary
2	chr12:63279400-63289200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:63281000-63293000	Weak transcription	Left Ventricle	heart
4	chr12:63281200-63293600	Weak transcription	Gastric	stomach
5	chr12:63282200-63295400	Weak transcription	Lung	lung
6	chr12:63284200-63291400	Weak transcription	Brain Angular Gyrus	brain
7	chr12:63284800-63289000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr12:63285600-63291400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr12:63286200-63291400	Weak transcription	Brain Anterior Caudate	brain
10	chr12:63286200-63291600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr12:63286200-63293600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr12:63286400-63291400	Weak transcription	Brain Substantia Nigra	brain
13	chr12:63286400-63291600	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr12:63286400-63291600	Weak transcription	Brain Hippocampus Middle	brain
15	chr12:63286400-63293400	Weak transcription	A549	lung
16	chr12:63286800-63291800	Weak transcription	Primary hematopoietic stem cells	blood
17	chr12:63286800-63291800	Weak transcription	Brain Cingulate Gyrus	brain
18	chr12:63287200-63289200	Enhancers	HepG2	liver
19	chr12:63287200-63289600	Weak transcription	K562	blood
20	chr12:63287400-63291200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr12:63287400-63293000	Weak transcription	Stomach Mucosa	stomach
22	chr12:63287400-63309000	Weak transcription	Pancreas	Pancrea
23	chr12:63287600-63291400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr12:63287600-63291600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr12:63287600-63292000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr12:63287800-63316400	Weak transcription	Fetal Intestine Small	intestine
27	chr12:63288000-63289000	Weak transcription	Placenta	Placenta
28	chr12:63288000-63289200	Weak transcription	Fetal Intestine Large	intestine
29	chr12:63289000-63289400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr12:63289000-63289400	Enhancers	Placenta	Placenta
31	chr12:63289000-63289600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr12:63289000-63289600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr12:63289000-63289600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr12:63289200-63289400	Enhancers	Fetal Intestine Large	intestine
35	chr12:63289200-63289400	Flanking Active TSS	HepG2	liver
36	chr12:63289200-63289600	Enhancers	H1 Cell Line	embryonic stem cell
37	chr12:63289200-63289600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr12:63289200-63289600	Enhancers	H9 Cell Line	embryonic stem cell
39	chr12:63289200-63289800	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr12:63289200-63289800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:63289400-63290000	Enhancers	HepG2	liver
42	chr12:63289400-63290400	Weak transcription	Fetal Intestine Large	intestine
43	chr12:63289400-63293000	Weak transcription	Placenta	Placenta
44	chr12:63289400-63293400	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr12:63289600-63293400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr12:63289600-63293800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr12:63289600-63294600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr12:63289600-63294600	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr12:63289600-63294600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr12:63289600-63306600	Weak transcription	H1 Cell Line	embryonic stem cell

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