Variant report

Variant	nsv1048199
Chromosome Location	chr12:64951666-65021700
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2346)
CpG islands
(count:1098)
Chromatin interactive
region (count:113)
LncRNA
region (count:4)
Mature miRNA
region (count: 3)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:64986928-64987049	K562	blood:	n/a	n/a
2	ARID3A	chr12:65019023-65019740	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:65002842-65003648	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:65012823-65013421	K562	blood:	n/a	n/a
5	ARID3A	chr12:65001932-65003917	K562	blood:	n/a	n/a
6	ARID3A	chr12:65018938-65019964	K562	blood:	n/a	n/a
7	ARID3A	chr12:65013732-65014147	K562	blood:	n/a	n/a
8	ARID3A	chr12:65004764-65004964	K562	blood:	n/a	n/a
9	ARID3A	chr12:65001997-65002366	HepG2	liver:	n/a	n/a
10	ARID3A	chr12:64981348-64981414	K562	blood:	n/a	n/a
11	ATF1	chr12:64951690-64951763	K562	blood:	n/a	n/a
12	ATF1	chr12:65019032-65019882	K562	blood:	n/a	n/a
13	ATF1	chr12:65012861-65013338	K562	blood:	n/a	n/a
14	ATF1	chr12:65002725-65003193	K562	blood:	n/a	n/a
15	ATF2	chr12:65012809-65013472	GM12878	blood:	n/a	n/a
16	ATF2	chr12:65014901-65015840	GM12878	blood:	n/a	n/a
17	ATF2	chr12:65003261-65003813	GM12878	blood:	n/a	n/a
18	ATF2	chr12:65007506-65007916	GM12878	blood:	n/a	n/a
19	ATF2	chr12:65003478-65004173	GM12878	blood:	n/a	n/a
20	ATF2	chr12:65018928-65019993	GM12878	blood:	n/a	n/a
21	ATF2	chr12:65018973-65019973	GM12878	blood:	n/a	n/a
22	ATF2	chr12:65012800-65013454	GM12878	blood:	n/a	n/a
23	ATF2	chr12:65014928-65015835	GM12878	blood:	n/a	n/a
24	ATF2	chr12:65004569-65005095	GM12878	blood:	n/a	n/a
25	ATF3	chr12:65002635-65003090	K562	blood:	n/a	n/a
26	ATF3	chr12:64970906-64971157	K562	blood:	n/a	n/a
27	BACH1	chr12:65003273-65004122	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr12:65004749-65005253	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr12:65002874-65003187	K562	blood:	n/a	chr12:65002878-65002892
30	BATF	chr12:65004772-65005024	GM12878	blood:	n/a	n/a
31	BATF	chr12:65015032-65015311	GM12878	blood:	n/a	n/a
32	BATF	chr12:65019124-65019893	GM12878	blood:	n/a	n/a
33	BCL11A	chr12:65014938-65015342	GM12878	blood:	n/a	n/a
34	BCL11A	chr12:65012871-65013307	GM12878	blood:	n/a	n/a
35	BCL3	chr12:65004592-65005294	A549	lung:	n/a	n/a
36	BCL3	chr12:64954646-64954944	GM12878	blood:	n/a	n/a
37	BCL3	chr12:65003670-65004172	GM12878	blood:	n/a	n/a
38	BCL3	chr12:65004612-65004925	GM12878	blood:	n/a	n/a
39	BCL3	chr12:65018952-65019624	A549	lung:	n/a	n/a
40	BCL3	chr12:64954524-64955072	GM12878	blood:	n/a	n/a
41	BCL3	chr12:65018853-65019864	A549	lung:	n/a	chr12:65019643-65019652 chr12:65019642-65019651
42	BCL3	chr12:65012816-65013390	A549	lung:	n/a	n/a
43	BCLAF1	chr12:65007558-65007996	GM12878	blood:	n/a	n/a
44	BCLAF1	chr12:65014877-65015656	GM12878	blood:	n/a	n/a
45	BCLAF1	chr12:65012782-65013345	GM12878	blood:	n/a	n/a
46	BCLAF1	chr12:65004508-65005426	GM12878	blood:	n/a	chr12:65004534-65004547 chr12:65004537-65004550 chr12:65004530-65004543 chr12:65004584-65004597
47	BCLAF1	chr12:65003605-65004188	GM12878	blood:	n/a	n/a
48	BCLAF1	chr12:65014892-65015485	GM12878	blood:	n/a	n/a
49	BCLAF1	chr12:65012818-65013490	GM12878	blood:	n/a	n/a
50	BCLAF1	chr12:65004486-65005163	GM12878	blood:	n/a	chr12:65004534-65004547 chr12:65004537-65004550 chr12:65004530-65004543 chr12:65004584-65004597

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:65015547-65015597	AG04449	skin:	fetal
2	chr12:65014995-65015045	AG04450	lung:	fetal
3	chr12:65003120-65003170	GM12891	blood:	n/a
4	chr12:64960957-64961007	A549	lung:	n/a
5	chr12:65003003-65003053	HEEpiC	esophagus:	n/a
6	chr12:65008851-65008901	HNPCEpiC	eye:	n/a
7	chr12:65014995-65015045	IMR90	lung:	fetal
8	chr12:65003032-65003082	CMK	blood:	n/a
9	chr12:64954729-64954779	AG04450	lung:	fetal
10	chr12:65004466-65004516	HCT-116	colon:	n/a
11	chr12:65003120-65003170	PFSK-1	brain:	n/a
12	chr12:65000487-65000537	HCPEpiC	choroid plexus:	n/a
13	chr12:65015486-65015536	HepG2	liver:	n/a
14	chr12:65015547-65015597	AoSMC	blood vessel:	n/a
15	chr12:64977593-64977643	HEK293	kidney:	embryo
16	chr12:64960957-64961007	HL-60	blood:	n/a
17	chr12:65003992-65004042	NT2-D1	testis:	n/a
18	chr12:65004898-65004948	HCPEpiC	choroid plexus:	n/a
19	chr12:65015547-65015597	BE2_C	brain:	n/a
20	chr12:65016129-65016179	HCF	heart:	n/a
21	chr12:65008851-65008901	U87	brain:	n/a
22	chr12:65019329-65019379	BJ	skin:	n/a
23	chr12:65019329-65019379	ECC-1	luminal epithelium:	n/a
24	chr12:65015486-65015536	ovcar-3	ovarian:	n/a
25	chr12:65000487-65000537	HCF	heart:	n/a
26	chr12:65019329-65019379	NHDF-neo	bronchial:	n/a
27	chr12:65015486-65015536	PrEC	prostate:	n/a
28	chr12:64960957-64961007	RPTEC	kidney:	n/a
29	chr12:65015547-65015597	GM19239	blood:	n/a
30	chr12:65003032-65003082	SAEC	small airway:	n/a
31	chr12:64977593-64977643	HPAEpiC	pulmonary alveolar:	n/a
32	chr12:65003992-65004042	HCF	heart:	n/a
33	chr12:65019329-65019379	HCT-116	colon:	n/a
34	chr12:65003794-65003844	SAEC	small airway:	n/a
35	chr12:65019329-65019379	HepG2	liver:	n/a
36	chr12:65008851-65008901	PFSK-1	brain:	n/a
37	chr12:64977593-64977643	NH-A	brain:	n/a
38	chr12:64960957-64961007	SAEC	small airway:	n/a
39	chr12:65004289-65004339	CMK	blood:	n/a
40	chr12:65003003-65003053	BJ	skin:	n/a
41	chr12:65003003-65003053	LNCaP	prostate:	n/a
42	chr12:65016129-65016179	PrEC	prostate:	n/a
43	chr12:65003120-65003170	AG04450	lung:	fetal
44	chr12:64960957-64961007	SKMC	muscle:	n/a
45	chr12:65004289-65004339	HRPEpiC	eye:	n/a
46	chr12:65000487-65000537	H1-hESC	embryonic stem cell:	embryo
47	chr12:65004466-65004516	HCPEpiC	choroid plexus:	n/a
48	chr12:65008851-65008901	Jurkat	blood:	n/a
49	chr12:65015486-65015536	HMEC	breast:	n/a
50	chr12:64960957-64961007	AG04449	skin:	fetal

(count:113 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:64955263..64957800-chr12:64960025..64962261,2	MCF-7	breast:
2	chr12:64992855..64995703-chr12:65002717..65005866,4	MCF-7	breast:
3	chr12:64949750..64952567-chr12:64952964..64956262,3	MCF-7	breast:
4	chr12:64962295..64965287-chr12:64977831..64979712,2	MCF-7	breast:
5	chr12:64798234..64800196-chr12:65021322..65023888,2	K562	blood:
6	chr12:64844696..64847501-chr12:65001513..65004366,3	K562	blood:
7	chr12:64980366..64983383-chr12:65001512..65004201,3	K562	blood:
8	chr12:65011462..65014885-chr12:65017332..65020916,6	MCF-7	breast:
9	chr12:65002574..65003271-chr4:103789942..103790730,2	Hela-S3	cervix:
10	chr12:64965065..64966977-chr12:64990883..64992397,2	MCF-7	breast:
11	chr12:65013056..65015741-chr12:65019440..65021647,2	MCF-7	breast:
12	chr12:65004967..65007120-chr12:65061292..65063041,2	K562	blood:
13	chr12:65004562..65005411-chr12:65018842..65019420,4	MCF-7	breast:
14	chr12:64796628..64799812-chr12:65002415..65005896,3	K562	blood:
15	chr12:65019590..65021389-chr12:65024467..65026055,3	K562	blood:
16	chr12:65018895..65020884-chr12:65086015..65088325,2	MCF-7	breast:
17	chr12:65011047..65013425-chr12:65022632..65024706,2	MCF-7	breast:
18	chr12:64943084..64943792-chr12:65002036..65002675,2	MCF-7	breast:
19	chr12:49525114..49525857-chr12:65004032..65004831,2	Hela-S3	cervix:
20	chr12:65019301..65021176-chr12:65062867..65064609,2	K562	blood:
21	chr12:65008925..65011325-chr12:65018761..65021697,3	MCF-7	breast:
22	chr12:65010556..65012937-chr12:65017376..65021348,4	K562	blood:
23	chr12:65004550..65006753-chr12:65173633..65175877,2	MCF-7	breast:
24	chr12:65001714..65006897-chr12:65088342..65093997,11	MCF-7	breast:
25	chr12:64950433..64954312-chr12:64959664..64962959,3	MCF-7	breast:
26	chr12:65001526..65007900-chr12:65015799..65021807,8	K562	blood:
27	chr12:65016442..65019284-chr12:65019658..65023232,4	MCF-7	breast:
28	chr12:65001678..65008078-chr12:65013108..65023657,17	MCF-7	breast:
29	chr12:65008839..65011429-chr12:65017334..65019705,2	MCF-7	breast:
30	chr12:65004562..65005411-chr12:65018842..65019420,4	MCF-7	breast:
31	chr12:64950051..64952899-chr12:64954686..64957659,2	K562	blood:
32	chr12:65001959..65007139-chr12:65021874..65025265,5	K562	blood:
33	chr12:64977051..64979186-chr12:65004019..65006616,2	K562	blood:
34	chr12:64949750..64952567-chr12:64952964..64956262,3	MCF-7	breast:
35	chr12:64989320..64990857-chr12:64990875..64993083,2	MCF-7	breast:
36	chr12:64966944..64968828-chr12:64983919..64985657,2	MCF-7	breast:
37	chr12:65006929..65009756-chr12:65024584..65028826,3	MCF-7	breast:
38	chr1:28974934..28975572-chr12:65004207..65004918,2	Hela-S3	cervix:
39	chr12:64989952..64991972-chr12:65050682..65053342,2	K562	blood:
40	chr12:65002182..65006670-chr12:65087134..65093452,10	MCF-7	breast:
41	chr12:64943164..64944020-chr12:65001607..65002572,3	K562	blood:
42	chr12:64960849..64962963-chr12:65011488..65013311,2	K562	blood:
43	chr12:65002667..65003975-chr15:72523179..72524331,3	Hela-S3	cervix:
44	chr12:64994040..64996773-chr12:65001474..65003410,2	K562	blood:
45	chr12:64990710..64993053-chr12:64998438..65000243,2	K562	blood:
46	chr12:65019263..65021039-chr12:65064985..65067371,4	MCF-7	breast:
47	chr12:65013129..65015693-chr12:65017473..65019068,2	K562	blood:
48	chr12:65011741..65013304-chr12:65014753..65016966,2	MCF-7	breast:
49	chr12:65014921..65016651-chr12:65088874..65091449,2	MCF-7	breast:
50	chr12:64960849..64962963-chr12:65011488..65013311,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNS-2	chr12:64992858-64992996	ENSG00000256670.1
2	lnc-TBK1-2	chr12:65004302-65004523	NONHSAT029155
3	lnc-GNS-2	chr12:65003125-65003239	ENSG00000256670.1
4	lnc-TBK1-2	chr12:65005218-65005430	NONHSAT029155

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548c-3p	chr12:65016349-65016370	MIMAT0003285
hsa-miR-548c-5p	chr12:65016313-65016334	MIMAT0004806
hsa-miR-548z	chr12:65016310-65016332	MIMAT0018446

No data

Variant related genes	Relation type
ENSG00000256670	TF binding region
MIR548C	TF binding region
ENSG00000223294	TF binding region
RASSF3	TF binding region
ENSG00000225195	TF binding region
ENSG00000256670	CpG island
MIR548C	CpG island
ENSG00000223294	CpG island
RASSF3	CpG island
ENSG00000225195	CpG island
ENSG00000270103	chromatin interactions
ENSG00000183735	chromatin interactions
ENSG00000258555	chromatin interactions
ENSG00000265020	chromatin interactions
ENSG00000153179	chromatin interactions
ENSG00000127948	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000207546	chromatin interactions
ENSG00000268028	chromatin interactions
ENSG00000184575	chromatin interactions
ENSG00000168476	chromatin interactions
ENSG00000100014	chromatin interactions
ENSG00000188290	chromatin interactions
ENSG00000123416	chromatin interactions
ENSG00000111490	chromatin interactions
ENSG00000145354	chromatin interactions
ENSG00000053501	chromatin interactions
ENSG00000135677	chromatin interactions
ENSG00000109332	chromatin interactions
ENSG00000256670	chromatin interactions
ENSG00000225195	chromatin interactions
ENSG00000067225	chromatin interactions
ENSG00000117139	chromatin interactions

Extended variants
information (count: 2620 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2620 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527884110	chr12:64951693-64951694	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs557422259	chr12:64951715-64951716	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs375053210	chr12:64951724-64951725	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs546221675	chr12:64951725-64951726	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553639550	chr12:64951733-64951734	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs184733574	chr12:64951806-64951807	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs542041183	chr12:64951828-64951829	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs561912103	chr12:64951852-64951853	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs530553861	chr12:64951865-64951866	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs144984584	chr12:64951907-64951908	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs73317530	chr12:64951909-64951910	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs532950304	chr12:64951914-64951915	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs546231683	chr12:64951978-64951979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188229639	chr12:64952006-64952007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377452553	chr12:64952016-64952017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147599126	chr12:64952063-64952064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs80016442	chr12:64952079-64952080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549790807	chr12:64952134-64952135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142060837	chr12:64952136-64952137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144441561	chr12:64952146-64952147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369125424	chr12:64952148-64952149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570818894	chr12:64952191-64952192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539825115	chr12:64952255-64952256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs55734450	chr12:64952266-64952267	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs558080961	chr12:64952275-64952276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573497477	chr12:64952284-64952285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571081901	chr12:64952312-64952313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535731921	chr12:64952345-64952346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527327936	chr12:64952360-64952361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs193174753	chr12:64952365-64952366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184654430	chr12:64952374-64952375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571814975	chr12:64952395-64952396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564209586	chr12:64952405-64952406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140267533	chr12:64952428-64952429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540236339	chr12:64952440-64952441	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534377868	chr12:64952516-64952517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559874649	chr12:64952533-64952534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529229546	chr12:64952550-64952551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549297553	chr12:64952572-64952573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562716260	chr12:64952606-64952607	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531547167	chr12:64952607-64952608	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551243164	chr12:64952728-64952729	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs369775931	chr12:64952737-64952738	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs570946615	chr12:64952747-64952748	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs374183487	chr12:64952808-64952809	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs555164623	chr12:64952903-64952904	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs377626053	chr12:64952912-64952913	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs116607998	chr12:64952913-64952914	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs574921068	chr12:64952919-64952920	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs547007358	chr12:64952942-64952943	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2245 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:64944800-64954000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr12:64946400-64952600	Weak transcription	Fetal Muscle Leg	muscle
3	chr12:64948200-64952400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr12:64951400-64960400	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr12:64952400-64953000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr12:64952400-64955800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr12:64952600-64952800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr12:64952600-64952800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr12:64952600-64952800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr12:64952600-64952800	Enhancers	Lung	lung
11	chr12:64952600-64953000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr12:64952600-64953000	Enhancers	Left Ventricle	heart
13	chr12:64952600-64953200	Enhancers	Fetal Muscle Leg	muscle
14	chr12:64952600-64953200	Enhancers	NHDF-Ad	bronchial
15	chr12:64952600-64955600	Enhancers	NHLF	lung
16	chr12:64952800-64953200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr12:64953000-64953800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr12:64953000-64953800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr12:64953000-64953800	Weak transcription	Lung	lung
20	chr12:64953200-64953600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr12:64953200-64953600	Weak transcription	Fetal Muscle Leg	muscle
22	chr12:64953200-64953600	Weak transcription	NHDF-Ad	bronchial
23	chr12:64953400-64954400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr12:64953600-64954200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr12:64953600-64954400	Enhancers	NHDF-Ad	bronchial
26	chr12:64953600-64955400	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr12:64953600-64955800	Enhancers	Fetal Muscle Leg	muscle
28	chr12:64953800-64954000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr12:64953800-64954000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr12:64953800-64954400	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr12:64953800-64955000	Enhancers	Lung	lung
32	chr12:64953800-64955600	Enhancers	HSMMtube	muscle
33	chr12:64953800-64956000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr12:64954000-64954200	Enhancers	NH-A	brain
35	chr12:64954000-64954400	Enhancers	Muscle Satellite Cultured Cells	--
36	chr12:64954000-64954400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr12:64954000-64954600	Enhancers	Hela-S3	cervix
38	chr12:64954000-64955000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr12:64954000-64955400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr12:64954000-64955400	Enhancers	Brain Anterior Caudate	brain
41	chr12:64954000-64955400	Enhancers	HMEC	breast
42	chr12:64954000-64955400	Enhancers	HSMM	muscle
43	chr12:64954000-64955600	Enhancers	Osteobl	bone
44	chr12:64954000-64955800	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr12:64954200-64954400	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr12:64954200-64954400	Flanking Active TSS	NH-A	brain
47	chr12:64954200-64954600	Enhancers	H1 Cell Line	embryonic stem cell
48	chr12:64954200-64954600	Enhancers	Brain Hippocampus Middle	brain
49	chr12:64954200-64954800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr12:64954200-64954800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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