Variant report

Variant	nsv898808
Chromosome Location	chr12:12463407-12549503
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2642)
CpG islands
(count:1956)
Chromatin interactive
region (count:120)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2642 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:12466883-12467373	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:12480753-12481084	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:12537535-12538151	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:12510182-12510546	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:12529544-12529933	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:12529578-12529897	K562	blood:	n/a	n/a
7	ARID3A	chr12:12487344-12487604	K562	blood:	n/a	n/a
8	ARID3A	chr12:12545008-12545232	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:12480758-12481101	K562	blood:	n/a	n/a
10	ARID3A	chr12:12545383-12545806	K562	blood:	n/a	n/a
11	ARID3A	chr12:12503398-12504581	HepG2	liver:	n/a	n/a
12	ARID3A	chr12:12489051-12489331	HepG2	liver:	n/a	n/a
13	ARID3A	chr12:12534087-12534699	HepG2	liver:	n/a	n/a
14	ARID3A	chr12:12487357-12487677	HepG2	liver:	n/a	n/a
15	ARID3A	chr12:12506748-12507137	K562	blood:	n/a	n/a
16	ARID3A	chr12:12501261-12501512	K562	blood:	n/a	n/a
17	ATF1	chr12:12506808-12507158	K562	blood:	n/a	n/a
18	ATF1	chr12:12487360-12487603	K562	blood:	n/a	n/a
19	ATF1	chr12:12501331-12501592	K562	blood:	n/a	n/a
20	ATF1	chr12:12545213-12545785	K562	blood:	n/a	n/a
21	ATF1	chr12:12480817-12481032	K562	blood:	n/a	n/a
22	ATF1	chr12:12509825-12510182	K562	blood:	n/a	n/a
23	ATF2	chr12:12509500-12510468	GM12878	blood:	n/a	n/a
24	ATF2	chr12:12509546-12510232	GM12878	blood:	n/a	n/a
25	ATF3	chr12:12509815-12510156	K562	blood:	n/a	n/a
26	ATF3	chr12:12487209-12487689	A549	lung:	n/a	n/a
27	BACH1	chr12:12545497-12545697	K562	blood:	n/a	n/a
28	BACH1	chr12:12509802-12510264	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr12:12503062-12503140	H1-hESC	embryonic stem cell:	n/a	n/a
30	BATF	chr12:12464721-12464983	GM12878	blood:	n/a	chr12:12464748-12464756
31	BATF	chr12:12509963-12510302	GM12878	blood:	n/a	n/a
32	BATF	chr12:12488948-12489314	GM12878	blood:	n/a	chr12:12489173-12489184
33	BATF	chr12:12488984-12489341	GM12878	blood:	n/a	chr12:12489173-12489184
34	BATF	chr12:12509293-12509509	GM12878	blood:	n/a	n/a
35	BCL11A	chr12:12509986-12510369	GM12878	blood:	n/a	chr12:12510259-12510272 chr12:12510326-12510339
36	BCL11A	chr12:12464735-12464957	GM12878	blood:	n/a	n/a
37	BCL11A	chr12:12509979-12510322	GM12878	blood:	n/a	chr12:12510259-12510272
38	BCL3	chr12:12486983-12487514	GM12878	blood:	n/a	chr12:12487446-12487455
39	BCL3	chr12:12509580-12510800	A549	lung:	n/a	chr12:12510259-12510272 chr12:12510326-12510339
40	BCLAF1	chr12:12529473-12530001	GM12878	blood:	n/a	n/a
41	BCLAF1	chr12:12509815-12510972	GM12878	blood:	n/a	chr12:12510259-12510272 chr12:12510326-12510339
42	BCLAF1	chr12:12509548-12510871	GM12878	blood:	n/a	chr12:12510259-12510272 chr12:12510326-12510339
43	BHLHE40	chr12:12545357-12545685	K562	blood:	n/a	n/a
44	BHLHE40	chr12:12502837-12503637	K562	blood:	n/a	chr12:12503027-12503043 chr12:12503142-12503158
45	BHLHE40	chr12:12537880-12538299	HepG2	liver:	n/a	chr12:12538104-12538113 chr12:12538104-12538113 chr12:12538105-12538114 chr12:12538098-12538119
46	BHLHE40	chr12:12537916-12538205	HepG2	liver:	n/a	chr12:12538104-12538113 chr12:12538104-12538113 chr12:12538105-12538114 chr12:12538098-12538119
47	BHLHE40	chr12:12480791-12481069	K562	blood:	n/a	n/a
48	BHLHE40	chr12:12537973-12538300	GM12878	blood:	n/a	chr12:12538104-12538113 chr12:12538104-12538113 chr12:12538105-12538114 chr12:12538098-12538119
49	BHLHE40	chr12:12532622-12533229	GM12878	blood:	n/a	n/a
50	BHLHE40	chr12:12463705-12463906	HepG2	liver:	n/a	n/a

(count:1956 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:12510001-12510051	HepG2	liver:	n/a
2	chr12:12502846-12502896	NT2-D1	testis:	n/a
3	chr12:12503186-12503236	BE2_C	brain:	n/a
4	chr12:12510007-12510057	RPTEC	kidney:	n/a
5	chr12:12510001-12510051	HepG2	liver:	n/a
6	chr12:12502846-12502896	NT2-D1	testis:	n/a
7	chr12:12503186-12503236	BE2_C	brain:	n/a
8	chr12:12510007-12510057	RPTEC	kidney:	n/a
9	chr12:12510155-12510205	HCT-116	colon:	n/a
10	chr12:12510155-12510205	HRE	kidney:	n/a
11	chr12:12503186-12503236	ECC-1	luminal epithelium:	n/a
12	chr12:12509930-12509980	HCM	heart:	n/a
13	chr12:12507213-12507263	AG04450	lung:	fetal
14	chr12:12510074-12510124	PANC-1	pancreas:	n/a
15	chr12:12503189-12503239	HUVEC	blood vessel:	n/a
16	chr12:12514228-12514278	MCF-7	breast:	n/a
17	chr12:12503544-12503594	NHDF-neo	bronchial:	n/a
18	chr12:12510064-12510114	GM12891	blood:	n/a
19	chr12:12509922-12509972	NHDF-neo	bronchial:	n/a
20	chr12:12518875-12518925	ProgFib	skin:	n/a
21	chr12:12503186-12503236	NB4	blood:	n/a
22	chr12:12510067-12510117	BE2_C	brain:	n/a
23	chr12:12510001-12510051	NHBE	bronchial:	n/a
24	chr12:12509705-12509755	AG09319	gingival:	n/a
25	chr12:12510074-12510124	GM12891	blood:	n/a
26	chr12:12484680-12484730	HRCEpiC	kidney:	n/a
27	chr12:12510155-12510205	AG10803	skin:	n/a
28	chr12:12503457-12503507	AG04449	skin:	fetal
29	chr12:12503030-12503080	RPTEC	kidney:	n/a
30	chr12:12510074-12510124	HCPEpiC	choroid plexus:	n/a
31	chr12:12509725-12509775	HNPCEpiC	eye:	n/a
32	chr12:12503186-12503236	LNCaP	prostate:	n/a
33	chr12:12509705-12509755	GM06990	blood:	n/a
34	chr12:12503544-12503594	HRE	kidney:	n/a
35	chr12:12503457-12503507	Hepatocyte	liver:	n/a
36	chr12:12510155-12510205	HMEC	breast:	n/a
37	chr12:12518875-12518925	NHDF-neo	bronchial:	n/a
38	chr12:12509940-12509990	HPAEpiC	pulmonary alveolar:	n/a
39	chr12:12510241-12510291	RPTEC	kidney:	n/a
40	chr12:12487500-12487550	BE2_C	brain:	n/a
41	chr12:12503544-12503594	NH-A	brain:	n/a
42	chr12:12503030-12503080	HAEpiC	amniotic membrane:	n/a
43	chr12:12503224-12503274	AG04450	lung:	fetal
44	chr12:12503224-12503274	SKMC	muscle:	n/a
45	chr12:12503189-12503239	HEK293	kidney:	embryo
46	chr12:12503189-12503239	U87	brain:	n/a
47	chr12:12503455-12503505	HRPEpiC	eye:	n/a
48	chr12:12510064-12510114	PANC-1	pancreas:	n/a
49	chr12:12510007-12510057	AoSMC	blood vessel:	n/a
50	chr12:12509725-12509775	H1-hESC	embryonic stem cell:	embryo

(count:120 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:12419210..12421739-chr12:12479012..12482155,4	MCF-7	breast:
2	chr12:12234308..12235009-chr12:12480762..12481311,2	MCF-7	breast:
3	chr12:12539967..12541683-chr12:12547549..12549266,2	MCF-7	breast:
4	chr12:12492591..12498034-chr12:12508387..12511659,4	K562	blood:
5	chr12:12509354..12513359-chr12:12517458..12522131,6	K562	blood:
6	chr12:12524724..12527440-chr12:12848940..12850671,2	MCF-7	breast:
7	chr12:12519688..12522989-chr12:12524598..12527681,3	K562	blood:
8	chr12:12479198..12480920-chr12:12483064..12485250,2	K562	blood:
9	chr12:12507394..12509953-chr12:12633944..12635631,2	MCF-7	breast:
10	chr12:12531073..12532698-chr12:12940131..12941983,2	K562	blood:
11	chr12:12419232..12421863-chr12:12485161..12488276,6	MCF-7	breast:
12	chr12:12515022..12517464-chr12:12520422..12522586,3	MCF-7	breast:
13	chr12:12419370..12422118-chr12:12510348..12512093,2	MCF-7	breast:
14	chr12:12480106..12480918-chr12:27090779..27091584,2	Hela-S3	cervix:
15	chr12:12509044..12511145-chr12:12512603..12514183,2	MCF-7	breast:
16	chr12:12510791..12511698-chrX:119797918..119798865,2	Hela-S3	cervix:
17	chr12:12509983..12510584-chr7:150020762..150021311,2	Hela-S3	cervix:
18	chr12:12510093..12511651-chr12:12512844..12515772,2	K562	blood:
19	chr12:12522631..12525556-chr12:12525783..12528472,2	MCF-7	breast:
20	chr12:12486786..12487683-chr12:12503028..12503718,2	K562	blood:
21	chr12:12493055..12495438-chr12:12763586..12765777,2	MCF-7	breast:
22	chr12:12510113..12510632-chr3:101405456..101406387,2	Hela-S3	cervix:
23	chr12:12502870..12505613-chr12:12507814..12511200,4	K562	blood:
24	chr12:12549500..12552302-chr12:12715831..12718057,2	MCF-7	breast:
25	chr12:12525607..12527513-chrX:39488072..39490988,2	MCF-7	breast:
26	chr12:12496602..12498278-chr12:12498388..12501729,3	K562	blood:
27	chr12:12479190..12481721-chr12:12482518..12485352,2	MCF-7	breast:
28	chr12:12531751..12533905-chr12:12536172..12537730,2	K562	blood:
29	chr12:12487375..12490317-chr12:12509840..12512376,2	MCF-7	breast:
30	chr12:12515022..12517464-chr12:12520422..12522586,3	MCF-7	breast:
31	chr12:12502767..12504788-chr12:12506780..12508303,2	MCF-7	breast:
32	chr12:12531370..12534398-chr12:12711544..12717276,8	MCF-7	breast:
33	chr12:12507988..12510235-chr12:12714031..12716523,2	MCF-7	breast:
34	chr12:12505582..12507087-chr12:12510779..12513309,2	MCF-7	breast:
35	chr12:12234594..12235634-chr12:12486774..12487917,3	MCF-7	breast:
36	chr12:12492591..12496628-chr12:12508387..12511489,3	K562	blood:
37	chr12:12493042..12496407-chr12:12508406..12511511,3	MCF-7	breast:
38	chr12:12501756..12503820-chr12:12509545..12511706,2	MCF-7	breast:
39	chr12:12502870..12505613-chr12:12507814..12511200,4	K562	blood:
40	chr12:12531757..12533450-chr12:12857670..12859223,2	MCF-7	breast:
41	chr12:12509843..12512441-chr12:12520561..12523436,3	MCF-7	breast:
42	chr12:12509503..12512182-chr12:12513037..12516438,6	MCF-7	breast:
43	chr12:12539967..12541683-chr12:12547549..12549266,2	MCF-7	breast:
44	chr12:12491237..12492051-chr12:12502345..12503099,2	MCF-7	breast:
45	chr12:12510200..12513346-chr12:12523638..12526361,3	K562	blood:
46	chr12:12510102..12510635-chr3:186500869..186501435,2	NB4	blood:
47	chr12:12479198..12480920-chr12:12483064..12485250,2	K562	blood:
48	chr12:12509599..12512153-chr12:12848294..12850312,2	MCF-7	breast:
49	chr12:12508678..12514314-chr12:12868637..12874427,7	K562	blood:
50	chr12:12497428..12499912-chr12:12500992..12503884,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC007621.1-1	chr12:12508342-12509739	NR_024061
2	lnc-AC007621.1-1	chr12:12508344-12509739	XLOC_010020
3	lnc-AC007621.1-1	chr12:12509862-12510001	NR_024061
4	lnc-AC007621.1-1	chr12:12509862-12510001	XLOC_010020
5	lnc-LOH12CR1-5	chr12:12491710-12492188	NONHSAT026968

No data

Variant related genes	Relation type
MANSC1	TF binding region
LOH12CR1	TF binding region
ENSG00000243141	TF binding region
LOH12CR2	TF binding region
MANSC1	CpG island
LOH12CR1	CpG island
ENSG00000243141	CpG island
LOH12CR2	CpG island
ENSG00000156976	chromatin interactions
ENSG00000121380	chromatin interactions
ENSG00000205791	chromatin interactions
ENSG00000114391	chromatin interactions
ENSG00000214078	chromatin interactions
ENSG00000106526	chromatin interactions
ENSG00000111790	chromatin interactions
ENSG00000111276	chromatin interactions
ENSG00000111266	chromatin interactions
ENSG00000244462	chromatin interactions
ENSG00000111269	chromatin interactions
ENSG00000183150	chromatin interactions
ENSG00000105483	chromatin interactions
ENSG00000243141	chromatin interactions
ENSG00000070018	chromatin interactions
ENSG00000064102	chromatin interactions
ENSG00000178878	chromatin interactions
ENSG00000256658	chromatin interactions
ENSG00000129932	chromatin interactions
ENSG00000165714	chromatin interactions
ENSG00000143933	chromatin interactions
ENSG00000111261	chromatin interactions

Extended variants
information (count: 3781 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:3781 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4763800	chr12:12463407-12463408	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs77100346	chr12:12463443-12463444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138376145	chr12:12463485-12463486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs4763801	chr12:12463488-12463489	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs4763802	chr12:12463494-12463495	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs73277410	chr12:12463518-12463519	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs371755517	chr12:12463539-12463540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373538774	chr12:12463554-12463555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74577586	chr12:12463564-12463565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142979730	chr12:12463572-12463573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11054790	chr12:12463592-12463593	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs11054791	chr12:12463601-12463602	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs190407301	chr12:12463602-12463603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs71452204	chr12:12463608-12463609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11054793	chr12:12463609-12463610	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs139879295	chr12:12463610-12463611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182043920	chr12:12463619-12463620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4763803	chr12:12463645-12463646	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs553676387	chr12:12463651-12463652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11054794	chr12:12463672-12463673	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs545414101	chr12:12463719-12463720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541576128	chr12:12463734-12463735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs4763804	chr12:12463799-12463800	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs575797747	chr12:12463836-12463837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370888148	chr12:12463839-12463840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543461878	chr12:12463873-12463874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113117388	chr12:12463903-12463904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200523088	chr12:12463913-12463914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs76569239	chr12:12463914-12463915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187596401	chr12:12463932-12463933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141059713	chr12:12463940-12463941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373442148	chr12:12463941-12463942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189073026	chr12:12463942-12463943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7976201	chr12:12463966-12463967	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs7973150	chr12:12463988-12463989	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs370582884	chr12:12463993-12463994	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533047005	chr12:12464015-12464016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551433328	chr12:12464026-12464027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs61922020	chr12:12464032-12464033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569785655	chr12:12464037-12464038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185270057	chr12:12464038-12464039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34196558	chr12:12464058-12464059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs374841888	chr12:12464061-12464062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140908924	chr12:12464067-12464068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535151846	chr12:12464081-12464082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150086058	chr12:12464106-12464107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571711400	chr12:12464126-12464127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539318501	chr12:12464146-12464147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113563326	chr12:12464175-12464176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557376846	chr12:12464194-12464195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Prostate cancer	21088497	CNVD

Chromatin state (count:2887 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:12459400-12469400	Enhancers	Liver	Liver
2	chr12:12460600-12465800	Enhancers	HepG2	liver
3	chr12:12461200-12465200	Enhancers	Fetal Intestine Large	intestine
4	chr12:12462000-12467000	Weak transcription	Stomach Mucosa	stomach
5	chr12:12462200-12464000	Enhancers	Rectal Mucosa Donor 29	rectum
6	chr12:12462400-12466800	Weak transcription	Pancreas	Pancrea
7	chr12:12462400-12472600	Weak transcription	Duodenum Mucosa	Duodenum
8	chr12:12462600-12463800	Weak transcription	Fetal Intestine Small	intestine
9	chr12:12462600-12463800	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr12:12463600-12467800	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr12:12463800-12465000	Enhancers	Fetal Intestine Small	intestine
12	chr12:12463800-12465000	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr12:12464000-12464400	Enhancers	Colonic Mucosa	Colon
14	chr12:12464000-12466800	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr12:12464400-12472400	Weak transcription	Colonic Mucosa	Colon
16	chr12:12465000-12465800	Weak transcription	Fetal Intestine Small	intestine
17	chr12:12465000-12465800	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr12:12465200-12465600	Weak transcription	Fetal Intestine Large	intestine
19	chr12:12465600-12466200	Enhancers	Hela-S3	cervix
20	chr12:12465600-12469400	Enhancers	Fetal Intestine Large	intestine
21	chr12:12465800-12466000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr12:12465800-12466200	Flanking Active TSS	HepG2	liver
23	chr12:12465800-12467200	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr12:12465800-12469400	Enhancers	Fetal Intestine Small	intestine
25	chr12:12466000-12484600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr12:12466200-12466600	Weak transcription	Hela-S3	cervix
27	chr12:12466200-12466800	Enhancers	HepG2	liver
28	chr12:12466600-12469400	Enhancers	Hela-S3	cervix
29	chr12:12466800-12467000	Enhancers	Small Intestine	intestine
30	chr12:12466800-12467200	Enhancers	Pancreas	Pancrea
31	chr12:12466800-12467600	Flanking Active TSS	HepG2	liver
32	chr12:12466800-12468400	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr12:12467000-12467400	Enhancers	Stomach Mucosa	stomach
34	chr12:12467000-12467400	Active TSS	A549	lung
35	chr12:12467000-12484400	Weak transcription	Small Intestine	intestine
36	chr12:12467200-12467400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr12:12467200-12467600	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr12:12467200-12468000	Weak transcription	Pancreas	Pancrea
39	chr12:12467400-12468800	Weak transcription	Stomach Mucosa	stomach
40	chr12:12467600-12468400	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr12:12467600-12469400	Enhancers	HepG2	liver
42	chr12:12467600-12472600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr12:12467800-12468000	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr12:12468000-12468400	Enhancers	Pancreas	Pancrea
45	chr12:12468000-12472800	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr12:12468400-12468600	Weak transcription	Pancreas	Pancrea
47	chr12:12468400-12468800	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr12:12468400-12468800	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr12:12468600-12469600	Enhancers	Pancreas	Pancrea
50	chr12:12468800-12469000	Enhancers	Rectal Mucosa Donor 29	rectum

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