Variant report

Variant	nsv541362
Chromosome Location	chr12:4627992-4689300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1233)
CpG islands
(count:1342)
Chromatin interactive
region (count:53)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1233 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:4636180-4636414	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:4681814-4682315	K562	blood:	n/a	n/a
3	ARID3A	chr12:4636251-4636437	K562	blood:	n/a	n/a
4	ARID3A	chr12:4648177-4648526	HepG2	liver:	n/a	n/a
5	ATF1	chr12:4681897-4682279	K562	blood:	n/a	n/a
6	ATF2	chr12:4647469-4648325	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr12:4647549-4648183	GM12878	blood:	n/a	n/a
8	ATF2	chr12:4647358-4648161	GM12878	blood:	n/a	n/a
9	ATF3	chr12:4647400-4648225	A549	lung:	n/a	n/a
10	ATF3	chr12:4647308-4648046	A549	lung:	n/a	n/a
11	BACH1	chr12:4682095-4682294	K562	blood:	n/a	n/a
12	BATF	chr12:4649361-4649660	GM12878	blood:	n/a	n/a
13	BCL3	chr12:4647290-4648348	A549	lung:	n/a	chr12:4647959-4647968 chr12:4648005-4648014
14	BCL3	chr12:4671772-4672077	GM12878	blood:	n/a	n/a
15	BCL3	chr12:4647427-4648113	A549	lung:	n/a	chr12:4647959-4647968 chr12:4648005-4648014
16	BHLHE40	chr12:4671260-4671648	K562	blood:	n/a	chr12:4671385-4671401 chr12:4671377-4671393 chr12:4671415-4671431
17	BHLHE40	chr12:4681807-4682170	K562	blood:	n/a	n/a
18	BHLHE40	chr12:4676584-4677265	GM12878	blood:	n/a	n/a
19	BHLHE40	chr12:4644257-4644652	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:4676768-4677129	K562	blood:	n/a	n/a
21	BHLHE40	chr12:4647539-4648217	GM12878	blood:	n/a	n/a
22	BHLHE40	chr12:4647451-4648358	K562	blood:	n/a	n/a
23	BHLHE40	chr12:4675711-4675854	GM12878	blood:	n/a	n/a
24	BRCA1	chr12:4647309-4647826	GM12878	blood:	n/a	n/a
25	BRCA1	chr12:4671285-4671703	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr12:4647424-4648673	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr12:4671172-4671660	K562	blood:	n/a	n/a
28	CCNT2	chr12:4671231-4671538	K562	blood:	n/a	n/a
29	CCNT2	chr12:4647801-4648173	K562	blood:	n/a	n/a
30	CCNT2	chr12:4681836-4682172	K562	blood:	n/a	n/a
31	CEBPB	chr12:4651288-4651409	HepG2	liver:	n/a	n/a
32	CEBPB	chr12:4667398-4667680	A549	lung:	n/a	chr12:4667533-4667544
33	CEBPB	chr12:4688661-4688815	MCF-7	breast:	n/a	n/a
34	CEBPB	chr12:4647503-4647995	K562	blood:	n/a	n/a
35	CEBPB	chr12:4667412-4667690	IMR90	lung:	n/a	chr12:4667533-4667544
36	CEBPB	chr12:4664974-4665312	HepG2	liver:	n/a	chr12:4664993-4665010
37	CEBPB	chr12:4665011-4665293	A549	lung:	n/a	n/a
38	CEBPB	chr12:4664969-4665339	IMR90	lung:	n/a	chr12:4664993-4665010
39	CEBPB	chr12:4671209-4671672	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr12:4688565-4688835	IMR90	lung:	n/a	n/a
41	CEBPB	chr12:4667396-4667714	HepG2	liver:	n/a	chr12:4667533-4667544
42	CEBPD	chr12:4681779-4682236	K562	blood:	n/a	n/a
43	CEBPD	chr12:4671352-4671548	HepG2	liver:	n/a	n/a
44	CEBPD	chr12:4681826-4682217	K562	blood:	n/a	n/a
45	CHD1	chr12:4647306-4648411	GM12878	blood:	n/a	n/a
46	CHD2	chr12:4647949-4648171	K562	blood:	n/a	n/a
47	CHD2	chr12:4647386-4648278	GM12878	blood:	n/a	n/a
48	CHD2	chr12:4671309-4671776	K562	blood:	n/a	chr12:4671418-4671428
49	CHD2	chr12:4675723-4675924	GM12878	blood:	n/a	n/a
50	CHD2	chr12:4647562-4648239	Hela-S3	cervix:	n/a	n/a

(count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:4659038-4659088	K562	blood:	n/a
2	chr12:4647856-4647906	BE2_C	brain:	n/a
3	chr12:4647560-4647610	NHDF-neo	bronchial:	n/a
4	chr12:4650518-4650568	HAEpiC	amniotic membrane:	n/a
5	chr12:4659038-4659088	HepG2	liver:	n/a
6	chr12:4648036-4648086	PANC-1	pancreas:	n/a
7	chr12:4659038-4659088	Jurkat	blood:	n/a
8	chr12:4671207-4671257	CMK	blood:	n/a
9	chr12:4647897-4647947	SAEC	small airway:	n/a
10	chr12:4647560-4647610	NHBE	bronchial:	n/a
11	chr12:4647928-4647978	SKMC	muscle:	n/a
12	chr12:4647911-4647961	BJ	skin:	n/a
13	chr12:4647856-4647906	MCF-7	breast:	n/a
14	chr12:4649136-4649186	HCPEpiC	choroid plexus:	n/a
15	chr12:4647897-4647947	AoSMC	blood vessel:	n/a
16	chr12:4647560-4647610	ECC-1	luminal epithelium:	n/a
17	chr12:4671207-4671257	AoSMC	blood vessel:	n/a
18	chr12:4647928-4647978	MCF-7	breast:	n/a
19	chr12:4659038-4659088	RPTEC	kidney:	n/a
20	chr12:4671731-4671781	Hepatocyte	liver:	n/a
21	chr12:4647911-4647961	GM06990	blood:	n/a
22	chr12:4671310-4671360	NB4	blood:	n/a
23	chr12:4648274-4648324	SK-N-MC	brain:	n/a
24	chr12:4650518-4650568	AG04449	skin:	fetal
25	chr12:4647845-4647895	SK-N-MC	brain:	n/a
26	chr12:4671207-4671257	NH-A	brain:	n/a
27	chr12:4647625-4647675	HEK293	kidney:	embryo
28	chr12:4647928-4647978	ovcar-3	ovarian:	n/a
29	chr12:4647911-4647961	NH-A	brain:	n/a
30	chr12:4675509-4675559	HRE	kidney:	n/a
31	chr12:4647856-4647906	BJ	skin:	n/a
32	chr12:4648009-4648059	HCM	heart:	n/a
33	chr12:4648052-4648102	ovcar-3	ovarian:	n/a
34	chr12:4647414-4647464	HUVEC	blood vessel:	n/a
35	chr12:4647897-4647947	HEK293	kidney:	embryo
36	chr12:4648052-4648102	HCM	heart:	n/a
37	chr12:4645224-4645274	RPTEC	kidney:	n/a
38	chr12:4649136-4649186	MCF-7	breast:	n/a
39	chr12:4648274-4648324	MCF-7	breast:	n/a
40	chr12:4659038-4659088	HCPEpiC	choroid plexus:	n/a
41	chr12:4659038-4659088	A549	lung:	n/a
42	chr12:4648052-4648102	NB4	blood:	n/a
43	chr12:4671310-4671360	A549	lung:	n/a
44	chr12:4649136-4649186	HUVEC	blood vessel:	n/a
45	chr12:4647560-4647610	HUVEC	blood vessel:	n/a
46	chr12:4647897-4647947	GM12891	blood:	n/a
47	chr12:4647414-4647464	HRPEpiC	eye:	n/a
48	chr12:4648052-4648102	IMR90	lung:	fetal
49	chr12:4648036-4648086	PFSK-1	brain:	n/a
50	chr12:4648052-4648102	SAEC	small airway:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:4671378..4673735-chr15:65588243..65590469,2	K562	blood:
2	chr12:4642107..4644935-chr12:4645402..4647439,3	K562	blood:
3	chr12:4663092..4664745-chr12:4674639..4676232,2	K562	blood:
4	chr12:4670212..4673171-chr12:4678079..4680577,3	K562	blood:
5	chr12:4664388..4668244-chr12:4668539..4671250,3	K562	blood:
6	chr12:4462645..4463521-chr12:4635539..4636424,3	MCF-7	breast:
7	chr12:4630575..4632650-chr12:4639446..4641631,2	K562	blood:
8	chr12:4688558..4689492-chr12:4866939..4867957,4	MCF-7	breast:
9	chr12:4656468..4659385-chr12:4664305..4666078,2	K562	blood:
10	chr12:4671177..4672797-chr12:4687364..4690356,2	K562	blood:
11	chr12:4671422..4673318-chr12:4674512..4676464,2	K562	blood:
12	chr12:4648277..4650261-chr12:4658631..4661516,2	K562	blood:
13	chr12:4638037..4640518-chr12:4647266..4649269,3	K562	blood:
14	chr12:4660124..4662897-chr12:4666466..4668044,2	K562	blood:
15	chr12:4657883..4658403-chr12:27090779..27091466,2	Hela-S3	cervix:
16	chr12:4664388..4668244-chr12:4668539..4671250,3	K562	blood:
17	chr12:4653671..4657442-chr12:4657770..4662457,4	K562	blood:
18	chr12:4416946..4417515-chr12:4635874..4636783,2	MCF-7	breast:
19	chr12:4530453..4531092-chr12:4635858..4636763,3	MCF-7	breast:
20	chr12:4637755..4640527-chr12:4643225..4645157,3	K562	blood:
21	chr12:4645218..4647616-chr12:4650193..4651787,2	K562	blood:
22	chr12:4671214..4672797-chr12:4688856..4690993,2	K562	blood:
23	chr12:4637116..4639367-chr12:4642465..4645295,2	MCF-7	breast:
24	chr12:4656468..4659385-chr12:4664305..4666078,2	K562	blood:
25	chr12:4464997..4465778-chr12:4635809..4636743,3	K562	blood:
26	chr12:4645218..4647616-chr12:4650193..4651787,2	K562	blood:
27	chr12:4647147..4649763-chr12:4649895..4651987,2	MCF-7	breast:
28	chr12:4630575..4632650-chr12:4639446..4641631,2	K562	blood:
29	chr12:4669709..4673171-chr12:4678079..4681060,3	K562	blood:
30	chr12:4651757..4653474-chr12:4666436..4667992,2	MCF-7	breast:
31	chr12:4635573..4636380-chr12:4646947..4647807,2	MCF-7	breast:
32	chr12:4651774..4653608-chr12:4656748..4658795,2	K562	blood:
33	chr12:4651331..4654199-chr12:4661820..4663364,2	K562	blood:
34	chr12:4646100..4649661-chr12:4665332..4668366,3	K562	blood:
35	chr12:4664294..4665889-chr12:4669852..4671734,2	K562	blood:
36	chr12:4642107..4644935-chr12:4645402..4647439,3	K562	blood:
37	chr12:4673631..4675136-chr12:4679453..4682428,2	K562	blood:
38	chr12:4646395..4648972-chr12:4672435..4674254,2	K562	blood:
39	chr12:4677609..4679805-chr12:4680922..4683723,3	K562	blood:
40	chr12:4647147..4649763-chr12:4649895..4651987,2	MCF-7	breast:
41	chr12:4660124..4662897-chr12:4666466..4668044,2	K562	blood:
42	chr12:4666221..4667808-chr12:4669530..4671066,2	K562	blood:
43	chr12:4666221..4667808-chr12:4669530..4671066,2	K562	blood:
44	chr12:4639152..4642726-chr12:4646208..4648490,3	MCF-7	breast:
45	chr12:4673631..4675136-chr12:4679453..4682428,2	K562	blood:
46	chr12:4671422..4673318-chr12:4674512..4676464,2	K562	blood:
47	chr12:4677609..4679805-chr12:4680922..4683723,3	K562	blood:
48	chr12:4664462..4667424-chr12:4914482..4915996,2	K562	blood:
49	chr12:4647472..4650149-chr12:4672435..4675119,3	K562	blood:
50	chr12:4638037..4640518-chr12:4647266..4649269,3	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAD51AP1-1	chr12:4673547-4673664	XLOC_009625
2	lnc-RAD51AP1-2	chr12:4676483-4676549	NONHSAT025959
3	lnc-AKAP3-8	chr12:4683605-4683724	ucscGeneNc_uc001qnd_2
4	lnc-RAD51AP1-2	chr12:4682012-4682364	NONHSAT025960
5	lnc-RAD51AP1-1	chr12:4675632-4675732	XLOC_009625
6	lnc-RAD51AP1-2	chr12:4677121-4677214	NONHSAT025959
7	lnc-RAD51AP1-2	chr12:4677121-4677214	NONHSAT025960
8	lnc-RAD51AP1-2	chr12:4682496-4682522	NONHSAT025959
9	lnc-AKAP3-8	chr12:4679847-4680606	ucscGeneNc_uc001qnd_2
10	lnc-RAD51AP1-1	chr12:4672223-4672342	XLOC_009625
11	lnc-AKAP3-8	chr12:4682740-4682867	ucscGeneNc_uc001qnd_2

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RAD51AP1	hsa-miR-124-3p	chr12:4668447-4668466

Variant related genes	Relation type
C12orf4	TF binding region
DYRK4	TF binding region
RAD51AP1	TF binding region
C12orf4	CpG island
DYRK4	CpG island
RAD51AP1	CpG island
ENSG00000047621	chromatin interactions
ENSG00000010219	chromatin interactions
ENSG00000111247	chromatin interactions
ENSG00000111790	chromatin interactions
ENSG00000064102	chromatin interactions
ENSG00000199568	chromatin interactions
C9orf40	miRNA target sites
C8orf55	miRNA target sites

Extended variants
information (count: 2206 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2206 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150579926	chr12:4627997-4627998	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs139574944	chr12:4628009-4628010	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs141697160	chr12:4628035-4628036	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs371115679	chr12:4628073-4628074	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs149321520	chr12:4628080-4628081	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs374663123	chr12:4628089-4628090	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs112323916	chr12:4628103-4628104	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs180687276	chr12:4628124-4628125	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs576863066	chr12:4628179-4628180	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568476608	chr12:4628223-4628224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144704062	chr12:4628266-4628267	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs559048733	chr12:4628274-4628275	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs368242846	chr12:4628289-4628290	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs572462032	chr12:4628344-4628345	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs367785664	chr12:4628409-4628410	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs535026992	chr12:4628435-4628436	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs528079862	chr12:4628469-4628470	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs150104109	chr12:4628490-4628491	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs369358246	chr12:4628491-4628492	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs370376321	chr12:4628492-4628493	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs372140339	chr12:4628566-4628567	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs558237775	chr12:4628610-4628611	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs542081983	chr12:4628620-4628621	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs562026821	chr12:4628633-4628634	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs16931500	chr12:4628649-4628650	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs578051387	chr12:4628650-4628651	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs16931503	chr12:4628696-4628697	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs533228449	chr12:4628703-4628704	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs111624270	chr12:4628720-4628721	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs547072640	chr12:4628730-4628731	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs74061935	chr12:4628737-4628738	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs566842581	chr12:4628781-4628782	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs535867173	chr12:4628829-4628830	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs186076846	chr12:4628832-4628833	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs551035124	chr12:4628851-4628852	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs189755397	chr12:4628871-4628872	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs2907498	chr12:4628899-4628900	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs539874927	chr12:4628908-4628909	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs2907497	chr12:4628918-4628919	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs553922743	chr12:4628925-4628926	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs181241267	chr12:4628938-4628939	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs368841282	chr12:4628950-4628951	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs567495436	chr12:4628968-4628969	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs143930983	chr12:4628971-4628972	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs185947159	chr12:4628981-4628982	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs115453124	chr12:4628985-4628986	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs372154175	chr12:4629072-4629073	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs34726430	chr12:4629083-4629084	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs558160351	chr12:4629146-4629147	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190362085	chr12:4629178-4629179	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Epilepsy	21858020	CNVD
Colorectal cancer	19359472	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1836 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:4590800-4631200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr12:4592400-4647200	Weak transcription	Esophagus	oesophagus
3	chr12:4593400-4628600	Weak transcription	Right Ventricle	heart
4	chr12:4594400-4646400	Weak transcription	NHLF	lung
5	chr12:4594800-4647000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr12:4595400-4628600	Weak transcription	A549	lung
7	chr12:4596000-4647200	Weak transcription	Small Intestine	intestine
8	chr12:4596400-4629000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr12:4596600-4633400	Weak transcription	Hela-S3	cervix
10	chr12:4596600-4640400	Weak transcription	Brain Angular Gyrus	brain
11	chr12:4598200-4647000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr12:4598400-4646800	Weak transcription	Fetal Brain Male	brain
13	chr12:4599200-4647200	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr12:4606200-4647200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr12:4608200-4647200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr12:4608600-4628800	Weak transcription	Gastric	stomach
17	chr12:4608600-4629000	Weak transcription	Brain Germinal Matrix	brain
18	chr12:4608600-4629400	Weak transcription	Spleen	Spleen
19	chr12:4609000-4633400	Weak transcription	Brain Cingulate Gyrus	brain
20	chr12:4609600-4640400	Weak transcription	Fetal Kidney	kidney
21	chr12:4609600-4642400	Weak transcription	Brain Substantia Nigra	brain
22	chr12:4609800-4640800	Weak transcription	Fetal Brain Female	brain
23	chr12:4610800-4647200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr12:4611200-4628800	Weak transcription	Fetal Stomach	stomach
25	chr12:4611200-4647000	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr12:4611600-4628800	Weak transcription	Brain Anterior Caudate	brain
27	chr12:4612600-4629000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr12:4613400-4628000	Weak transcription	Stomach Smooth Muscle	stomach
29	chr12:4613600-4631000	Weak transcription	HUVEC	blood vessel
30	chr12:4614200-4628800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr12:4614400-4628600	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr12:4614400-4628600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr12:4615000-4633200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr12:4615000-4642200	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr12:4615000-4646400	Weak transcription	Fetal Heart	heart
36	chr12:4616200-4630600	Weak transcription	Fetal Lung	lung
37	chr12:4616400-4628800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr12:4616400-4629400	Weak transcription	Fetal Intestine Small	intestine
39	chr12:4616400-4634600	Weak transcription	Primary hematopoietic stem cells	blood
40	chr12:4616400-4640600	Weak transcription	HSMMtube	muscle
41	chr12:4616400-4646000	Weak transcription	HepG2	liver
42	chr12:4617000-4628800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr12:4617000-4633600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr12:4617000-4639800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr12:4617000-4646600	Weak transcription	NHEK	skin
46	chr12:4617400-4631600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr12:4617600-4628800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr12:4617600-4628800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr12:4617600-4631400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr12:4617600-4639800	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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