Variant report

Variant	nsv1050547
Chromosome Location	chr12:67122154-67314886
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:798)
CpG islands
(count:490)
Chromatin interactive
region (count:74)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:67254981-67255261	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:67314051-67314273	K562	blood:	n/a	n/a
3	ARID3A	chr12:67254992-67255139	K562	blood:	n/a	n/a
4	ATF2	chr12:67170642-67171041	GM12878	blood:	n/a	n/a
5	BACH1	chr12:67263777-67263803	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr12:67170708-67171069	GM12878	blood:	n/a	n/a
7	BATF	chr12:67293386-67293615	GM12878	blood:	n/a	n/a
8	BATF	chr12:67170761-67171074	GM12878	blood:	n/a	n/a
9	BCL11A	chr12:67170790-67171069	GM12878	blood:	n/a	n/a
10	BCL11A	chr12:67170768-67171000	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:67314035-67314327	K562	blood:	n/a	n/a
12	BHLHE40	chr12:67279238-67279595	K562	blood:	n/a	n/a
13	CCNT2	chr12:67314049-67314384	K562	blood:	n/a	n/a
14	CCNT2	chr12:67302677-67302878	K562	blood:	n/a	n/a
15	CEBPB	chr12:67271645-67272006	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr12:67267895-67268214	HepG2	liver:	n/a	chr12:67268066-67268079 chr12:67267913-67267924 chr12:67267911-67267924 chr12:67268066-67268077 chr12:67268068-67268077
17	CEBPB	chr12:67138715-67138996	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:67272457-67272773	A549	lung:	n/a	chr12:67272606-67272617
19	CEBPB	chr12:67217733-67218325	MCF-7	breast:	n/a	n/a
20	CEBPB	chr12:67178069-67178104	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:67138611-67139048	MCF-7	breast:	n/a	n/a
22	CEBPB	chr12:67272501-67272773	H1-hESC	embryonic stem cell:	n/a	chr12:67272606-67272617
23	CEBPB	chr12:67216689-67217186	MCF-7	breast:	n/a	chr12:67216932-67216943
24	CEBPB	chr12:67130864-67131019	HepG2	liver:	n/a	n/a
25	CEBPB	chr12:67252792-67252817	A549	lung:	n/a	chr12:67252801-67252812 chr12:67252799-67252812
26	CEBPB	chr12:67216755-67217217	IMR90	lung:	n/a	chr12:67216932-67216943
27	CEBPB	chr12:67267962-67268207	IMR90	lung:	n/a	chr12:67268066-67268079 chr12:67268066-67268077 chr12:67268068-67268077
28	CEBPB	chr12:67205932-67205978	K562	blood:	n/a	n/a
29	CEBPB	chr12:67216756-67217273	Hela-S3	cervix:	n/a	chr12:67216932-67216943
30	CEBPB	chr12:67271748-67271978	K562	blood:	n/a	n/a
31	CEBPB	chr12:67271680-67271954	HepG2	liver:	n/a	n/a
32	CEBPB	chr12:67138648-67139144	MCF-7	breast:	n/a	n/a
33	CEBPB	chr12:67238386-67238695	HepG2	liver:	n/a	chr12:67238537-67238548
34	CEBPB	chr12:67207257-67207342	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr12:67138687-67139031	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr12:67216752-67217214	HepG2	liver:	n/a	chr12:67216932-67216943
37	CEBPB	chr12:67217673-67218383	MCF-7	breast:	n/a	n/a
38	CEBPB	chr12:67272481-67272773	HepG2	liver:	n/a	chr12:67272606-67272617
39	CEBPB	chr12:67313908-67314351	K562	blood:	n/a	n/a
40	CEBPB	chr12:67267907-67268104	H1-hESC	embryonic stem cell:	n/a	chr12:67268066-67268079 chr12:67267913-67267924 chr12:67267911-67267924 chr12:67268066-67268077 chr12:67268068-67268077
41	CEBPB	chr12:67131609-67131785	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr12:67216766-67217108	K562	blood:	n/a	chr12:67216932-67216943
43	CEBPB	chr12:67238358-67238680	A549	lung:	n/a	chr12:67238537-67238548
44	CEBPB	chr12:67217824-67218366	A549	lung:	n/a	n/a
45	CEBPB	chr12:67229596-67229628	A549	lung:	n/a	n/a
46	CEBPB	chr12:67131490-67131690	K562	blood:	n/a	n/a
47	CEBPB	chr12:67138695-67138991	K562	blood:	n/a	n/a
48	CEBPB	chr12:67216684-67217075	MCF-7	breast:	n/a	chr12:67216932-67216943
49	CEBPB	chr12:67313970-67314307	K562	blood:	n/a	n/a
50	CEBPB	chr12:67216767-67217265	A549	lung:	n/a	chr12:67216932-67216943

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:67127781-67127831	T-47D	breast:	n/a
2	chr12:67197851-67197901	AG04449	skin:	fetal
3	chr12:67127781-67127831	T-47D	breast:	n/a
4	chr12:67197851-67197901	AG04449	skin:	fetal
5	chr12:67197851-67197901	BJ	skin:	n/a
6	chr12:67127781-67127831	HCF	heart:	n/a
7	chr12:67192853-67192903	HepG2	liver:	n/a
8	chr12:67160208-67160258	GM12892	blood:	n/a
9	chr12:67197851-67197901	ProgFib	skin:	n/a
10	chr12:67160208-67160258	GM12878	blood:	n/a
11	chr12:67197936-67197986	HRPEpiC	eye:	n/a
12	chr12:67192853-67192903	Hela-S3	cervix:	n/a
13	chr12:67160208-67160258	AG10803	skin:	n/a
14	chr12:67127781-67127831	AG09309	skin:	n/a
15	chr12:67197851-67197901	GM06990	blood:	n/a
16	chr12:67197936-67197986	Hepatocyte	liver:	n/a
17	chr12:67272574-67272624	ProgFib	skin:	n/a
18	chr12:67278182-67278232	K562	blood:	n/a
19	chr12:67197984-67198034	HEK293	kidney:	embryo
20	chr12:67127781-67127831	GM12892	blood:	n/a
21	chr12:67160208-67160258	AG04449	skin:	fetal
22	chr12:67192853-67192903	HRPEpiC	eye:	n/a
23	chr12:67197936-67197986	BJ	skin:	n/a
24	chr12:67278182-67278232	AG09309	skin:	n/a
25	chr12:67197984-67198034	ovcar-3	ovarian:	n/a
26	chr12:67278182-67278232	HEEpiC	esophagus:	n/a
27	chr12:67160208-67160258	HNPCEpiC	eye:	n/a
28	chr12:67272574-67272624	K562	blood:	n/a
29	chr12:67197984-67198034	NHDF-neo	bronchial:	n/a
30	chr12:67192853-67192903	HUVEC	blood vessel:	n/a
31	chr12:67278182-67278232	HCT-116	colon:	n/a
32	chr12:67197984-67198034	K562	blood:	n/a
33	chr12:67272574-67272624	HPAEpiC	pulmonary alveolar:	n/a
34	chr12:67197936-67197986	HEEpiC	esophagus:	n/a
35	chr12:67192853-67192903	BJ	skin:	n/a
36	chr12:67127781-67127831	NHDF-neo	bronchial:	n/a
37	chr12:67197984-67198034	IMR90	lung:	fetal
38	chr12:67127781-67127831	BJ	skin:	n/a
39	chr12:67127781-67127831	HEK293	kidney:	embryo
40	chr12:67197936-67197986	Caco-2	colon:	n/a
41	chr12:67197984-67198034	HEEpiC	esophagus:	n/a
42	chr12:67127781-67127831	ECC-1	luminal epithelium:	n/a
43	chr12:67197851-67197901	HL-60	blood:	n/a
44	chr12:67197936-67197986	H1-hESC	embryonic stem cell:	embryo
45	chr12:67127781-67127831	NH-A	brain:	n/a
46	chr12:67278182-67278232	PFSK-1	brain:	n/a
47	chr12:67272574-67272624	GM12878	blood:	n/a
48	chr12:67197936-67197986	ECC-1	luminal epithelium:	n/a
49	chr12:67197851-67197901	AoSMC	blood vessel:	n/a
50	chr12:67192853-67192903	Caco-2	colon:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:67184228..67185827-chr12:67187513..67190445,3	MCF-7	breast:
2	chr12:67197849..67199448-chr12:67204005..67205599,2	K562	blood:
3	chr12:67253380..67256928-chr12:67258329..67261239,3	K562	blood:
4	chr12:67181348..67184002-chr12:67184358..67185894,2	K562	blood:
5	chr12:67255252..67257877-chr12:67460950..67463258,3	MCF-7	breast:
6	chr12:67132372..67134745-chr12:67135516..67139525,4	MCF-7	breast:
7	chr12:67193227..67194822-chr12:67197221..67199274,2	MCF-7	breast:
8	chr12:67109144..67111332-chr12:67122763..67125755,2	K562	blood:
9	chr12:67306567..67308676-chr12:67310361..67312988,2	K562	blood:
10	chr12:67174375..67176870-chr12:67178960..67180503,2	K562	blood:
11	chr12:67133078..67135278-chr12:67140129..67142008,2	MCF-7	breast:
12	chr12:67314700..67316458-chr12:67662314..67664044,2	MCF-7	breast:
13	chr12:67270133..67270911-chr12:67613617..67614322,2	MCF-7	breast:
14	chr12:67296029..67298947-chr12:67402634..67404774,2	K562	blood:
15	chr12:67298346..67300741-chr12:67305071..67306583,2	MCF-7	breast:
16	chr12:67314178..67315962-chr12:67342919..67344851,2	K562	blood:
17	chr12:67308306..67310520-chr12:67311991..67314710,2	K562	blood:
18	chr12:67235225..67237663-chr12:67242475..67245104,2	MCF-7	breast:
19	chr12:67082410..67083294-chr12:67254648..67255604,5	MCF-7	breast:
20	chr12:67169597..67171791-chr2:190019336..190021927,2	MCF-7	breast:
21	chr12:67267602..67269180-chr12:67272677..67275456,2	MCF-7	breast:
22	chr12:67267602..67269180-chr12:67272677..67275456,2	MCF-7	breast:
23	chr12:67228648..67230716-chr12:67231553..67234052,2	K562	blood:
24	chr12:67306214..67308962-chr12:67318247..67321230,2	MCF-7	breast:
25	chr12:67289479..67291060-chr12:67301635..67303898,2	K562	blood:
26	chr12:67263616..67266720-chr12:67267325..67269969,3	MCF-7	breast:
27	chr12:67263616..67266720-chr12:67267325..67269969,3	MCF-7	breast:
28	chr12:67297065..67298731-chr12:67613597..67614634,5	MCF-7	breast:
29	chr12:67110006..67111455-chr12:67254721..67255586,6	MCF-7	breast:
30	chr12:67308306..67310520-chr12:67311991..67314710,2	K562	blood:
31	chr12:67132372..67134745-chr12:67135516..67139525,4	MCF-7	breast:
32	chr12:67133078..67135278-chr12:67140129..67142008,2	MCF-7	breast:
33	chr12:67110471..67111538-chr12:67254403..67256131,14	MCF-7	breast:
34	chr12:67300543..67302588-chr12:67306675..67309652,2	MCF-7	breast:
35	chr12:67184228..67185827-chr12:67187513..67190445,3	MCF-7	breast:
36	chr12:67298346..67300741-chr12:67305071..67306583,2	MCF-7	breast:
37	chr12:67216740..67218475-chr12:67222220..67224061,2	MCF-7	breast:
38	chr12:67297865..67298411-chr12:67461007..67461777,2	MCF-7	breast:
39	chr12:67306567..67308676-chr12:67310361..67312988,2	K562	blood:
40	chr12:67216740..67218475-chr12:67222220..67224061,2	MCF-7	breast:
41	chr12:67174375..67176870-chr12:67178960..67180503,2	K562	blood:
42	chr12:67109764..67110463-chr12:67254735..67255402,2	MCF-7	breast:
43	chr12:67310671..67312914-chr12:67463080..67465006,2	MCF-7	breast:
44	chr12:67235225..67237663-chr12:67242475..67245104,2	MCF-7	breast:
45	chr12:67289452..67290999-chr12:67296445..67299201,2	MCF-7	breast:
46	chr12:67253647..67256314-chr12:67565336..67566847,2	K562	blood:
47	chr12:67075881..67076642-chr12:67254630..67255196,2	MCF-7	breast:
48	chr12:67297515..67298406-chr12:67615824..67616730,3	MCF-7	breast:
49	chr12:67253380..67256928-chr12:67258329..67261239,3	K562	blood:
50	chr12:67296511..67299023-chr12:67323435..67324974,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRIP1-1	chr12:67301276-67301326	XLOC_010109
2	lnc-TMBIM4-4	chr12:67122111-67122188	l_672_chr12:67111893-67114021_adrenal
3	lnc-GRIP1-1	chr12:67285656-67285734	ENSG00000256248
4	lnc-GRIP1-1	chr12:67285593-67290880	XLOC_010109
5	lnc-TMBIM4-4	chr12:67131414-67131624	l_672_chr12:67111893-67114021_adrenal

No data

Variant related genes	Relation type
GRIP1	TF binding region
GRIP1	CpG island
ENSG00000155974	chromatin interactions
ENSG00000256248	chromatin interactions
ENSG00000111530	chromatin interactions
ENSG00000163636	chromatin interactions
DCBLD2	miRNA target sites

Extended variants
information (count: 6768 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:6768 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558381049	chr12:67122186-67122187	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs150273488	chr12:67126220-67126221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs1480028	chr12:67126228-67126229	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs565500810	chr12:67126232-67126233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189060981	chr12:67126233-67126234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551217243	chr12:67126256-67126257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79028050	chr12:67126311-67126312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs193259661	chr12:67126312-67126313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185411508	chr12:67126317-67126318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs565165609	chr12:67126339-67126340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534745476	chr12:67126343-67126344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546476922	chr12:67126472-67126473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545468110	chr12:67126511-67126512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368239993	chr12:67126512-67126513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571459716	chr12:67126719-67126720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555178479	chr12:67126721-67126722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538464513	chr12:67126773-67126774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190409903	chr12:67126783-67126784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1383110	chr12:67126802-67126803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs117934321	chr12:67126846-67126847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145795404	chr12:67126852-67126853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536611904	chr12:67126939-67126940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555034429	chr12:67126944-67126945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181595808	chr12:67127068-67127069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575568797	chr12:67127087-67127088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369893536	chr12:67127106-67127107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs202212185	chr12:67127118-67127119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568233774	chr12:67127129-67127130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148986465	chr12:67127137-67127138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs147095170	chr12:67127141-67127142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577323514	chr12:67127169-67127170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544504481	chr12:67127191-67127192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs78916354	chr12:67127209-67127210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185828415	chr12:67127224-67127225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542195783	chr12:67127245-67127246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs560597598	chr12:67127270-67127271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547640025	chr12:67127277-67127278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570353519	chr12:67127308-67127309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs546632934	chr12:67127312-67127313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs137997414	chr12:67127330-67127331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532306058	chr12:67127430-67127431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs374890066	chr12:67127477-67127478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563776612	chr12:67127512-67127513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188731153	chr12:67127628-67127629	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs536575630	chr12:67127688-67127689	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs181156071	chr12:67127755-67127756	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs566820326	chr12:67127761-67127762	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs143548405	chr12:67127763-67127764	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs533945567	chr12:67127767-67127768	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs558984742	chr12:67127851-67127852	Enhancers Flanking Active TSS	n/a	n/a	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
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
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
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
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21364760	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	22048815	CNVD
Congenital anomalies of the kidney and urinary tract	21113617	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Myxofibrosarcoma	16751306	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Lung cancer	17925434	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	21569311	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:948 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:67126200-67127600	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr12:67126400-67128400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr12:67126600-67127600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr12:67126600-67128400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr12:67127200-67128400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr12:67127200-67129400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:67127600-67128000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
8	chr12:67127600-67128200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr12:67127600-67128200	Enhancers	H1 Cell Line	embryonic stem cell
10	chr12:67127600-67128200	Enhancers	H9 Cell Line	embryonic stem cell
11	chr12:67127600-67128200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr12:67127600-67128200	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr12:67127600-67128200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr12:67127600-67128200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr12:67127600-67129000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr12:67127800-67128400	Enhancers	Fetal Brain Female	brain
17	chr12:67128000-67129000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr12:67128200-67129200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr12:67128200-67129400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr12:67128200-67129400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr12:67128400-67133800	Weak transcription	Fetal Brain Female	brain
22	chr12:67129200-67129600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr12:67129400-67131000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:67129600-67132600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr12:67131000-67131800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:67132400-67134400	Enhancers	Fetal Heart	heart
27	chr12:67132600-67133000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr12:67133000-67134200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr12:67133600-67134000	Enhancers	Rectal Smooth Muscle	rectum
30	chr12:67133600-67134200	Enhancers	Fetal Brain Male	brain
31	chr12:67133600-67134400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr12:67133800-67134200	Enhancers	Esophagus	oesophagus
33	chr12:67133800-67134200	Enhancers	Right Atrium	heart
34	chr12:67133800-67134400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr12:67133800-67134400	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr12:67133800-67134400	Enhancers	Colon Smooth Muscle	Colon
37	chr12:67133800-67134800	Enhancers	Fetal Brain Female	brain
38	chr12:67134000-67134200	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
39	chr12:67134000-67136400	Weak transcription	Rectal Smooth Muscle	rectum
40	chr12:67134200-67135200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr12:67134400-67135800	Weak transcription	Colon Smooth Muscle	Colon
42	chr12:67135200-67135600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr12:67135400-67137600	Enhancers	Primary T cells from cord blood	blood
44	chr12:67135600-67137000	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr12:67135600-67137200	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr12:67135600-67137200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr12:67135600-67137200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr12:67135600-67139000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr12:67135800-67136400	Enhancers	Colon Smooth Muscle	Colon
50	chr12:67135800-67136600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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