Variant report

Variant	nsv559156
Chromosome Location	chr12:62893199-62959137
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:347)
CpG islands
(count:61)
Chromatin interactive
region (count:50)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr12:62936941-62936943	Hela-S3	cervix:	n/a	n/a
2	CBX3	chr12:62907942-62908234	K562	blood:	n/a	n/a
3	CBX3	chr12:62907886-62908248	K562	blood:	n/a	n/a
4	CEBPB	chr12:62956760-62957120	IMR90	lung:	n/a	chr12:62956928-62956941
5	CEBPB	chr12:62935055-62935244	A549	lung:	n/a	n/a
6	CEBPB	chr12:62934970-62935203	MCF-7	breast:	n/a	n/a
7	CEBPB	chr12:62935078-62935214	K562	blood:	n/a	n/a
8	CHD2	chr12:62908825-62908902	GM12878	blood:	n/a	n/a
9	CHD2	chr12:62906816-62906903	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chr12:62912899-62913119	A549	lung:	n/a	n/a
11	CTCF	chr12:62916740-62916890	BE2_C	brain:	n/a	n/a
12	CTCF	chr12:62916880-62917030	HEK293	kidney:	n/a	chr12:62916923-62916944
13	CTCF	chr12:62916800-62916950	GM12865	blood:	n/a	chr12:62916923-62916944
14	CTCF	chr12:62950980-62951130	A549	lung:	n/a	n/a
15	CTCF	chr12:62956780-62956930	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr12:62918820-62918970	HPAF	blood vessel:	n/a	n/a
17	CTCF	chr12:62916937-62916940	Gliobla	brain:	n/a	n/a
18	CTCF	chr12:62916740-62916890	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr12:62916827-62917092	A549	lung:	n/a	chr12:62916923-62916944
20	CTCF	chr12:62916760-62917050	HCM	heart:	n/a	chr12:62916923-62916944
21	CTCF	chr12:62949840-62949990	MCF-7	breast:	n/a	n/a
22	CTCF	chr12:62916860-62917010	HPAF	blood vessel:	n/a	chr12:62916923-62916944
23	CTCF	chr12:62918820-62918970	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr12:62918960-62919110	RPTEC	kidney:	n/a	n/a
25	CTCF	chr12:62918940-62919090	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr12:62918880-62919030	GM12872	blood:	n/a	n/a
27	CTCF	chr12:62916761-62917057	MCF-7	breast:	n/a	chr12:62916923-62916944
28	CTCF	chr12:62918960-62919110	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr12:62916858-62916967	K562	blood:	n/a	chr12:62916923-62916944
30	CTCF	chr12:62916780-62916930	GM12869	blood:	n/a	n/a
31	CTCF	chr12:62918920-62919070	GM06990	blood:	n/a	n/a
32	CTCF	chr12:62916820-62916970	GM12872	blood:	n/a	chr12:62916923-62916944
33	CTCF	chr12:62916877-62916967	MCF-7	breast:	n/a	chr12:62916923-62916944
34	CTCF	chr12:62916800-62916950	AoAF	blood vessel:	n/a	chr12:62916923-62916944
35	CTCF	chr12:62916827-62917080	K562	blood:	n/a	chr12:62916923-62916944
36	CTCF	chr12:62916960-62917110	HCT-116	colon:	n/a	n/a
37	CTCF	chr12:62916800-62916950	GM12871	blood:	n/a	chr12:62916923-62916944
38	CTCF	chr12:62916820-62916970	GM12878	blood:	n/a	chr12:62916923-62916944
39	CTCF	chr12:62916780-62916930	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr12:62918880-62919030	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr12:62918920-62919070	AG09319	gingival:	n/a	n/a
42	CTCF	chr12:62918880-62919030	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr12:62916800-62916950	AG10803	skin:	n/a	chr12:62916923-62916944
44	CTCF	chr12:62916860-62917010	GM12874	blood:	n/a	chr12:62916923-62916944
45	CTCF	chr12:62916960-62917110	HMEC	breast:	n/a	n/a
46	CTCF	chr12:62956740-62956890	AG09319	gingival:	n/a	n/a
47	CTCF	chr12:62918880-62919030	HMF	breast:	n/a	n/a
48	CTCF	chr12:62916780-62916930	GM12866	blood:	n/a	n/a
49	CTCF	chr12:62916880-62917030	AG04450	lung:	n/a	chr12:62916923-62916944
50	CTCF	chr12:62916860-62917010	AG09319	gingival:	n/a	chr12:62916923-62916944

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:62918364-62918414	NB4	blood:	n/a
2	chr12:62918364-62918414	HAEpiC	amniotic membrane:	n/a
3	chr12:62918364-62918414	A549	lung:	n/a
4	chr12:62918364-62918414	PrEC	prostate:	n/a
5	chr12:62918364-62918414	AG09319	gingival:	n/a
6	chr12:62918364-62918414	HCT-116	colon:	n/a
7	chr12:62918364-62918414	GM12878	blood:	n/a
8	chr12:62918364-62918414	PANC-1	pancreas:	n/a
9	chr12:62918364-62918414	HEK293	kidney:	embryo
10	chr12:62918364-62918414	T-47D	breast:	n/a
11	chr12:62918364-62918414	Jurkat	blood:	n/a
12	chr12:62918364-62918414	H1-hESC	embryonic stem cell:	embryo
13	chr12:62918364-62918414	HRE	kidney:	n/a
14	chr12:62918364-62918414	MCF-7	breast:	n/a
15	chr12:62918364-62918414	IMR90	lung:	fetal
16	chr12:62918364-62918414	ProgFib	skin:	n/a
17	chr12:62918364-62918414	HepG2	liver:	n/a
18	chr12:62918364-62918414	SKMC	muscle:	n/a
19	chr12:62918364-62918414	HIPEpiC	eye:	n/a
20	chr12:62918364-62918414	NT2-D1	testis:	n/a
21	chr12:62918364-62918414	U87	brain:	n/a
22	chr12:62918364-62918414	ovcar-3	ovarian:	n/a
23	chr12:62918364-62918414	AG09309	skin:	n/a
24	chr12:62918364-62918414	SAEC	small airway:	n/a
25	chr12:62918364-62918414	HL-60	blood:	n/a
26	chr12:62918364-62918414	HCPEpiC	choroid plexus:	n/a
27	chr12:62918364-62918414	GM06990	blood:	n/a
28	chr12:62918364-62918414	HMEC	breast:	n/a
29	chr12:62918364-62918414	NH-A	brain:	n/a
30	chr12:62918364-62918414	GM12891	blood:	n/a
31	chr12:62918364-62918414	AG04449	skin:	fetal
32	chr12:62918364-62918414	LNCaP	prostate:	n/a
33	chr12:62918364-62918414	NHDF-neo	bronchial:	n/a
34	chr12:62918364-62918414	CMK	blood:	n/a
35	chr12:62918364-62918414	ECC-1	luminal epithelium:	n/a
36	chr12:62918364-62918414	PFSK-1	brain:	n/a
37	chr12:62918364-62918414	BE2_C	brain:	n/a
38	chr12:62918364-62918414	MCF10A-Er-Src	breast:	n/a
39	chr12:62918364-62918414	AG10803	skin:	n/a
40	chr12:62918364-62918414	K562	blood:	n/a
41	chr12:62918364-62918414	Hepatocyte	liver:	n/a
42	chr12:62918364-62918414	AG04450	lung:	fetal
43	chr12:62918364-62918414	HNPCEpiC	eye:	n/a
44	chr12:62918364-62918414	NHBE	bronchial:	n/a
45	chr12:62918364-62918414	HUVEC	blood vessel:	n/a
46	chr12:62918364-62918414	AoSMC	blood vessel:	n/a
47	chr12:62918364-62918414	HRCEpiC	kidney:	n/a
48	chr12:62918364-62918414	SK-N-SH_RA	brain:	n/a
49	chr12:62918364-62918414	RPTEC	kidney:	n/a
50	chr12:62918364-62918414	GM12892	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:62954746..62957075-chr12:62963284..62964948,2	K562	blood:
2	chr12:62915089..62916755-chr12:62920315..62922629,2	MCF-7	breast:
3	chr12:62879324..62880981-chr12:62954743..62956272,2	K562	blood:
4	chr12:62920513..62925358-chr12:62927927..62931461,4	K562	blood:
5	chr12:62929084..62931888-chr12:62931989..62935552,3	MCF-7	breast:
6	chr12:62940703..62942604-chr12:62944482..62947077,2	MCF-7	breast:
7	chr12:62892704..62894662-chr12:62995139..62997140,2	K562	blood:
8	chr12:62922843..62924770-chr12:62994956..62997093,2	K562	blood:
9	chr12:62936384..62938344-chr12:62940152..62942077,2	MCF-7	breast:
10	chr12:62914778..62916591-chr12:62918347..62920592,2	K562	blood:
11	chr1:116960059..116961967-chr12:62941015..62944003,2	MCF-7	breast:
12	chr12:62956004..62957777-chr12:62965289..62967550,2	K562	blood:
13	chr12:62897832..62899888-chr12:62900613..62903392,2	K562	blood:
14	chr12:62937527..62940044-chr12:62996050..62998265,2	MCF-7	breast:
15	chr12:62939712..62942391-chr12:62948706..62950538,2	K562	blood:
16	chr12:62889593..62891337-chr12:62894794..62897430,2	K562	blood:
17	chr12:62920932..62923566-chr12:62937495..62939485,2	MCF-7	breast:
18	chr12:62901029..62903305-chr12:62910983..62913530,2	MCF-7	breast:
19	chr12:62897832..62899888-chr12:62900613..62903392,2	K562	blood:
20	chr12:62874210..62877124-chr12:62898589..62900755,2	K562	blood:
21	chr12:62936384..62938344-chr12:62940152..62942077,2	MCF-7	breast:
22	chr12:62914162..62916402-chr12:63001500..63003390,2	K562	blood:
23	chr12:62939712..62942391-chr12:62948706..62950538,2	K562	blood:
24	chr12:62935650..62938196-chr7:138541897..138543397,2	MCF-7	breast:
25	chr12:62918451..62921309-chr12:62921578..62923186,2	MCF-7	breast:
26	chr12:62916495..62918610-chr12:62994074..62996393,2	MCF-7	breast:
27	chr12:62953650..62956031-chr12:62956662..62959616,2	MCF-7	breast:
28	chr12:62887479..62889929-chr12:62903301..62905417,2	MCF-7	breast:
29	chr12:62919040..62922013-chr12:62927125..62929427,2	K562	blood:
30	chr12:62931071..62933138-chr12:62938483..62940782,2	MCF-7	breast:
31	chr12:62940703..62942604-chr12:62944482..62947077,2	MCF-7	breast:
32	chr12:62929084..62931888-chr12:62931989..62935552,3	MCF-7	breast:
33	chr12:62947795..62949989-chr12:62996507..62998854,2	MCF-7	breast:
34	chr12:62955537..62958369-chr12:62958968..62960475,2	K562	blood:
35	chr12:62927109..62929930-chr12:63090186..63092753,2	K562	blood:
36	chr12:62859503..62861171-chr12:62910614..62912246,2	MCF-7	breast:
37	chr12:62918451..62921309-chr12:62921578..62923186,2	MCF-7	breast:
38	chr12:62914778..62916591-chr12:62918347..62920592,2	K562	blood:
39	chr12:62948110..62949717-chr12:62994806..62996596,2	K562	blood:
40	chr12:62920513..62925358-chr12:62927927..62931461,4	K562	blood:
41	chr12:62860005..62861659-chr12:62903072..62905027,2	MCF-7	breast:
42	chr12:62916535..62917392-chr12:63192666..63193171,2	K562	blood:
43	chr12:62957949..62960640-chr14:99946332..99949190,2	MCF-7	breast:
44	chr12:62887087..62888673-chr12:62894503..62897008,2	K562	blood:
45	chr12:62901029..62903305-chr12:62910983..62913530,2	MCF-7	breast:
46	chr12:62953650..62956031-chr12:62956662..62959616,2	MCF-7	breast:
47	chr12:62919040..62922013-chr12:62927125..62929427,2	K562	blood:
48	chr12:62873508..62875169-chr12:62896381..62898756,2	K562	blood:
49	chr12:62915089..62916755-chr12:62920315..62922629,2	MCF-7	breast:
50	chr12:62828192..62830358-chr12:62897908..62900786,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-399P	TF binding region
MON2	TF binding region
RNU6-399P	CpG island
MON2	CpG island
ENSG00000061987	chromatin interactions
ENSG00000203865	chromatin interactions
ENSG00000221949	chromatin interactions
ENSG00000202034	chromatin interactions
ENSG00000183576	chromatin interactions
ENSG00000199179	chromatin interactions
ENSG00000257354	chromatin interactions
ENSG00000090061	chromatin interactions

Extended variants
information (count: 2274 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2274 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10877864	chr12:62893199-62893200	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs533936911	chr12:62893228-62893229	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs138072439	chr12:62893252-62893253	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs180979701	chr12:62893305-62893306	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs536349993	chr12:62893306-62893307	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs185372834	chr12:62893351-62893352	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs556163215	chr12:62893382-62893383	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs190665016	chr12:62893481-62893482	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs564262629	chr12:62893482-62893483	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs532143985	chr12:62893520-62893521	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs565412822	chr12:62893526-62893527	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs182005678	chr12:62893529-62893530	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs541187761	chr12:62893577-62893578	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs563854969	chr12:62893652-62893653	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs201274871	chr12:62893664-62893665	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs113471494	chr12:62893665-62893666	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs7309087	chr12:62893673-62893674	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs78737719	chr12:62893676-62893677	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs543503662	chr12:62893709-62893710	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs563738720	chr12:62893796-62893797	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs373275851	chr12:62893846-62893847	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs551667941	chr12:62893855-62893856	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs7298046	chr12:62893881-62893882	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs201587957	chr12:62893920-62893921	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs527483334	chr12:62893932-62893933	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs143747810	chr12:62893963-62893964	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs377636105	chr12:62894038-62894039	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs10784303	chr12:62894058-62894059	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs536386752	chr12:62894113-62894114	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs555964094	chr12:62894118-62894119	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs569655843	chr12:62894206-62894207	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs538221616	chr12:62894285-62894286	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs201677867	chr12:62894394-62894395	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559213204	chr12:62894408-62894409	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs74095804	chr12:62894414-62894415	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs190608016	chr12:62894451-62894452	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs143913309	chr12:62894462-62894463	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs574678759	chr12:62894523-62894524	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs372969306	chr12:62894529-62894530	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs201434593	chr12:62894533-62894534	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs115864448	chr12:62894540-62894541	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs532546106	chr12:62894544-62894545	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs200692514	chr12:62894558-62894559	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs202015814	chr12:62894583-62894584	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568074105	chr12:62894617-62894618	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs201958152	chr12:62894635-62894636	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs17120341	chr12:62894636-62894637	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs112159926	chr12:62894697-62894698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557056811	chr12:62894720-62894721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140022963	chr12:62894781-62894782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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	19602461	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
Hodgkin''s lymphoma	18179710	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
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Man infertility	21397064	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1957 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62861800-62902200	Weak transcription	Fetal Kidney	kidney
2	chr12:62862800-62895400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:62863200-62895200	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr12:62863200-62896800	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr12:62863200-62901800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr12:62863200-62937400	Weak transcription	Pancreas	Pancrea
7	chr12:62863400-62895400	Weak transcription	Stomach Smooth Muscle	stomach
8	chr12:62863400-62902000	Weak transcription	HUVEC	blood vessel
9	chr12:62863400-62911000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr12:62863600-62926400	Weak transcription	Colon Smooth Muscle	Colon
11	chr12:62864000-62894400	Weak transcription	Spleen	Spleen
12	chr12:62864000-62899200	Weak transcription	Brain Germinal Matrix	brain
13	chr12:62864000-62901600	Weak transcription	Lung	lung
14	chr12:62864000-62901600	Weak transcription	Rectal Smooth Muscle	rectum
15	chr12:62864000-62906200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr12:62866000-62895400	Weak transcription	Left Ventricle	heart
17	chr12:62866200-62897000	Weak transcription	K562	blood
18	chr12:62866200-62899200	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr12:62866200-62906200	Weak transcription	Aorta	Aorta
20	chr12:62866600-62896000	Weak transcription	Fetal Brain Female	brain
21	chr12:62866600-62906200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr12:62866600-62912400	Weak transcription	NHLF	lung
23	chr12:62866600-62953200	Weak transcription	Psoas Muscle	Psoas
24	chr12:62867200-62898600	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr12:62869000-62904400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr12:62871000-62910800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr12:62871200-62895200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr12:62871800-62895200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr12:62871800-62895400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr12:62871800-62897200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr12:62871800-62926200	Weak transcription	Fetal Brain Male	brain
32	chr12:62872000-62894200	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr12:62872200-62895400	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr12:62872600-62901600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr12:62873400-62895400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr12:62874000-62895800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr12:62874600-62898800	Weak transcription	Fetal Muscle Trunk	muscle
38	chr12:62874600-62917400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr12:62874800-62895200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr12:62874800-62896000	Weak transcription	HMEC	breast
41	chr12:62875600-62901200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr12:62876000-62902000	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr12:62876000-62905800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr12:62876000-62937400	Weak transcription	Gastric	stomach
45	chr12:62876200-62895600	Weak transcription	HSMM	muscle
46	chr12:62876200-62913000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr12:62876400-62902000	Weak transcription	Brain Anterior Caudate	brain
48	chr12:62876800-62897000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr12:62877400-62899200	Weak transcription	Ovary	ovary
50	chr12:62877800-62896800	Weak transcription	Brain Hippocampus Middle	brain

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