Variant report

Variant	nsv1013553
Chromosome Location	chr2:52010500-52471153
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1335)
CpG islands
(count:366)
Chromatin interactive
region (count:46)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1335 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:52467445-52467547	K562	blood:	n/a	n/a
2	BACH1	chr2:52196504-52196856	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:52362389-52362723	K562	blood:	n/a	n/a
4	BACH1	chr2:52013621-52013717	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:52362395-52362744	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:52185802-52185829	K562	blood:	n/a	n/a
7	BACH1	chr2:52196504-52196867	K562	blood:	n/a	n/a
8	BACH1	chr2:52208991-52209296	H1-hESC	embryonic stem cell:	n/a	chr2:52209155-52209169
9	BATF	chr2:52304385-52304596	GM12878	blood:	n/a	n/a
10	BRCA1	chr2:52259388-52259484	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr2:52412674-52412755	GM12878	blood:	n/a	n/a
12	CBX3	chr2:52309795-52311146	HCT-116	colon:	n/a	n/a
13	CBX3	chr2:52310166-52311117	HCT-116	colon:	n/a	n/a
14	CBX3	chr2:52040441-52040852	HCT-116	colon:	n/a	n/a
15	CEBPB	chr2:52231435-52231623	A549	lung:	n/a	n/a
16	CEBPB	chr2:52317611-52317713	H1-hESC	embryonic stem cell:	n/a	chr2:52317668-52317679
17	CEBPB	chr2:52331040-52331249	HepG2	liver:	n/a	chr2:52331137-52331148
18	CEBPB	chr2:52020231-52020456	A549	lung:	n/a	chr2:52020327-52020338 chr2:52020277-52020288
19	CEBPB	chr2:52222367-52222678	H1-hESC	embryonic stem cell:	n/a	chr2:52222524-52222537 chr2:52222524-52222535
20	CEBPB	chr2:52262546-52262937	Hela-S3	cervix:	n/a	chr2:52262762-52262773
21	CEBPB	chr2:52130882-52131188	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr2:52057394-52057709	IMR90	lung:	n/a	n/a
23	CEBPB	chr2:52117644-52117838	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:52424571-52424862	HepG2	liver:	n/a	chr2:52424680-52424691
25	CEBPB	chr2:52040436-52040772	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr2:52324255-52324571	A549	lung:	n/a	chr2:52324407-52324416 chr2:52324407-52324416 chr2:52324407-52324416
27	CEBPB	chr2:52447446-52447926	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr2:52020223-52020461	HepG2	liver:	n/a	chr2:52020327-52020338 chr2:52020277-52020288
29	CEBPB	chr2:52145319-52145566	IMR90	lung:	n/a	n/a
30	CEBPB	chr2:52193961-52194229	Hela-S3	cervix:	n/a	chr2:52194121-52194132
31	CEBPB	chr2:52126935-52126947	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:52324253-52324595	H1-hESC	embryonic stem cell:	n/a	chr2:52324407-52324416 chr2:52324407-52324416 chr2:52324407-52324416
33	CEBPB	chr2:52324223-52324560	A549	lung:	n/a	chr2:52324407-52324416 chr2:52324407-52324416 chr2:52324407-52324416
34	CEBPB	chr2:52057437-52057715	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:52170578-52170756	HepG2	liver:	n/a	chr2:52170622-52170633
36	CEBPB	chr2:52146526-52146921	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:52130970-52131211	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:52324224-52324581	IMR90	lung:	n/a	chr2:52324407-52324416 chr2:52324407-52324416 chr2:52324407-52324416
39	CEBPB	chr2:52284272-52284554	IMR90	lung:	n/a	chr2:52284412-52284421 chr2:52284412-52284423 chr2:52284410-52284423 chr2:52284410-52284421
40	CEBPB	chr2:52222401-52222715	Hela-S3	cervix:	n/a	chr2:52222524-52222537 chr2:52222524-52222535
41	CEBPB	chr2:52222480-52222649	K562	blood:	n/a	chr2:52222524-52222537 chr2:52222524-52222535
42	CEBPB	chr2:52284303-52284564	A549	lung:	n/a	chr2:52284412-52284421 chr2:52284412-52284423 chr2:52284410-52284423 chr2:52284410-52284421
43	CEBPB	chr2:52437849-52438049	IMR90	lung:	n/a	n/a
44	CEBPB	chr2:52107350-52107669	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:52130863-52131276	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr2:52222336-52222779	IMR90	lung:	n/a	chr2:52222749-52222761 chr2:52222524-52222537 chr2:52222524-52222535
47	CEBPB	chr2:52017155-52017401	IMR90	lung:	n/a	n/a
48	CEBPB	chr2:52130909-52131253	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPB	chr2:52104076-52104488	HCT-116	colon:	n/a	n/a
50	CEBPB	chr2:52306763-52307073	IMR90	lung:	n/a	chr2:52306925-52306936 chr2:52306927-52306936

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52281777-52281827	NHBE	bronchial:	n/a
2	chr2:52272404-52272454	AG04449	skin:	fetal
3	chr2:52221668-52221718	Caco-2	colon:	n/a
4	chr2:52234104-52234154	AG09319	gingival:	n/a
5	chr2:52281777-52281827	NHDF-neo	bronchial:	n/a
6	chr2:52234104-52234154	GM19239	blood:	n/a
7	chr2:52235062-52235112	NH-A	brain:	n/a
8	chr2:52234104-52234154	PFSK-1	brain:	n/a
9	chr2:52235062-52235112	BJ	skin:	n/a
10	chr2:52221668-52221718	AG04449	skin:	fetal
11	chr2:52281777-52281827	HCF	heart:	n/a
12	chr2:52221668-52221718	HEEpiC	esophagus:	n/a
13	chr2:52039654-52039704	Caco-2	colon:	n/a
14	chr2:52039654-52039704	HIPEpiC	eye:	n/a
15	chr2:52234104-52234154	AG04450	lung:	fetal
16	chr2:52272404-52272454	U87	brain:	n/a
17	chr2:52272404-52272454	HPAEpiC	pulmonary alveolar:	n/a
18	chr2:52039654-52039704	BE2_C	brain:	n/a
19	chr2:52234104-52234154	HAEpiC	amniotic membrane:	n/a
20	chr2:52039654-52039704	NH-A	brain:	n/a
21	chr2:52272404-52272454	T-47D	breast:	n/a
22	chr2:52234104-52234154	Caco-2	colon:	n/a
23	chr2:52272404-52272454	HNPCEpiC	eye:	n/a
24	chr2:52272404-52272454	ECC-1	luminal epithelium:	n/a
25	chr2:52221668-52221718	HepG2	liver:	n/a
26	chr2:52039654-52039704	GM12892	blood:	n/a
27	chr2:52221668-52221718	HAEpiC	amniotic membrane:	n/a
28	chr2:52234104-52234154	AG10803	skin:	n/a
29	chr2:52281777-52281827	U87	brain:	n/a
30	chr2:52235062-52235112	GM06990	blood:	n/a
31	chr2:52221668-52221718	AG09319	gingival:	n/a
32	chr2:52039654-52039704	SK-N-SH_RA	brain:	n/a
33	chr2:52039654-52039704	HRCEpiC	kidney:	n/a
34	chr2:52234104-52234154	T-47D	breast:	n/a
35	chr2:52235062-52235112	HUVEC	blood vessel:	n/a
36	chr2:52281777-52281827	AG09309	skin:	n/a
37	chr2:52234104-52234154	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:52234104-52234154	PANC-1	pancreas:	n/a
39	chr2:52272404-52272454	SK-N-SH_RA	brain:	n/a
40	chr2:52039654-52039704	K562	blood:	n/a
41	chr2:52235062-52235112	AG09309	skin:	n/a
42	chr2:52234104-52234154	AG04449	skin:	fetal
43	chr2:52281777-52281827	RPTEC	kidney:	n/a
44	chr2:52281777-52281827	Hepatocyte	liver:	n/a
45	chr2:52235062-52235112	HIPEpiC	eye:	n/a
46	chr2:52272404-52272454	NH-A	brain:	n/a
47	chr2:52235062-52235112	MCF-7	breast:	n/a
48	chr2:52235062-52235112	MCF10A-Er-Src	breast:	n/a
49	chr2:52221668-52221718	NH-A	brain:	n/a
50	chr2:52039654-52039704	Hela-S3	cervix:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:52063384..52066305-chr2:52068038..52070794,3	K562	blood:
2	chr2:52097711..52099315-chr2:52104533..52106401,2	K562	blood:
3	chr11:63952383..63953021-chr2:52077502..52078002,2	Hela-S3	cervix:
4	chr2:52444137..52446093-chr2:52447228..52448981,2	K562	blood:
5	2:51664217-51674289..2:52132828-52140118	H1-hESC	embryonic stem cell:	embryo
6	2:52132828-52140118..2:52144960-52145427	GM12878	blood:
7	2:51755125-51764739..2:52034460-52043624	K562	blood:
8	chr2:52045177..52047183-chr2:52049220..52051220,2	K562	blood:
9	chr2:52367783..52370728-chr2:52370744..52372935,2	K562	blood:
10	chr2:52045177..52047313-chr2:52049220..52051486,2	K562	blood:
11	chr2:52367783..52370728-chr2:52370744..52372935,2	K562	blood:
12	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
13	2:52043909-52049825..2:52049825-52050373	K562	blood:
14	2:51664217-51674289..2:52034460-52043624	GM12878	blood:
15	2:51785137-51786126..2:52106672-52112664	GM12878	blood:
16	2:51745267-51754233..2:52043624-52043909	K562	blood:
17	chr2:52097711..52099315-chr2:52104533..52106401,2	K562	blood:
18	chr2:52344101..52346354-chr2:52360940..52363061,2	MCF-7	breast:
19	chr2:52444137..52446093-chr2:52447228..52448981,2	K562	blood:
20	chr2:52045177..52047183-chr2:52049220..52051220,2	K562	blood:
21	2:51664217-51674289..2:52043909-52049825	H1-hESC	embryonic stem cell:	embryo
22	2:51675236-51679533..2:52132828-52140118	GM12878	blood:
23	2:51745267-51754233..2:52106672-52112664	GM12878	blood:
24	2:52132828-52140118..2:52144960-52145427	GM12878	blood:
25	chr2:52335533..52337278-chr2:52346386..52348387,2	K562	blood:
26	chr2:52013693..52015857-chr2:52040010..52042547,2	K562	blood:
27	chr2:52002782..52005199-chr2:52008928..52011159,2	K562	blood:
28	2:52043909-52049825..2:52049825-52050373	K562	blood:
29	chr2:52069239..52070064-chr8:36656303..36657160,2	MCF-7	breast:
30	2:51664217-51674289..2:52100874-52104046	H1-hESC	embryonic stem cell:	embryo
31	chr2:52063384..52066305-chr2:52068038..52070794,3	K562	blood:
32	chr2:52045177..52047313-chr2:52049220..52051486,2	K562	blood:
33	chr2:52239790..52242380-chr2:52244407..52246519,2	K562	blood:
34	2:51664217-51674289..2:52112664-52117037	K562	blood:
35	chr2:52321532..52323280-chr2:52325089..52327796,2	K562	blood:
36	2:51664217-51674289..2:52055539-52058793	H1-hESC	embryonic stem cell:	embryo
37	chr2:52344101..52346354-chr2:52360940..52363061,2	MCF-7	breast:
38	chr2:50756714..50757394-chr2:52022672..52023233,2	MCF-7	breast:
39	chr2:52261393..52263430-chr2:52272675..52274372,2	K562	blood:
40	chr2:52261393..52263430-chr2:52272675..52274372,2	K562	blood:
41	chr2:52013693..52015857-chr2:52040010..52042547,2	K562	blood:
42	chr2:52321532..52323280-chr2:52325089..52327796,2	K562	blood:
43	chr2:50763606..50764181-chr2:52224822..52225393,2	MCF-7	breast:
44	chr2:52239790..52242380-chr2:52244407..52246519,2	K562	blood:
45	chr2:52357469..52360071-chr20:52739539..52742222,2	MCF-7	breast:
46	chr2:52335533..52337278-chr2:52346386..52348387,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHAC2-10	chr2:52470105-52470654	NONHSAT070667
2	lnc-CHAC2-11	chr2:52304140-52304335	NONHSAT070666
3	lnc-CHAC2-11	chr2:52302622-52302775	NONHSAT070666
4	lnc-CHAC2-4	chr2:52088587-52088626	ENSG00000231918.1
5	lnc-CHAC2-11	chr2:52298493-52298559	NONHSAT070666
6	lnc-CHAC2-10	chr2:52453760-52453813	NONHSAT070667

No data

Variant related genes	Relation type
ZNF863P	TF binding region
ENSG00000226366	TF binding region
ENSG00000230840	TF binding region
ZNF863P	CpG island
ENSG00000226366	CpG island
ENSG00000230840	CpG island
ENSG00000168439	chromatin interactions

Extended variants
information (count: 8284 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:8284 , 50 per page) page: 1 2 3 4 5 6 7 ... 166

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540786068	chr2:52010529-52010530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562170967	chr2:52010530-52010531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541119808	chr2:52010544-52010545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11563140	chr2:52010562-52010563	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs372636490	chr2:52010573-52010574	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544529465	chr2:52010574-52010575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562908382	chr2:52010585-52010586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144801193	chr2:52010597-52010598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs28965210	chr2:52010599-52010600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560362996	chr2:52010620-52010621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376918606	chr2:52010658-52010659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564796201	chr2:52010674-52010675	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188960976	chr2:52010689-52010690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548722345	chr2:52010697-52010698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567120691	chr2:52010712-52010713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs149011087	chr2:52010725-52010726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549450696	chr2:52010786-52010787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182011462	chr2:52010803-52010804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538598735	chr2:52010812-52010813	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187331679	chr2:52010813-52010814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567112801	chr2:52010859-52010860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534130758	chr2:52010904-52010905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190946294	chr2:52010933-52010934	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574272737	chr2:52010938-52010939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544749168	chr2:52010947-52010948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs77548250	chr2:52010954-52010955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577973305	chr2:52010973-52010974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371582010	chr2:52010981-52010982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549949809	chr2:52010988-52010989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545348788	chr2:52011001-52011002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147811228	chr2:52011028-52011029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs72790132	chr2:52011069-52011070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374195598	chr2:52011071-52011072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527631048	chr2:52011084-52011085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs578215378	chr2:52011099-52011100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142959354	chr2:52011125-52011126	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372050936	chr2:52011128-52011129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542506015	chr2:52011154-52011155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540409111	chr2:52011167-52011168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34029048	chr2:52011173-52011174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs151143339	chr2:52011176-52011177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531379754	chr2:52011183-52011184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549485567	chr2:52011206-52011207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs951189	chr2:52011225-52011226	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs532666372	chr2:52011231-52011232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538755203	chr2:52011246-52011247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140049685	chr2:52011261-52011262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145386893	chr2:52011262-52011263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370504647	chr2:52011328-52011329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534536516	chr2:52011347-52011348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52006800-52011000	Weak transcription	Right Atrium	heart
2	chr2:52009000-52012000	Enhancers	Fetal Heart	heart
3	chr2:52009400-52010800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr2:52009800-52011400	Enhancers	Fetal Brain Male	brain
5	chr2:52010000-52010600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:52010000-52010600	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr2:52010000-52010600	Enhancers	HMEC	breast
8	chr2:52010200-52010600	Enhancers	NHDF-Ad	bronchial
9	chr2:52010200-52010800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr2:52010200-52010800	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr2:52010200-52011000	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr2:52011000-52011600	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr2:52011600-52011800	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr2:52016800-52018000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr2:52017000-52017400	Enhancers	Osteobl	bone
16	chr2:52017000-52017600	Enhancers	Adipose Nuclei	Adipose
17	chr2:52018000-52019000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr2:52019000-52019200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr2:52022000-52022400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr2:52022000-52022600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr2:52022000-52022800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr2:52022200-52022600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr2:52022400-52022800	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr2:52022400-52023000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:52032400-52032800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:52032400-52032800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
27	chr2:52032800-52035200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr2:52035200-52035400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr2:52037200-52037600	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr2:52037600-52038400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr2:52038200-52039200	Enhancers	Hela-S3	cervix
32	chr2:52038400-52039600	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr2:52038800-52040800	Enhancers	Osteobl	bone
34	chr2:52039000-52041200	Enhancers	Muscle Satellite Cultured Cells	--
35	chr2:52039200-52039400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr2:52039200-52039400	Flanking Active TSS	Hela-S3	cervix
37	chr2:52039200-52041000	Enhancers	HMEC	breast
38	chr2:52039200-52041000	Enhancers	NH-A	brain
39	chr2:52039200-52041200	Enhancers	NHDF-Ad	bronchial
40	chr2:52039200-52041600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr2:52039200-52042400	Enhancers	HUVEC	blood vessel
42	chr2:52039400-52039600	Enhancers	Hela-S3	cervix
43	chr2:52039400-52039800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr2:52039400-52040400	Enhancers	NHLF	lung
45	chr2:52039400-52041000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr2:52039600-52039800	Flanking Active TSS	Hela-S3	cervix
47	chr2:52039600-52043400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr2:52039800-52040200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr2:52039800-52041000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr2:52039800-52041600	Enhancers	Hela-S3	cervix

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