Variant report

Variant	nsv1021193
Chromosome Location	chr9:978833-1020933
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1291)
CpG islands
(count:549)
Chromatin interactive
region (count:47)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1291 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:1009225-1009309	K562	blood:	n/a	n/a
2	ATF1	chr9:1013083-1013384	K562	blood:	n/a	n/a
3	ATF3	chr9:1018242-1018408	K562	blood:	n/a	n/a
4	ATF3	chr9:1018219-1018540	HepG2	liver:	n/a	n/a
5	BACH1	chr9:1005054-1005459	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr9:998485-999029	GM12878	blood:	n/a	n/a
7	BATF	chr9:998447-999060	GM12878	blood:	n/a	n/a
8	BCL11A	chr9:998476-999059	GM12878	blood:	n/a	n/a
9	BCL11A	chr9:998478-999038	GM12878	blood:	n/a	n/a
10	BHLHE40	chr9:1018136-1018550	HepG2	liver:	n/a	chr9:1018361-1018370 chr9:1018359-1018372 chr9:1018362-1018371 chr9:1018361-1018370 chr9:1018360-1018369 chr9:1018355-1018376
11	BHLHE40	chr9:1009153-1009539	GM12878	blood:	n/a	chr9:1009235-1009251
12	BHLHE40	chr9:1018181-1018542	GM12878	blood:	n/a	chr9:1018361-1018370 chr9:1018359-1018372 chr9:1018362-1018371 chr9:1018361-1018370 chr9:1018360-1018369 chr9:1018355-1018376
13	BHLHE40	chr9:1009111-1009469	HepG2	liver:	n/a	chr9:1009235-1009251
14	BHLHE40	chr9:1018168-1018552	K562	blood:	n/a	chr9:1018361-1018370 chr9:1018359-1018372 chr9:1018362-1018371 chr9:1018361-1018370 chr9:1018360-1018369 chr9:1018355-1018376
15	BHLHE40	chr9:1018311-1018500	A549	lung:	n/a	chr9:1018361-1018370 chr9:1018359-1018372 chr9:1018362-1018371 chr9:1018361-1018370 chr9:1018360-1018369 chr9:1018355-1018376
16	BHLHE40	chr9:1009121-1009447	K562	blood:	n/a	chr9:1009235-1009251
17	BHLHE40	chr9:998476-999116	HepG2	liver:	n/a	n/a
18	BHLHE40	chr9:1005037-1005437	GM12878	blood:	n/a	n/a
19	BRCA1	chr9:1009179-1009384	HepG2	liver:	n/a	n/a
20	BRCA1	chr9:1009140-1009395	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr9:998488-999102	K562	blood:	n/a	n/a
22	CBX3	chr9:998426-999145	K562	blood:	n/a	n/a
23	CEBPB	chr9:1007173-1007672	MCF-7	breast:	n/a	chr9:1007420-1007431
24	CEBPB	chr9:1007119-1007701	MCF-7	breast:	n/a	chr9:1007420-1007431
25	CEBPB	chr9:1006646-1006667	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr9:1007270-1007577	IMR90	lung:	n/a	chr9:1007420-1007431
27	CEBPB	chr9:1005051-1005367	A549	lung:	n/a	n/a
28	CEBPB	chr9:1008314-1008607	A549	lung:	n/a	n/a
29	CEBPB	chr9:1007275-1007607	A549	lung:	n/a	chr9:1007420-1007431
30	CEBPB	chr9:1005027-1005521	MCF-7	breast:	n/a	n/a
31	CEBPB	chr9:1018102-1018487	MCF-7	breast:	n/a	n/a
32	CEBPB	chr9:1005104-1005356	HepG2	liver:	n/a	n/a
33	CEBPB	chr9:1008255-1008623	IMR90	lung:	n/a	n/a
34	CEBPB	chr9:1007275-1007605	HepG2	liver:	n/a	chr9:1007420-1007431
35	CEBPB	chr9:1009159-1009464	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr9:1005008-1005372	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr9:1009154-1009437	GM12878	blood:	n/a	n/a
38	CHD2	chr9:1009169-1009480	HepG2	liver:	n/a	n/a
39	CHD2	chr9:1009154-1009544	GM12878	blood:	n/a	n/a
40	CREB1	chr9:1009145-1009543	A549	lung:	n/a	n/a
41	CTCF	chr9:999020-999170	HEK293	kidney:	n/a	n/a
42	CTCF	chr9:1018140-1018290	GM12866	blood:	n/a	n/a
43	CTCF	chr9:998400-998550	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr9:1005180-1005330	GM12874	blood:	n/a	n/a
45	CTCF	chr9:1009240-1009390	HUVEC	blood vessel:	n/a	chr9:1009272-1009288 chr9:1009273-1009286 chr9:1009271-1009289 chr9:1009276-1009284 chr9:1009266-1009287
46	CTCF	chr9:1009147-1009437	ProgFib	skin:	n/a	chr9:1009272-1009288 chr9:1009273-1009286 chr9:1009271-1009289 chr9:1009276-1009284 chr9:1009266-1009287
47	CTCF	chr9:999020-999170	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr9:999020-999170	HCFaa	heart:	n/a	n/a
49	CTCF	chr9:1005168-1005392	GM10266	blood:	n/a	n/a
50	CTCF	chr9:1018220-1018370	NHLF	lung:	n/a	chr9:1018297-1018315 chr9:1018300-1018309 chr9:1018299-1018320

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:997475-997525	H1-hESC	embryonic stem cell:	embryo
2	chr9:998261-998311	MCF10A-Er-Src	breast:	n/a
3	chr9:990692-990742	ProgFib	skin:	n/a
4	chr9:990260-990310	HCT-116	colon:	n/a
5	chr9:990260-990310	HepG2	liver:	n/a
6	chr9:991047-991097	HL-60	blood:	n/a
7	chr9:990260-990310	ovcar-3	ovarian:	n/a
8	chr9:998261-998311	K562	blood:	n/a
9	chr9:990692-990742	NH-A	brain:	n/a
10	chr9:998261-998311	GM06990	blood:	n/a
11	chr9:991047-991097	BJ	skin:	n/a
12	chr9:998533-998583	AG04449	skin:	fetal
13	chr9:998533-998583	HNPCEpiC	eye:	n/a
14	chr9:990260-990310	HRE	kidney:	n/a
15	chr9:990618-990668	GM19239	blood:	n/a
16	chr9:995579-995629	HAEpiC	amniotic membrane:	n/a
17	chr9:997475-997525	HAEpiC	amniotic membrane:	n/a
18	chr9:998547-998597	Caco-2	colon:	n/a
19	chr9:990692-990742	PFSK-1	brain:	n/a
20	chr9:997475-997525	HRCEpiC	kidney:	n/a
21	chr9:998261-998311	H1-hESC	embryonic stem cell:	embryo
22	chr9:998261-998311	GM12892	blood:	n/a
23	chr9:990692-990742	T-47D	breast:	n/a
24	chr9:995579-995629	Caco-2	colon:	n/a
25	chr9:998547-998597	SAEC	small airway:	n/a
26	chr9:990618-990668	HRPEpiC	eye:	n/a
27	chr9:990692-990742	HRPEpiC	eye:	n/a
28	chr9:990618-990668	BJ	skin:	n/a
29	chr9:990618-990668	HUVEC	blood vessel:	n/a
30	chr9:990618-990668	HepG2	liver:	n/a
31	chr9:990692-990742	HPAEpiC	pulmonary alveolar:	n/a
32	chr9:990618-990668	PFSK-1	brain:	n/a
33	chr9:998547-998597	ECC-1	luminal epithelium:	n/a
34	chr9:997475-997525	HCT-116	colon:	n/a
35	chr9:997475-997525	IMR90	lung:	fetal
36	chr9:998547-998597	HCF	heart:	n/a
37	chr9:990260-990310	SAEC	small airway:	n/a
38	chr9:990260-990310	AG09319	gingival:	n/a
39	chr9:990618-990668	T-47D	breast:	n/a
40	chr9:990692-990742	GM19239	blood:	n/a
41	chr9:990260-990310	HCM	heart:	n/a
42	chr9:990692-990742	HCPEpiC	choroid plexus:	n/a
43	chr9:998547-998597	GM12892	blood:	n/a
44	chr9:990692-990742	HCF	heart:	n/a
45	chr9:998547-998597	RPTEC	kidney:	n/a
46	chr9:990260-990310	SK-N-SH_RA	brain:	n/a
47	chr9:991047-991097	HRE	kidney:	n/a
48	chr9:997475-997525	T-47D	breast:	n/a
49	chr9:990618-990668	ECC-1	luminal epithelium:	n/a
50	chr9:990692-990742	ovcar-3	ovarian:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:995490..996572-chr9:1050045..1050642,3	MCF-7	breast:
2	chr9:899986..901721-chr9:992328..994954,2	MCF-7	breast:
3	chr9:910762..911411-chr9:998511..999239,3	MCF-7	breast:
4	chr9:892914..894635-chr9:997792..999398,19	MCF-7	breast:
5	chr9:1017795..1018400-chr9:1429068..1429992,2	MCF-7	breast:
6	chr9:892827..894783-chr9:997829..1000001,46	MCF-7	breast:
7	chr9:979709..982475-chr9:990921..992536,2	MCF-7	breast:
8	chr9:1017784..1019327-chr9:1158625..1160475,2	MCF-7	breast:
9	chr9:988079..991446-chr9:991820..996186,5	MCF-7	breast:
10	chr9:979709..982475-chr9:990921..992536,2	MCF-7	breast:
11	chr9:982152..984016-chr9:986443..989260,2	MCF-7	breast:
12	chr9:979898..983032-chr9:983503..985277,3	MCF-7	breast:
13	chr9:893903..894431-chr9:1004790..1005383,2	K562	blood:
14	chr9:893090..895102-chr9:997642..1000257,3	MCF-7	breast:
15	chr9:1017972..1018656-chr9:1527877..1528623,2	MCF-7	breast:
16	chr9:887794..889918-chr9:1005357..1008295,2	MCF-7	breast:
17	chr9:994727..996463-chr9:998360..1001251,2	K562	blood:
18	chr9:892413..895344-chr9:995955..997519,2	MCF-7	breast:
19	chr9:892531..895372-chr9:1005273..1008806,3	MCF-7	breast:
20	chr9:982598..984781-chr9:987934..990176,2	MCF-7	breast:
21	chr9:581649..582215-chr9:998516..999103,2	MCF-7	breast:
22	chr9:893739..894732-chr9:1008819..1009733,5	MCF-7	breast:
23	chr9:979898..983032-chr9:983503..985277,3	MCF-7	breast:
24	chr9:1009051..1010072-chr9:1017840..1018709,4	MCF-7	breast:
25	chr9:826413..827016-chr9:1004866..1005745,2	MCF-7	breast:
26	chr9:893937..894571-chr9:1000555..1001318,2	MCF-7	breast:
27	chr9:890713..892471-chr9:1006171..1008763,2	MCF-7	breast:
28	chr9:998424..999235-chr9:1008893..1009451,2	MCF-7	breast:
29	chr9:994727..996463-chr9:998360..1001251,2	K562	blood:
30	chr9:893523..894096-chr9:1008794..1009361,2	MCF-7	breast:
31	chr9:893804..894399-chr9:1008894..1009774,3	K562	blood:
32	chr9:385756..386457-chr9:1008777..1009377,2	MCF-7	breast:
33	chr6:89674376..89674876-chr9:1017838..1018522,2	MCF-7	breast:
34	chr2:238421116..238421980-chr9:998514..999134,2	MCF-7	breast:
35	chr9:978343..980542-chr9:980897..983519,2	K562	blood:
36	chr9:1017910..1018696-chr9:1429132..1429802,2	MCF-7	breast:
37	chr9:891599..892777-chr9:998523..999622,4	MCF-7	breast:
38	chr9:982152..984016-chr9:986443..989260,2	MCF-7	breast:
39	chr9:1017828..1018465-chr9:1337011..1337699,2	MCF-7	breast:
40	chr9:763938..764768-chr9:1004823..1005723,3	MCF-7	breast:
41	chr9:613814..614512-chr9:1017801..1018342,2	MCF-7	breast:
42	chr9:978343..980542-chr9:980897..983519,2	K562	blood:
43	chr9:892287..894400-chr9:997529..999081,2	MCF-7	breast:
44	chr9:889496..890427-chr9:998557..999062,2	MCF-7	breast:
45	chr9:1007423..1009287-chr9:1045081..1047981,2	MCF-7	breast:
46	chr9:1009051..1010072-chr9:1017840..1018709,4	MCF-7	breast:
47	chr9:998424..999235-chr9:1008893..1009451,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMRT3-4	chr9:1011085-1011386	NONHSAT129956
2	lnc-DMRT3-4	chr9:1011710-1011799	NONHSAT129956

No data

Variant related genes	Relation type
ENSG00000228783	TF binding region
RNU6-1073P	TF binding region
DMRT3	TF binding region
ENSG00000228783	CpG island
RNU6-1073P	CpG island
DMRT3	CpG island
ENSG00000173253	chromatin interactions
ENSG00000064218	chromatin interactions

Extended variants
information (count: 1627 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:1627 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs279888	chr9:978833-978834	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182772579	chr9:978863-978864	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs370803647	chr9:978923-978924	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs559700775	chr9:978950-978951	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs113593372	chr9:978967-978968	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs532285429	chr9:978979-978980	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs563667550	chr9:979023-979024	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs542154989	chr9:979024-979025	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs377290808	chr9:979042-979043	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs529267989	chr9:979071-979072	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs279887	chr9:979080-979081	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs111623849	chr9:979115-979116	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs60301829	chr9:979131-979132	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs188888489	chr9:979149-979150	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs551842848	chr9:979192-979193	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs565718030	chr9:979209-979210	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs534907099	chr9:979222-979223	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs548538350	chr9:979255-979256	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs552801260	chr9:979290-979291	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs568241042	chr9:979305-979306	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs373866747	chr9:979315-979316	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs61021481	chr9:979322-979323	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs537207655	chr9:979334-979335	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs75600641	chr9:979343-979344	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs577220584	chr9:979357-979358	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs190877648	chr9:979372-979373	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs553080781	chr9:979383-979384	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs71509982	chr9:979409-979410	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs572932819	chr9:979414-979415	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs542094331	chr9:979496-979497	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs111872162	chr9:979501-979502	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs575550143	chr9:979524-979525	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs183024989	chr9:979529-979530	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs564708726	chr9:979530-979531	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs532107534	chr9:979561-979562	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs552291196	chr9:979577-979578	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs279886	chr9:979585-979586	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs438293	chr9:979610-979611	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs438294	chr9:979611-979612	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs568320657	chr9:979612-979613	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs279885	chr9:979640-979641	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs550498357	chr9:979693-979694	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs570665432	chr9:979726-979727	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs569624002	chr9:979735-979736	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs1509189	chr9:979809-979810	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs113001562	chr9:979819-979820	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs75809511	chr9:979841-979842	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs573021384	chr9:979883-979884	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs1912019	chr9:979896-979897	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs426119	chr9:979919-979920	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	21272361	CNVD
Non-small cell lung cancer	16651412	CNVD
Ovarian cancer	21781307	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Autism	22495311	CNVD

Chromatin state (count:195 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:978800-979800	Bivalent Enhancer	Adipose Nuclei	Adipose
2	chr9:979200-979400	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:979400-979600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
4	chr9:979800-980200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:980800-981000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
6	chr9:980800-981000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
7	chr9:980800-981000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:980800-981000	Bivalent Enhancer	Fetal Kidney	kidney
9	chr9:980800-981200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr9:981000-981200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
11	chr9:981200-983000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr9:981400-981600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
13	chr9:981400-982000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
14	chr9:981400-983000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:981600-981800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
16	chr9:981600-981800	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr9:981600-981800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr9:981600-981800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr9:981600-981800	Flanking Bivalent TSS/Enh	Spleen	Spleen
20	chr9:981600-982400	Bivalent Enhancer	Lung	lung
21	chr9:981600-983000	Bivalent Enhancer	Fetal Muscle Leg	muscle
22	chr9:981800-982000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
23	chr9:981800-982000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
24	chr9:981800-982200	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
25	chr9:982000-982200	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
26	chr9:982200-982400	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr9:982200-982400	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
28	chr9:982200-983200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr9:982200-984000	Enhancers	Adipose Nuclei	Adipose
30	chr9:982400-983000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr9:982400-983200	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr9:982800-983000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr9:982800-983000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
34	chr9:983200-983400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr9:983200-983800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr9:983400-983600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr9:990200-990400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr9:991200-994000	Weak transcription	Adipose Nuclei	Adipose
39	chr9:991800-992000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
40	chr9:992000-992200	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr9:992600-995600	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr9:993400-994800	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr9:993600-994800	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr9:994000-994600	Enhancers	GM12878-XiMat	blood
45	chr9:994000-995000	Enhancers	Adipose Nuclei	Adipose
46	chr9:994200-994400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
47	chr9:994200-996400	Enhancers	NHDF-Ad	bronchial
48	chr9:994600-995000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr9:994600-996800	Enhancers	HSMM	muscle
50	chr9:994800-995400	Enhancers	Muscle Satellite Cultured Cells	--

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