Variant report

Variant	nsv871494
Chromosome Location	chr1:103354138-103466917
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:103424463-103424755	HepG2	liver:	n/a	n/a
2	BRCA1	chr1:103436155-103436294	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr1:103363004-103363495	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr1:103385312-103385827	Hela-S3	cervix:	n/a	chr1:103385694-103385707 chr1:103385696-103385707 chr1:103385694-103385707 chr1:103385696-103385707 chr1:103385694-103385707
5	CEBPB	chr1:103385285-103385812	IMR90	lung:	n/a	chr1:103385694-103385707 chr1:103385696-103385707 chr1:103385694-103385707 chr1:103385696-103385707 chr1:103385694-103385707
6	CEBPB	chr1:103457286-103457644	H1-hESC	embryonic stem cell:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
7	CEBPB	chr1:103420192-103420551	H1-hESC	embryonic stem cell:	n/a	chr1:103420350-103420361
8	CEBPB	chr1:103363066-103363488	A549	lung:	n/a	n/a
9	CEBPB	chr1:103462260-103462460	HepG2	liver:	n/a	chr1:103462355-103462366 chr1:103462357-103462368
10	CEBPB	chr1:103420205-103420542	A549	lung:	n/a	chr1:103420350-103420361
11	CEBPB	chr1:103420187-103420500	HepG2	liver:	n/a	chr1:103420350-103420361
12	CEBPB	chr1:103463557-103463788	A549	lung:	n/a	chr1:103463691-103463704 chr1:103463691-103463702 chr1:103463691-103463702 chr1:103463712-103463725 chr1:103463691-103463704
13	CEBPB	chr1:103424437-103424754	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:103420192-103420500	IMR90	lung:	n/a	chr1:103420350-103420361
15	CEBPB	chr1:103457305-103457616	HepG2	liver:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
16	CHD2	chr1:103363173-103363438	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr1:103436153-103436432	GM20000	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
18	CTCF	chr1:103436540-103436690	BJ	skin:	n/a	n/a
19	CTCF	chr1:103436127-103436380	GM13977	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
20	CTCF	chr1:103436540-103436690	HFF-Myc	foreskin:	n/a	n/a
21	CTCF	chr1:103436428-103436540	Fibrobl	skin:	n/a	n/a
22	CTCF	chr1:103436180-103436330	NHEK	skin:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
23	CTCF	chr1:103436160-103436310	HRPEpiC	eye:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
24	CTCF	chr1:103436180-103436330	GM12871	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
25	CTCF	chr1:103436140-103436290	GM12878	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
26	CTCF	chr1:103436140-103436290	NHDF-neo	bronchial:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
27	CTCF	chr1:103436140-103436290	HMEC	breast:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
28	CTCF	chr1:103436108-103436355	HepG2	liver:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
29	CTCF	chr1:103436260-103436410	A549	lung:	n/a	n/a
30	CTCF	chr1:103436180-103436330	GM12865	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
31	CTCF	chr1:103436080-103436427	K562	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
32	CTCF	chr1:103436240-103436390	HEK293	kidney:	n/a	chr1:103436240-103436253 chr1:103436243-103436251
33	CTCF	chr1:103436171-103436402	ProgFib	skin:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
34	CTCF	chr1:103436180-103436330	GM12864	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
35	CTCF	chr1:103436063-103436357	H1-hESC	embryonic stem cell:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
36	CTCF	chr1:103435994-103436641	SK-N-SH	brain:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
37	CTCF	chr1:103436140-103436290	HPAF	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
38	CTCF	chr1:103436200-103436350	SAEC	small airway:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
39	CTCF	chr1:103436120-103436270	HVMF	connective:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
40	CTCF	chr1:103436462-103436507	ProgFib	skin:	n/a	n/a
41	CTCF	chr1:103436149-103436360	Spleen_OC	spleen:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
42	CTCF	chr1:103436140-103436290	GM12864	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
43	CTCF	chr1:103436140-103436290	AG09319	gingival:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
44	CTCF	chr1:103436140-103436290	Hela-S3	cervix:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
45	CTCF	chr1:103436045-103436353	A549	lung:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
46	CTCF	chr1:103436220-103436370	Hela-S3	cervix:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
47	CTCF	chr1:103436180-103436330	GM12873	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
48	CTCF	chr1:103436180-103436330	GM12867	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
49	CTCF	chr1:103436138-103436362	LNCaP	prostate:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
50	CTCF	chr1:103436141-103436369	K562	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:103399388-103399438	ovcar-3	ovarian:	n/a
2	chr1:103399388-103399438	SK-N-MC	brain:	n/a
3	chr1:103399388-103399438	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:103399388-103399438	AG04449	skin:	fetal
5	chr1:103399388-103399438	Caco-2	colon:	n/a
6	chr1:103399388-103399438	GM19239	blood:	n/a
7	chr1:103399388-103399438	HCM	heart:	n/a
8	chr1:103399388-103399438	GM12891	blood:	n/a
9	chr1:103399388-103399438	NH-A	brain:	n/a
10	chr1:103399388-103399438	BJ	skin:	n/a
11	chr1:103399388-103399438	MCF10A-Er-Src	breast:	n/a
12	chr1:103399388-103399438	NB4	blood:	n/a
13	chr1:103399388-103399438	HMEC	breast:	n/a
14	chr1:103399388-103399438	H1-hESC	embryonic stem cell:	embryo
15	chr1:103399388-103399438	SK-N-SH	brain:	n/a
16	chr1:103399388-103399438	AoSMC	blood vessel:	n/a
17	chr1:103399388-103399438	AG10803	skin:	n/a
18	chr1:103399388-103399438	Hela-S3	cervix:	n/a
19	chr1:103399388-103399438	GM06990	blood:	n/a
20	chr1:103399388-103399438	SKMC	muscle:	n/a
21	chr1:103399388-103399438	T-47D	breast:	n/a
22	chr1:103399388-103399438	IMR90	lung:	fetal
23	chr1:103399388-103399438	GM12878	blood:	n/a
24	chr1:103399388-103399438	HRPEpiC	eye:	n/a
25	chr1:103399388-103399438	PANC-1	pancreas:	n/a
26	chr1:103399388-103399438	NHBE	bronchial:	n/a
27	chr1:103399388-103399438	AG04450	lung:	fetal
28	chr1:103399388-103399438	CMK	blood:	n/a
29	chr1:103399388-103399438	GM12892	blood:	n/a
30	chr1:103399388-103399438	PFSK-1	brain:	n/a
31	chr1:103399388-103399438	Hepatocyte	liver:	n/a
32	chr1:103399388-103399438	ECC-1	luminal epithelium:	n/a
33	chr1:103399388-103399438	HCT-116	colon:	n/a
34	chr1:103399388-103399438	HCPEpiC	choroid plexus:	n/a
35	chr1:103399388-103399438	HNPCEpiC	eye:	n/a
36	chr1:103399388-103399438	AG09309	skin:	n/a
37	chr1:103399388-103399438	BE2_C	brain:	n/a
38	chr1:103399388-103399438	A549	lung:	n/a
39	chr1:103399388-103399438	AG09319	gingival:	n/a
40	chr1:103399388-103399438	NT2-D1	testis:	n/a
41	chr1:103399388-103399438	HEK293	kidney:	embryo
42	chr1:103399388-103399438	HEEpiC	esophagus:	n/a
43	chr1:103399388-103399438	PrEC	prostate:	n/a
44	chr1:103399388-103399438	RPTEC	kidney:	n/a
45	chr1:103399388-103399438	MCF-7	breast:	n/a
46	chr1:103399388-103399438	SK-N-SH_RA	brain:	n/a
47	chr1:103399388-103399438	HCF	heart:	n/a
48	chr1:103399388-103399438	LNCaP	prostate:	n/a
49	chr1:103399388-103399438	Jurkat	blood:	n/a
50	chr1:103399388-103399438	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:103373284..103376255-chr1:103376543..103379257,2	K562	blood:
2	chr1:103373284..103376255-chr1:103376543..103379257,2	K562	blood:
3	chr1:103303886..103305574-chr1:103404633..103406434,2	MCF-7	breast:
4	chr1:103016225..103017019-chr1:103436153..103436688,2	MCF-7	breast:
5	chr1:103426177..103428144-chr1:103433364..103435643,2	K562	blood:
6	chr1:103435891..103438484-chr1:103439465..103441994,2	K562	blood:
7	chr1:103259174..103259873-chr1:103435676..103436665,2	MCF-7	breast:
8	chr1:103435891..103438484-chr1:103439465..103441994,2	K562	blood:
9	chr1:103426177..103428144-chr1:103433364..103435643,2	K562	blood:

Variant related genes	Relation type
COL11A1	TF binding region
COL11A1	CpG island

Extended variants
information (count: 4651 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:4651 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1676486	chr1:103354138-103354139	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140954784	chr1:103354147-103354148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs578137786	chr1:103354155-103354156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146997967	chr1:103354160-103354161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370574925	chr1:103354169-103354170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375198724	chr1:103354242-103354243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545281542	chr1:103354245-103354246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369145108	chr1:103354247-103354248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200793857	chr1:103354260-103354261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372206712	chr1:103354271-103354272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575231157	chr1:103354288-103354289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542653794	chr1:103354323-103354324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1763347	chr1:103354428-103354429	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs528529875	chr1:103354432-103354433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs199952288	chr1:103354445-103354446	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145901197	chr1:103354472-103354473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201511614	chr1:103354492-103354493	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369961901	chr1:103354522-103354523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142473371	chr1:103354537-103354538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150545115	chr1:103354540-103354541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188319192	chr1:103354579-103354580	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139504614	chr1:103354710-103354711	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567278514	chr1:103354729-103354730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534388693	chr1:103354730-103354731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs61813926	chr1:103354736-103354737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571728021	chr1:103354761-103354762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150048187	chr1:103354798-103354799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564353217	chr1:103354854-103354855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374288103	chr1:103354875-103354876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536617466	chr1:103354909-103354910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531716806	chr1:103354920-103354921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113226085	chr1:103354939-103354940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs71094579	chr1:103354966-103354967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376841140	chr1:103355050-103355051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369947899	chr1:103355057-103355058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs55821405	chr1:103355059-103355060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs202194245	chr1:103355087-103355088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs180734278	chr1:103355095-103355096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184965786	chr1:103355112-103355113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573203662	chr1:103355116-103355117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540354456	chr1:103355166-103355167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113682635	chr1:103355204-103355205	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565404949	chr1:103355207-103355208	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577906907	chr1:103355212-103355213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs60484126	chr1:103355222-103355223	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs145341276	chr1:103355250-103355251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189479411	chr1:103355303-103355304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562208677	chr1:103355315-103355316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148800226	chr1:103355318-103355319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549278423	chr1:103355327-103355328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	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	chr1:103338400-103369400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:103338800-103357200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr1:103343400-103355800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr1:103343400-103356200	Weak transcription	Fetal Heart	heart
5	chr1:103343400-103366000	Weak transcription	Fetal Brain Female	brain
6	chr1:103345600-103385600	Weak transcription	HSMMtube	muscle
7	chr1:103345800-103357200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:103346200-103357400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr1:103346200-103357400	Weak transcription	NH-A	brain
10	chr1:103348200-103357400	Weak transcription	HSMM	muscle
11	chr1:103348200-103357400	Weak transcription	Osteobl	bone
12	chr1:103349800-103356000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr1:103350000-103369400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:103350400-103355400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:103350400-103380200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr1:103350800-103378600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr1:103352200-103354800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:103352200-103355200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr1:103352600-103354600	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr1:103352600-103357600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:103352600-103362400	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr1:103352600-103403200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr1:103352800-103357400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr1:103353400-103355000	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr1:103353600-103357200	Weak transcription	HMEC	breast
26	chr1:103353600-103357400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr1:103354000-103354800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:103354800-103357800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr1:103354800-103377400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr1:103355000-103378000	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr1:103355200-103357000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr1:103355400-103360400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:103356400-103356800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr1:103357000-103357400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr1:103357000-103358400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr1:103357200-103357400	Active TSS	A549	lung
37	chr1:103357200-103358200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:103357200-103358200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr1:103357200-103358200	Enhancers	HMEC	breast
40	chr1:103357200-103358400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr1:103357200-103358400	Enhancers	NHDF-Ad	bronchial
42	chr1:103357200-103358600	Enhancers	HUVEC	blood vessel
43	chr1:103357200-103359600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr1:103357400-103357600	Enhancers	Muscle Satellite Cultured Cells	--
45	chr1:103357400-103357600	Flanking Active TSS	A549	lung
46	chr1:103357400-103358200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr1:103357400-103358200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr1:103357400-103358200	Enhancers	HSMM	muscle
49	chr1:103357400-103358400	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:103357400-103358400	Enhancers	NH-A	brain

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