Variant report

Variant	nsv871263
Chromosome Location	chr1:93196273-93248228
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:557)
CpG islands
(count:61)
Chromatin interactive
region (count:44)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:557 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:93214645-93214948	K562	blood:	n/a	n/a
2	ARID3A	chr1:93214634-93214893	HepG2	liver:	n/a	n/a
3	BCL3	chr1:93221333-93221668	GM12878	blood:	n/a	n/a
4	BHLHE40	chr1:93213897-93213901	K562	blood:	n/a	n/a
5	CBX3	chr1:93219921-93220333	K562	blood:	n/a	n/a
6	CEBPB	chr1:93224930-93225299	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:93220310-93220564	IMR90	lung:	n/a	chr1:93220467-93220478 chr1:93220467-93220478 chr1:93220467-93220480
8	CEBPB	chr1:93224935-93225304	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr1:93204905-93205227	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:93204969-93205204	K562	blood:	n/a	n/a
11	CEBPB	chr1:93211456-93211671	A549	lung:	n/a	n/a
12	CEBPB	chr1:93220345-93220608	K562	blood:	n/a	chr1:93220467-93220478 chr1:93220467-93220478 chr1:93220467-93220480
13	CEBPB	chr1:93211423-93211728	IMR90	lung:	n/a	n/a
14	CEBPB	chr1:93220979-93221288	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:93233181-93233381	IMR90	lung:	n/a	chr1:93233277-93233290 chr1:93233277-93233288 chr1:93233277-93233290
16	CEBPB	chr1:93229642-93230087	K562	blood:	n/a	chr1:93229793-93229805
17	CEBPB	chr1:93211445-93211703	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:93204969-93205122	A549	lung:	n/a	n/a
19	CEBPB	chr1:93211465-93211717	HepG2	liver:	n/a	n/a
20	CHD2	chr1:93214675-93214875	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr1:93214700-93214850	GM12871	blood:	n/a	n/a
22	CTCF	chr1:93202040-93202190	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr1:93213800-93213950	HEK293	kidney:	n/a	n/a
24	CTCF	chr1:93214668-93214834	GM13976	blood:	n/a	n/a
25	CTCF	chr1:93213840-93213990	GM12866	blood:	n/a	n/a
26	CTCF	chr1:93214680-93214830	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr1:93202040-93202190	SAEC	small airway:	n/a	n/a
28	CTCF	chr1:93214280-93214430	GM12872	blood:	n/a	n/a
29	CTCF	chr1:93214634-93214883	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr1:93214733-93214842	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr1:93214660-93214810	AG04450	lung:	n/a	n/a
32	CTCF	chr1:93213760-93213910	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr1:93214240-93214390	AG09319	gingival:	n/a	n/a
34	CTCF	chr1:93202060-93202210	HCM	heart:	n/a	n/a
35	CTCF	chr1:93202120-93202270	HMEC	breast:	n/a	n/a
36	CTCF	chr1:93214680-93214830	GM06990	blood:	n/a	n/a
37	CTCF	chr1:93214485-93215096	A549	lung:	n/a	n/a
38	CTCF	chr1:93202060-93202210	MCF-7	breast:	n/a	n/a
39	CTCF	chr1:93214680-93214830	HPF	lung:	n/a	n/a
40	CTCF	chr1:93202040-93202190	GM12878	blood:	n/a	n/a
41	CTCF	chr1:93202040-93202190	K562	blood:	n/a	n/a
42	CTCF	chr1:93213860-93214010	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr1:93214658-93214865	LNCaP	prostate:	n/a	n/a
44	CTCF	chr1:93213840-93213990	AG09309	skin:	n/a	n/a
45	CTCF	chr1:93201981-93202251	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr1:93214680-93214830	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr1:93202157-93202204	GM10266	blood:	n/a	n/a
48	CTCF	chr1:93202160-93202310	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr1:93214629-93214891	Medullo	brain:	n/a	n/a
50	CTCF	chr1:93202062-93202229	SK-N-SH_RA	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:93246698-93246748	HRE	kidney:	n/a
2	chr1:93246698-93246748	ECC-1	luminal epithelium:	n/a
3	chr1:93246698-93246748	GM06990	blood:	n/a
4	chr1:93246698-93246748	HRCEpiC	kidney:	n/a
5	chr1:93246698-93246748	HCM	heart:	n/a
6	chr1:93246698-93246748	H1-hESC	embryonic stem cell:	embryo
7	chr1:93246698-93246748	HMEC	breast:	n/a
8	chr1:93246698-93246748	HCT-116	colon:	n/a
9	chr1:93246698-93246748	ovcar-3	ovarian:	n/a
10	chr1:93246698-93246748	AoSMC	blood vessel:	n/a
11	chr1:93246698-93246748	K562	blood:	n/a
12	chr1:93246698-93246748	GM12891	blood:	n/a
13	chr1:93246698-93246748	SK-N-SH_RA	brain:	n/a
14	chr1:93246698-93246748	SK-N-SH	brain:	n/a
15	chr1:93246698-93246748	NHDF-neo	bronchial:	n/a
16	chr1:93246698-93246748	GM12892	blood:	n/a
17	chr1:93246698-93246748	RPTEC	kidney:	n/a
18	chr1:93246698-93246748	NB4	blood:	n/a
19	chr1:93246698-93246748	Hela-S3	cervix:	n/a
20	chr1:93246698-93246748	HUVEC	blood vessel:	n/a
21	chr1:93246698-93246748	BE2_C	brain:	n/a
22	chr1:93246698-93246748	HL-60	blood:	n/a
23	chr1:93246698-93246748	PANC-1	pancreas:	n/a
24	chr1:93246698-93246748	SK-N-MC	brain:	n/a
25	chr1:93246698-93246748	A549	lung:	n/a
26	chr1:93246698-93246748	PFSK-1	brain:	n/a
27	chr1:93246698-93246748	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:93246698-93246748	T-47D	breast:	n/a
29	chr1:93246698-93246748	Jurkat	blood:	n/a
30	chr1:93246698-93246748	CMK	blood:	n/a
31	chr1:93246698-93246748	SKMC	muscle:	n/a
32	chr1:93246698-93246748	Hepatocyte	liver:	n/a
33	chr1:93246698-93246748	GM12878	blood:	n/a
34	chr1:93246698-93246748	NH-A	brain:	n/a
35	chr1:93246698-93246748	GM19239	blood:	n/a
36	chr1:93246698-93246748	MCF-7	breast:	n/a
37	chr1:93246698-93246748	SAEC	small airway:	n/a
38	chr1:93246698-93246748	Caco-2	colon:	n/a
39	chr1:93246698-93246748	HEEpiC	esophagus:	n/a
40	chr1:93246698-93246748	ProgFib	skin:	n/a
41	chr1:93246698-93246748	NT2-D1	testis:	n/a
42	chr1:93246698-93246748	HCF	heart:	n/a
43	chr1:93246698-93246748	AG04449	skin:	fetal
44	chr1:93246698-93246748	MCF10A-Er-Src	breast:	n/a
45	chr1:93246698-93246748	NHBE	bronchial:	n/a
46	chr1:93246698-93246748	AG09319	gingival:	n/a
47	chr1:93246698-93246748	HepG2	liver:	n/a
48	chr1:93246698-93246748	LNCaP	prostate:	n/a
49	chr1:93246698-93246748	HNPCEpiC	eye:	n/a
50	chr1:93246698-93246748	AG04450	lung:	fetal

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:93219197..93221453-chr1:93249271..93251757,2	K562	blood:
2	chr1:93229641..93232894-chr1:93233646..93238232,4	K562	blood:
3	chr1:93243984..93247027-chr1:93248183..93251287,3	MCF-7	breast:
4	chr1:93218168..93220841-chr1:93296877..93299515,3	K562	blood:
5	chr1:93216027..93217718-chr1:93282953..93285543,2	MCF-7	breast:
6	chr1:93208801..93211728-chr1:93211944..93214074,2	K562	blood:
7	chr1:93208387..93210301-chr1:93211944..93214241,2	K562	blood:
8	chr1:93225286..93227993-chr1:93232044..93233868,2	K562	blood:
9	chr1:93208387..93210301-chr1:93211944..93214241,2	K562	blood:
10	chr1:93242184..93247777-chr1:93248755..93252044,8	K562	blood:
11	chr1:93212729..93214501-chr1:93296404..93298744,2	MCF-7	breast:
12	chr1:93215740..93218576-chr1:93300666..93305068,4	K562	blood:
13	chr1:93214862..93218519-chr1:93302722..93305780,4	K562	blood:
14	chr1:93243993..93246087-chr1:93282223..93283796,2	K562	blood:
15	chr1:93214790..93219134-chr1:93222182..93225825,4	K562	blood:
16	chr1:93220670..93222907-chr1:93296640..93299176,3	MCF-7	breast:
17	chr1:93204366..93207086-chr1:93298267..93300832,2	MCF-7	breast:
18	chr1:93213628..93216369-chr1:93216676..93218192,2	K562	blood:
19	chr1:93215411..93218590-chr1:93221864..93223911,3	MCF-7	breast:
20	chr1:93199006..93201048-chr1:93203256..93205414,2	K562	blood:
21	chr1:93225286..93227993-chr1:93232044..93233868,2	K562	blood:
22	chr1:93208801..93211728-chr1:93211944..93214074,2	K562	blood:
23	chr1:93165186..93167884-chr1:93200897..93202411,2	K562	blood:
24	chr1:93209945..93212352-chr1:93296707..93299344,2	K562	blood:
25	chr1:93217706..93221127-chr1:93297522..93299381,3	K562	blood:
26	chr1:93203847..93205464-chr1:93207057..93209940,2	K562	blood:
27	chr1:93199006..93201048-chr1:93203256..93205414,2	K562	blood:
28	chr1:93222826..93225248-chr1:93296209..93297825,2	MCF-7	breast:
29	chr1:93214671..93215199-chr1:93250016..93250945,2	K562	blood:
30	chr1:93222521..93225056-chr1:93227048..93229710,2	K562	blood:
31	chr1:93244037..93247777-chr1:93248755..93251898,4	K562	blood:
32	chr1:93212530..93215412-chr1:93297450..93301173,3	K562	blood:
33	chr1:93215411..93218590-chr1:93221864..93223911,3	MCF-7	breast:
34	chr1:93211573..93213718-chr1:93306717..93309071,2	K562	blood:
35	chr1:93203847..93205464-chr1:93207057..93209940,2	K562	blood:
36	chr1:93243157..93245780-chr1:93300781..93303678,2	K562	blood:
37	chr1:93213561..93216239-chr1:93249509..93251766,2	K562	blood:
38	chr1:93230295..93232894-chr1:93233646..93235757,2	K562	blood:
39	chr1:93229641..93232894-chr1:93233646..93238232,4	K562	blood:
40	chr1:93230295..93232894-chr1:93233646..93235757,2	K562	blood:
41	chr1:93175208..93177703-chr1:93227101..93229847,2	K562	blood:
42	chr1:93224973..93225919-chr6:153207877..153208672,2	K562	blood:
43	chr1:93227169..93228688-chr1:93249929..93251675,2	MCF-7	breast:
44	chr1:93222521..93225056-chr1:93227048..93229710,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPL5-4	chr1:93198634-93198814	NONHSAT004464
2	lnc-RPL5-4	chr1:93197557-93198172	NONHSAT004464
3	lnc-RPL5-2	chr1:93221351-93222513	NONHSAT004467

No data

Variant related genes	Relation type
CCNJP2	TF binding region
ENSG00000225505	TF binding region
ENSG00000234202	TF binding region
CCNJP2	CpG island
ENSG00000225505	CpG island
ENSG00000234202	CpG island
ENSG00000251795	chromatin interactions
ENSG00000201317	chromatin interactions
ENSG00000122406	chromatin interactions
ENSG00000067208	chromatin interactions
ENSG00000206680	chromatin interactions
ENSG00000234202	chromatin interactions

Extended variants
information (count: 1868 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1868 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7516141	chr1:93196273-93196274	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184390838	chr1:93196329-93196330	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs565827898	chr1:93196331-93196332	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs188261760	chr1:93196351-93196352	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs34026414	chr1:93196396-93196397	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs554323262	chr1:93196415-93196416	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs193280153	chr1:93196434-93196435	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs149420521	chr1:93196439-93196440	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs7549844	chr1:93196493-93196494	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs576727709	chr1:93196506-93196507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200243439	chr1:93196520-93196521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376485497	chr1:93196617-93196618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541016819	chr1:93196623-93196624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573918291	chr1:93196647-93196648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs71652503	chr1:93196654-93196655	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs147980979	chr1:93196724-93196725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs375335687	chr1:93196735-93196736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561496760	chr1:93196742-93196743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs12564537	chr1:93196806-93196807	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs185491187	chr1:93196854-93196855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565438758	chr1:93196891-93196892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189611170	chr1:93196892-93196893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545242578	chr1:93196900-93196901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547374746	chr1:93196919-93196920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141697830	chr1:93196930-93196931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536319806	chr1:93196935-93196936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs6661600	chr1:93196961-93196962	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs527387826	chr1:93197034-93197035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569792263	chr1:93197058-93197059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115954500	chr1:93197074-93197075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs147162464	chr1:93197094-93197095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs180837774	chr1:93197119-93197120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112772562	chr1:93197128-93197129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140364698	chr1:93197205-93197206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs6664425	chr1:93197296-93197297	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs183597284	chr1:93197342-93197343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs201561784	chr1:93197349-93197350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541903288	chr1:93197358-93197359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142806804	chr1:93197390-93197391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188702494	chr1:93197398-93197399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543647139	chr1:93197403-93197404	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565608457	chr1:93197431-93197432	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34761380	chr1:93197485-93197486	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs547411888	chr1:93197515-93197516	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs75940005	chr1:93197548-93197549	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530143691	chr1:93197559-93197560	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs147393918	chr1:93197603-93197604	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
48	rs139221486	chr1:93197608-93197609	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
49	rs537285128	chr1:93197613-93197614	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
50	rs552064787	chr1:93197711-93197712	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:765 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:93098400-93205400	Weak transcription	NHLF	lung
2	chr1:93123600-93213400	Weak transcription	Gastric	stomach
3	chr1:93155800-93213400	Weak transcription	Lung	lung
4	chr1:93161000-93197400	Weak transcription	Primary B cells from cord blood	blood
5	chr1:93161000-93197800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr1:93161000-93199000	Weak transcription	Left Ventricle	heart
7	chr1:93174400-93202000	Weak transcription	Fetal Heart	heart
8	chr1:93175800-93199400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:93177800-93197600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr1:93181800-93196600	Weak transcription	HepG2	liver
11	chr1:93182600-93200000	Weak transcription	Primary B cells from peripheral blood	blood
12	chr1:93186600-93205600	Weak transcription	Ovary	ovary
13	chr1:93186800-93197800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr1:93186800-93213400	Weak transcription	K562	blood
15	chr1:93188400-93202000	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr1:93188400-93205400	Weak transcription	Small Intestine	intestine
17	chr1:93188600-93199200	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr1:93188600-93203800	Weak transcription	HMEC	breast
19	chr1:93188800-93201000	Weak transcription	Stomach Smooth Muscle	stomach
20	chr1:93189000-93197800	Weak transcription	Fetal Muscle Trunk	muscle
21	chr1:93189000-93203800	Weak transcription	Hela-S3	cervix
22	chr1:93189000-93213400	Weak transcription	Fetal Lung	lung
23	chr1:93189400-93204200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr1:93189400-93206000	Weak transcription	Brain Anterior Caudate	brain
25	chr1:93189800-93199200	Weak transcription	NH-A	brain
26	chr1:93190000-93221800	Weak transcription	Rectal Smooth Muscle	rectum
27	chr1:93190200-93198000	Weak transcription	Primary hematopoietic stem cells	blood
28	chr1:93190200-93220000	Weak transcription	Fetal Muscle Leg	muscle
29	chr1:93190400-93198400	Weak transcription	Fetal Stomach	stomach
30	chr1:93190400-93199200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:93190600-93197000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr1:93190800-93197800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr1:93191200-93221600	Weak transcription	Fetal Intestine Large	intestine
34	chr1:93191600-93199400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr1:93192400-93221200	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr1:93192400-93226400	Weak transcription	Esophagus	oesophagus
37	chr1:93193000-93200600	Weak transcription	Brain Hippocampus Middle	brain
38	chr1:93193000-93203800	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr1:93193000-93223800	Weak transcription	Duodenum Mucosa	Duodenum
40	chr1:93193600-93200600	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr1:93193600-93213200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:93193800-93196800	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr1:93194200-93196800	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr1:93194200-93197600	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr1:93194200-93199200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr1:93194600-93197600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr1:93194600-93199400	Weak transcription	Adipose Nuclei	Adipose
48	chr1:93194600-93200600	Weak transcription	HSMM	muscle
49	chr1:93194600-93207400	Weak transcription	Osteobl	bone
50	chr1:93194600-93218000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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