Variant report

Variant	nsv873069
Chromosome Location	chr1:197055925-197109042
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:376)
CpG islands
(count:61)
Chromatin interactive
region (count:43)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:376 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:197072339-197072887	K562	blood:	n/a	n/a
2	BACH1	chr1:197073109-197073136	K562	blood:	n/a	n/a
3	BATF	chr1:197061784-197062055	GM12878	blood:	n/a	n/a
4	BATF	chr1:197065302-197065518	GM12878	blood:	n/a	chr1:197065444-197065455
5	BCL11A	chr1:197098823-197099125	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr1:197067276-197067321	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:197079129-197079230	IMR90	lung:	n/a	n/a
8	CEBPB	chr1:197062761-197062934	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr1:197059128-197059372	HepG2	liver:	n/a	chr1:197059287-197059298
10	CEBPB	chr1:197062726-197062961	K562	blood:	n/a	n/a
11	CEBPB	chr1:197062650-197062984	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:197070552-197070638	K562	blood:	n/a	n/a
13	CEBPB	chr1:197088028-197088299	Hela-S3	cervix:	n/a	chr1:197088188-197088197 chr1:197088186-197088199 chr1:197088186-197088197 chr1:197088186-197088197 chr1:197088188-197088197 chr1:197088188-197088197 chr1:197088187-197088198 chr1:197088186-197088199 chr1:197088188-197088197
14	CEBPB	chr1:197096691-197096985	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:197062475-197062999	A549	lung:	n/a	n/a
16	CEBPB	chr1:197096716-197096938	A549	lung:	n/a	n/a
17	CEBPB	chr1:197075977-197076481	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr1:197062629-197063024	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:197106586-197106785	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr1:197088031-197088342	K562	blood:	n/a	chr1:197088188-197088197 chr1:197088186-197088199 chr1:197088186-197088197 chr1:197088186-197088197 chr1:197088188-197088197 chr1:197088188-197088197 chr1:197088187-197088198 chr1:197088186-197088199 chr1:197088188-197088197 chr1:197088294-197088311
21	CEBPB	chr1:197088012-197088373	HepG2	liver:	n/a	chr1:197088188-197088197 chr1:197088186-197088199 chr1:197088186-197088197 chr1:197088186-197088197 chr1:197088188-197088197 chr1:197088188-197088197 chr1:197088187-197088198 chr1:197088186-197088199 chr1:197088188-197088197 chr1:197088294-197088311
22	CEBPB	chr1:197088024-197088365	A549	lung:	n/a	chr1:197088188-197088197 chr1:197088186-197088199 chr1:197088186-197088197 chr1:197088186-197088197 chr1:197088188-197088197 chr1:197088188-197088197 chr1:197088187-197088198 chr1:197088186-197088199 chr1:197088188-197088197 chr1:197088294-197088311
23	CEBPB	chr1:197076040-197076417	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr1:197099839-197100779	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr1:197088037-197088366	IMR90	lung:	n/a	chr1:197088188-197088197 chr1:197088186-197088199 chr1:197088186-197088197 chr1:197088186-197088197 chr1:197088188-197088197 chr1:197088188-197088197 chr1:197088187-197088198 chr1:197088186-197088199 chr1:197088188-197088197 chr1:197088294-197088311
26	CEBPB	chr1:197062648-197063000	IMR90	lung:	n/a	n/a
27	CHD2	chr1:197071837-197071866	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr1:197070875-197071307	K562	blood:	n/a	n/a
29	CHD2	chr1:197072318-197072793	K562	blood:	n/a	n/a
30	CHD2	chr1:197072563-197073085	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr1:197070949-197071464	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr1:197099920-197100070	AG10803	skin:	n/a	n/a
33	CTCF	chr1:197099960-197100110	AG04449	skin:	n/a	n/a
34	CTCF	chr1:197099920-197100070	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr1:197099960-197100110	HPF	lung:	n/a	n/a
36	CTCF	chr1:197100000-197100150	HMEC	breast:	n/a	n/a
37	CTCF	chr1:197099840-197099990	AG04450	lung:	n/a	n/a
38	CTCF	chr1:197065446-197065665	K562	blood:	n/a	n/a
39	CTCF	chr1:197100020-197100170	HAc	cerebellar:	n/a	n/a
40	CTCF	chr1:197099940-197100090	AoAF	blood vessel:	n/a	n/a
41	CTCF	chr1:197099960-197100110	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:197099940-197100090	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr1:197099920-197100070	SAEC	small airway:	n/a	n/a
44	CTCF	chr1:197100000-197100150	NHEK	skin:	n/a	n/a
45	CTCF	chr1:197099940-197100090	AG10803	skin:	n/a	n/a
46	CTCF	chr1:197099960-197100110	HCFaa	heart:	n/a	n/a
47	CTCF	chr1:197099980-197100130	AG04450	lung:	n/a	n/a
48	CTCF	chr1:197099980-197100130	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr1:197100060-197100210	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr1:197100040-197100190	BJ	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:197099113-197099163	SAEC	small airway:	n/a
2	chr1:197099113-197099163	ECC-1	luminal epithelium:	n/a
3	chr1:197099113-197099163	SK-N-SH_RA	brain:	n/a
4	chr1:197099113-197099163	HRCEpiC	kidney:	n/a
5	chr1:197099113-197099163	HAEpiC	amniotic membrane:	n/a
6	chr1:197099113-197099163	GM12892	blood:	n/a
7	chr1:197099113-197099163	GM19239	blood:	n/a
8	chr1:197099113-197099163	AG10803	skin:	n/a
9	chr1:197099113-197099163	K562	blood:	n/a
10	chr1:197099113-197099163	ProgFib	skin:	n/a
11	chr1:197099113-197099163	LNCaP	prostate:	n/a
12	chr1:197099113-197099163	HMEC	breast:	n/a
13	chr1:197099113-197099163	AG09309	skin:	n/a
14	chr1:197099113-197099163	SK-N-SH	brain:	n/a
15	chr1:197099113-197099163	HUVEC	blood vessel:	n/a
16	chr1:197099113-197099163	HepG2	liver:	n/a
17	chr1:197099113-197099163	RPTEC	kidney:	n/a
18	chr1:197099113-197099163	CMK	blood:	n/a
19	chr1:197099113-197099163	Hela-S3	cervix:	n/a
20	chr1:197099113-197099163	HPAEpiC	pulmonary alveolar:	n/a
21	chr1:197099113-197099163	HL-60	blood:	n/a
22	chr1:197099113-197099163	MCF10A-Er-Src	breast:	n/a
23	chr1:197099113-197099163	BJ	skin:	n/a
24	chr1:197099113-197099163	HCF	heart:	n/a
25	chr1:197099113-197099163	U87	brain:	n/a
26	chr1:197099113-197099163	NHBE	bronchial:	n/a
27	chr1:197099113-197099163	HEK293	kidney:	embryo
28	chr1:197099113-197099163	HEEpiC	esophagus:	n/a
29	chr1:197099113-197099163	H1-hESC	embryonic stem cell:	embryo
30	chr1:197099113-197099163	MCF-7	breast:	n/a
31	chr1:197099113-197099163	PFSK-1	brain:	n/a
32	chr1:197099113-197099163	HIPEpiC	eye:	n/a
33	chr1:197099113-197099163	HCPEpiC	choroid plexus:	n/a
34	chr1:197099113-197099163	HNPCEpiC	eye:	n/a
35	chr1:197099113-197099163	Hepatocyte	liver:	n/a
36	chr1:197099113-197099163	HRE	kidney:	n/a
37	chr1:197099113-197099163	AG04450	lung:	fetal
38	chr1:197099113-197099163	Jurkat	blood:	n/a
39	chr1:197099113-197099163	AoSMC	blood vessel:	n/a
40	chr1:197099113-197099163	NT2-D1	testis:	n/a
41	chr1:197099113-197099163	IMR90	lung:	fetal
42	chr1:197099113-197099163	AG04449	skin:	fetal
43	chr1:197099113-197099163	HRPEpiC	eye:	n/a
44	chr1:197099113-197099163	NHDF-neo	bronchial:	n/a
45	chr1:197099113-197099163	SKMC	muscle:	n/a
46	chr1:197099113-197099163	PANC-1	pancreas:	n/a
47	chr1:197099113-197099163	HCT-116	colon:	n/a
48	chr1:197099113-197099163	BE2_C	brain:	n/a
49	chr1:197099113-197099163	PrEC	prostate:	n/a
50	chr1:197099113-197099163	AG09319	gingival:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:197098436..197100309-chr1:197101264..197103559,2	K562	blood:
2	chr1:197098436..197100309-chr1:197101264..197103559,2	K562	blood:
3	chr1:197086007..197087668-chr1:197097835..197099382,2	K562	blood:
4	chr1:197063964..197065535-chr1:197110090..197112434,2	K562	blood:
5	chr1:197090506..197092545-chr1:197093003..197095180,2	MCF-7	breast:
6	chr1:197093674..197095835-chr1:197097163..197099418,3	K562	blood:
7	chr1:197068919..197071341-chr1:197120763..197122532,2	K562	blood:
8	chr1:197083131..197085209-chr1:197097769..197099515,2	K562	blood:
9	chr1:197075217..197076795-chr1:197101256..197102905,2	K562	blood:
10	chr1:197086007..197089050-chr1:197097882..197101609,3	K562	blood:
11	chr1:197075415..197078387-chr1:197103819..197106746,2	K562	blood:
12	chr1:197090506..197092545-chr1:197093003..197095180,2	MCF-7	breast:
13	chr1:197083131..197085209-chr1:197097769..197099515,2	K562	blood:
14	chr1:197082888..197084637-chr1:197110135..197112878,2	K562	blood:
15	chr1:197057862..197060422-chr16:85387668..85389752,2	MCF-7	breast:
16	chr1:197073799..197075979-chr1:197077836..197079355,2	K562	blood:
17	chr1:197090849..197092576-chr1:197169357..197171640,2	K562	blood:
18	chr1:197086007..197087668-chr1:197097835..197099382,2	K562	blood:
19	chr1:197086007..197089050-chr1:197097882..197101609,3	K562	blood:
20	chr1:197093048..197099045-chr1:197107378..197117076,12	K562	blood:
21	chr1:197075217..197076795-chr1:197101256..197102905,2	K562	blood:
22	chr1:197092500..197094237-chr1:197110834..197113696,2	K562	blood:
23	chr1:197108980..197111975-chr1:197160260..197161833,2	K562	blood:
24	chr1:197071674..197075370-chr1:197103633..197105995,3	K562	blood:
25	chr1:197102908..197105277-chr1:197113696..197116665,2	MCF-7	breast:
26	chr1:196993317..196995109-chr1:197057738..197060458,2	K562	blood:
27	chr1:197055379..197060712-chr1:197061077..197065456,6	K562	blood:
28	chr1:197055911..197057601-chr1:197071905..197074191,2	K562	blood:
29	chr1:197088400..197091064-chr1:197110423..197113146,2	K562	blood:
30	chr1:197096123..197098122-chr1:197113804..197115489,2	K562	blood:
31	chr1:197089752..197091362-chr1:197102516..197104850,2	K562	blood:
32	chr1:197093674..197095835-chr1:197097163..197099418,3	K562	blood:
33	chr1:197073799..197075979-chr1:197077836..197079355,2	K562	blood:
34	chr1:197094788..197098380-chr1:197102598..197105893,5	K562	blood:
35	chr1:197100050..197103962-chr1:197110434..197115621,7	K562	blood:
36	chr1:197056210..197058041-chr1:197063459..197065342,2	K562	blood:
37	chr1:197086992..197089260-chr1:197103012..197104578,2	K562	blood:
38	chr1:196988548..196990975-chr1:197072466..197074203,2	K562	blood:
39	chr1:197080735..197084388-chr1:197109840..197112878,3	K562	blood:
40	chr1:197056210..197058041-chr1:197063459..197065342,2	K562	blood:
41	chr1:197095850..197097444-chr1:197103656..197105716,2	K562	blood:
42	chr1:197055379..197060712-chr1:197061077..197065456,6	K562	blood:
43	chr1:197055911..197057601-chr1:197071905..197074191,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASPM-1	chr1:197062778-197062807	l_160_chr1:197043319-197062807_placenta
2	lnc-ZBTB41-2	chr1:197107878-197108437	NONHSAT008613
3	lnc-ASPM-1	chr1:197062778-197062968	NONHSAT008611

No data

Variant related genes	Relation type
ENSG00000235748	TF binding region
ASPM	TF binding region
ENSG00000235748	CpG island
ASPM	CpG island
ENSG00000134376	chromatin interactions
ENSG00000066279	chromatin interactions
ENSG00000177888	chromatin interactions
ENSG00000235748	chromatin interactions

Extended variants
information (count: 2252 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2252 , 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	rs10754213	chr1:197055925-197055926	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs368843607	chr1:197055928-197055929	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376500383	chr1:197055932-197055933	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140231146	chr1:197055934-197055935	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs137887134	chr1:197055976-197055977	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370856504	chr1:197055980-197055981	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555541926	chr1:197055981-197055982	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201191528	chr1:197056003-197056004	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565430593	chr1:197056044-197056045	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372574057	chr1:197056071-197056072	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376905328	chr1:197056072-197056073	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200083138	chr1:197056087-197056088	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370380433	chr1:197056099-197056100	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141402675	chr1:197056109-197056110	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368313435	chr1:197056136-197056137	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs149864217	chr1:197056175-197056176	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546054669	chr1:197056207-197056208	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564253652	chr1:197056243-197056244	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145454968	chr1:197056259-197056260	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs180769803	chr1:197056307-197056308	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561580294	chr1:197056319-197056320	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528930192	chr1:197056359-197056360	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550296007	chr1:197056363-197056364	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569566079	chr1:197056408-197056409	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112882154	chr1:197056463-197056464	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551628878	chr1:197056485-197056486	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532787122	chr1:197056486-197056487	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143472412	chr1:197056532-197056533	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186494710	chr1:197056578-197056579	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192236248	chr1:197056605-197056606	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs71675127	chr1:197056662-197056663	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs199537982	chr1:197056675-197056676	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567654456	chr1:197056678-197056679	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538280753	chr1:197056689-197056690	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529643079	chr1:197056763-197056764	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556268581	chr1:197056764-197056765	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575638807	chr1:197056768-197056769	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs71631881	chr1:197056778-197056779	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183620702	chr1:197056860-197056861	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188614785	chr1:197056905-197056906	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191411994	chr1:197056948-197056949	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138033028	chr1:197056949-197056950	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553896882	chr1:197056997-197056998	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561861857	chr1:197057066-197057067	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371311147	chr1:197057072-197057073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538763468	chr1:197057079-197057080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183282274	chr1:197057172-197057173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562164221	chr1:197057202-197057203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75268113	chr1:197057242-197057243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551665275	chr1:197057247-197057248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20962326	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:892 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:197050400-197065600	Weak transcription	Stomach Mucosa	stomach
2	chr1:197050600-197059600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr1:197050600-197064400	Weak transcription	Fetal Heart	heart
4	chr1:197050800-197057200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:197051400-197063000	Strong transcription	HUVEC	blood vessel
6	chr1:197051400-197069600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr1:197051600-197057000	Strong transcription	Fetal Muscle Trunk	muscle
8	chr1:197051600-197057200	Strong transcription	NHDF-Ad	bronchial
9	chr1:197051600-197065600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:197051600-197066200	Strong transcription	Hela-S3	cervix
11	chr1:197051800-197057000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr1:197051800-197061000	Strong transcription	Osteobl	bone
13	chr1:197051800-197069800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr1:197052000-197062000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr1:197052000-197064200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:197052200-197057000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
17	chr1:197052200-197057000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr1:197052200-197058000	Strong transcription	H1 Cell Line	embryonic stem cell
19	chr1:197052200-197061400	Strong transcription	Primary neutrophils fromperipheralblood	blood
20	chr1:197052200-197062200	Weak transcription	Fetal Intestine Small	intestine
21	chr1:197052200-197063200	Strong transcription	Primary hematopoietic stem cells	blood
22	chr1:197052200-197063600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr1:197052200-197064600	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr1:197052200-197065400	Weak transcription	Duodenum Mucosa	Duodenum
25	chr1:197052200-197065400	Weak transcription	Fetal Brain Female	brain
26	chr1:197052200-197074400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr1:197052200-197076200	Weak transcription	NHLF	lung
28	chr1:197052200-197083600	Weak transcription	Fetal Stomach	stomach
29	chr1:197052200-197106600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr1:197052200-197114200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr1:197052400-197057800	Strong transcription	Cortex derived primary cultured neurospheres	brain
32	chr1:197052400-197063000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr1:197052400-197063000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr1:197052400-197063200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:197052400-197065400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr1:197052400-197068800	Weak transcription	Primary T cells from cord blood	blood
37	chr1:197052400-197069200	Strong transcription	Fetal Thymus	thymus
38	chr1:197052600-197068600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr1:197052800-197063000	Strong transcription	A549	lung
40	chr1:197052800-197063200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:197052800-197067000	Strong transcription	HUES6 Cell Line	embryonic stem cell
42	chr1:197053000-197060800	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr1:197053000-197064800	Strong transcription	K562	blood
44	chr1:197053000-197066800	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr1:197053000-197067000	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr1:197053800-197060400	Strong transcription	Fetal Lung	lung
47	chr1:197054000-197059400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr1:197054000-197071200	Weak transcription	Brain Germinal Matrix	brain
49	chr1:197054200-197063600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr1:197054200-197066600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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