Variant report

Variant	nsv541179
Chromosome Location	chr11:119842515-119898368
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:679)
CpG islands
(count:490)
Chromatin interactive
region (count:28)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:679 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr11:119883865-119884317	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr11:119883955-119884284	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr11:119884035-119884235	K562	blood:	n/a	n/a
4	BRCA1	chr11:119887432-119887433	HepG2	liver:	n/a	n/a
5	BRCA1	chr11:119884084-119884362	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr11:119869053-119869350	HepG2	liver:	n/a	chr11:119869201-119869212
7	CEBPB	chr11:119884088-119884289	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr11:119886597-119886715	Hela-S3	cervix:	n/a	chr11:119886628-119886639 chr11:119886630-119886641 chr11:119886628-119886641
9	CEBPB	chr11:119842494-119842782	HepG2	liver:	n/a	chr11:119842611-119842622
10	CEBPB	chr11:119869183-119869254	H1-hESC	embryonic stem cell:	n/a	chr11:119869201-119869212
11	CEBPB	chr11:119886544-119886721	H1-hESC	embryonic stem cell:	n/a	chr11:119886628-119886639 chr11:119886630-119886641 chr11:119886628-119886641
12	CEBPB	chr11:119886477-119886822	HepG2	liver:	n/a	chr11:119886628-119886639 chr11:119886630-119886641 chr11:119886628-119886641
13	CEBPB	chr11:119886515-119886784	IMR90	lung:	n/a	chr11:119886628-119886639 chr11:119886630-119886641 chr11:119886628-119886641
14	CEBPB	chr11:119876410-119876514	HepG2	liver:	n/a	n/a
15	CEBPB	chr11:119886569-119886769	K562	blood:	n/a	chr11:119886628-119886639 chr11:119886630-119886641 chr11:119886628-119886641
16	CHD1	chr11:119873499-119873589	GM12878	blood:	n/a	n/a
17	CHD2	chr11:119883958-119884349	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr11:119854182-119854307	GM12878	blood:	n/a	n/a
19	CTCF	chr11:119870041-119870264	HepG2	liver:	n/a	n/a
20	CTCF	chr11:119870060-119870210	HVMF	connective:	n/a	n/a
21	CTCF	chr11:119884060-119884210	SAEC	small airway:	n/a	chr11:119884123-119884136
22	CTCF	chr11:119866600-119866750	SAEC	small airway:	n/a	chr11:119866665-119866674
23	CTCF	chr11:119884080-119884230	HMEC	breast:	n/a	chr11:119884123-119884136
24	CTCF	chr11:119888067-119888145	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr11:119854162-119854278	NHEK	skin:	n/a	n/a
26	CTCF	chr11:119870040-119870190	SAEC	small airway:	n/a	n/a
27	CTCF	chr11:119866614-119866716	MCF-7	breast:	n/a	chr11:119866665-119866674
28	CTCF	chr11:119864628-119864695	LNCaP	prostate:	n/a	chr11:119864634-119864647 chr11:119864632-119864650
29	CTCF	chr11:119864600-119864750	HCPEpiC	choroid plexus:	n/a	chr11:119864634-119864647 chr11:119864632-119864650
30	CTCF	chr11:119870109-119870186	A549	lung:	n/a	n/a
31	CTCF	chr11:119883968-119884279	MCF-7	breast:	n/a	chr11:119884123-119884136
32	CTCF	chr11:119884040-119884190	GM12874	blood:	n/a	chr11:119884123-119884136
33	CTCF	chr11:119854240-119854390	K562	blood:	n/a	n/a
34	CTCF	chr11:119864600-119864750	HEK293	kidney:	n/a	chr11:119864634-119864647 chr11:119864632-119864650
35	CTCF	chr11:119864580-119864730	WERI-Rb-1	eye:	n/a	chr11:119864634-119864647 chr11:119864632-119864650
36	CTCF	chr11:119870060-119870210	NHEK	skin:	n/a	n/a
37	CTCF	chr11:119883911-119884372	H1-hESC	embryonic stem cell:	n/a	chr11:119884123-119884136
38	CTCF	chr11:119854172-119854313	GM19240	blood:	n/a	n/a
39	CTCF	chr11:119862620-119862770	WERI-Rb-1	eye:	n/a	chr11:119862739-119862747
40	CTCF	chr11:119884060-119884210	RPTEC	kidney:	n/a	chr11:119884123-119884136
41	CTCF	chr11:119883936-119884311	K562	blood:	n/a	chr11:119884123-119884136
42	CTCF	chr11:119870112-119870209	MCF-7	breast:	n/a	n/a
43	CTCF	chr11:119869920-119870070	HCT-116	colon:	n/a	n/a
44	CTCF	chr11:119864600-119864750	K562	blood:	n/a	chr11:119864634-119864647 chr11:119864632-119864650
45	CTCF	chr11:119869972-119870322	K562	blood:	n/a	n/a
46	CTCF	chr11:119884100-119884250	Hela-S3	cervix:	n/a	chr11:119884123-119884136
47	CTCF	chr11:119854135-119854333	K562	blood:	n/a	n/a
48	CTCF	chr11:119884040-119884190	HepG2	liver:	n/a	chr11:119884123-119884136
49	CTCF	chr11:119884040-119884190	AG04449	skin:	n/a	chr11:119884123-119884136
50	CTCF	chr11:119864600-119864750	GM06990	blood:	n/a	chr11:119864634-119864647 chr11:119864632-119864650

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:119846564-119846614	HEEpiC	esophagus:	n/a
2	chr11:119881616-119881666	AG04449	skin:	fetal
3	chr11:119846564-119846614	HEEpiC	esophagus:	n/a
4	chr11:119881616-119881666	AG04449	skin:	fetal
5	chr11:119872718-119872768	SKMC	muscle:	n/a
6	chr11:119897708-119897758	NB4	blood:	n/a
7	chr11:119872718-119872768	SK-N-MC	brain:	n/a
8	chr11:119872718-119872768	HEK293	kidney:	embryo
9	chr11:119881616-119881666	BJ	skin:	n/a
10	chr11:119881616-119881666	HEK293	kidney:	embryo
11	chr11:119897708-119897758	HL-60	blood:	n/a
12	chr11:119887950-119888000	NHDF-neo	bronchial:	n/a
13	chr11:119862409-119862459	HUVEC	blood vessel:	n/a
14	chr11:119893672-119893722	CMK	blood:	n/a
15	chr11:119862409-119862459	SAEC	small airway:	n/a
16	chr11:119897638-119897688	HepG2	liver:	n/a
17	chr11:119897708-119897758	SAEC	small airway:	n/a
18	chr11:119893672-119893722	PFSK-1	brain:	n/a
19	chr11:119893672-119893722	HEK293	kidney:	embryo
20	chr11:119893672-119893722	ECC-1	luminal epithelium:	n/a
21	chr11:119846564-119846614	HIPEpiC	eye:	n/a
22	chr11:119862409-119862459	GM12878	blood:	n/a
23	chr11:119887950-119888000	HEEpiC	esophagus:	n/a
24	chr11:119862409-119862459	AG09309	skin:	n/a
25	chr11:119897708-119897758	HNPCEpiC	eye:	n/a
26	chr11:119862409-119862459	Hela-S3	cervix:	n/a
27	chr11:119897708-119897758	SK-N-SH_RA	brain:	n/a
28	chr11:119893672-119893722	ProgFib	skin:	n/a
29	chr11:119846564-119846614	T-47D	breast:	n/a
30	chr11:119887950-119888000	GM12892	blood:	n/a
31	chr11:119897638-119897688	AG04450	lung:	fetal
32	chr11:119881616-119881666	IMR90	lung:	fetal
33	chr11:119881616-119881666	AG09309	skin:	n/a
34	chr11:119897708-119897758	LNCaP	prostate:	n/a
35	chr11:119887950-119888000	NH-A	brain:	n/a
36	chr11:119881616-119881666	HCF	heart:	n/a
37	chr11:119846564-119846614	HRE	kidney:	n/a
38	chr11:119897638-119897688	HCPEpiC	choroid plexus:	n/a
39	chr11:119893672-119893722	HCM	heart:	n/a
40	chr11:119846564-119846614	Hepatocyte	liver:	n/a
41	chr11:119887950-119888000	SAEC	small airway:	n/a
42	chr11:119862409-119862459	T-47D	breast:	n/a
43	chr11:119887950-119888000	BJ	skin:	n/a
44	chr11:119887950-119888000	CMK	blood:	n/a
45	chr11:119897638-119897688	NH-A	brain:	n/a
46	chr11:119846564-119846614	AG10803	skin:	n/a
47	chr11:119881616-119881666	HCT-116	colon:	n/a
48	chr11:119887950-119888000	AG09319	gingival:	n/a
49	chr11:119887950-119888000	PFSK-1	brain:	n/a
50	chr11:119846564-119846614	HL-60	blood:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:119867354..119869206-chr11:119872754..119874804,2	K562	blood:
2	chr11:119599184..119600753-chr11:119861551..119864175,2	MCF-7	breast:
3	chr11:119886138..119888688-chr11:119891563..119894396,2	K562	blood:
4	chr11:119846486..119848999-chr11:119849174..119851937,3	K562	blood:
5	chr11:119853779..119856334-chr11:119866020..119869388,3	K562	blood:
6	chr11:119536949..119537719-chr11:119883693..119884201,2	MCF-7	breast:
7	chr11:119600000..119600710-chr11:119883945..119884504,2	MCF-7	breast:
8	chr11:119536835..119537469-chr11:119883617..119884436,2	MCF-7	breast:
9	chr11:119893105..119894802-chr11:119896511..119898254,2	K562	blood:
10	chr11:119881383..119883433-chr11:119886474..119889218,2	K562	blood:
11	chr11:119886138..119888688-chr11:119891563..119894396,2	K562	blood:
12	chr11:119847784..119851574-chr11:119854250..119856305,4	K562	blood:
13	chr11:119599746..119600613-chr11:119883658..119884285,2	MCF-7	breast:
14	chr11:119848644..119851574-chr11:119854250..119856097,2	K562	blood:
15	chr11:119883883..119884665-chr11:119978239..119979557,5	MCF-7	breast:
16	chr11:119853779..119856334-chr11:119866020..119869388,3	K562	blood:
17	chr11:119867354..119869206-chr11:119872754..119874804,2	K562	blood:
18	chr11:119880494..119882883-chr11:119885315..119887974,2	K562	blood:
19	chr11:119875923..119878520-chr11:119878673..119880916,2	K562	blood:
20	chr11:119855228..119858162-chr11:119871012..119872668,2	K562	blood:
21	chr11:119848644..119851574-chr11:119854250..119856097,2	K562	blood:
22	chr11:119846486..119848999-chr11:119849174..119851937,3	K562	blood:
23	chr11:119875923..119878520-chr11:119878673..119880916,2	K562	blood:
24	chr11:119855228..119858162-chr11:119871012..119872668,2	K562	blood:
25	chr11:119847784..119851574-chr11:119854250..119856305,4	K562	blood:
26	chr11:119893105..119894802-chr11:119896511..119898254,2	K562	blood:
27	chr11:119833649..119836146-chr11:119840215..119843105,2	MCF-7	breast:
28	chr11:119865550..119868461-chr11:119874925..119876802,2	K562	blood:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-831A10.1.1-1	chr11:119859300-119859513	NONHSAT024699
2	lnc-RP11-831A10.1.1-1	chr11:119858663-119858936	ENSG00000254863
3	lnc-RP11-831A10.1.1-1	chr11:119859473-119859610	ENSG00000254863
4	lnc-RP11-831A10.1.1-1	chr11:119865303-119865413	NONHSAT024698
5	lnc-RP11-831A10.1.1-1	chr11:119859300-119859543	ENSG00000254863
6	lnc-RP11-831A10.1.1-1	chr11:119859990-119860165	ENSG00000254863
7	lnc-RP11-831A10.1.1-2	chr11:119879313-119879808	ENSG00000255216.1
8	lnc-RP11-831A10.1.1-1	chr11:119858675-119858936	NONHSAT024699
9	lnc-RP11-831A10.1.1-1	chr11:119858675-119858936	NONHSAT024700
10	lnc-RP11-831A10.1.1-1	chr11:119859990-119860175	NONHSAT024699
11	lnc-RP11-831A10.1.1-1	chr11:119863386-119863425	XLOC_009578
12	lnc-RP11-831A10.1.1-1	chr11:119859300-119859589	NONHSAT024698
13	lnc-RP11-831A10.1.1-1	chr11:119860166-119860388	ENSG00000254863
14	lnc-RP11-831A10.1.1-1	chr11:119865303-119865400	XLOC_009578
15	lnc-RP11-831A10.1.1-1	chr11:119865303-119865411	XLOC_009578
16	lnc-RP11-831A10.1.1-1	chr11:119859990-119860134	NONHSAT024697
17	lnc-RP11-831A10.1.1-1	chr11:119865597-119865746	ENSG00000254863
18	lnc-RP11-831A10.1.1-1	chr11:119859889-119860165	XLOC_009578
19	lnc-RP11-831A10.1.1-1	chr11:119859297-119859589	XLOC_009578
20	lnc-RP11-831A10.1.1-2	chr11:119882802-119882867	ENSG00000255216.1
21	lnc-RP11-831A10.1.1-1	chr11:119858517-119859513	XLOC_009578
22	lnc-RP11-831A10.1.1-1	chr11:119858675-119858936	NONHSAT024698
23	lnc-RP11-831A10.1.1-1	chr11:119859300-119859513	NONHSAT024700
24	lnc-RP11-831A10.1.1-1	chr11:119859374-119859513	ENSG00000254863
25	lnc-RP11-831A10.1.1-1	chr11:119858675-119858936	NONHSAT024697
26	lnc-RP11-831A10.1.1-1	chr11:119859300-119859589	NONHSAT024697
27	lnc-RP11-831A10.1.1-1	chr11:119865303-119865413	NONHSAT024700
28	lnc-RP11-831A10.1.1-1	chr11:119865303-119865418	ENSG00000254863
29	lnc-RP11-831A10.1.1-1	chr11:119861913-119862015	NONHSAT024697

No data

Variant related genes	Relation type
ENSG00000255216	TF binding region
ENSG00000254863	TF binding region
ENSG00000255216	CpG island
ENSG00000254863	CpG island
ENSG00000254863	chromatin interactions
ENSG00000255216	chromatin interactions
ENSG00000110400	chromatin interactions
ENSG00000254854	chromatin interactions
MITF	miRNA target sites

Extended variants
information (count: 2370 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:2370 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116893335	chr11:119842560-119842561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145521353	chr11:119842561-119842562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570166311	chr11:119842602-119842603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567190929	chr11:119842604-119842605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138815394	chr11:119842651-119842652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549126535	chr11:119842697-119842698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs17123506	chr11:119842708-119842709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs535035131	chr11:119842730-119842731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551890956	chr11:119842741-119842742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571787719	chr11:119842773-119842774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7944850	chr11:119842786-119842787	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs552554398	chr11:119842798-119842799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189388070	chr11:119842828-119842829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140470986	chr11:119842829-119842830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539661124	chr11:119842833-119842834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555100891	chr11:119842863-119842864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573580693	chr11:119842909-119842910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182064281	chr11:119843004-119843005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185724248	chr11:119843023-119843024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145634773	chr11:119843042-119843043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114983350	chr11:119843054-119843055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563438479	chr11:119843107-119843108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531062656	chr11:119843149-119843150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549435983	chr11:119843154-119843155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561171320	chr11:119843156-119843157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528476518	chr11:119843200-119843201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs60316181	chr11:119843202-119843203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1944504	chr11:119843219-119843220	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs538915095	chr11:119843220-119843221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148126866	chr11:119843259-119843260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570522400	chr11:119843263-119843264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536794399	chr11:119843278-119843279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544935106	chr11:119843301-119843302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563119454	chr11:119843313-119843314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141881258	chr11:119843319-119843320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534618250	chr11:119843351-119843352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537929270	chr11:119843358-119843359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150676180	chr11:119843373-119843374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs578010693	chr11:119843384-119843385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111261083	chr11:119843438-119843439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563505466	chr11:119843456-119843457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574083450	chr11:119843466-119843467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544587238	chr11:119843469-119843470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542793902	chr11:119843483-119843484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542744924	chr11:119843488-119843489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561442760	chr11:119843503-119843504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368868406	chr11:119843507-119843508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138874317	chr11:119843587-119843588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190436899	chr11:119843626-119843627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143340152	chr11:119843645-119843646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Emanuel syndrome	21549014	CNVD
Emanuel syndrome	18184694	CNVD
Non-syndromic sensorineural hearing loss	18184694	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Ovarian neoplasms	16753589	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Retinoblastoma	22278416	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-syndromic sensorineural hearing loss	16829213	CNVD
Non-syndromic sensorineural hearing loss	16760666	CNVD
Squamous cell cancer	20885788	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Neurocytoma	17123091	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Central neurocytomas	17123091	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Acute myeloid leukemia	19651601	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	20409316	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	22543975	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21509527	CNVD
Ductal carcinoma	22052326	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:598 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119836200-119845600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:119837400-119844200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr11:119841600-119844400	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr11:119841600-119844400	Weak transcription	Brain Substantia Nigra	brain
5	chr11:119841600-119845600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr11:119841800-119844400	Weak transcription	Brain Angular Gyrus	brain
7	chr11:119841800-119844400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr11:119841800-119844400	Weak transcription	Brain Hippocampus Middle	brain
9	chr11:119842000-119844600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:119842200-119844400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr11:119842200-119844400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr11:119844200-119846200	Enhancers	Fetal Muscle Trunk	muscle
13	chr11:119844200-119847800	Enhancers	Fetal Muscle Leg	muscle
14	chr11:119844200-119849600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr11:119844400-119844800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:119844400-119844800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
17	chr11:119844400-119846000	Enhancers	Brain Anterior Caudate	brain
18	chr11:119844400-119846200	Enhancers	Brain Cingulate Gyrus	brain
19	chr11:119844400-119846200	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr11:119844400-119846400	Enhancers	Brain Angular Gyrus	brain
21	chr11:119844400-119846600	Enhancers	Brain Hippocampus Middle	brain
22	chr11:119844400-119846600	Enhancers	Brain Substantia Nigra	brain
23	chr11:119844400-119847000	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr11:119844400-119847000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr11:119844400-119847200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr11:119844600-119844800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr11:119844600-119846000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr11:119844600-119846200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr11:119844600-119846800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr11:119844600-119846800	Enhancers	Adipose Nuclei	Adipose
31	chr11:119844600-119847200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr11:119844600-119847400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr11:119844800-119845200	Enhancers	Psoas Muscle	Psoas
34	chr11:119844800-119845800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr11:119844800-119846200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr11:119845200-119845400	Enhancers	Fetal Brain Female	brain
37	chr11:119845200-119846200	Enhancers	Fetal Stomach	stomach
38	chr11:119845200-119846200	Weak transcription	Right Atrium	heart
39	chr11:119845200-119846400	Weak transcription	Psoas Muscle	Psoas
40	chr11:119845200-119847200	Enhancers	Fetal Brain Male	brain
41	chr11:119845200-119847800	Enhancers	Brain Germinal Matrix	brain
42	chr11:119845400-119846000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
43	chr11:119845400-119846400	Weak transcription	Fetal Brain Female	brain
44	chr11:119845400-119846800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
45	chr11:119845600-119847000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:119845600-119847000	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr11:119845600-119847000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
48	chr11:119845600-119847200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
49	chr11:119845600-119847800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr11:119845800-119846000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell

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