Variant report

Variant	nsv897910
Chromosome Location	chr11:72154529-72281884
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2080)
CpG islands
(count:428)
Chromatin interactive
region (count:72)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2080 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:72204817-72205763	K562	blood:	n/a	n/a
2	ARID3A	chr11:72157943-72158351	K562	blood:	n/a	n/a
3	ARID3A	chr11:72157941-72158357	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:72163674-72163874	K562	blood:	n/a	n/a
5	ARID3A	chr11:72193378-72193521	K562	blood:	n/a	n/a
6	ARID3A	chr11:72194675-72194697	K562	blood:	n/a	n/a
7	ATF1	chr11:72204892-72205204	K562	blood:	n/a	n/a
8	ATF1	chr11:72163609-72163837	K562	blood:	n/a	n/a
9	ATF1	chr11:72227396-72227445	K562	blood:	n/a	n/a
10	ATF1	chr11:72155913-72155914	K562	blood:	n/a	n/a
11	ATF1	chr11:72158067-72158243	K562	blood:	n/a	n/a
12	ATF3	chr11:72222446-72222794	K562	blood:	n/a	n/a
13	BACH1	chr11:72245661-72246557	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr11:72182317-72182696	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr11:72205148-72205487	K562	blood:	n/a	n/a
16	BACH1	chr11:72156523-72156824	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr11:72229728-72229764	K562	blood:	n/a	n/a
18	BACH1	chr11:72270887-72271158	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr11:72230773-72231082	GM12878	blood:	n/a	chr11:72230933-72230941
20	BATF	chr11:72230751-72231141	GM12878	blood:	n/a	chr11:72230933-72230941
21	BATF	chr11:72162989-72163369	GM12878	blood:	n/a	n/a
22	BATF	chr11:72163110-72163410	GM12878	blood:	n/a	n/a
23	BCL3	chr11:72255580-72256061	GM12878	blood:	n/a	n/a
24	BCL3	chr11:72234899-72235317	GM12878	blood:	n/a	n/a
25	BCL3	chr11:72255633-72256093	GM12878	blood:	n/a	n/a
26	BDP1	chr11:72247212-72247547	Hela-S3	cervix:	n/a	n/a
27	BHLHE40	chr11:72204870-72205190	K562	blood:	n/a	n/a
28	BHLHE40	chr11:72182457-72182658	A549	lung:	n/a	n/a
29	BHLHE40	chr11:72158069-72158517	K562	blood:	n/a	n/a
30	BHLHE40	chr11:72249437-72249634	K562	blood:	n/a	chr11:72249557-72249566 chr11:72249557-72249566 chr11:72249556-72249565
31	BHLHE40	chr11:72194738-72195100	K562	blood:	n/a	n/a
32	BHLHE40	chr11:72182371-72182681	K562	blood:	n/a	n/a
33	BHLHE40	chr11:72193407-72193584	K562	blood:	n/a	n/a
34	BHLHE40	chr11:72182397-72182696	GM12878	blood:	n/a	n/a
35	BRCA1	chr11:72202834-72203037	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr11:72183169-72184784	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr11:72245367-72246521	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr11:72259492-72259888	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr11:72280907-72283068	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr11:72222836-72223149	K562	blood:	n/a	n/a
41	CBX3	chr11:72222807-72223194	K562	blood:	n/a	n/a
42	CBX3	chr11:72264772-72265095	K562	blood:	n/a	n/a
43	CBX3	chr11:72204807-72205222	K562	blood:	n/a	n/a
44	CBX3	chr11:72212010-72212277	K562	blood:	n/a	n/a
45	CBX3	chr11:72211982-72212333	K562	blood:	n/a	n/a
46	CBX3	chr11:72222295-72222788	K562	blood:	n/a	n/a
47	CBX3	chr11:72222356-72222861	HCT-116	colon:	n/a	n/a
48	CCNT2	chr11:72204617-72205274	K562	blood:	n/a	chr11:72205107-72205127
49	CEBPB	chr11:72194912-72195018	HepG2	liver:	n/a	chr11:72194973-72194984
50	CEBPB	chr11:72194773-72195189	MCF-7	breast:	n/a	chr11:72194973-72194984

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:72237341-72237391	HUVEC	blood vessel:	n/a
2	chr11:72237341-72237391	HUVEC	blood vessel:	n/a
3	chr11:72280409-72280459	T-47D	breast:	n/a
4	chr11:72213993-72214043	H1-hESC	embryonic stem cell:	embryo
5	chr11:72246863-72246913	HCPEpiC	choroid plexus:	n/a
6	chr11:72214332-72214382	HPAEpiC	pulmonary alveolar:	n/a
7	chr11:72213993-72214043	HCF	heart:	n/a
8	chr11:72237341-72237391	GM19239	blood:	n/a
9	chr11:72182728-72182778	ovcar-3	ovarian:	n/a
10	chr11:72280409-72280459	PFSK-1	brain:	n/a
11	chr11:72214332-72214382	Hepatocyte	liver:	n/a
12	chr11:72281327-72281377	GM19239	blood:	n/a
13	chr11:72214332-72214382	SK-N-MC	brain:	n/a
14	chr11:72214332-72214382	HCF	heart:	n/a
15	chr11:72246863-72246913	HCT-116	colon:	n/a
16	chr11:72213993-72214043	HL-60	blood:	n/a
17	chr11:72237341-72237391	HL-60	blood:	n/a
18	chr11:72213993-72214043	SK-N-SH	brain:	n/a
19	chr11:72246863-72246913	NHBE	bronchial:	n/a
20	chr11:72237341-72237391	AG09319	gingival:	n/a
21	chr11:72246863-72246913	AG04450	lung:	fetal
22	chr11:72214332-72214382	CMK	blood:	n/a
23	chr11:72280409-72280459	IMR90	lung:	fetal
24	chr11:72182728-72182778	HL-60	blood:	n/a
25	chr11:72246863-72246913	HAEpiC	amniotic membrane:	n/a
26	chr11:72237341-72237391	SAEC	small airway:	n/a
27	chr11:72281327-72281377	NT2-D1	testis:	n/a
28	chr11:72280409-72280459	HepG2	liver:	n/a
29	chr11:72281327-72281377	ProgFib	skin:	n/a
30	chr11:72237341-72237391	HRE	kidney:	n/a
31	chr11:72214332-72214382	BJ	skin:	n/a
32	chr11:72280409-72280459	HL-60	blood:	n/a
33	chr11:72237341-72237391	IMR90	lung:	fetal
34	chr11:72246863-72246913	AG04449	skin:	fetal
35	chr11:72237341-72237391	AG04449	skin:	fetal
36	chr11:72280409-72280459	AG04449	skin:	fetal
37	chr11:72246863-72246913	SK-N-SH_RA	brain:	n/a
38	chr11:72237341-72237391	NHBE	bronchial:	n/a
39	chr11:72213993-72214043	K562	blood:	n/a
40	chr11:72182728-72182778	GM06990	blood:	n/a
41	chr11:72214332-72214382	MCF10A-Er-Src	breast:	n/a
42	chr11:72246863-72246913	U87	brain:	n/a
43	chr11:72214332-72214382	NB4	blood:	n/a
44	chr11:72213993-72214043	MCF-7	breast:	n/a
45	chr11:72237341-72237391	Hela-S3	cervix:	n/a
46	chr11:72213993-72214043	U87	brain:	n/a
47	chr11:72280409-72280459	A549	lung:	n/a
48	chr11:72182728-72182778	Hepatocyte	liver:	n/a
49	chr11:72280409-72280459	Jurkat	blood:	n/a
50	chr11:72182728-72182778	AG09309	skin:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:72246038..72248152-chr11:72252483..72254260,2	K562	blood:
2	chr11:72145271..72146910-chr11:72154563..72157956,3	MCF-7	breast:
3	chr11:72253701..72256576-chr11:72263470..72265138,2	MCF-7	breast:
4	chr11:72141748..72142617-chr11:72158017..72158572,2	MCF-7	breast:
5	chr11:72159747..72162636-chr11:72268105..72269694,2	K562	blood:
6	chr11:72157990..72159779-chr11:72162354..72164537,2	K562	blood:
7	chr11:72266439..72269266-chr11:72274057..72276635,2	K562	blood:
8	chr11:72228545..72231064-chr11:72236824..72239786,2	MCF-7	breast:
9	chr11:72193362..72195099-chr11:72256516..72259028,2	K562	blood:
10	chr11:71812827..71814983-chr11:72157130..72160023,3	MCF-7	breast:
11	chr11:72176161..72177730-chr11:72182280..72185148,2	MCF-7	breast:
12	chr11:72193156..72193932-chr11:72353772..72354286,2	K562	blood:
13	chr11:72182101..72182698-chr11:72264110..72265089,3	MCF-7	breast:
14	chr11:72223975..72225851-chr11:72235004..72237826,2	K562	blood:
15	chr11:72262899..72264765-chr11:72267921..72270295,2	MCF-7	breast:
16	chr11:72264900..72266912-chr11:72268181..72270017,2	MCF-7	breast:
17	chr11:72157990..72159779-chr11:72162354..72164537,2	K562	blood:
18	chr11:72193379..72193985-chr11:72264593..72265698,3	MCF-7	breast:
19	chr11:72193362..72195099-chr11:72256516..72259028,2	K562	blood:
20	chr11:72182044..72183015-chr11:72284099..72284984,4	K562	blood:
21	chr11:72193243..72193909-chr11:72319827..72320926,3	K562	blood:
22	chr11:72248824..72251874-chr11:72254465..72256611,3	K562	blood:
23	chr11:72193020..72194195-chr11:72264566..72265474,7	MCF-7	breast:
24	chr11:72182051..72183095-chr11:72284054..72285050,11	MCF-7	breast:
25	chr11:72220916..72223040-chr11:72228194..72229797,2	K562	blood:
26	chr11:72264900..72266912-chr11:72268181..72270017,2	MCF-7	breast:
27	chr11:72144772..72145877-chr11:72157260..72158587,8	MCF-7	breast:
28	chr11:72181031..72183647-chr11:72184728..72186447,2	K562	blood:
29	chr11:72246038..72248152-chr11:72252483..72254260,2	K562	blood:
30	chr11:72193284..72193993-chr11:72284096..72285030,3	K562	blood:
31	chr11:72192993..72193929-chr11:72284110..72285074,4	MCF-7	breast:
32	chr11:72168860..72170475-chr11:72364322..72366473,2	MCF-7	breast:
33	chr11:72250374..72253358-chr11:72254465..72256986,3	K562	blood:
34	chr11:72150565..72152924-chr11:72165968..72167789,2	K562	blood:
35	chr11:72248183..72250191-chr11:72262749..72265384,2	K562	blood:
36	chr11:72193379..72193985-chr11:72264593..72265698,3	MCF-7	breast:
37	chr11:72220916..72223040-chr11:72228194..72229797,2	K562	blood:
38	chr11:72266439..72269266-chr11:72274057..72276635,2	K562	blood:
39	chr11:72182259..72183014-chr11:72353467..72354664,3	MCF-7	breast:
40	chr11:72144882..72145842-chr11:72157717..72158559,5	MCF-7	breast:
41	chr11:72281234..72282064-chr13:111364772..111365743,2	Hela-S3	cervix:
42	chr11:72253701..72256576-chr11:72263470..72265138,2	MCF-7	breast:
43	chr11:72223975..72225851-chr11:72235004..72237826,2	K562	blood:
44	chr11:72233870..72236471-chr11:72306547..72308962,2	K562	blood:
45	chr11:72258665..72259621-chr20:52596884..52597756,2	MCF-7	breast:
46	chr11:72173490..72176344-chr11:72294292..72296426,2	K562	blood:
47	chr11:72182101..72182698-chr11:72264110..72265089,3	MCF-7	breast:
48	chr11:72150961..72153899-chr11:72155415..72157907,2	MCF-7	breast:
49	chr11:72138473..72140807-chr11:72156234..72158136,2	MCF-7	breast:
50	chr11:72193020..72194195-chr11:72264566..72265474,7	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDE2A-1	chr11:72239231-72239457	XLOC_009497
2	lnc-PDE2A-1	chr11:72245991-72246063	XLOC_009497
3	lnc-PDE2A-6	chr11:72246412-72246880	NONHSAT022775
4	lnc-PDE2A-6	chr11:72247176-72247305	NONHSAT022775
5	lnc-INPPL1-5	chr11:72189265-72189282	NONHSAT022772
6	lnc-PDE2A-6	chr11:72247176-72247188	FPKM1_group_4927_transcript_1
7	lnc-PDE2A-6	chr11:72246412-72246880	FPKM1_group_4927_transcript_1
8	lnc-ATG16L2-6	chr11:72281704-72281951	ENSG00000227467
9	lnc-INPPL1-6	chr11:72231986-72232777	NONHSAT022773
10	lnc-INPPL1-5	chr11:72189801-72190281	NONHSAT022772
11	lnc-INPPL1-6	chr11:72231030-72231059	NONHSAT022773

No data

Variant related genes	Relation type
ENSG00000237408	TF binding region
ENSG00000227467	TF binding region
ENSG00000238048	TF binding region
ENSG00000237408	CpG island
ENSG00000227467	CpG island
ENSG00000238048	CpG island
ENSG00000237408	chromatin interactions
ENSG00000255808	chromatin interactions
ENSG00000186642	chromatin interactions
ENSG00000149357	chromatin interactions
ENSG00000162129	chromatin interactions
ENSG00000227467	chromatin interactions
ENSG00000238048	chromatin interactions
ENSG00000256633	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000134905	chromatin interactions

Extended variants
information (count: 4509 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:4509 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7129167	chr11:72154529-72154530	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149668428	chr11:72154558-72154559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527857768	chr11:72154560-72154561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs150394505	chr11:72154585-72154586	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs540141664	chr11:72154604-72154605	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs559317967	chr11:72154644-72154645	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs555218272	chr11:72154658-72154659	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs566337862	chr11:72154677-72154678	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs111746272	chr11:72154730-72154731	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs558825363	chr11:72154732-72154733	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs138647398	chr11:72154802-72154803	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs73532646	chr11:72154810-72154811	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs76403159	chr11:72154861-72154862	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs574406198	chr11:72154905-72154906	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs565406940	chr11:72154933-72154934	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs141810819	chr11:72154976-72154977	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs368366672	chr11:72154987-72154988	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs371496529	chr11:72154992-72154993	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs552243555	chr11:72154995-72154996	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs189044885	chr11:72155001-72155002	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs535478535	chr11:72155045-72155046	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs530928711	chr11:72155091-72155092	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs12277254	chr11:72155137-72155138	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs549812651	chr11:72155198-72155199	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs146270501	chr11:72155240-72155241	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs536922199	chr11:72155287-72155288	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs548931687	chr11:72155322-72155323	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs567060697	chr11:72155339-72155340	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs556683990	chr11:72155365-72155366	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs192699374	chr11:72155387-72155388	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs551117912	chr11:72155388-72155389	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs558960090	chr11:72155463-72155464	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs59133090	chr11:72155511-72155512	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs543172157	chr11:72155545-72155546	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs533785300	chr11:72155581-72155582	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs577273896	chr11:72155677-72155678	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs138078109	chr11:72155768-72155769	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs556158574	chr11:72155769-72155770	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs568793321	chr11:72155781-72155782	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs574523270	chr11:72155782-72155783	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs541707872	chr11:72155791-72155792	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs142538004	chr11:72155808-72155809	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs143971181	chr11:72155815-72155816	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs7122350	chr11:72155852-72155853	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs184742434	chr11:72155881-72155882	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs564168329	chr11:72155891-72155892	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs148629016	chr11:72155905-72155906	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs71477727	chr11:72155965-72155966	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs547360077	chr11:72156034-72156035	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs142062464	chr11:72156076-72156077	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	19153074	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:810 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:72150400-72154800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr11:72150800-72158000	Weak transcription	Hela-S3	cervix
3	chr11:72153000-72156000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr11:72153200-72154600	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr11:72153200-72158400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr11:72153400-72158200	Weak transcription	K562	blood
7	chr11:72154400-72158200	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr11:72154600-72156200	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr11:72154800-72156200	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr11:72156000-72156400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr11:72156200-72156600	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr11:72156200-72156600	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr11:72156200-72156800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
14	chr11:72156400-72158400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr11:72156600-72158000	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr11:72156600-72158200	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr11:72158000-72158200	Enhancers	Hela-S3	cervix
18	chr11:72158000-72159200	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr11:72158200-72158600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr11:72158200-72158600	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr11:72158200-72158600	Flanking Active TSS	Hela-S3	cervix
22	chr11:72158200-72158600	Enhancers	K562	blood
23	chr11:72158200-72158800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
24	chr11:72158400-72158600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr11:72158400-72158600	Enhancers	HMEC	breast
26	chr11:72158400-72158800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr11:72158600-72159200	Enhancers	Hela-S3	cervix
28	chr11:72158800-72159200	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr11:72158800-72163400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr11:72159200-72160600	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr11:72160600-72161200	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
32	chr11:72162800-72163600	Enhancers	Brain Hippocampus Middle	brain
33	chr11:72163000-72164200	Enhancers	K562	blood
34	chr11:72163400-72163800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr11:72164200-72166000	Weak transcription	K562	blood
36	chr11:72166200-72166400	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr11:72166200-72166400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
38	chr11:72166200-72166400	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr11:72166200-72166400	Enhancers	K562	blood
40	chr11:72168400-72168600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr11:72170000-72170200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr11:72170000-72170400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr11:72174800-72175400	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr11:72175000-72175400	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr11:72175400-72175600	Flanking Active TSS	HSMM	muscle
46	chr11:72175600-72181800	Weak transcription	HSMM	muscle
47	chr11:72177400-72177600	Bivalent Enhancer	Fetal Muscle Leg	muscle
48	chr11:72177400-72177800	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr11:72179400-72179600	Bivalent Enhancer	Fetal Muscle Leg	muscle
50	chr11:72181000-72182800	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood

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