Variant report

Variant	nsv898046
Chromosome Location	chr11:85180409-85300458
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:810)
CpG islands
(count:305)
Chromatin interactive
region (count:64)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:85194846-85195386	K562	blood:	n/a	n/a
2	ARID3A	chr11:85194849-85195394	HepG2	liver:	n/a	n/a
3	ATF1	chr11:85194845-85195356	K562	blood:	n/a	n/a
4	ATF2	chr11:85194922-85195282	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr11:85194862-85195290	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr11:85194913-85195295	GM12878	blood:	n/a	n/a
7	ATF3	chr11:85194862-85195351	A549	lung:	n/a	n/a
8	ATF3	chr11:85194944-85195261	HepG2	liver:	n/a	n/a
9	ATF3	chr11:85194963-85195250	K562	blood:	n/a	n/a
10	ATF3	chr11:85194934-85195312	K562	blood:	n/a	n/a
11	ATF3	chr11:85194909-85195394	A549	lung:	n/a	n/a
12	BACH1	chr11:85194841-85195358	K562	blood:	n/a	n/a
13	BCL11A	chr11:85194950-85195351	GM12878	blood:	n/a	n/a
14	BCL11A	chr11:85194942-85195269	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr11:85194954-85195284	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr11:85194895-85195358	A549	lung:	n/a	n/a
17	BCL3	chr11:85194883-85195274	K562	blood:	n/a	n/a
18	BCL3	chr11:85194898-85195403	A549	lung:	n/a	n/a
19	BCL3	chr11:85194858-85195272	GM12878	blood:	n/a	n/a
20	BCL3	chr11:85194945-85195256	K562	blood:	n/a	n/a
21	BCLAF1	chr11:85194905-85195306	GM12878	blood:	n/a	n/a
22	BCLAF1	chr11:85194857-85195305	K562	blood:	n/a	n/a
23	BCLAF1	chr11:85194896-85195401	K562	blood:	n/a	n/a
24	BCLAF1	chr11:85194932-85195302	GM12878	blood:	n/a	n/a
25	BHLHE40	chr11:85194841-85195394	K562	blood:	n/a	n/a
26	BHLHE40	chr11:85194906-85195256	HepG2	liver:	n/a	n/a
27	BRCA1	chr11:85194846-85195361	HepG2	liver:	n/a	n/a
28	BRCA1	chr11:85194838-85195396	GM12878	blood:	n/a	n/a
29	BRCA1	chr11:85284159-85284164	GM12878	blood:	n/a	n/a
30	BRCA1	chr11:85194843-85195389	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr11:85194935-85195248	K562	blood:	n/a	n/a
32	CBX3	chr11:85233281-85233544	K562	blood:	n/a	n/a
33	CCNT2	chr11:85194837-85195401	K562	blood:	n/a	n/a
34	CEBPB	chr11:85294764-85295064	IMR90	lung:	n/a	n/a
35	CEBPB	chr11:85194965-85195283	A549	lung:	n/a	n/a
36	CEBPB	chr11:85194846-85195392	K562	blood:	n/a	n/a
37	CEBPB	chr11:85194923-85195275	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:85194933-85195343	A549	lung:	n/a	n/a
39	CEBPB	chr11:85294754-85295048	HepG2	liver:	n/a	n/a
40	CEBPB	chr11:85185152-85185164	A549	lung:	n/a	n/a
41	CEBPB	chr11:85181841-85182182	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr11:85294763-85294963	A549	lung:	n/a	n/a
43	CEBPD	chr11:85194948-85195262	HepG2	liver:	n/a	n/a
44	CEBPD	chr11:85194945-85195305	K562	blood:	n/a	n/a
45	CEBPD	chr11:85194929-85195282	HepG2	liver:	n/a	n/a
46	CEBPD	chr11:85194950-85195320	K562	blood:	n/a	n/a
47	CHD1	chr11:85194841-85195391	GM12878	blood:	n/a	n/a
48	CHD2	chr11:85194840-85195405	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr11:85194839-85195395	K562	blood:	n/a	n/a
50	CHD2	chr11:85194841-85195395	HepG2	liver:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:85236929-85236979	LNCaP	prostate:	n/a
2	chr11:85236929-85236979	ECC-1	luminal epithelium:	n/a
3	chr11:85195094-85195144	ECC-1	luminal epithelium:	n/a
4	chr11:85195094-85195144	HEEpiC	esophagus:	n/a
5	chr11:85195094-85195144	ovcar-3	ovarian:	n/a
6	chr11:85195100-85195150	HRCEpiC	kidney:	n/a
7	chr11:85195094-85195144	MCF-7	breast:	n/a
8	chr11:85242554-85242604	GM19239	blood:	n/a
9	chr11:85195094-85195144	HIPEpiC	eye:	n/a
10	chr11:85242554-85242604	HCM	heart:	n/a
11	chr11:85236929-85236979	HCM	heart:	n/a
12	chr11:85242554-85242604	HCT-116	colon:	n/a
13	chr11:85236929-85236979	AG04449	skin:	fetal
14	chr11:85236929-85236979	HEEpiC	esophagus:	n/a
15	chr11:85195205-85195255	HCF	heart:	n/a
16	chr11:85195100-85195150	HNPCEpiC	eye:	n/a
17	chr11:85195205-85195255	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:85242554-85242604	PANC-1	pancreas:	n/a
19	chr11:85195100-85195150	U87	brain:	n/a
20	chr11:85236929-85236979	H1-hESC	embryonic stem cell:	embryo
21	chr11:85195094-85195144	GM06990	blood:	n/a
22	chr11:85242554-85242604	BJ	skin:	n/a
23	chr11:85195205-85195255	GM12878	blood:	n/a
24	chr11:85195205-85195255	A549	lung:	n/a
25	chr11:85195205-85195255	HUVEC	blood vessel:	n/a
26	chr11:85195100-85195150	MCF-7	breast:	n/a
27	chr11:85236929-85236979	SAEC	small airway:	n/a
28	chr11:85195205-85195255	IMR90	lung:	fetal
29	chr11:85195205-85195255	PrEC	prostate:	n/a
30	chr11:85195100-85195150	BJ	skin:	n/a
31	chr11:85195205-85195255	BE2_C	brain:	n/a
32	chr11:85195205-85195255	RPTEC	kidney:	n/a
33	chr11:85236929-85236979	BJ	skin:	n/a
34	chr11:85236929-85236979	HCT-116	colon:	n/a
35	chr11:85195205-85195255	PFSK-1	brain:	n/a
36	chr11:85242554-85242604	PFSK-1	brain:	n/a
37	chr11:85195205-85195255	HepG2	liver:	n/a
38	chr11:85195205-85195255	HRPEpiC	eye:	n/a
39	chr11:85195094-85195144	NT2-D1	testis:	n/a
40	chr11:85236929-85236979	SKMC	muscle:	n/a
41	chr11:85195094-85195144	GM12891	blood:	n/a
42	chr11:85236929-85236979	HRCEpiC	kidney:	n/a
43	chr11:85195094-85195144	NB4	blood:	n/a
44	chr11:85242554-85242604	HL-60	blood:	n/a
45	chr11:85195100-85195150	SK-N-SH	brain:	n/a
46	chr11:85195094-85195144	HRCEpiC	kidney:	n/a
47	chr11:85195205-85195255	CMK	blood:	n/a
48	chr11:85195205-85195255	PANC-1	pancreas:	n/a
49	chr11:85195094-85195144	HCT-116	colon:	n/a
50	chr11:85195094-85195144	PANC-1	pancreas:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:91851562..91854585-chr11:85195040..85196753,3	K562	blood:
2	chr11:85193664..85196579-chr19:24184471..24186975,3	MCF-7	breast:
3	chr11:85195169..85196687-chr19:24184953..24186982,2	MCF-7	breast:
4	chr1:206858043..206859563-chr11:85195223..85196734,2	K562	blood:
5	chr11:85193550..85196726-chr21:9824306..9828726,11	K562	blood:
6	chr11:85195109..85196717-chr16:33964349..33967903,4	K562	blood:
7	chr11:85194574..85195759-chr19:24184744..24186176,10	MCF-7	breast:
8	chr11:85283403..85286347-chr11:85339640..85342131,2	MCF-7	breast:
9	chr11:85195041..85196746-chr2:230044008..230046987,2	K562	blood:
10	chr11:85193576..85195251-chr17:33476660..33478297,7	MCF-7	breast:
11	chr11:85194519..85195599-chr17:33477658..33478328,13	MCF-7	breast:
12	chr11:85280987..85284444-chr11:85284671..85287173,3	MCF-7	breast:
13	chr11:85193587..85195104-chr4:187024539..187026040,2	K562	blood:
14	chr11:85195086..85195758-chr4:169753807..169754327,3	MCF-7	breast:
15	chr11:85194537..85195256-chr17:33477651..33478689,13	K562	blood:
16	chr11:85194634..85195770-chr21:9826689..9827668,3	MCF-7	breast:
17	chr10:24497863..24498383-chr11:85195069..85195755,2	MCF-7	breast:
18	chr11:85193624..85196703-chr2:133010749..133014388,3	K562	blood:
19	chr11:85194556..85195599-chr21:9825626..9826659,3	MCF-7	breast:
20	chr11:85193727..85196636-chr17:31148107..31149878,3	MCF-7	breast:
21	chr11:85195071..85195734-chr6:137143975..137144475,2	K562	blood:
22	chr11:85195106..85195725-chr16:33963665..33964258,2	MCF-7	breast:
23	chr11:85193511..85196736-chr17:33476657..33479798,16	K562	blood:
24	chr11:85194566..85195163-chr12:109181096..109181616,2	MCF-7	breast:
25	chr11:85299211..85301979-chr11:85303362..85305385,2	K562	blood:
26	chr11:85193566..85195120-chr16:33965483..33967840,2	MCF-7	breast:
27	chr11:85194679..85195667-chr19:24185002..24186153,3	MCF-7	breast:
28	chr11:85195036..85195776-chr2:71565795..71566299,2	MCF-7	breast:
29	chr11:85194707..85195726-chr19:24185012..24186176,4	MCF-7	breast:
30	chr1:156184765..156186541-chr11:85195122..85196659,2	K562	blood:
31	chr11:85193649..85195183-chrX:108296303..108299199,2	K562	blood:
32	chr11:85195239..85196758-chr17:31148351..31151120,3	K562	blood:
33	chr11:85195583..85198227-chr8:113682885..113684772,2	MCF-7	breast:
34	chr11:85193623..85195251-chr6:110677855..110679355,2	MCF-7	breast:
35	chr11:85195161..85196755-chr12:20702902..20704406,2	K562	blood:
36	chr11:85194535..85195243-chr17:33477642..33478335,12	MCF-7	breast:
37	chr11:85195015..85195732-chr21:9826213..9827241,3	MCF-7	breast:
38	chr11:85195049..85196754-chr19:24184306..24186751,3	K562	blood:
39	chr11:85193729..85196593-chr2:133010514..133013451,3	K562	blood:
40	chr11:85195062..85195778-chr6:144328873..144329374,2	HCT-116	colon:
41	chr11:85193525..85196750-chr20:26187839..26191543,6	K562	blood:
42	chr11:85193511..85196736-chr17:33476647..33479728,15	K562	blood:
43	chr11:85194519..85195708-chr17:33477647..33478310,15	MCF-7	breast:
44	chr11:85193597..85195196-chr17:33476655..33478347,10	MCF-7	breast:
45	chr11:85193511..85195081-chr16:33965594..33967907,2	MCF-7	breast:
46	chr11:84494003..84496842-chr11:85300062..85301679,2	MCF-7	breast:
47	chr11:85194541..85195128-chr16:33965453..33966369,3	MCF-7	breast:
48	chr1:156186383..156187035-chr11:85195090..85195711,2	MCF-7	breast:
49	chr11:85193537..85196743-chr16:33959805..33967587,15	K562	blood:
50	chr11:85193550..85196769-chr21:9824428..9828726,11	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CREBZF-1	chr11:85180382-85180766	NONHSAT023435
2	lnc-CREBZF-1	chr11:85236035-85236066	NONHSAT023435

No data

Variant related genes	Relation type
RNU6-1292P	TF binding region
DLG2	TF binding region
RNU6-1292P	CpG island
DLG2	CpG island
ENSG00000120549	chromatin interactions
ENSG00000256642	chromatin interactions
ENSG00000053328	chromatin interactions
ENSG00000226958	chromatin interactions
ENSG00000207986	chromatin interactions
ENSG00000162889	chromatin interactions
ENSG00000200434	chromatin interactions
ENSG00000171204	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000264462	chromatin interactions
ENSG00000109794	chromatin interactions
ENSG00000249609	chromatin interactions
ENSG00000202174	chromatin interactions
ENSG00000227195	chromatin interactions
ENSG00000201966	chromatin interactions

Extended variants
information (count: 5207 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5207 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55670704	chr11:85180409-85180410	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs570998617	chr11:85180437-85180438	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs367883934	chr11:85180515-85180516	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs538392077	chr11:85180517-85180518	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs553680424	chr11:85180565-85180566	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs565548713	chr11:85180616-85180617	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs75744851	chr11:85180650-85180651	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs538869040	chr11:85180657-85180658	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs553781404	chr11:85180698-85180699	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs77848294	chr11:85180709-85180710	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs118121257	chr11:85180725-85180726	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs73503527	chr11:85180732-85180733	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs147630507	chr11:85180752-85180753	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs142263204	chr11:85180753-85180754	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs536112359	chr11:85180754-85180755	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs560505823	chr11:85180758-85180759	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs572373867	chr11:85180762-85180763	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs543032704	chr11:85180788-85180789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542630835	chr11:85180886-85180887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561006906	chr11:85180926-85180927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs117753716	chr11:85180930-85180931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7118963	chr11:85180943-85180944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576178957	chr11:85181003-85181004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532036907	chr11:85181047-85181048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543546068	chr11:85181082-85181083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182376392	chr11:85181095-85181096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565642175	chr11:85181110-85181111	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs59818906	chr11:85181116-85181117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565031946	chr11:85181137-85181138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573058011	chr11:85181147-85181148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188707984	chr11:85181158-85181159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374861672	chr11:85181159-85181160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567958855	chr11:85181166-85181167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533121148	chr11:85181191-85181192	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538542904	chr11:85181197-85181198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556756811	chr11:85181201-85181202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113051824	chr11:85181256-85181257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77148502	chr11:85181257-85181258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539097737	chr11:85181295-85181296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201076582	chr11:85181297-85181298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553956177	chr11:85181320-85181321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs61907127	chr11:85181349-85181350	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs542644572	chr11:85181363-85181364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs7951307	chr11:85181382-85181383	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs141159606	chr11:85181415-85181416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150316224	chr11:85181430-85181431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564703020	chr11:85181438-85181439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185155754	chr11:85181445-85181446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547603608	chr11:85181502-85181503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7130354	chr11:85181528-85181529	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	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
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	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
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	20844748	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Colorectal cancer	16912164	CNVD
Mental retardation	17847001	CNVD
Melanoma	19509136	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Bipolar disorder	19114987	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ductal carcinoma	22052326	CNVD
Obesity	20622171	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Attention deficit hyperactivity disorder	22241247	CNVD
Breast cancer	21958427	CNVD

Chromatin state (count:542 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85171400-85182800	Weak transcription	Ovary	ovary
2	chr11:85180400-85181000	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr11:85180600-85180800	Enhancers	H9 Cell Line	embryonic stem cell
4	chr11:85180600-85181800	Enhancers	H1 Cell Line	embryonic stem cell
5	chr11:85180600-85181800	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr11:85180600-85181800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr11:85180600-85181800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr11:85180600-85182800	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr11:85180800-85183800	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr11:85181000-85181800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr11:85181000-85182200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr11:85181200-85181800	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr11:85181400-85182600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr11:85181400-85182800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr11:85181600-85181800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr11:85181800-85182000	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr11:85181800-85182200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr11:85181800-85182200	Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr11:85181800-85182400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
20	chr11:85181800-85182600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
21	chr11:85181800-85183200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr11:85181800-85194800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr11:85182000-85184400	Enhancers	H1 Cell Line	embryonic stem cell
24	chr11:85182200-85182600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr11:85182200-85182800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr11:85182200-85183400	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr11:85182400-85184200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr11:85182600-85183400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr11:85182600-85184200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr11:85182800-85183800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr11:85182800-85184200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
32	chr11:85183000-85184400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr11:85183200-85184400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr11:85183400-85183600	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr11:85183400-85183800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr11:85183600-85184400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
37	chr11:85183600-85184400	ZNF genes & repeats	Aorta	Aorta
38	chr11:85183800-85184000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr11:85183800-85184200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr11:85183800-85184200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
41	chr11:85183800-85184400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr11:85184000-85184200	Enhancers	Fetal Lung	lung
43	chr11:85184000-85184400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr11:85184000-85184400	ZNF genes & repeats	Pancreas	Pancrea
45	chr11:85184000-85194800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr11:85184200-85187000	Weak transcription	Fetal Lung	lung
47	chr11:85184200-85194800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr11:85184400-85192600	Weak transcription	Pancreas	Pancrea
49	chr11:85184400-85194800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr11:85184400-85194800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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