Variant report

Variant	nsv898394
Chromosome Location	chr11:113298339-113341391
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:113318698-113319075	K562	blood:	n/a	n/a
2	BATF	chr11:113316940-113317222	GM12878	blood:	n/a	chr11:113317033-113317043 chr11:113317036-113317047
3	BATF	chr11:113310486-113310745	GM12878	blood:	n/a	chr11:113310619-113310630
4	BATF	chr11:113310411-113310851	GM12878	blood:	n/a	chr11:113310619-113310630
5	BATF	chr11:113316916-113317242	GM12878	blood:	n/a	chr11:113317033-113317043 chr11:113317036-113317047
6	BCL11A	chr11:113310489-113310723	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:113333705-113333805	K562	blood:	n/a	chr11:113333748-113333757 chr11:113333746-113333759 chr11:113333748-113333757 chr11:113333747-113333756
8	BHLHE40	chr11:113318815-113318900	K562	blood:	n/a	n/a
9	CEBPB	chr11:113324492-113324660	HepG2	liver:	n/a	chr11:113324606-113324619 chr11:113324607-113324618 chr11:113324606-113324617
10	CEBPD	chr11:113300181-113300520	K562	blood:	n/a	n/a
11	CHD1	chr11:113326915-113326996	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr11:113341120-113341270	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr11:113307660-113307810	SK-N-SH_RA	brain:	n/a	chr11:113307764-113307782 chr11:113307767-113307775 chr11:113307767-113307780
14	CTCF	chr11:113329584-113329647	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr11:113307734-113307908	GM12878	blood:	n/a	chr11:113307764-113307782 chr11:113307767-113307775 chr11:113307767-113307780
16	CTCF	chr11:113307660-113307810	WERI-Rb-1	eye:	n/a	chr11:113307764-113307782 chr11:113307767-113307775 chr11:113307767-113307780
17	CTCF	chr11:113341120-113341270	BE2_C	brain:	n/a	n/a
18	CTCF	chr11:113328440-113328590	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr11:113307640-113307790	GM12871	blood:	n/a	chr11:113307764-113307782 chr11:113307767-113307775 chr11:113307767-113307780
20	CTCF	chr11:113307680-113307830	SK-N-SH_RA	brain:	n/a	chr11:113307764-113307782 chr11:113307767-113307775 chr11:113307767-113307780
21	CTCF	chr11:113307800-113307803	K562	blood:	n/a	n/a
22	CTCF	chr11:113330932-113330959	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr11:113307739-113307791	GM19239	blood:	n/a	chr11:113307764-113307782 chr11:113307767-113307775 chr11:113307767-113307780
24	CTCF	chr11:113307680-113307830	GM12873	blood:	n/a	chr11:113307764-113307782 chr11:113307767-113307775 chr11:113307767-113307780
25	CTCF	chr11:113307800-113307950	GM12873	blood:	n/a	n/a
26	CTCF	chr11:113341140-113341290	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr11:113307680-113307830	Caco-2	colon:	n/a	chr11:113307764-113307782 chr11:113307767-113307775 chr11:113307767-113307780
28	CTCF	chr11:113307740-113307890	Caco-2	colon:	n/a	chr11:113307764-113307782 chr11:113307767-113307775 chr11:113307767-113307780
29	CTCF	chr11:113307660-113307810	BE2_C	brain:	n/a	chr11:113307764-113307782 chr11:113307767-113307775 chr11:113307767-113307780
30	CTCF	chr11:113307729-113307816	GM12892	blood:	n/a	chr11:113307764-113307782 chr11:113307767-113307775 chr11:113307767-113307780
31	CTCF	chr11:113307740-113307890	HEK293	kidney:	n/a	chr11:113307764-113307782 chr11:113307767-113307775 chr11:113307767-113307780
32	CTCF	chr11:113307680-113307830	K562	blood:	n/a	chr11:113307764-113307782 chr11:113307767-113307775 chr11:113307767-113307780
33	CTCF	chr11:113307700-113307850	BE2_C	brain:	n/a	chr11:113307764-113307782 chr11:113307767-113307775 chr11:113307767-113307780
34	CTCF	chr11:113307700-113307850	HBMEC	blood vessel:	n/a	chr11:113307764-113307782 chr11:113307767-113307775 chr11:113307767-113307780
35	CTCF	chr11:113341220-113341370	BE2_C	brain:	n/a	n/a
36	CTCF	chr11:113329600-113329750	HEK293	kidney:	n/a	n/a
37	CTCF	chr11:113307728-113307799	K562	blood:	n/a	chr11:113307764-113307782 chr11:113307767-113307775 chr11:113307767-113307780
38	E2F4	chr11:113317867-113318032	MCF10A-Er-Src	breast:	n/a	chr11:113317887-113317897
39	E2F4	chr11:113317016-113317244	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr11:113337925-113337945	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr11:113326849-113327140	MCF10A-Er-Src	breast:	n/a	n/a
42	EGR1	chr11:113334193-113334447	K562	blood:	n/a	chr11:113334369-113334380 chr11:113334371-113334380 chr11:113334371-113334381 chr11:113334367-113334382 chr11:113334368-113334381 chr11:113334370-113334380 chr11:113334368-113334381 chr11:113334370-113334380 chr11:113334368-113334381 chr11:113334368-113334381 chr11:113334373-113334383 chr11:113334368-113334382
43	EGR1	chr11:113334233-113334439	K562	blood:	n/a	chr11:113334369-113334380 chr11:113334371-113334380 chr11:113334371-113334381 chr11:113334367-113334382 chr11:113334368-113334381 chr11:113334370-113334380 chr11:113334368-113334381 chr11:113334370-113334380 chr11:113334368-113334381 chr11:113334368-113334381 chr11:113334373-113334383 chr11:113334368-113334382
44	EGR1	chr11:113320470-113320672	K562	blood:	n/a	chr11:113320597-113320610
45	ELF1	chr11:113318730-113318988	K562	blood:	n/a	n/a
46	EP300	chr11:113318805-113318943	K562	blood:	n/a	chr11:113318858-113318871
47	EP300	chr11:113300250-113300347	K562	blood:	n/a	n/a
48	FOS	chr11:113339595-113339602	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr11:113310512-113310715	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr11:113300548-113300793	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:113329026-113329076	AG04450	lung:	fetal
2	chr11:113329026-113329076	NB4	blood:	n/a
3	chr11:113329026-113329076	AG09309	skin:	n/a
4	chr11:113329026-113329076	HRCEpiC	kidney:	n/a
5	chr11:113329026-113329076	K562	blood:	n/a
6	chr11:113329026-113329076	ProgFib	skin:	n/a
7	chr11:113329026-113329076	SAEC	small airway:	n/a
8	chr11:113329026-113329076	T-47D	breast:	n/a
9	chr11:113329026-113329076	LNCaP	prostate:	n/a
10	chr11:113329026-113329076	HL-60	blood:	n/a
11	chr11:113329026-113329076	HEEpiC	esophagus:	n/a
12	chr11:113329026-113329076	NT2-D1	testis:	n/a
13	chr11:113329026-113329076	HAEpiC	amniotic membrane:	n/a
14	chr11:113329026-113329076	HCM	heart:	n/a
15	chr11:113329026-113329076	GM12878	blood:	n/a
16	chr11:113329026-113329076	HUVEC	blood vessel:	n/a
17	chr11:113329026-113329076	Caco-2	colon:	n/a
18	chr11:113329026-113329076	HNPCEpiC	eye:	n/a
19	chr11:113329026-113329076	SK-N-MC	brain:	n/a
20	chr11:113329026-113329076	PrEC	prostate:	n/a
21	chr11:113329026-113329076	SK-N-SH	brain:	n/a
22	chr11:113329026-113329076	HMEC	breast:	n/a
23	chr11:113329026-113329076	ovcar-3	ovarian:	n/a
24	chr11:113329026-113329076	HIPEpiC	eye:	n/a
25	chr11:113329026-113329076	AoSMC	blood vessel:	n/a
26	chr11:113329026-113329076	NHBE	bronchial:	n/a
27	chr11:113329026-113329076	NHDF-neo	bronchial:	n/a
28	chr11:113329026-113329076	AG04449	skin:	fetal
29	chr11:113329026-113329076	HCF	heart:	n/a
30	chr11:113329026-113329076	SKMC	muscle:	n/a
31	chr11:113329026-113329076	ECC-1	luminal epithelium:	n/a
32	chr11:113329026-113329076	HCT-116	colon:	n/a
33	chr11:113329026-113329076	Hepatocyte	liver:	n/a
34	chr11:113329026-113329076	H1-hESC	embryonic stem cell:	embryo
35	chr11:113329026-113329076	Jurkat	blood:	n/a
36	chr11:113329026-113329076	GM12892	blood:	n/a
37	chr11:113329026-113329076	CMK	blood:	n/a
38	chr11:113329026-113329076	HCPEpiC	choroid plexus:	n/a
39	chr11:113329026-113329076	BE2_C	brain:	n/a
40	chr11:113329026-113329076	U87	brain:	n/a
41	chr11:113329026-113329076	HepG2	liver:	n/a
42	chr11:113329026-113329076	A549	lung:	n/a
43	chr11:113329026-113329076	HPAEpiC	pulmonary alveolar:	n/a
44	chr11:113329026-113329076	PFSK-1	brain:	n/a
45	chr11:113329026-113329076	HRPEpiC	eye:	n/a
46	chr11:113329026-113329076	NH-A	brain:	n/a
47	chr11:113329026-113329076	MCF-7	breast:	n/a
48	chr11:113329026-113329076	PANC-1	pancreas:	n/a
49	chr11:113329026-113329076	GM12891	blood:	n/a
50	chr11:113329026-113329076	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:113325314..113328227-chr11:113331410..113333770,2	K562	blood:
2	chr11:113305667..113307415-chr11:113325184..113328085,2	K562	blood:
3	chr11:113299352..113300914-chr11:113306077..113308061,2	K562	blood:
4	chr11:113325314..113328227-chr11:113331410..113333770,2	K562	blood:
5	chr11:113257045..113259527-chr11:113302176..113303690,2	MCF-7	breast:
6	chr11:113299352..113300914-chr11:113306077..113308061,2	K562	blood:
7	chr11:113331579..113333762-chr11:113334872..113336624,2	K562	blood:
8	chr11:113338240..113340526-chr11:113343673..113346425,2	K562	blood:
9	chr11:113289401..113292081-chr11:113309563..113312385,2	K562	blood:
10	chr11:113334895..113337509-chr11:113366189..113367772,2	K562	blood:
11	chr11:113313898..113316743-chr11:113318799..113320535,2	K562	blood:
12	chr11:113305667..113307415-chr11:113325184..113328085,2	K562	blood:
13	chr11:113331579..113333762-chr11:113334872..113336624,2	K562	blood:
14	chr11:113334256..113337805-chr11:113341499..113343738,3	K562	blood:
15	chr11:113304576..113307222-chr11:113336806..113338535,2	MCF-7	breast:
16	chr11:113295023..113297766-chr11:113300499..113303337,2	K562	blood:
17	chr11:113341089..113342617-chr11:113343236..113346107,2	K562	blood:
18	chr11:113314007..113315614-chr11:113410459..113413373,2	K562	blood:
19	chr11:113293105..113295955-chr11:113297557..113300361,2	K562	blood:
20	chr11:113304576..113307222-chr11:113336806..113338535,2	MCF-7	breast:
21	chr11:113306892..113309143-chr11:113347013..113349045,2	K562	blood:
22	chr11:113312410..113314479-chr11:113316189..113318543,2	MCF-7	breast:
23	chr11:113313898..113316743-chr11:113318799..113320535,2	K562	blood:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4301	chr11:113320781-113320800	MIMAT0016850

Variant related genes	Relation type
DRD2	TF binding region
MIR4301	TF binding region
DRD2	CpG island
MIR4301	CpG island
ENSG00000149295	chromatin interactions
ENSG00000170209	chromatin interactions

Extended variants
information (count: 1571 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:1571 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2471857	chr11:113298339-113298340	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs117861690	chr11:113298386-113298387	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs530625985	chr11:113298448-113298449	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs111632069	chr11:113298496-113298497	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs570409704	chr11:113298513-113298514	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs561455856	chr11:113298530-113298531	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs539378098	chr11:113298566-113298567	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs141490076	chr11:113298600-113298601	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs566396522	chr11:113298627-113298628	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs535280402	chr11:113298650-113298651	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs555098310	chr11:113298680-113298681	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs530416151	chr11:113298682-113298683	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs146981961	chr11:113298726-113298727	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs550597572	chr11:113298788-113298789	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs369997267	chr11:113298819-113298820	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs372067076	chr11:113298857-113298858	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs138054337	chr11:113298868-113298869	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs557901075	chr11:113298885-113298886	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs577948753	chr11:113298923-113298924	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs540237401	chr11:113298933-113298934	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs560774660	chr11:113298957-113298958	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs149090837	chr11:113298983-113298984	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs192784945	chr11:113298992-113298993	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs12798900	chr11:113298996-113298997	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs530551517	chr11:113299068-113299069	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs12799083	chr11:113299070-113299071	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs369393580	chr11:113299082-113299083	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs34535530	chr11:113299117-113299118	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs79027564	chr11:113299125-113299126	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566435277	chr11:113299142-113299143	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs566230294	chr11:113299164-113299165	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs141125385	chr11:113299177-113299178	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs184415246	chr11:113299180-113299181	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs2471856	chr11:113299201-113299202	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs537983765	chr11:113299213-113299214	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs377472703	chr11:113299227-113299228	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs190527179	chr11:113299251-113299252	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs75349786	chr11:113299273-113299274	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs538838456	chr11:113299352-113299353	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs373038387	chr11:113299387-113299388	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs543324857	chr11:113299418-113299419	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs556506388	chr11:113299420-113299421	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs576597331	chr11:113299473-113299474	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs2471855	chr11:113299500-113299501	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs182146306	chr11:113299528-113299529	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs532844103	chr11:113299559-113299560	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539890447	chr11:113299560-113299561	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs559711882	chr11:113299564-113299565	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs556826991	chr11:113299589-113299590	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs568913427	chr11:113299596-113299597	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	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
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Urothelial carcinoma	21177765	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
Cancer	20164920	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Cancer	21129771	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
Neuroblastoma	20406844	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Mantle cell lymphoma	19029149	CNVD
Squamous cell cancer	19047905	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Multiple myeloma	16616336	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	21385341	CNVD
Hepatocellular carcinoma	16750200	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:222 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:113278600-113300200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr11:113298200-113301800	Weak transcription	Right Atrium	heart
3	chr11:113299000-113299400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr11:113299800-113300600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:113300200-113301200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr11:113300200-113301200	Enhancers	NHEK	skin
7	chr11:113300200-113307000	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr11:113300400-113301000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr11:113300400-113301200	Enhancers	HMEC	breast
10	chr11:113300400-113301400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr11:113300400-113301400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr11:113300600-113300800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr11:113300600-113301000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:113300800-113313200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr11:113301000-113304400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr11:113301200-113301400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr11:113301200-113304600	Weak transcription	HMEC	breast
18	chr11:113301400-113301600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr11:113302000-113302400	Enhancers	Fetal Stomach	stomach
20	chr11:113302600-113304000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr11:113302800-113303600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:113302800-113303800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr11:113303000-113303600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr11:113303000-113303600	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr11:113303000-113303600	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr11:113303000-113304000	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr11:113303200-113303600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr11:113303200-113303800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr11:113303200-113303800	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr11:113303400-113303600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr11:113303400-113303800	Enhancers	H9 Cell Line	embryonic stem cell
32	chr11:113303400-113304000	Enhancers	H1 Cell Line	embryonic stem cell
33	chr11:113303600-113303800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr11:113303600-113303800	Enhancers	Brain Anterior Caudate	brain
35	chr11:113303600-113304200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr11:113303800-113304600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:113304200-113305400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr11:113304400-113304600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr11:113304600-113304800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr11:113304600-113305000	Enhancers	HMEC	breast
41	chr11:113305000-113306400	Weak transcription	HMEC	breast
42	chr11:113305400-113306000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr11:113305600-113306800	Enhancers	Brain Anterior Caudate	brain
44	chr11:113305800-113307000	Enhancers	Ovary	ovary
45	chr11:113306200-113306600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr11:113306200-113307800	Enhancers	Adipose Nuclei	Adipose
47	chr11:113306400-113307200	Enhancers	HMEC	breast
48	chr11:113306600-113306800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr11:113306800-113307200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr11:113306800-113307800	Weak transcription	Brain Anterior Caudate	brain

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