Variant report

Variant	esv3478707
Chromosome Location	chr11:74782633-74842791
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:811)
CpG islands
(count:489)
Chromatin interactive
region (count:49)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:811 , 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	chr11:74812912-74813525	K562	blood:	n/a	n/a
2	ARID3A	chr11:74814299-74815109	K562	blood:	n/a	n/a
3	ARID3A	chr11:74807950-74808543	K562	blood:	n/a	n/a
4	ARID3A	chr11:74797336-74797572	K562	blood:	n/a	n/a
5	ARID3A	chr11:74797976-74798342	K562	blood:	n/a	n/a
6	ARID3A	chr11:74798550-74799308	K562	blood:	n/a	n/a
7	ARID3A	chr11:74816411-74816752	K562	blood:	n/a	n/a
8	ATF1	chr11:74811380-74811717	K562	blood:	n/a	n/a
9	ATF1	chr11:74807827-74808247	K562	blood:	n/a	n/a
10	ATF1	chr11:74814433-74814973	K562	blood:	n/a	n/a
11	ATF2	chr11:74814570-74814866	GM12878	blood:	n/a	n/a
12	ATF3	chr11:74814412-74815106	K562	blood:	n/a	n/a
13	ATF3	chr11:74816345-74816730	K562	blood:	n/a	n/a
14	ATF3	chr11:74789276-74789456	K562	blood:	n/a	n/a
15	ATF3	chr11:74811290-74811675	K562	blood:	n/a	n/a
16	BACH1	chr11:74814608-74814808	K562	blood:	n/a	chr11:74814692-74814706
17	BACH1	chr11:74811044-74811657	K562	blood:	n/a	n/a
18	BACH1	chr11:74824475-74824605	K562	blood:	n/a	n/a
19	BACH1	chr11:74816387-74816824	K562	blood:	n/a	n/a
20	BACH1	chr11:74807850-74808373	K562	blood:	n/a	n/a
21	BATF	chr11:74814549-74814814	GM12878	blood:	n/a	chr11:74814691-74814702
22	BATF	chr11:74811327-74811691	GM12878	blood:	n/a	chr11:74811500-74811511
23	BATF	chr11:74814471-74814871	GM12878	blood:	n/a	chr11:74814691-74814702
24	BCL3	chr11:74814547-74814982	K562	blood:	n/a	n/a
25	BCL3	chr11:74811189-74811855	A549	lung:	n/a	chr11:74811689-74811698 chr11:74811556-74811565
26	BCL3	chr11:74811229-74811928	A549	lung:	n/a	chr11:74811689-74811698 chr11:74811556-74811565
27	BHLHE40	chr11:74807512-74808211	K562	blood:	n/a	n/a
28	BHLHE40	chr11:74808538-74808624	K562	blood:	n/a	n/a
29	BHLHE40	chr11:74806458-74806487	K562	blood:	n/a	n/a
30	BHLHE40	chr11:74811264-74811815	K562	blood:	n/a	n/a
31	BHLHE40	chr11:74814574-74814959	GM12878	blood:	n/a	n/a
32	BHLHE40	chr11:74816373-74817014	K562	blood:	n/a	n/a
33	BHLHE40	chr11:74814521-74815141	K562	blood:	n/a	n/a
34	BHLHE40	chr11:74798454-74798668	K562	blood:	n/a	n/a
35	BHLHE40	chr11:74811021-74811650	GM12878	blood:	n/a	n/a
36	CBX3	chr11:74814494-74815055	K562	blood:	n/a	n/a
37	CBX3	chr11:74839739-74840126	K562	blood:	n/a	n/a
38	CBX3	chr11:74829591-74830147	K562	blood:	n/a	n/a
39	CBX3	chr11:74823242-74823625	K562	blood:	n/a	n/a
40	CBX3	chr11:74807649-74808735	K562	blood:	n/a	n/a
41	CBX3	chr11:74814306-74815021	K562	blood:	n/a	n/a
42	CBX3	chr11:74811226-74811840	K562	blood:	n/a	n/a
43	CBX3	chr11:74802184-74802545	K562	blood:	n/a	n/a
44	CBX3	chr11:74823283-74823608	K562	blood:	n/a	n/a
45	CBX3	chr11:74829582-74830019	K562	blood:	n/a	n/a
46	CBX3	chr11:74816217-74816996	K562	blood:	n/a	n/a
47	CCNT2	chr11:74811373-74811828	K562	blood:	n/a	n/a
48	CCNT2	chr11:74807743-74808424	K562	blood:	n/a	chr11:74808092-74808112 chr11:74807807-74807827
49	CCNT2	chr11:74816426-74816890	K562	blood:	n/a	n/a
50	CCNT2	chr11:74814456-74815009	K562	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:74809555-74809605	HEEpiC	esophagus:	n/a
2	chr11:74809555-74809605	HEEpiC	esophagus:	n/a
3	chr11:74810020-74810070	LNCaP	prostate:	n/a
4	chr11:74801987-74802037	SK-N-SH_RA	brain:	n/a
5	chr11:74810020-74810070	HRPEpiC	eye:	n/a
6	chr11:74802047-74802097	SK-N-SH_RA	brain:	n/a
7	chr11:74801987-74802037	HCPEpiC	choroid plexus:	n/a
8	chr11:74810020-74810070	HL-60	blood:	n/a
9	chr11:74809555-74809605	GM12878	blood:	n/a
10	chr11:74810020-74810070	HMEC	breast:	n/a
11	chr11:74801987-74802037	HUVEC	blood vessel:	n/a
12	chr11:74800716-74800766	HRCEpiC	kidney:	n/a
13	chr11:74800716-74800766	SAEC	small airway:	n/a
14	chr11:74802047-74802097	AG04450	lung:	fetal
15	chr11:74809555-74809605	NH-A	brain:	n/a
16	chr11:74800716-74800766	LNCaP	prostate:	n/a
17	chr11:74801987-74802037	SKMC	muscle:	n/a
18	chr11:74809555-74809605	BJ	skin:	n/a
19	chr11:74810020-74810070	PrEC	prostate:	n/a
20	chr11:74809555-74809605	HEK293	kidney:	embryo
21	chr11:74809354-74809404	H1-hESC	embryonic stem cell:	embryo
22	chr11:74810020-74810070	SK-N-MC	brain:	n/a
23	chr11:74809354-74809404	NHBE	bronchial:	n/a
24	chr11:74802047-74802097	K562	blood:	n/a
25	chr11:74809354-74809404	AG09309	skin:	n/a
26	chr11:74802047-74802097	HRE	kidney:	n/a
27	chr11:74810020-74810070	T-47D	breast:	n/a
28	chr11:74800379-74800429	HRCEpiC	kidney:	n/a
29	chr11:74810020-74810070	GM12891	blood:	n/a
30	chr11:74809354-74809404	U87	brain:	n/a
31	chr11:74800716-74800766	BE2_C	brain:	n/a
32	chr11:74810020-74810070	GM19239	blood:	n/a
33	chr11:74800716-74800766	HEEpiC	esophagus:	n/a
34	chr11:74800716-74800766	PANC-1	pancreas:	n/a
35	chr11:74802047-74802097	HUVEC	blood vessel:	n/a
36	chr11:74809562-74809612	GM12891	blood:	n/a
37	chr11:74810020-74810070	Caco-2	colon:	n/a
38	chr11:74800379-74800429	AG09309	skin:	n/a
39	chr11:74809354-74809404	GM12892	blood:	n/a
40	chr11:74809562-74809612	PANC-1	pancreas:	n/a
41	chr11:74809354-74809404	SK-N-SH	brain:	n/a
42	chr11:74800716-74800766	HCT-116	colon:	n/a
43	chr11:74809555-74809605	T-47D	breast:	n/a
44	chr11:74809354-74809404	HIPEpiC	eye:	n/a
45	chr11:74809555-74809605	ECC-1	luminal epithelium:	n/a
46	chr11:74809555-74809605	HRCEpiC	kidney:	n/a
47	chr11:74800379-74800429	CMK	blood:	n/a
48	chr11:74800716-74800766	GM12891	blood:	n/a
49	chr11:74800716-74800766	ProgFib	skin:	n/a
50	chr11:74809562-74809612	HCM	heart:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:74732304..74734096-chr11:74818351..74820380,2	K562	blood:
2	chr11:74802545..74804894-chr11:74822489..74824628,2	K562	blood:
3	chr11:74669969..74672134-chr11:74806047..74808621,2	K562	blood:
4	chr11:74835442..74838144-chr11:74838497..74840020,2	K562	blood:
5	chr11:74835782..74837327-chr11:74848239..74850752,2	K562	blood:
6	chr11:74816527..74818557-chr11:74820136..74822463,4	K562	blood:
7	chr11:74815946..74818124-chr11:74820163..74822127,2	K562	blood:
8	chr11:74813208..74814840-chr11:74819763..74821471,2	K562	blood:
9	chr11:74638553..74640492-chr11:74816821..74818911,2	K562	blood:
10	chr11:74812003..74816154-chr11:74816263..74818470,5	K562	blood:
11	chr11:74818635..74821800-chr11:74824211..74827439,3	K562	blood:
12	chr11:74795794..74798553-chr11:74813017..74814712,2	K562	blood:
13	chr11:74733675..74734283-chr11:74784742..74785495,2	MCF-7	breast:
14	chr11:74773998..74776628-chr11:74806307..74808054,2	K562	blood:
15	chr11:74742464..74743172-chr11:74783405..74784082,2	K562	blood:
16	chr11:74702670..74704894-chr11:74816765..74819731,2	K562	blood:
17	chr11:74775844..74777522-chr11:74789368..74791115,2	K562	blood:
18	chr11:74723507..74725888-chr11:74813976..74816359,2	K562	blood:
19	chr11:74818635..74821800-chr11:74824211..74827439,3	K562	blood:
20	chr11:74823031..74824915-chr11:74846084..74847848,2	K562	blood:
21	chr11:74740096..74742646-chr11:74811856..74813625,2	K562	blood:
22	chr11:74776958..74778685-chr11:74780199..74782834,2	MCF-7	breast:
23	chr11:74734239..74737191-chr11:74823772..74825545,2	K562	blood:
24	chr11:74805066..74808860-chr11:74814569..74816963,4	K562	blood:
25	chr11:74805066..74808860-chr11:74814569..74816963,4	K562	blood:
26	chr11:74790844..74792497-chr11:74804407..74806198,2	MCF-7	breast:
27	chr11:74790767..74792368-chr11:74814886..74816678,2	K562	blood:
28	chr11:74813734..74816663-chr11:74951389..74954189,2	K562	blood:
29	chr11:74815946..74818124-chr11:74820163..74822127,2	K562	blood:
30	chr11:74802408..74809371-chr11:74811514..74814356,7	K562	blood:
31	chr11:74813208..74814840-chr11:74819763..74821471,2	K562	blood:
32	chr11:74795794..74798553-chr11:74813017..74814712,2	K562	blood:
33	chr11:74798344..74800296-chr11:74811269..74812884,2	K562	blood:
34	chr11:74781895..74783678-chr11:74787128..74789596,2	K562	blood:
35	chr11:74816527..74818557-chr11:74820136..74822463,4	K562	blood:
36	chr11:74784418..74786926-chr11:74788706..74790951,2	K562	blood:
37	chr11:74699188..74701842-chr11:74822279..74824034,2	K562	blood:
38	chr11:74807810..74809325-chr11:74810000..74811512,2	K562	blood:
39	chr11:74807810..74809325-chr11:74810000..74811512,2	K562	blood:
40	chr11:74796178..74800020-chr11:74800917..74805286,4	K562	blood:
41	chr11:74835442..74838144-chr11:74838497..74840020,2	K562	blood:
42	chr11:74658596..74660669-chr11:74813822..74816180,2	K562	blood:
43	chr11:74775986..74778736-chr11:74786345..74788649,2	K562	blood:
44	chr11:74812003..74816154-chr11:74816263..74818470,5	K562	blood:
45	chr11:74784418..74786926-chr11:74788706..74790951,2	K562	blood:
46	chr11:74796178..74800020-chr11:74800917..74805286,4	K562	blood:
47	chr11:74802545..74804894-chr11:74822489..74824628,2	K562	blood:
48	chr11:74810124..74813291-chr11:74818623..74822146,3	MCF-7	breast:
49	chr11:74809645..74812912-chr11:74813164..74816030,5	K562	blood:

No data

Variant related genes	Relation type
SLCO2B1	TF binding region
NPM1P50	TF binding region
OR2AT2P	TF binding region
OR2AT4	TF binding region
SLCO2B1	CpG island
NPM1P50	CpG island
OR2AT2P	CpG island
OR2AT4	CpG island
ENSG00000213333	chromatin interactions
ENSG00000166435	chromatin interactions
ENSG00000234611	chromatin interactions
ENSG00000162139	chromatin interactions
ENSG00000118363	chromatin interactions
ENSG00000261594	chromatin interactions
ENSG00000137491	chromatin interactions
ENSG00000255136	chromatin interactions

Extended variants
information (count: 1564 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1564 , 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	rs562930352	chr11:74782642-74782643	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs531695799	chr11:74782670-74782671	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs34983444	chr11:74782708-74782709	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143694923	chr11:74782740-74782741	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374906674	chr11:74782750-74782751	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529918490	chr11:74782757-74782758	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546872650	chr11:74782859-74782860	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566785433	chr11:74782890-74782891	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs72992691	chr11:74782989-74782990	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs112947659	chr11:74782995-74782996	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181646759	chr11:74782999-74783000	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568877294	chr11:74783007-74783008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537542946	chr11:74783022-74783023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183981396	chr11:74783067-74783068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs75824342	chr11:74783159-74783160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs113322162	chr11:74783221-74783222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554016502	chr11:74783246-74783247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148116987	chr11:74783502-74783503	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs539779092	chr11:74783555-74783556	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs556272650	chr11:74783584-74783585	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs372516693	chr11:74783588-74783589	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs189857661	chr11:74783643-74783644	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs529949980	chr11:74783771-74783772	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs141922059	chr11:74783816-74783817	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs548358118	chr11:74783832-74783833	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs368659850	chr11:74783869-74783870	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs180719905	chr11:74783897-74783898	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs112565307	chr11:74783923-74783924	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs186158012	chr11:74783993-74783994	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs375419921	chr11:74784247-74784248	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs34285574	chr11:74784271-74784272	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs532684906	chr11:74784299-74784300	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs150667297	chr11:74784311-74784312	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs532430440	chr11:74784358-74784359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs372683241	chr11:74784431-74784432	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs574498208	chr11:74784473-74784474	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs551897451	chr11:74784518-74784519	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs570395678	chr11:74784553-74784554	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs191879317	chr11:74784556-74784557	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs547946314	chr11:74784607-74784608	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs139289073	chr11:74784641-74784642	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs533670828	chr11:74784642-74784643	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs11820818	chr11:74784653-74784654	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs368377760	chr11:74784723-74784724	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs552679868	chr11:74784783-74784784	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs181863210	chr11:74784834-74784835	Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs556817960	chr11:74784900-74784901	Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs576317919	chr11:74784906-74784907	Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs186551725	chr11:74784937-74784938	Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs12417378	chr11:74784946-74784947	Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	21364760	CNVD
Hodgkin''s lymphoma	17606441	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
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
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:213 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74779600-74783600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr11:74781400-74785000	Enhancers	K562	blood
3	chr11:74782200-74783000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr11:74782600-74782800	Weak transcription	Gastric	stomach
5	chr11:74783000-74783800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr11:74783000-74784200	Enhancers	HepG2	liver
7	chr11:74783400-74784200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr11:74783400-74784200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr11:74783400-74784600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr11:74783600-74784200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr11:74783600-74784200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr11:74783800-74784000	Enhancers	Brain Cingulate Gyrus	brain
13	chr11:74783800-74784200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr11:74783800-74784200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr11:74783800-74784200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr11:74783800-74784800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr11:74784800-74785400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr11:74785000-74787000	Weak transcription	K562	blood
19	chr11:74785400-74785600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr11:74785600-74788200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr11:74787000-74788600	Strong transcription	K562	blood
22	chr11:74788200-74788400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr11:74788200-74788400	Bivalent Enhancer	NH-A	brain
24	chr11:74788400-74788800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr11:74788400-74788800	Enhancers	Adipose Nuclei	Adipose
26	chr11:74788600-74790000	Enhancers	Osteobl	bone
27	chr11:74788600-74794000	Weak transcription	K562	blood
28	chr11:74788800-74789000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr11:74789000-74793800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr11:74790000-74790200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr11:74790600-74793600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr11:74793600-74794400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr11:74793800-74794200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr11:74794000-74794600	Enhancers	K562	blood
35	chr11:74794200-74802000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr11:74794600-74797600	Weak transcription	K562	blood
37	chr11:74797600-74799400	Genic enhancers	K562	blood
38	chr11:74799400-74801800	Strong transcription	K562	blood
39	chr11:74800000-74800600	Enhancers	Gastric	stomach
40	chr11:74801800-74803200	ZNF genes & repeats	K562	blood
41	chr11:74802000-74802400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr11:74802400-74805000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr11:74803200-74804200	Weak transcription	K562	blood
44	chr11:74804200-74805800	Enhancers	K562	blood
45	chr11:74804400-74804800	Active TSS	A549	lung
46	chr11:74804800-74806200	Weak transcription	A549	lung
47	chr11:74805000-74805400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr11:74805400-74805600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr11:74805600-74805800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr11:74805800-74806600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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