Variant report

Variant	nsv886940
Chromosome Location	chr6:166881023-166895934
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	BHLHE40	chr6:166891641-166891785	K562	blood:	n/a	chr6:166891719-166891740
2	BHLHE40	chr6:166888791-166889071	K562	blood:	n/a	chr6:166888947-166888956
3	CTCF	chr6:166881140-166881290	WERI-Rb-1	eye:	n/a	n/a
4	EGR1	chr6:166891465-166891734	K562	blood:	n/a	chr6:166891629-166891642 chr6:166891628-166891643 chr6:166891629-166891643 chr6:166891627-166891637 chr6:166891629-166891642 chr6:166891629-166891642 chr6:166891629-166891642 chr6:166891632-166891641
5	EGR1	chr6:166891504-166891700	K562	blood:	n/a	chr6:166891629-166891642 chr6:166891628-166891643 chr6:166891629-166891643 chr6:166891627-166891637 chr6:166891629-166891642 chr6:166891629-166891642 chr6:166891629-166891642 chr6:166891632-166891641
6	ELF1	chr6:166893503-166893836	K562	blood:	n/a	chr6:166893657-166893670
7	EP300	chr6:166885331-166885617	SK-N-SH_RA	brain:	n/a	n/a
8	EP300	chr6:166885246-166885616	SK-N-SH_RA	brain:	n/a	n/a
9	EP300	chr6:166881587-166881614	HepG2	liver:	n/a	n/a
10	EP300	chr6:166884183-166886015	SK-N-SH	brain:	n/a	chr6:166884655-166884668
11	FOS	chr6:166891251-166891428	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr6:166891250-166891439	MCF10A-Er-Src	breast:	n/a	n/a
13	GATA2	chr6:166894967-166895339	SH-SY5Y	brain:	n/a	n/a
14	GATA3	chr6:166894759-166895335	SH-SY5Y	brain:	n/a	chr6:166894797-166894818
15	IRF1	chr6:166882363-166882425	K562	blood:	n/a	chr6:166882372-166882385 chr6:166882372-166882385 chr6:166882370-166882384 chr6:166882374-166882385 chr6:166882374-166882388 chr6:166882375-166882386 chr6:166882374-166882384 chr6:166882373-166882385 chr6:166882366-166882386 chr6:166882371-166882385 chr6:166882371-166882388 chr6:166882373-166882390 chr6:166882372-166882385
16	MAFK	chr6:166889829-166889961	HepG2	liver:	n/a	n/a
17	MYC	chr6:166883895-166883963	MCF10A-Er-Src	breast:	n/a	n/a
18	MYC	chr6:166889688-166889737	H1-hESC	embryonic stem cell:	n/a	n/a
19	NR3C1	chr6:166885470-166885849	A549	lung:	n/a	chr6:166885673-166885687
20	NR3C1	chr6:166885599-166885780	A549	lung:	n/a	chr6:166885673-166885687
21	NR3C1	chr6:166885440-166885849	A549	lung:	n/a	chr6:166885673-166885687
22	NR3C1	chr6:166885562-166885848	A549	lung:	n/a	chr6:166885673-166885687
23	POLR2A	chr6:166888749-166890119	PFSK-1	brain:	n/a	n/a
24	POLR2A	chr6:166889609-166889633	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr6:166887088-166887212	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr6:166889466-166889836	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr6:166891976-166892958	PFSK-1	brain:	n/a	n/a
28	POLR2A	chr6:166889323-166889931	PFSK-1	brain:	n/a	n/a
29	POLR2A	chr6:166888913-166889071	HUVEC	blood vessel:	n/a	n/a
30	POLR2A	chr6:166893782-166893878	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr6:166885733-166885735	HUVEC	blood vessel:	n/a	n/a
32	POLR2A	chr6:166890521-166890735	HUVEC	blood vessel:	n/a	n/a
33	POLR2A	chr6:166883110-166884808	PFSK-1	brain:	n/a	n/a
34	POLR2A	chr6:166878145-166882263	PFSK-1	brain:	n/a	n/a
35	POLR2A	chr6:166891431-166891765	HUVEC	blood vessel:	n/a	n/a
36	POLR2A	chr6:166886368-166886441	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr6:166888713-166888876	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr6:166883903-166883992	HUVEC	blood vessel:	n/a	n/a
39	POLR2A	chr6:166886965-166887023	HUVEC	blood vessel:	n/a	n/a
40	POLR2A	chr6:166889576-166889961	K562	blood:	n/a	n/a
41	POLR2A	chr6:166878957-166882136	PFSK-1	brain:	n/a	n/a
42	SPI1	chr6:166891390-166891561	K562	blood:	n/a	chr6:166891515-166891528
43	STAT3	chr6:166895096-166895272	MCF10A-Er-Src	breast:	n/a	n/a
44	STAT3	chr6:166891579-166891670	MCF10A-Er-Src	breast:	n/a	n/a
45	STAT3	chr6:166883741-166883941	MCF10A-Er-Src	breast:	n/a	chr6:166883834-166883843 chr6:166883833-166883842 chr6:166883831-166883845 chr6:166883828-166883848
46	TAF1	chr6:166879595-166881068	PFSK-1	brain:	n/a	n/a
47	TAL1	chr6:166890226-166890488	K562	blood:	n/a	chr6:166890356-166890365 chr6:166890434-166890449 chr6:166890434-166890449 chr6:166890331-166890349
48	USF2	chr6:166883756-166883881	H1-hESC	embryonic stem cell:	n/a	n/a
49	WRNIP1	chr6:166889860-166889915	GM12878	blood:	n/a	n/a
50	ZNF263	chr6:166891171-166891549	HEK293-T-REx	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:166880989-166881039	AG04449	skin:	fetal
2	chr6:166880989-166881039	AG04449	skin:	fetal
3	chr6:166891902-166891952	H1-hESC	embryonic stem cell:	embryo
4	chr6:166887879-166887929	HCPEpiC	choroid plexus:	n/a
5	chr6:166887879-166887929	SAEC	small airway:	n/a
6	chr6:166892762-166892812	AG09309	skin:	n/a
7	chr6:166892362-166892412	BE2_C	brain:	n/a
8	chr6:166892921-166892971	HCT-116	colon:	n/a
9	chr6:166892216-166892266	GM12878	blood:	n/a
10	chr6:166880989-166881039	HIPEpiC	eye:	n/a
11	chr6:166892438-166892488	HCPEpiC	choroid plexus:	n/a
12	chr6:166891650-166891700	SK-N-SH_RA	brain:	n/a
13	chr6:166892438-166892488	GM19239	blood:	n/a
14	chr6:166892921-166892971	HRE	kidney:	n/a
15	chr6:166892649-166892699	ECC-1	luminal epithelium:	n/a
16	chr6:166891650-166891700	MCF10A-Er-Src	breast:	n/a
17	chr6:166891959-166892009	HAEpiC	amniotic membrane:	n/a
18	chr6:166891650-166891700	AG04450	lung:	fetal
19	chr6:166892438-166892488	AG09309	skin:	n/a
20	chr6:166892216-166892266	U87	brain:	n/a
21	chr6:166892921-166892971	ECC-1	luminal epithelium:	n/a
22	chr6:166892649-166892699	BJ	skin:	n/a
23	chr6:166892921-166892971	H1-hESC	embryonic stem cell:	embryo
24	chr6:166887879-166887929	Jurkat	blood:	n/a
25	chr6:166887879-166887929	NT2-D1	testis:	n/a
26	chr6:166891902-166891952	PANC-1	pancreas:	n/a
27	chr6:166891902-166891952	SAEC	small airway:	n/a
28	chr6:166892216-166892266	AG09309	skin:	n/a
29	chr6:166892216-166892266	BJ	skin:	n/a
30	chr6:166891617-166891667	MCF-7	breast:	n/a
31	chr6:166892649-166892699	HCT-116	colon:	n/a
32	chr6:166891729-166891779	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:166884430-166884480	CMK	blood:	n/a
34	chr6:166891959-166892009	HRCEpiC	kidney:	n/a
35	chr6:166892216-166892266	HCPEpiC	choroid plexus:	n/a
36	chr6:166891959-166892009	SK-N-SH	brain:	n/a
37	chr6:166891902-166891952	LNCaP	prostate:	n/a
38	chr6:166884430-166884480	HEEpiC	esophagus:	n/a
39	chr6:166892649-166892699	H1-hESC	embryonic stem cell:	embryo
40	chr6:166892438-166892488	SK-N-SH	brain:	n/a
41	chr6:166892921-166892971	HCM	heart:	n/a
42	chr6:166891650-166891700	PFSK-1	brain:	n/a
43	chr6:166891650-166891700	SAEC	small airway:	n/a
44	chr6:166892762-166892812	PFSK-1	brain:	n/a
45	chr6:166891617-166891667	AG09319	gingival:	n/a
46	chr6:166891902-166891952	HMEC	breast:	n/a
47	chr6:166891617-166891667	Hela-S3	cervix:	n/a
48	chr6:166884430-166884480	HCT-116	colon:	n/a
49	chr6:166892438-166892488	HepG2	liver:	n/a
50	chr6:166892216-166892266	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:166881013..166882996-chr6:166884544..166886077,2	K562	blood:
2	chr6:166871889..166873613-chr6:166879410..166881105,2	K562	blood:
3	chr6:166881013..166882996-chr6:166884544..166886077,2	K562	blood:
4	chr6:166893774..166896880-chr6:166897771..166899718,3	MCF-7	breast:
5	chr6:166754479..166756533-chr6:166881640..166884124,2	MCF-7	breast:
6	chr6:166892327..166894616-chr6:166897228..166898880,2	K562	blood:
7	chr6:166877740..166880123-chr6:166885130..166887516,2	K562	blood:
8	chr6:166877343..166879705-chr6:166880050..166881798,2	MCF-7	breast:

Variant related genes	Relation type
RPS6KA2-IT1	TF binding region
RPS6KA2-IT1	CpG island
ENSG00000198818	chromatin interactions
ENSG00000232082	chromatin interactions
ENSG00000071242	chromatin interactions

Extended variants
information (count: 709 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:709 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2281046	chr6:166881023-166881024	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs570176599	chr6:166881048-166881049	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs537644475	chr6:166881072-166881073	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs541346371	chr6:166881107-166881108	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs370910104	chr6:166881109-166881110	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs143023294	chr6:166881125-166881126	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs386708474	chr6:166881146-166881147	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs114983443	chr6:166881147-166881148	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs572075914	chr6:166881165-166881166	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs116134459	chr6:166881169-166881170	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs369337579	chr6:166881191-166881192	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs530555404	chr6:166881209-166881210	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs576114930	chr6:166881293-166881294	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs192768452	chr6:166881298-166881299	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs114286671	chr6:166881306-166881307	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs146124844	chr6:166881307-166881308	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs547687904	chr6:166881309-166881310	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs559283610	chr6:166881331-166881332	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs372845661	chr6:166881332-166881333	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs548613304	chr6:166881361-166881362	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs562147198	chr6:166881363-166881364	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs148757470	chr6:166881372-166881373	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs537587946	chr6:166881413-166881414	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs536654287	chr6:166881414-166881415	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs549680042	chr6:166881511-166881512	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs141518986	chr6:166881515-166881516	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs538891576	chr6:166881535-166881536	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs552229409	chr6:166881548-166881549	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs554097052	chr6:166881587-166881588	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs377604988	chr6:166881591-166881592	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs536232139	chr6:166881627-166881628	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs554583013	chr6:166881628-166881629	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs386708475	chr6:166881645-166881646	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs116800870	chr6:166881646-166881647	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs150862668	chr6:166881722-166881723	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs529559962	chr6:166881725-166881726	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs541267739	chr6:166881735-166881736	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs559619351	chr6:166881750-166881751	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs116951827	chr6:166881758-166881759	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs544810173	chr6:166881797-166881798	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs563718520	chr6:166881886-166881887	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs567188201	chr6:166881964-166881965	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs530860047	chr6:166882001-166882002	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs552648353	chr6:166882014-166882015	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs570995836	chr6:166882017-166882018	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs111906033	chr6:166882029-166882030	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs547640576	chr6:166882040-166882041	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs565964222	chr6:166882041-166882042	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs16898962	chr6:166882049-166882050	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs554240744	chr6:166882074-166882075	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166808200-166911800	Weak transcription	Psoas Muscle	Psoas
2	chr6:166824000-166901400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr6:166862400-166900600	Weak transcription	Primary T cells from cord blood	blood
4	chr6:166862400-166920600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:166862600-166883000	Weak transcription	Aorta	Aorta
6	chr6:166862600-166883000	Weak transcription	Duodenum Mucosa	Duodenum
7	chr6:166863600-166900200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr6:166863600-166902000	Weak transcription	Small Intestine	intestine
9	chr6:166864600-166883000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:166864800-166899800	Weak transcription	Esophagus	oesophagus
11	chr6:166867400-166892800	Weak transcription	Fetal Brain Male	brain
12	chr6:166867600-166900000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr6:166870400-166898400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:166871000-166901400	Weak transcription	Stomach Mucosa	stomach
15	chr6:166872000-166900400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr6:166872200-166900400	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr6:166873000-166902800	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr6:166874200-166885200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr6:166874800-166903000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr6:166875000-166900800	Weak transcription	Fetal Heart	heart
21	chr6:166875400-166881200	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr6:166875400-166885400	Strong transcription	Cortex derived primary cultured neurospheres	brain
23	chr6:166875600-166884200	Strong transcription	Gastric	stomach
24	chr6:166875800-166883000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr6:166875800-166883200	Weak transcription	HMEC	breast
26	chr6:166875800-166887000	Strong transcription	Primary neutrophils fromperipheralblood	blood
27	chr6:166875800-166894000	Strong transcription	Skeletal Muscle Male	skeletal muscle
28	chr6:166876000-166881200	Strong transcription	Fetal Brain Female	brain
29	chr6:166876000-166883800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr6:166876000-166885000	Strong transcription	Right Ventricle	heart
31	chr6:166876000-166888800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr6:166876000-166901400	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr6:166876200-166886600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr6:166877000-166885200	Strong transcription	Spleen	Spleen
35	chr6:166877200-166904400	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr6:166877200-166908800	Weak transcription	Colonic Mucosa	Colon
37	chr6:166877400-166883800	Strong transcription	Brain Germinal Matrix	brain
38	chr6:166877600-166885200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr6:166877800-166881800	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr6:166878200-166902000	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr6:166879000-166881200	Genic enhancers	Pancreas	Pancrea
42	chr6:166879000-166881400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr6:166879000-166900600	Weak transcription	Primary B cells from cord blood	blood
44	chr6:166879200-166881400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr6:166879400-166881800	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr6:166879400-166882000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr6:166879400-166882800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr6:166879400-166883600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr6:166879400-166883600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr6:166879600-166883600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain

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