Variant report

Variant	esv1834245
Chromosome Location	chr7:70193768-70202993
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	ATF2	chr7:70194222-70194708	GM12878	blood:	n/a	n/a
2	ATF2	chr7:70193730-70194787	GM12878	blood:	n/a	n/a
3	BATF	chr7:70195849-70196064	GM12878	blood:	n/a	chr7:70195970-70195981
4	BATF	chr7:70195779-70196118	GM12878	blood:	n/a	chr7:70195970-70195981
5	BCL11A	chr7:70193763-70194026	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr7:70194287-70194666	GM12878	blood:	n/a	n/a
7	BCL3	chr7:70194233-70194787	GM12878	blood:	n/a	n/a
8	BCLAF1	chr7:70194201-70194815	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:70201669-70201693	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:70193857-70194815	GM12878	blood:	n/a	n/a
11	CEBPB	chr7:70201659-70202017	HepG2	liver:	n/a	chr7:70201840-70201851 chr7:70201841-70201850 chr7:70201841-70201850 chr7:70201839-70201850 chr7:70201841-70201850 chr7:70201839-70201852 chr7:70201841-70201850
12	CEBPB	chr7:70201668-70201974	K562	blood:	n/a	chr7:70201840-70201851 chr7:70201841-70201850 chr7:70201841-70201850 chr7:70201839-70201850 chr7:70201841-70201850 chr7:70201839-70201852 chr7:70201841-70201850
13	CEBPB	chr7:70201715-70202034	H1-hESC	embryonic stem cell:	n/a	chr7:70201840-70201851 chr7:70201841-70201850 chr7:70201841-70201850 chr7:70201839-70201850 chr7:70201841-70201850 chr7:70201839-70201852 chr7:70201841-70201850
14	CEBPB	chr7:70201625-70202591	IMR90	lung:	n/a	chr7:70201840-70201851 chr7:70201841-70201850 chr7:70201841-70201850 chr7:70201839-70201850 chr7:70201841-70201850 chr7:70201839-70201852 chr7:70201841-70201850
15	CEBPB	chr7:70201664-70202020	A549	lung:	n/a	chr7:70201840-70201851 chr7:70201841-70201850 chr7:70201841-70201850 chr7:70201839-70201850 chr7:70201841-70201850 chr7:70201839-70201852 chr7:70201841-70201850
16	CEBPB	chr7:70194815-70195004	HepG2	liver:	n/a	chr7:70194924-70194935
17	CEBPB	chr7:70201697-70201948	Hela-S3	cervix:	n/a	chr7:70201840-70201851 chr7:70201841-70201850 chr7:70201841-70201850 chr7:70201839-70201850 chr7:70201841-70201850 chr7:70201839-70201852 chr7:70201841-70201850
18	CEBPB	chr7:70201772-70201910	HepG2	liver:	n/a	chr7:70201840-70201851 chr7:70201841-70201850 chr7:70201841-70201850 chr7:70201839-70201850 chr7:70201841-70201850 chr7:70201839-70201852 chr7:70201841-70201850
19	CEBPB	chr7:70201763-70201984	A549	lung:	n/a	chr7:70201840-70201851 chr7:70201841-70201850 chr7:70201841-70201850 chr7:70201839-70201850 chr7:70201841-70201850 chr7:70201839-70201852 chr7:70201841-70201850
20	CEBPB	chr7:70201595-70202106	A549	lung:	n/a	chr7:70201840-70201851 chr7:70201841-70201850 chr7:70201841-70201850 chr7:70201839-70201850 chr7:70201841-70201850 chr7:70201839-70201852 chr7:70201841-70201850
21	CEBPB	chr7:70198141-70198507	IMR90	lung:	n/a	n/a
22	CEBPB	chr7:70194793-70195081	HepG2	liver:	n/a	chr7:70194924-70194935
23	CHD1	chr7:70193869-70194679	GM12878	blood:	n/a	n/a
24	CHD2	chr7:70193835-70194085	GM12878	blood:	n/a	n/a
25	CTBP2	chr7:70193894-70194317	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr7:70193840-70193955	GM12878	blood:	n/a	n/a
27	CTCF	chr7:70193920-70194070	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr7:70202259-70202355	GM12878	blood:	n/a	n/a
29	CTCF	chr7:70202976-70203396	MCF-7	breast:	n/a	n/a
30	CUX1	chr7:70193791-70194663	GM12878	blood:	n/a	n/a
31	E2F6	chr7:70201929-70202649	H1-hESC	embryonic stem cell:	n/a	chr7:70202309-70202321
32	E2F6	chr7:70202092-70202523	H1-hESC	embryonic stem cell:	n/a	chr7:70202309-70202321
33	EBF1	chr7:70194173-70194724	GM12878	blood:	n/a	chr7:70194434-70194445 chr7:70194351-70194361
34	EBF1	chr7:70193712-70194140	GM12878	blood:	n/a	n/a
35	EBF1	chr7:70199618-70199681	GM12878	blood:	n/a	n/a
36	EBF1	chr7:70202136-70202266	GM12878	blood:	n/a	n/a
37	EBF1	chr7:70193751-70194136	GM12878	blood:	n/a	n/a
38	EBF1	chr7:70194148-70194690	GM12878	blood:	n/a	chr7:70194434-70194445 chr7:70194351-70194361
39	EBF1	chr7:70193706-70194834	GM12878	blood:	n/a	chr7:70194434-70194445 chr7:70194351-70194361
40	EBF1	chr7:70195872-70195991	GM12878	blood:	n/a	n/a
41	ELF1	chr7:70193895-70194411	GM12878	blood:	n/a	n/a
42	ELK1	chr7:70201653-70201733	GM12878	blood:	n/a	n/a
43	ELK1	chr7:70193975-70193997	GM12878	blood:	n/a	n/a
44	EP300	chr7:70193937-70194557	GM12878	blood:	n/a	chr7:70194393-70194407
45	EP300	chr7:70201643-70202285	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr7:70199372-70199726	SK-N-SH_RA	brain:	n/a	n/a
47	EP300	chr7:70201791-70202219	GM12878	blood:	n/a	n/a
48	EP300	chr7:70199430-70199749	SK-N-SH_RA	brain:	n/a	n/a
49	EP300	chr7:70199324-70200100	SK-N-SH	brain:	n/a	n/a
50	EP300	chr7:70201582-70202098	SK-N-SH_RA	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70200532-70200582	HIPEpiC	eye:	n/a
2	chr7:70194602-70194652	Caco-2	colon:	n/a
3	chr7:70198123-70198173	U87	brain:	n/a
4	chr7:70200532-70200582	HAEpiC	amniotic membrane:	n/a
5	chr7:70198123-70198173	ovcar-3	ovarian:	n/a
6	chr7:70198123-70198173	T-47D	breast:	n/a
7	chr7:70200532-70200582	Hela-S3	cervix:	n/a
8	chr7:70194602-70194652	H1-hESC	embryonic stem cell:	embryo
9	chr7:70198123-70198173	PANC-1	pancreas:	n/a
10	chr7:70194602-70194652	HEEpiC	esophagus:	n/a
11	chr7:70198123-70198173	SK-N-SH	brain:	n/a
12	chr7:70200532-70200582	SAEC	small airway:	n/a
13	chr7:70198123-70198173	HIPEpiC	eye:	n/a
14	chr7:70200532-70200582	MCF10A-Er-Src	breast:	n/a
15	chr7:70200532-70200582	HNPCEpiC	eye:	n/a
16	chr7:70194602-70194652	A549	lung:	n/a
17	chr7:70200532-70200582	SK-N-SH	brain:	n/a
18	chr7:70198123-70198173	NHDF-neo	bronchial:	n/a
19	chr7:70200532-70200582	HUVEC	blood vessel:	n/a
20	chr7:70198123-70198173	SAEC	small airway:	n/a
21	chr7:70194602-70194652	GM12891	blood:	n/a
22	chr7:70194602-70194652	ProgFib	skin:	n/a
23	chr7:70198123-70198173	NB4	blood:	n/a
24	chr7:70194602-70194652	CMK	blood:	n/a
25	chr7:70200532-70200582	HMEC	breast:	n/a
26	chr7:70200532-70200582	AG04450	lung:	fetal
27	chr7:70200532-70200582	BJ	skin:	n/a
28	chr7:70194602-70194652	PANC-1	pancreas:	n/a
29	chr7:70194602-70194652	HEK293	kidney:	embryo
30	chr7:70198123-70198173	AG10803	skin:	n/a
31	chr7:70200532-70200582	AoSMC	blood vessel:	n/a
32	chr7:70200532-70200582	AG04449	skin:	fetal
33	chr7:70200532-70200582	GM12878	blood:	n/a
34	chr7:70200532-70200582	HCT-116	colon:	n/a
35	chr7:70194602-70194652	IMR90	lung:	fetal
36	chr7:70200532-70200582	PrEC	prostate:	n/a
37	chr7:70200532-70200582	NHDF-neo	bronchial:	n/a
38	chr7:70194602-70194652	NHDF-neo	bronchial:	n/a
39	chr7:70200532-70200582	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:70194602-70194652	HCF	heart:	n/a
41	chr7:70198123-70198173	AG09319	gingival:	n/a
42	chr7:70194602-70194652	BJ	skin:	n/a
43	chr7:70194602-70194652	PFSK-1	brain:	n/a
44	chr7:70198123-70198173	GM12891	blood:	n/a
45	chr7:70198123-70198173	SK-N-SH_RA	brain:	n/a
46	chr7:70200532-70200582	MCF-7	breast:	n/a
47	chr7:70194602-70194652	SK-N-SH	brain:	n/a
48	chr7:70198123-70198173	NHBE	bronchial:	n/a
49	chr7:70200532-70200582	SKMC	muscle:	n/a
50	chr7:70200532-70200582	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:70184183..70185798-chr7:70197589..70200298,2	MCF-7	breast:

Variant related genes	Relation type
AUTS2	TF binding region
AUTS2	CpG island

Extended variants
information (count: 420 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7807160	chr7:70193768-70193769	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs539062369	chr7:70193825-70193826	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs530892694	chr7:70193826-70193827	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs565461104	chr7:70193890-70193891	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs370470121	chr7:70193907-70193908	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs4718987	chr7:70193932-70193933	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs569676030	chr7:70193953-70193954	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs10259549	chr7:70194005-70194006	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs570855242	chr7:70194021-70194022	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs4718988	chr7:70194024-70194025	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs534831813	chr7:70194044-70194045	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs553230295	chr7:70194049-70194050	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs574969214	chr7:70194098-70194099	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs542383034	chr7:70194099-70194100	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs557073761	chr7:70194108-70194109	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs575597407	chr7:70194169-70194170	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546140514	chr7:70194170-70194171	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139700878	chr7:70194191-70194192	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371314167	chr7:70194215-70194216	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs528649592	chr7:70194228-70194229	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs377203356	chr7:70194229-70194230	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs540406784	chr7:70194245-70194246	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs143578000	chr7:70194253-70194254	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs73181075	chr7:70194277-70194278	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs529733734	chr7:70194289-70194290	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs534792377	chr7:70194298-70194299	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs554385701	chr7:70194330-70194331	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs190898430	chr7:70194345-70194346	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs568184048	chr7:70194357-70194358	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs569505556	chr7:70194360-70194361	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs149604760	chr7:70194369-70194370	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs73443101	chr7:70194384-70194385	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs73706458	chr7:70194441-70194442	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs536727858	chr7:70194446-70194447	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs534950481	chr7:70194485-70194486	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs546807289	chr7:70194526-70194527	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs568306726	chr7:70194530-70194531	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs182376250	chr7:70194542-70194543	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs186616257	chr7:70194543-70194544	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs368447841	chr7:70194625-70194626	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs191811049	chr7:70194653-70194654	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs539843263	chr7:70194787-70194788	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs149246147	chr7:70194838-70194839	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs199570693	chr7:70194839-70194840	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs557895481	chr7:70194845-70194846	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs71077676	chr7:70194868-70194869	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs57582549	chr7:70194872-70194873	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs184846109	chr7:70194878-70194879	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs56233310	chr7:70194880-70194881	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs76701116	chr7:70194883-70194884	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:553 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70162200-70201600	Weak transcription	Primary B cells from cord blood	blood
2	chr7:70176200-70201600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr7:70176400-70193800	Weak transcription	NH-A	brain
4	chr7:70179800-70201600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr7:70180200-70193800	Weak transcription	Fetal Intestine Small	intestine
6	chr7:70182600-70194000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr7:70183000-70194000	Weak transcription	Fetal Stomach	stomach
8	chr7:70183000-70201600	Weak transcription	Fetal Muscle Leg	muscle
9	chr7:70183200-70193800	Weak transcription	Thymus	Thymus
10	chr7:70183200-70194000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr7:70183200-70200200	Weak transcription	Ovary	ovary
12	chr7:70183200-70201800	Weak transcription	Pancreas	Pancrea
13	chr7:70183400-70193800	Weak transcription	Fetal Muscle Trunk	muscle
14	chr7:70183400-70194000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr7:70183400-70195400	Weak transcription	HSMM	muscle
16	chr7:70183600-70197600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr7:70184400-70195200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr7:70185800-70197600	Weak transcription	HSMMtube	muscle
19	chr7:70186000-70195400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr7:70186400-70198200	Weak transcription	Dnd41	blood
21	chr7:70187000-70201200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr7:70189200-70193800	Weak transcription	Lung	lung
23	chr7:70189800-70193800	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr7:70189800-70194000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr7:70190200-70194600	Enhancers	H1 Cell Line	embryonic stem cell
26	chr7:70190200-70201400	Weak transcription	Fetal Kidney	kidney
27	chr7:70190600-70193800	Weak transcription	Fetal Lung	lung
28	chr7:70190600-70199400	Weak transcription	Left Ventricle	heart
29	chr7:70190600-70199600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr7:70190600-70201600	Weak transcription	Fetal Intestine Large	intestine
31	chr7:70190800-70193800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr7:70190800-70194000	Weak transcription	Gastric	stomach
33	chr7:70190800-70194200	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr7:70190800-70195400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr7:70190800-70198000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr7:70190800-70199400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr7:70191000-70194200	Weak transcription	Esophagus	oesophagus
38	chr7:70191000-70197400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr7:70191400-70195000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr7:70191600-70195000	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr7:70191800-70194000	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr7:70191800-70194200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr7:70192000-70193800	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr7:70192000-70193800	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr7:70192200-70193800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:70192200-70193800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr7:70192200-70193800	Weak transcription	Psoas Muscle	Psoas
48	chr7:70192200-70194000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr7:70192200-70197400	Weak transcription	Brain Anterior Caudate	brain
50	chr7:70192200-70200200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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