Variant report

Variant	nsv889550
Chromosome Location	chr7:153640474-153671450
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	CEBPB	chr7:153653827-153654031	K562	blood:	n/a	chr7:153653924-153653933
2	CEBPB	chr7:153653846-153654075	A549	lung:	n/a	chr7:153653924-153653933
3	CEBPB	chr7:153649223-153649552	HepG2	liver:	n/a	chr7:153649388-153649399
4	CEBPB	chr7:153650331-153650429	K562	blood:	n/a	n/a
5	CEBPB	chr7:153661713-153661899	HepG2	liver:	n/a	n/a
6	CEBPB	chr7:153649215-153649575	A549	lung:	n/a	chr7:153649388-153649399
7	CHD2	chr7:153653758-153653916	HepG2	liver:	n/a	n/a
8	CTCF	chr7:153645332-153645347	Hela-S3	cervix:	n/a	chr7:153645332-153645340
9	CTCF	chr7:153645108-153645544	MCF-7	breast:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
10	CTCF	chr7:153645260-153645410	MCF-7	breast:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
11	CTCF	chr7:153645272-153645418	HepG2	liver:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
12	CTCF	chr7:153645200-153645350	WERI-Rb-1	eye:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340
13	CTCF	chr7:153645243-153645248	LNCaP	prostate:	n/a	n/a
14	CTCF	chr7:153645220-153645370	BE2_C	brain:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
15	CTCF	chr7:153645200-153645350	Caco-2	colon:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340
16	CTCF	chr7:153645260-153645410	K562	blood:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
17	CTCF	chr7:153657784-153657790	GM19239	blood:	n/a	n/a
18	CTCF	chr7:153668897-153668985	GM20000	blood:	n/a	n/a
19	CTCF	chr7:153645255-153645431	MCF-7	breast:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
20	CTCF	chr7:153643759-153643799	GM20000	blood:	n/a	n/a
21	CTCF	chr7:153656264-153656311	LNCaP	prostate:	n/a	n/a
22	CTCF	chr7:153645250-153645405	LNCaP	prostate:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
23	CTCF	chr7:153645320-153645470	HepG2	liver:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
24	CTCF	chr7:153645206-153645506	HepG2	liver:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
25	CTCF	chr7:153645257-153645434	LNCaP	prostate:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
26	CTCF	chr7:153645260-153645410	A549	lung:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
27	CTCF	chr7:153645240-153645390	MCF-7	breast:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
28	CTCF	chr7:153656565-153656620	Medullo	brain:	n/a	n/a
29	CTCF	chr7:153645240-153645390	SK-N-SH_RA	brain:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
30	CTCF	chr7:153645243-153645423	K562	blood:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
31	CTCF	chr7:153645280-153645430	BE2_C	brain:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
32	CTCF	chr7:153645352-153645361	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr7:153645254-153645428	HepG2	liver:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
34	CTCF	chr7:153659757-153659816	LNCaP	prostate:	n/a	n/a
35	CTCF	chr7:153645220-153645370	HEK293	kidney:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
36	CTCF	chr7:153645220-153645370	NB4	blood:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
37	CTCF	chr7:153645280-153645411	MCF-7	breast:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
38	CTCF	chr7:153645248-153645411	Medullo	brain:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
39	CTCF	chr7:153645311-153645353	Kidney_OC	kidney:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
40	CTCF	chr7:153657792-153657823	GM19239	blood:	n/a	n/a
41	CTCF	chr7:153655901-153655912	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr7:153645220-153645370	SK-N-SH_RA	brain:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
43	CTCF	chr7:153645140-153645290	A549	lung:	n/a	n/a
44	CTCF	chr7:153645280-153645430	K562	blood:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
45	CTCF	chr7:153645320-153645331	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr7:153645240-153645390	HRE	kidney:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
47	CTCF	chr7:153645153-153645562	MCF-7	breast:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
48	CTCF	chr7:153645141-153645515	K562	blood:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
49	CUX1	chr7:153640708-153640825	K562	blood:	n/a	n/a
50	FOXA1	chr7:153645163-153645399	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:153641242-153641292	NB4	blood:	n/a
2	chr7:153641242-153641292	HCF	heart:	n/a
3	chr7:153641267-153641317	AG04450	lung:	fetal
4	chr7:153641267-153641317	Caco-2	colon:	n/a
5	chr7:153641307-153641357	PANC-1	pancreas:	n/a
6	chr7:153641242-153641292	AG09309	skin:	n/a
7	chr7:153641307-153641357	ProgFib	skin:	n/a
8	chr7:153641242-153641292	HRPEpiC	eye:	n/a
9	chr7:153641307-153641357	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:153641267-153641317	NHBE	bronchial:	n/a
11	chr7:153641242-153641292	HCT-116	colon:	n/a
12	chr7:153641267-153641317	HCF	heart:	n/a
13	chr7:153641267-153641317	SKMC	muscle:	n/a
14	chr7:153641267-153641317	LNCaP	prostate:	n/a
15	chr7:153641242-153641292	MCF10A-Er-Src	breast:	n/a
16	chr7:153641307-153641357	HRE	kidney:	n/a
17	chr7:153641267-153641317	MCF-7	breast:	n/a
18	chr7:153641267-153641317	Hepatocyte	liver:	n/a
19	chr7:153641242-153641292	SAEC	small airway:	n/a
20	chr7:153641242-153641292	Jurkat	blood:	n/a
21	chr7:153641242-153641292	A549	lung:	n/a
22	chr7:153641307-153641357	NB4	blood:	n/a
23	chr7:153641267-153641317	T-47D	breast:	n/a
24	chr7:153641242-153641292	HEK293	kidney:	embryo
25	chr7:153641242-153641292	ECC-1	luminal epithelium:	n/a
26	chr7:153641307-153641357	Hela-S3	cervix:	n/a
27	chr7:153641267-153641317	HIPEpiC	eye:	n/a
28	chr7:153641242-153641292	AG10803	skin:	n/a
29	chr7:153641307-153641357	SK-N-SH	brain:	n/a
30	chr7:153641242-153641292	NHBE	bronchial:	n/a
31	chr7:153641242-153641292	HepG2	liver:	n/a
32	chr7:153641267-153641317	HRPEpiC	eye:	n/a
33	chr7:153641267-153641317	A549	lung:	n/a
34	chr7:153641267-153641317	AG04449	skin:	fetal
35	chr7:153641307-153641357	HCF	heart:	n/a
36	chr7:153641242-153641292	NHDF-neo	bronchial:	n/a
37	chr7:153641242-153641292	PrEC	prostate:	n/a
38	chr7:153641307-153641357	HMEC	breast:	n/a
39	chr7:153641307-153641357	A549	lung:	n/a
40	chr7:153641242-153641292	BJ	skin:	n/a
41	chr7:153641267-153641317	HNPCEpiC	eye:	n/a
42	chr7:153641307-153641357	HepG2	liver:	n/a
43	chr7:153641242-153641292	LNCaP	prostate:	n/a
44	chr7:153641307-153641357	T-47D	breast:	n/a
45	chr7:153641307-153641357	NT2-D1	testis:	n/a
46	chr7:153641307-153641357	HL-60	blood:	n/a
47	chr7:153641242-153641292	PFSK-1	brain:	n/a
48	chr7:153641307-153641357	HIPEpiC	eye:	n/a
49	chr7:153641307-153641357	GM12892	blood:	n/a
50	chr7:153641267-153641317	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:153646257..153648420-chr7:153652652..153654403,2	K562	blood:
2	chr7:153636379..153638876-chr7:153641967..153644697,4	K562	blood:
3	chr7:153646257..153648420-chr7:153652652..153654403,2	K562	blood:
4	chr7:153636605..153638915-chr7:153643180..153645983,3	K562	blood:

Variant related genes	Relation type
ENSG00000226509	TF binding region
ENSG00000226509	CpG island

Extended variants
information (count: 738 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:738 , 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	rs10487687	chr7:153640474-153640475	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs118146583	chr7:153640495-153640496	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs183797292	chr7:153640527-153640528	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs188021889	chr7:153640537-153640538	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs560016669	chr7:153640547-153640548	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs149726713	chr7:153640574-153640575	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs536667040	chr7:153640588-153640589	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs527364521	chr7:153640597-153640598	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs28447406	chr7:153640605-153640606	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs549239889	chr7:153640635-153640636	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs114989028	chr7:153640641-153640642	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs376502239	chr7:153640672-153640673	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs553325806	chr7:153640760-153640761	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs572021176	chr7:153640761-153640762	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs542495806	chr7:153640785-153640786	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs561060849	chr7:153640805-153640806	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs190762062	chr7:153640853-153640854	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs34209360	chr7:153640939-153640940	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs67059255	chr7:153640942-153640943	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs182050135	chr7:153640970-153640971	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs543934962	chr7:153640973-153640974	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs117002942	chr7:153640996-153640997	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs532592242	chr7:153641004-153641005	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs547496533	chr7:153641052-153641053	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs545838933	chr7:153641066-153641067	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs60481350	chr7:153641123-153641124	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs372901936	chr7:153641129-153641130	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs376902975	chr7:153641162-153641163	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs58548160	chr7:153641182-153641183	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs377099048	chr7:153641210-153641211	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370380728	chr7:153641211-153641212	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs58418946	chr7:153641222-153641223	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6948322	chr7:153641228-153641229	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs187042631	chr7:153641235-153641236	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs57100178	chr7:153641240-153641241	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs536195627	chr7:153641243-153641244	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6464377	chr7:153641247-153641248	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs191540602	chr7:153641260-153641261	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543255923	chr7:153641295-153641296	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566895166	chr7:153641303-153641304	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534027270	chr7:153641307-153641308	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs61456764	chr7:153641308-153641309	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs58068307	chr7:153641332-153641333	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs6952540	chr7:153641346-153641347	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs527875516	chr7:153641355-153641356	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376504872	chr7:153641364-153641365	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7785600	chr7:153641366-153641367	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs78322563	chr7:153641384-153641385	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573232606	chr7:153641395-153641396	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201010534	chr7:153641397-153641398	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Ovarian cancer	21720365	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Myelofibrosis	22110671	CNVD
Nasopharyngeal cancer	20548289	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Autism	22102821	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495309	CNVD

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:153628200-153640600	Weak transcription	Stomach Smooth Muscle	stomach
2	chr7:153631000-153643000	Weak transcription	Right Atrium	heart
3	chr7:153632200-153641200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:153638600-153640800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr7:153639000-153640600	Enhancers	Brain Angular Gyrus	brain
6	chr7:153639000-153642200	Enhancers	Fetal Brain Male	brain
7	chr7:153639200-153640600	Enhancers	Brain Substantia Nigra	brain
8	chr7:153639400-153641800	Enhancers	Fetal Stomach	stomach
9	chr7:153639800-153641400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr7:153640000-153640600	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr7:153640200-153640600	Enhancers	Fetal Kidney	kidney
12	chr7:153640200-153641400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr7:153640200-153641400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr7:153640400-153640600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
15	chr7:153640400-153640600	Flanking Active TSS	Brain Germinal Matrix	brain
16	chr7:153640400-153640600	Flanking Active TSS	Brain Hippocampus Middle	brain
17	chr7:153640400-153640600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
18	chr7:153640400-153640600	Flanking Active TSS	Fetal Brain Female	brain
19	chr7:153640400-153641200	Active TSS	Brain Anterior Caudate	brain
20	chr7:153640400-153641200	Enhancers	Colon Smooth Muscle	Colon
21	chr7:153640400-153641400	Enhancers	Rectal Smooth Muscle	rectum
22	chr7:153640400-153641600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr7:153640400-153641600	Flanking Active TSS	Brain Cingulate Gyrus	brain
24	chr7:153640400-153642200	Enhancers	Fetal Muscle Leg	muscle
25	chr7:153640600-153640800	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr7:153640600-153640800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
27	chr7:153640600-153640800	Active TSS	Brain Substantia Nigra	brain
28	chr7:153640600-153640800	Enhancers	Fetal Brain Female	brain
29	chr7:153640600-153640800	Flanking Active TSS	Stomach Smooth Muscle	stomach
30	chr7:153640600-153641000	Active TSS	Brain Germinal Matrix	brain
31	chr7:153640600-153641200	Active TSS	Brain Hippocampus Middle	brain
32	chr7:153640600-153641200	Weak transcription	Fetal Kidney	kidney
33	chr7:153640600-153641400	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr7:153640600-153641400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr7:153640600-153641600	Active TSS	Brain Angular Gyrus	brain
36	chr7:153640800-153641000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
37	chr7:153640800-153641000	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr7:153640800-153641000	Flanking Active TSS	Brain Substantia Nigra	brain
39	chr7:153640800-153641200	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr7:153640800-153641200	Active TSS	Stomach Smooth Muscle	stomach
41	chr7:153640800-153641400	Flanking Active TSS	Fetal Brain Female	brain
42	chr7:153641000-153641200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr7:153641000-153641400	Active TSS	Brain Substantia Nigra	brain
44	chr7:153641000-153641600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr7:153641000-153641600	Flanking Active TSS	Brain Germinal Matrix	brain
46	chr7:153641000-153641600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
47	chr7:153641000-153642200	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr7:153641200-153641400	Flanking Active TSS	Brain Anterior Caudate	brain
49	chr7:153641200-153641400	Flanking Active TSS	Brain Hippocampus Middle	brain
50	chr7:153641200-153641600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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