Variant report

Variant	esv1792538
Chromosome Location	chr8:11888999-12026635
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	BATF	chr8:11973137-11973394	GM12878	blood:	n/a	n/a
2	BATF	chr8:11921281-11921530	GM12878	blood:	n/a	n/a
3	BATF	chr8:11965355-11965780	GM12878	blood:	n/a	n/a
4	BATF	chr8:11921283-11921507	GM12878	blood:	n/a	n/a
5	BATF	chr8:11895971-11896326	GM12878	blood:	n/a	n/a
6	BATF	chr8:11970251-11970426	GM12878	blood:	n/a	chr8:11970334-11970345
7	BATF	chr8:11970194-11970485	GM12878	blood:	n/a	chr8:11970334-11970345
8	BCL11A	chr8:11965424-11965597	GM12878	blood:	n/a	n/a
9	BCL11A	chr8:11958839-11959052	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:11965306-11965766	GM12878	blood:	n/a	n/a
11	BCL3	chr8:11998133-11998417	GM12878	blood:	n/a	n/a
12	CEBPB	chr8:12006770-12006998	K562	blood:	n/a	n/a
13	CEBPB	chr8:11909083-11909117	A549	lung:	n/a	chr8:11909099-11909108 chr8:11909099-11909108 chr8:11909097-11909110 chr8:11909097-11909110 chr8:11909099-11909108
14	CEBPB	chr8:11908914-11909287	Hela-S3	cervix:	n/a	chr8:11909099-11909108 chr8:11909099-11909108 chr8:11909097-11909110 chr8:11909097-11909110 chr8:11909099-11909108
15	CTCF	chr8:11908779-11908816	Pancreas_OC	pancreas:	n/a	n/a
16	CTCF	chr8:11921276-11921427	GM19240	blood:	n/a	n/a
17	CTCF	chr8:11918021-11918104	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr8:11973120-11973270	HRPEpiC	eye:	n/a	chr8:11973230-11973248 chr8:11973225-11973246 chr8:11973244-11973260 chr8:11973245-11973266 chr8:11973243-11973261
19	CTCF	chr8:11973100-11973250	SAEC	small airway:	n/a	chr8:11973230-11973248 chr8:11973225-11973246
20	CTCF	chr8:11913991-11914034	LNCaP	prostate:	n/a	n/a
21	CTCF	chr8:11921327-11921483	Lung_OC	lung:	n/a	n/a
22	CTCF	chr8:11973059-11973435	GM12878	blood:	n/a	chr8:11973230-11973248 chr8:11973225-11973246 chr8:11973244-11973260 chr8:11973245-11973266 chr8:11973243-11973261
23	CTCF	chr8:11921198-11921498	LNCaP	prostate:	n/a	n/a
24	CTCF	chr8:11995479-11995525	GM13977	blood:	n/a	n/a
25	CTCF	chr8:11973100-11973250	BJ	skin:	n/a	chr8:11973230-11973248 chr8:11973225-11973246
26	CTCF	chr8:11989880-11990030	K562	blood:	n/a	n/a
27	CTCF	chr8:11973120-11973270	HCFaa	heart:	n/a	chr8:11973230-11973248 chr8:11973225-11973246 chr8:11973244-11973260 chr8:11973245-11973266 chr8:11973243-11973261
28	CTCF	chr8:12004460-12004610	GM12878	blood:	n/a	chr8:12004569-12004577 chr8:12004568-12004576
29	CTCF	chr8:11973140-11973290	NHLF	lung:	n/a	chr8:11973230-11973248 chr8:11973225-11973246 chr8:11973244-11973260 chr8:11973245-11973266 chr8:11973243-11973261
30	CTCF	chr8:11973140-11973290	HAc	cerebellar:	n/a	chr8:11973230-11973248 chr8:11973225-11973246 chr8:11973244-11973260 chr8:11973245-11973266 chr8:11973243-11973261
31	CTCF	chr8:11901028-11901082	GM13976	blood:	n/a	n/a
32	CTCF	chr8:12004512-12004551	GM20000	blood:	n/a	n/a
33	CTCF	chr8:12004460-12004610	HPAF	blood vessel:	n/a	chr8:12004569-12004577 chr8:12004568-12004576
34	CTCF	chr8:12004169-12004215	GM20000	blood:	n/a	n/a
35	CTCF	chr8:12004340-12004490	RPTEC	kidney:	n/a	n/a
36	CTCF	chr8:12004440-12004590	GM12870	blood:	n/a	chr8:12004569-12004577 chr8:12004568-12004576
37	CTCF	chr8:11933378-11933476	Lung_OC	lung:	n/a	n/a
38	CTCF	chr8:11973146-11973359	A549	lung:	n/a	chr8:11973230-11973248 chr8:11973225-11973246 chr8:11973244-11973260 chr8:11973245-11973266 chr8:11973243-11973261
39	CTCF	chr8:11927957-11927994	GM10248	blood:	n/a	n/a
40	CTCF	chr8:11973100-11973250	HBMEC	blood vessel:	n/a	chr8:11973230-11973248 chr8:11973225-11973246
41	CTCF	chr8:11973187-11973330	MCF-7	breast:	n/a	chr8:11973230-11973248 chr8:11973225-11973246 chr8:11973244-11973260 chr8:11973245-11973266 chr8:11973243-11973261
42	CTCF	chr8:11973024-11973465	A549	lung:	n/a	chr8:11973230-11973248 chr8:11973225-11973246 chr8:11973244-11973260 chr8:11973245-11973266 chr8:11973243-11973261
43	CTCF	chr8:11921282-11921450	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:11973114-11973385	Lung_OC	lung:	n/a	chr8:11973230-11973248 chr8:11973225-11973246 chr8:11973244-11973260 chr8:11973245-11973266 chr8:11973243-11973261
45	CTCF	chr8:11973134-11973319	Medullo	brain:	n/a	chr8:11973230-11973248 chr8:11973225-11973246 chr8:11973244-11973260 chr8:11973245-11973266 chr8:11973243-11973261
46	CTCF	chr8:11970362-11970429	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr8:11973178-11973324	MCF-7	breast:	n/a	chr8:11973230-11973248 chr8:11973225-11973246 chr8:11973244-11973260 chr8:11973245-11973266 chr8:11973243-11973261
48	CTCF	chr8:11917900-11918050	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr8:11889431-11889487	GM10248	blood:	n/a	n/a
50	CTCF	chr8:12004440-12004670	HRPEpiC	eye:	n/a	chr8:12004569-12004577 chr8:12004568-12004576

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11996937-11996987	A549	lung:	n/a
2	chr8:11986933-11986983	HRPEpiC	eye:	n/a
3	chr8:11996937-11996987	A549	lung:	n/a
4	chr8:11986933-11986983	HRPEpiC	eye:	n/a
5	chr8:11995002-11995052	MCF-7	breast:	n/a
6	chr8:11972998-11973048	NH-A	brain:	n/a
7	chr8:11946498-11946548	GM12878	blood:	n/a
8	chr8:11996937-11996987	K562	blood:	n/a
9	chr8:11992857-11992907	HRE	kidney:	n/a
10	chr8:11993449-11993499	GM06990	blood:	n/a
11	chr8:11986864-11986914	HUVEC	blood vessel:	n/a
12	chr8:11977206-11977256	RPTEC	kidney:	n/a
13	chr8:11996358-11996408	AG09319	gingival:	n/a
14	chr8:11986864-11986914	GM12891	blood:	n/a
15	chr8:11946498-11946548	CMK	blood:	n/a
16	chr8:11977206-11977256	SAEC	small airway:	n/a
17	chr8:11986876-11986926	PrEC	prostate:	n/a
18	chr8:11993787-11993837	SK-N-SH_RA	brain:	n/a
19	chr8:11991521-11991571	CMK	blood:	n/a
20	chr8:11996327-11996377	NH-A	brain:	n/a
21	chr8:11996358-11996408	HRE	kidney:	n/a
22	chr8:11972998-11973048	AG04450	lung:	fetal
23	chr8:11991521-11991571	HCPEpiC	choroid plexus:	n/a
24	chr8:11995002-11995052	GM12878	blood:	n/a
25	chr8:11993787-11993837	AG10803	skin:	n/a
26	chr8:11986813-11986863	NB4	blood:	n/a
27	chr8:11986813-11986863	IMR90	lung:	fetal
28	chr8:11986501-11986551	HPAEpiC	pulmonary alveolar:	n/a
29	chr8:11993449-11993499	HRE	kidney:	n/a
30	chr8:11973223-11973273	Hepatocyte	liver:	n/a
31	chr8:11991521-11991571	IMR90	lung:	fetal
32	chr8:11997496-11997546	SK-N-MC	brain:	n/a
33	chr8:11993787-11993837	BJ	skin:	n/a
34	chr8:11993449-11993499	GM19239	blood:	n/a
35	chr8:11992857-11992907	HRPEpiC	eye:	n/a
36	chr8:11895252-11895302	NT2-D1	testis:	n/a
37	chr8:11996937-11996987	Hela-S3	cervix:	n/a
38	chr8:11946498-11946548	HPAEpiC	pulmonary alveolar:	n/a
39	chr8:11986876-11986926	SKMC	muscle:	n/a
40	chr8:11973029-11973079	HCF	heart:	n/a
41	chr8:11986501-11986551	MCF-7	breast:	n/a
42	chr8:11986501-11986551	Hepatocyte	liver:	n/a
43	chr8:11970655-11970705	HAEpiC	amniotic membrane:	n/a
44	chr8:11993449-11993499	HEEpiC	esophagus:	n/a
45	chr8:11996327-11996377	HEEpiC	esophagus:	n/a
46	chr8:11986864-11986914	HMEC	breast:	n/a
47	chr8:11993449-11993499	HEK293	kidney:	embryo
48	chr8:11991521-11991571	SKMC	muscle:	n/a
49	chr8:11994639-11994689	HRE	kidney:	n/a
50	chr8:11986933-11986983	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:101006536..101007134-chr8:11906757..11907257,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF705D-2	chr8:11998190-11998224	NONHSAT125119
2	lnc-ZNF705D-2	chr8:11973699-11973834	NONHSAT125117
3	lnc-ZNF705D-2	chr8:12003148-12003209	NONHSAT125117
4	lnc-USP17L2-2	chr8:12008404-12008643	NONHSAT125120
5	lnc-ZNF705D-2	chr8:12002932-12003055	NONHSAT125117
6	lnc-ZNF705D-2	chr8:11979496-11979559	NONHSAT125117
7	lnc-USP17L2-1	chr8:11985367-11986806	NONHSAT125118
8	lnc-ZNF705D-2	chr8:12002932-12003176	NONHSAT125119

Variant related genes	Relation type
ENSG00000254923	TF binding region
DEFB109P3	TF binding region
DEFB108P3	TF binding region
ENSG00000233050	TF binding region
RNA5SP253	TF binding region
USP17L7	TF binding region
USP17L2	TF binding region
OR7E160P	TF binding region
ENSG00000254700	TF binding region
FAM66D	TF binding region
ZNF705D	TF binding region
ENSG00000254923	CpG island
DEFB109P3	CpG island
DEFB108P3	CpG island
ENSG00000233050	CpG island
RNA5SP253	CpG island
USP17L7	CpG island
USP17L2	CpG island
OR7E160P	CpG island
ENSG00000254700	CpG island
FAM66D	CpG island
ZNF705D	CpG island

Extended variants
information (count: 2564 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:2564 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558322586	chr8:11888999-11889000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370936023	chr8:11889015-11889016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568136594	chr8:11889017-11889018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535508779	chr8:11889023-11889024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557041990	chr8:11889026-11889027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374350416	chr8:11889137-11889138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575686553	chr8:11889140-11889141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537245435	chr8:11889154-11889155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531029867	chr8:11889155-11889156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368199609	chr8:11889163-11889164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558497716	chr8:11889179-11889180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577053368	chr8:11889198-11889199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371656345	chr8:11889201-11889202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559365311	chr8:11889202-11889203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574491203	chr8:11889222-11889223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs386722357	chr8:11889226-11889227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs34754650	chr8:11889227-11889228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190254868	chr8:11889237-11889238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111870654	chr8:11889238-11889239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564538626	chr8:11889245-11889246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554139319	chr8:11889266-11889267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546892520	chr8:11889273-11889274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184253269	chr8:11889276-11889277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188673130	chr8:11889288-11889289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs111955344	chr8:11889298-11889299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs4841673	chr8:11889310-11889311	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs186129464	chr8:11889316-11889317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539584768	chr8:11889319-11889320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543295353	chr8:11889322-11889323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375753360	chr8:11889323-11889324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138809944	chr8:11889328-11889329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113341391	chr8:11889330-11889331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553314124	chr8:11889357-11889358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189466129	chr8:11889375-11889376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs372568223	chr8:11889376-11889377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs55798400	chr8:11889386-11889387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs72603918	chr8:11889387-11889388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545600519	chr8:11889393-11889394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112967058	chr8:11889395-11889396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576932204	chr8:11889418-11889419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528688159	chr8:11889421-11889422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs571231732	chr8:11889424-11889425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs562039132	chr8:11889427-11889428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs78343468	chr8:11889428-11889429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs370456422	chr8:11889431-11889432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs180716859	chr8:11889461-11889462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187462445	chr8:11889470-11889471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs533439581	chr8:11889476-11889477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551589802	chr8:11889477-11889478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190950963	chr8:11889480-11889481	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:144)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11887600-11889200	Weak transcription	Pancreas	Pancrea
2	chr8:11889200-11889600	Enhancers	Pancreas	Pancrea
3	chr8:11973200-11973400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr8:11973200-11973600	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr8:11973200-11973600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr8:11973200-11973600	Active TSS	Cortex derived primary cultured neurospheres	brain
7	chr8:11973200-11973600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr8:11973200-11973600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
9	chr8:11973200-11973600	Active TSS	Colonic Mucosa	Colon
10	chr8:11973200-11973600	Active TSS	Duodenum Smooth Muscle	Duodenum
11	chr8:11973200-11973600	Active TSS	Esophagus	oesophagus
12	chr8:11973200-11973600	Active TSS	Placenta	Placenta
13	chr8:11973200-11973600	Active TSS	Fetal Stomach	stomach
14	chr8:11973200-11973600	Active TSS	Fetal Thymus	thymus
15	chr8:11973200-11973600	Active TSS	Left Ventricle	heart
16	chr8:11973200-11973600	Active TSS	Thymus	Thymus
17	chr8:11973200-11973600	Active TSS	A549	lung
18	chr8:11973200-11973600	Active TSS	Monocytes-CD14+_RO01746	blood
19	chr8:11973200-11973600	Active TSS	NHLF	lung
20	chr8:11973200-11973600	Active TSS	Osteobl	bone
21	chr8:11973200-11973800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr8:11973200-11973800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr8:11973200-11973800	Active TSS	Ovary	ovary
24	chr8:11973200-11973800	Active TSS	Psoas Muscle	Psoas
25	chr8:11973200-11973800	Active TSS	Right Ventricle	heart
26	chr8:11973200-11974000	Active TSS	H1 Cell Line	embryonic stem cell
27	chr8:11973200-11974000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr8:11973200-11974000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:11973200-11974000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr8:11973200-11974000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr8:11973200-11974000	Active TSS	Primary T regulatory cells fromperipheralblood	blood
32	chr8:11973200-11974000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr8:11973200-11974000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr8:11973200-11974000	Active TSS	Muscle Satellite Cultured Cells	--
35	chr8:11973200-11974000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr8:11973200-11974000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr8:11973200-11974000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr8:11973200-11974000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr8:11973200-11974000	Active TSS	Adipose Nuclei	Adipose
40	chr8:11973200-11974000	Active TSS	Brain Germinal Matrix	brain
41	chr8:11973200-11974000	Active TSS	Fetal Brain Female	brain
42	chr8:11973200-11974000	Active TSS	Fetal Muscle Leg	muscle
43	chr8:11973200-11974000	Active TSS	Stomach Smooth Muscle	stomach
44	chr8:11973400-11973600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr8:11973400-11973800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr8:11973400-11973800	Active TSS	Rectal Mucosa Donor 31	rectum
47	chr8:11973400-11974000	Active TSS	Brain Hippocampus Middle	brain
48	chr8:11973400-11974000	Active TSS	NHDF-Ad	bronchial
49	chr8:11973600-11973800	Flanking Active TSS	Colonic Mucosa	Colon
50	chr8:11973600-11974000	Enhancers	Brain Angular Gyrus	brain

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