Variant report

Variant	esv1811226
Chromosome Location	chr8:7169416-7855756
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3339)
CpG islands
(count:6291)
Chromatin interactive
region (count:4)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3339 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:7277768-7278018	K562	blood:	n/a	n/a
2	ATF1	chr8:7771027-7771432	K562	blood:	n/a	n/a
3	ATF1	chr8:7694221-7694565	K562	blood:	n/a	n/a
4	ATF1	chr8:7255409-7255636	K562	blood:	n/a	n/a
5	BACH1	chr8:7265686-7265994	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:7771106-7771311	K562	blood:	n/a	n/a
7	BATF	chr8:7564517-7564858	GM12878	blood:	n/a	n/a
8	BATF	chr8:7220356-7220781	GM12878	blood:	n/a	n/a
9	BATF	chr8:7564552-7564860	GM12878	blood:	n/a	n/a
10	BATF	chr8:7215669-7216199	GM12878	blood:	n/a	n/a
11	BATF	chr8:7809440-7809731	GM12878	blood:	n/a	chr8:7809580-7809591
12	BATF	chr8:7215685-7216141	GM12878	blood:	n/a	n/a
13	BATF	chr8:7744485-7744737	GM12878	blood:	n/a	n/a
14	BATF	chr8:7812383-7812672	GM12878	blood:	n/a	n/a
15	BATF	chr8:7255357-7255599	GM12878	blood:	n/a	n/a
16	BATF	chr8:7809497-7809672	GM12878	blood:	n/a	chr8:7809580-7809591
17	BATF	chr8:7448204-7448611	GM12878	blood:	n/a	n/a
18	BATF	chr8:7212714-7213011	GM12878	blood:	n/a	n/a
19	BATF	chr8:7804596-7805021	GM12878	blood:	n/a	n/a
20	BATF	chr8:7448268-7448576	GM12878	blood:	n/a	n/a
21	BATF	chr8:7281851-7282075	GM12878	blood:	n/a	n/a
22	BCL11A	chr8:7804547-7805007	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:7220370-7220830	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:7468589-7468841	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:7212700-7212924	GM12878	blood:	n/a	n/a
26	BCL11A	chr8:7458367-7458546	GM12878	blood:	n/a	chr8:7458446-7458459
27	BCL11A	chr8:7537480-7537668	GM12878	blood:	n/a	n/a
28	BCL11A	chr8:7228613-7228840	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:7554560-7554739	GM12878	blood:	n/a	chr8:7554682-7554695
30	BCL11A	chr8:7804665-7804838	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:7215704-7215862	GM12878	blood:	n/a	n/a
32	BCL11A	chr8:7213997-7214166	GM12878	blood:	n/a	n/a
33	BCL3	chr8:7199106-7199270	GM12878	blood:	n/a	chr8:7199138-7199147
34	BHLHE40	chr8:7770999-7771207	GM12878	blood:	n/a	n/a
35	BHLHE40	chr8:7212714-7213011	GM12878	blood:	n/a	n/a
36	BHLHE40	chr8:7770946-7771148	K562	blood:	n/a	n/a
37	BHLHE40	chr8:7744443-7744699	HepG2	liver:	n/a	n/a
38	BHLHE40	chr8:7212724-7213120	K562	blood:	n/a	n/a
39	BHLHE40	chr8:7468640-7468924	HepG2	liver:	n/a	chr8:7468879-7468895
40	BRCA1	chr8:7771100-7771544	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr8:7770582-7771313	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr8:7212733-7213463	GM12878	blood:	n/a	n/a
43	BRCA1	chr8:7255419-7255821	H1-hESC	embryonic stem cell:	n/a	n/a
44	CBX3	chr8:7378825-7379598	K562	blood:	n/a	n/a
45	CBX3	chr8:7641288-7641775	K562	blood:	n/a	n/a
46	CBX3	chr8:7656260-7657147	K562	blood:	n/a	n/a
47	CBX3	chr8:7656542-7657115	K562	blood:	n/a	n/a
48	CBX3	chr8:7394220-7394817	K562	blood:	n/a	n/a
49	CBX3	chr8:7641140-7641830	K562	blood:	n/a	n/a
50	CBX3	chr8:7378829-7379412	K562	blood:	n/a	n/a

(count:6291 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:7213526-7213576	HRCEpiC	kidney:	n/a
2	chr8:7572749-7572799	ProgFib	skin:	n/a
3	chr8:7465756-7465806	AoSMC	blood vessel:	n/a
4	chr8:7396283-7396333	HUVEC	blood vessel:	n/a
5	chr8:7320532-7320582	HCT-116	colon:	n/a
6	chr8:7430856-7430906	BJ	skin:	n/a
7	chr8:7328654-7328704	HRE	kidney:	n/a
8	chr8:7622631-7622681	NHBE	bronchial:	n/a
9	chr8:7213526-7213576	HRCEpiC	kidney:	n/a
10	chr8:7572749-7572799	ProgFib	skin:	n/a
11	chr8:7465756-7465806	AoSMC	blood vessel:	n/a
12	chr8:7396283-7396333	HUVEC	blood vessel:	n/a
13	chr8:7320532-7320582	HCT-116	colon:	n/a
14	chr8:7430856-7430906	BJ	skin:	n/a
15	chr8:7328654-7328704	HRE	kidney:	n/a
16	chr8:7622631-7622681	NHBE	bronchial:	n/a
17	chr8:7833268-7833318	IMR90	lung:	fetal
18	chr8:7191953-7192003	AoSMC	blood vessel:	n/a
19	chr8:7333711-7333761	T-47D	breast:	n/a
20	chr8:7537473-7537523	Jurkat	blood:	n/a
21	chr8:7434722-7434772	LNCaP	prostate:	n/a
22	chr8:7275380-7275430	U87	brain:	n/a
23	chr8:7275380-7275430	HCM	heart:	n/a
24	chr8:7208812-7208862	Caco-2	colon:	n/a
25	chr8:7436707-7436757	A549	lung:	n/a
26	chr8:7192145-7192195	RPTEC	kidney:	n/a
27	chr8:7328654-7328704	Hepatocyte	liver:	n/a
28	chr8:7308492-7308542	K562	blood:	n/a
29	chr8:7221471-7221521	HCPEpiC	choroid plexus:	n/a
30	chr8:7813144-7813194	AG04450	lung:	fetal
31	chr8:7320520-7320570	AG04450	lung:	fetal
32	chr8:7441660-7441710	HIPEpiC	eye:	n/a
33	chr8:7385970-7386020	MCF10A-Er-Src	breast:	n/a
34	chr8:7344471-7344521	RPTEC	kidney:	n/a
35	chr8:7332257-7332307	PrEC	prostate:	n/a
36	chr8:7537473-7537523	NB4	blood:	n/a
37	chr8:7543899-7543949	HCF	heart:	n/a
38	chr8:7572749-7572799	GM12878	blood:	n/a
39	chr8:7657022-7657072	U87	brain:	n/a
40	chr8:7332851-7332901	K562	blood:	n/a
41	chr8:7406299-7406349	HIPEpiC	eye:	n/a
42	chr8:7834142-7834192	HPAEpiC	pulmonary alveolar:	n/a
43	chr8:7405502-7405552	ovcar-3	ovarian:	n/a
44	chr8:7639801-7639851	K562	blood:	n/a
45	chr8:7833268-7833318	CMK	blood:	n/a
46	chr8:7441660-7441710	SK-N-SH	brain:	n/a
47	chr8:7585573-7585623	HRPEpiC	eye:	n/a
48	chr8:7407308-7407358	ECC-1	luminal epithelium:	n/a
49	chr8:7275380-7275430	GM12891	blood:	n/a
50	chr8:7465756-7465806	HIPEpiC	eye:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:8332362..8333276-chr8:7212481..7212992,2	MCF-7	breast:
2	chr8:7255181..7256067-chr8:7770740..7771265,2	MCF-7	breast:
3	chr8:7079344..7079857-chr8:7537961..7538472,3	MCF-7	breast:
4	chr8:7255181..7256067-chr8:7770740..7771265,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB104B-1	chr8:7333626-7334120	XLOC_006991
2	lnc-DEFB105B-1	chr8:7234859-7235022	NONHSAT124827
3	lnc-DEFB104B-1	chr8:7334999-7335170	XLOC_006991
4	lnc-DEFB105B-1	chr8:7230636-7230723	NONHSAT124827
5	lnc-ZNF705G-1	chr8:7206593-7206668	NONHSAT124826
6	lnc-DEFB104B-1	chr8:7334988-7335170	XLOC_006991
7	lnc-ZNF705G-1	chr8:7212333-7212511	NONHSAT124824
8	lnc-DEFB105B-3	chr8:7170368-7170425	NONHSAT124823
9	lnc-DEFB105B-3	chr8:7177268-7177473	NONHSAT124823
10	lnc-ZNF705G-1	chr8:7206605-7206668	NONHSAT124824
11	lnc-ZNF705G-1	chr8:7180835-7180882	NONHSAT124824
12	lnc-ZNF705G-1	chr8:7181819-7181886	NONHSAT124824
13	lnc-DEFB105A-4	chr8:7847937-7848142	NONHSAT124844
14	lnc-ZNF705G-1	chr8:7212333-7212574	NONHSAT124826
15	lnc-DEFB105A-4	chr8:7854986-7855043	NONHSAT124844
16	lnc-DEFB104B-1	chr8:7337502-7337622	XLOC_006991
17	lnc-ZNF705G-1	chr8:7182659-7182720	NONHSAT124824
18	lnc-ZNF705G-1	chr8:7182344-7182411	NONHSAT124824
19	lnc-DEFB105A-1	chr8:7748525-7750077	NONHSAT124838

No data

Variant related genes	Relation type
DEFB108P2	TF binding region
DEFB107A	TF binding region
SPAG11B	TF binding region
FAM90A7P	TF binding region
OR7E157P	TF binding region
FAM90A14P	TF binding region
ZNF705G	TF binding region
FAM90A19P	TF binding region
FAM66E	TF binding region
DEFB103A	TF binding region
DEFB109P1B	TF binding region
DEFB104A	TF binding region
OR7E154P	TF binding region
FAM90A9P	TF binding region
ENSG00000235778	TF binding region
ENSG00000254889	TF binding region
ENSG00000254776	TF binding region
FAM90A23P	TF binding region
DEFB4B	TF binding region
ENSG00000254796	TF binding region
FAM66B	TF binding region
FAM90A22P	TF binding region
DEFB105A	TF binding region
DEFB106B	TF binding region
DEFB104B	TF binding region
FAM90A6P	TF binding region
ENSG00000216194	TF binding region
HSPD1P2	TF binding region
ZNF705B	TF binding region
PRR23D2	TF binding region
FAM90A21P	TF binding region
FAM90A10P	TF binding region
ENSG00000215977	TF binding region
USP17L1P	TF binding region
USP17L4	TF binding region
PRR23D1	TF binding region
DEFB4A	TF binding region
FAM90A18P	TF binding region
FAM90A16P	TF binding region
FAM90A8P	TF binding region
DEFB105B	TF binding region
DEFB108P1	TF binding region
ENSG00000255211	TF binding region
USP17L8	TF binding region
DEFB107B	TF binding region
HSPD1P3	TF binding region
ENSG00000205989	TF binding region
DEFB106A	TF binding region
SPAG11A	TF binding region
DEFB103B	TF binding region
USP17L3	TF binding region
FAM90A17P	TF binding region
DEFB108P2	CpG island
DEFB107A	CpG island
SPAG11B	CpG island
FAM90A7P	CpG island
OR7E157P	CpG island
FAM90A14P	CpG island
ZNF705G	CpG island
FAM90A19P	CpG island
FAM66E	CpG island
DEFB103A	CpG island
DEFB109P1B	CpG island
DEFB104A	CpG island
OR7E154P	CpG island
FAM90A9P	CpG island
ENSG00000235778	CpG island
ENSG00000254889	CpG island
ENSG00000254776	CpG island
FAM90A23P	CpG island
DEFB4B	CpG island
ENSG00000254796	CpG island
FAM66B	CpG island
FAM90A22P	CpG island
DEFB105A	CpG island
DEFB106B	CpG island
DEFB104B	CpG island
FAM90A6P	CpG island
ENSG00000216194	CpG island
HSPD1P2	CpG island
ZNF705B	CpG island
PRR23D2	CpG island
FAM90A21P	CpG island
FAM90A10P	CpG island
ENSG00000215977	CpG island
USP17L1P	CpG island
USP17L4	CpG island
PRR23D1	CpG island
DEFB4A	CpG island
FAM90A18P	CpG island
FAM90A16P	CpG island
FAM90A8P	CpG island
DEFB105B	CpG island
DEFB108P1	CpG island
ENSG00000255211	CpG island
USP17L8	CpG island
DEFB107B	CpG island
HSPD1P3	CpG island
ENSG00000205989	CpG island
DEFB106A	CpG island
SPAG11A	CpG island
DEFB103B	CpG island
USP17L3	CpG island
FAM90A17P	CpG island
ENSG00000226711	chromatin interactions
JARID2	miRNA target sites

Extended variants
information (count: 4447 )
Associated
traits (count: 160 )

Variant overlapped rSNPs/rCNVs (count:4447 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550566259	chr8:7170372-7170373	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs201259211	chr8:7170378-7170379	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs529715643	chr8:7170408-7170409	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs182044766	chr8:7177270-7177271	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs537604998	chr8:7177277-7177278	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs557639939	chr8:7177301-7177302	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs574225399	chr8:7177313-7177314	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs550699244	chr8:7177322-7177323	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs536667403	chr8:7177341-7177342	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs553127891	chr8:7177376-7177377	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs572881405	chr8:7177417-7177418	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs62488805	chr8:7182702-7182703	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs558894102	chr8:7185265-7185266	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs553450503	chr8:7186450-7186451	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs576499826	chr8:7186461-7186462	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs563808361	chr8:7186462-7186463	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs563126727	chr8:7186481-7186482	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs576560368	chr8:7186530-7186531	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs542553516	chr8:7186531-7186532	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs562204257	chr8:7186533-7186534	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs527690515	chr8:7186535-7186536	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs62488807	chr8:7186637-7186638	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs111755036	chr8:7187766-7187767	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs549983277	chr8:7187793-7187794	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs569080568	chr8:7187796-7187797	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs531395550	chr8:7187874-7187875	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs111798709	chr8:7187876-7187877	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs112172362	chr8:7187906-7187907	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs548471631	chr8:7187908-7187909	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs567966132	chr8:7187922-7187923	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs369002778	chr8:7187925-7187926	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs138910436	chr8:7187941-7187942	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs372574850	chr8:7189624-7189625	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs571914943	chr8:7189646-7189647	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs540799660	chr8:7189719-7189720	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs564055600	chr8:7189734-7189735	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs559420869	chr8:7189745-7189746	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs558999074	chr8:7190653-7190654	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs577770663	chr8:7190670-7190671	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs543555499	chr8:7190671-7190672	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs556996544	chr8:7190679-7190680	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs567507668	chr8:7191281-7191282	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs536406580	chr8:7191287-7191288	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs369451964	chr8:7191292-7191293	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs553328557	chr8:7191294-7191295	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs573142893	chr8:7191295-7191296	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs201803133	chr8:7191296-7191297	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs554177915	chr8:7191922-7191923	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs567693019	chr8:7191953-7191954	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs554690655	chr8:7191954-7191955	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:160)

Disease	PMID	Source
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
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
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	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
Colorectal cancer	16774939	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
Bladder cancer	21909424	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Cognitive impairment	21505072	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	20369283	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD
Barrett''s syndrome	19417022	CNVD
Schizophrenia	23813976	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	21364760	CNVD
Developmental disorder	20461109	CNVD
Pancreatic cancer	17952125	CNVD
Crohn''s disease	17953491	CNVD
Immune disease	21076436	CNVD
Crohn''s disease	21956041	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	22302058	CNVD

Chromatin state (count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:7206000-7212200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr8:7209200-7212200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr8:7209600-7212200	Weak transcription	Gastric	stomach
4	chr8:7210200-7212400	Weak transcription	Brain Substantia Nigra	brain
5	chr8:7210600-7210800	Enhancers	Right Atrium	heart
6	chr8:7210600-7210800	Enhancers	Right Ventricle	heart
7	chr8:7210800-7212200	Weak transcription	Right Atrium	heart
8	chr8:7210800-7212200	Weak transcription	Right Ventricle	heart
9	chr8:7212000-7213000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr8:7212000-7213000	Active TSS	Primary T helper cells fromperipheralblood	blood
11	chr8:7212000-7213000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr8:7212000-7213800	Active TSS	Brain Anterior Caudate	brain
13	chr8:7212200-7212400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr8:7212200-7212400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr8:7212200-7212400	Enhancers	Gastric	stomach
16	chr8:7212200-7212400	Flanking Active TSS	Right Atrium	heart
17	chr8:7212200-7212400	Flanking Active TSS	Right Ventricle	heart
18	chr8:7212200-7212400	Enhancers	NHEK	skin
19	chr8:7212200-7212600	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr8:7212200-7212600	Enhancers	Placenta	Placenta
21	chr8:7212200-7213000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:7212200-7213000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr8:7212200-7213000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr8:7212200-7213000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr8:7212200-7213000	Active TSS	Breast Myoepithelial Primary Cells	Breast
26	chr8:7212200-7213000	Active TSS	Primary B cells from peripheral blood	blood
27	chr8:7212200-7213000	Active TSS	Primary T cells from cord blood	blood
28	chr8:7212200-7213000	Active TSS	Primary T cells fromperipheralblood	blood
29	chr8:7212200-7213000	Active TSS	Primary T helper cells PMA-I stimulated	--
30	chr8:7212200-7213000	Active TSS	Primary T regulatory cells fromperipheralblood	blood
31	chr8:7212200-7213000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr8:7212200-7213000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
33	chr8:7212200-7213000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr8:7212200-7213000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr8:7212200-7213000	Active TSS	Muscle Satellite Cultured Cells	--
36	chr8:7212200-7213000	Active TSS	Cortex derived primary cultured neurospheres	brain
37	chr8:7212200-7213000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr8:7212200-7213000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr8:7212200-7213000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr8:7212200-7213000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr8:7212200-7213000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr8:7212200-7213000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr8:7212200-7213000	Active TSS	Adipose Nuclei	Adipose
44	chr8:7212200-7213000	Active TSS	Aorta	Aorta
45	chr8:7212200-7213000	Active TSS	Liver	Liver
46	chr8:7212200-7213000	Active TSS	Brain Germinal Matrix	brain
47	chr8:7212200-7213000	Active TSS	Brain Hippocampus Middle	brain
48	chr8:7212200-7213000	Active TSS	Colonic Mucosa	Colon
49	chr8:7212200-7213000	Active TSS	Colon Smooth Muscle	Colon
50	chr8:7212200-7213000	Active TSS	Duodenum Mucosa	Duodenum

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