Variant report

Variant	nsv1019489
Chromosome Location	chr8:11802328-11858466
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:992)
CpG islands
(count:1342)
Chromatin interactive
region (count:30)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:992 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:11813783-11814113	HepG2	liver:	n/a	n/a
2	ATF1	chr8:11807083-11807365	K562	blood:	n/a	n/a
3	BACH1	chr8:11815300-11815374	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:11816433-11816692	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr8:11822405-11822652	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:11812950-11813081	K562	blood:	n/a	n/a
7	BHLHE40	chr8:11815181-11815494	K562	blood:	n/a	n/a
8	BHLHE40	chr8:11815192-11815513	HepG2	liver:	n/a	n/a
9	BHLHE40	chr8:11816398-11816683	K562	blood:	n/a	n/a
10	BHLHE40	chr8:11806929-11807352	K562	blood:	n/a	n/a
11	CBX3	chr8:11805093-11805433	K562	blood:	n/a	n/a
12	CBX3	chr8:11839401-11840135	HCT-116	colon:	n/a	n/a
13	CCNT2	chr8:11843856-11844050	K562	blood:	n/a	n/a
14	CCNT2	chr8:11807053-11807488	K562	blood:	n/a	chr8:11807360-11807369 chr8:11807248-11807268
15	CEBPB	chr8:11816152-11816521	HepG2	liver:	n/a	chr8:11816330-11816341
16	CEBPB	chr8:11854282-11854495	HepG2	liver:	n/a	chr8:11854359-11854368 chr8:11854357-11854368 chr8:11854359-11854370
17	CEBPB	chr8:11816243-11816470	K562	blood:	n/a	chr8:11816330-11816341
18	CEBPB	chr8:11858214-11858354	IMR90	lung:	n/a	n/a
19	CEBPB	chr8:11816165-11816600	A549	lung:	n/a	chr8:11816330-11816341
20	CEBPB	chr8:11813757-11814093	K562	blood:	n/a	chr8:11813929-11813940
21	CEBPB	chr8:11854216-11854508	IMR90	lung:	n/a	chr8:11854359-11854368 chr8:11854357-11854368 chr8:11854359-11854370
22	CEBPB	chr8:11852658-11853061	IMR90	lung:	n/a	chr8:11852980-11852993
23	CEBPB	chr8:11816146-11816622	A549	lung:	n/a	chr8:11816330-11816341
24	CEBPB	chr8:11858214-11858439	A549	lung:	n/a	n/a
25	CEBPB	chr8:11816168-11816706	Hela-S3	cervix:	n/a	chr8:11816330-11816341
26	CEBPB	chr8:11816144-11816589	K562	blood:	n/a	chr8:11816330-11816341
27	CEBPB	chr8:11858243-11858418	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:11816146-11816527	MCF-7	breast:	n/a	chr8:11816330-11816341
29	CEBPB	chr8:11816198-11816767	A549	lung:	n/a	chr8:11816330-11816341
30	CEBPB	chr8:11813778-11814109	A549	lung:	n/a	chr8:11813929-11813940
31	CEBPB	chr8:11816251-11816631	H1-hESC	embryonic stem cell:	n/a	chr8:11816330-11816341
32	CEBPB	chr8:11816175-11816712	K562	blood:	n/a	chr8:11816330-11816341
33	CEBPB	chr8:11816162-11816603	IMR90	lung:	n/a	chr8:11816330-11816341
34	CEBPB	chr8:11813744-11814114	HepG2	liver:	n/a	chr8:11813929-11813940
35	CEBPB	chr8:11854319-11854398	H1-hESC	embryonic stem cell:	n/a	chr8:11854359-11854368 chr8:11854357-11854368 chr8:11854359-11854370
36	CEBPB	chr8:11816229-11816539	HepG2	liver:	n/a	chr8:11816330-11816341
37	CEBPB	chr8:11816235-11816570	ECC-1	luminal epithelium:	n/a	chr8:11816330-11816341
38	CEBPB	chr8:11821309-11821507	HepG2	liver:	n/a	chr8:11821395-11821406
39	CEBPB	chr8:11852501-11853120	HCT-116	colon:	n/a	chr8:11852980-11852993
40	CEBPB	chr8:11816261-11816393	HepG2	liver:	n/a	chr8:11816330-11816341
41	CEBPB	chr8:11813825-11814061	K562	blood:	n/a	chr8:11813929-11813940
42	CEBPB	chr8:11813814-11814090	A549	lung:	n/a	chr8:11813929-11813940
43	CEBPB	chr8:11813806-11814094	Hela-S3	cervix:	n/a	chr8:11813929-11813940
44	CEBPB	chr8:11813778-11814105	IMR90	lung:	n/a	chr8:11813929-11813940
45	CEBPB	chr8:11854194-11854540	K562	blood:	n/a	chr8:11854359-11854368 chr8:11854357-11854368 chr8:11854359-11854370
46	CEBPD	chr8:11807025-11807456	K562	blood:	n/a	n/a
47	CHD2	chr8:11832848-11832898	K562	blood:	n/a	n/a
48	CHD2	chr8:11844195-11844527	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr8:11816501-11816691	K562	blood:	n/a	n/a
50	CREB1	chr8:11816331-11816758	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11843807-11843857	AoSMC	blood vessel:	n/a
2	chr8:11839780-11839830	GM12878	blood:	n/a
3	chr8:11835607-11835657	GM12891	blood:	n/a
4	chr8:11832261-11832311	NB4	blood:	n/a
5	chr8:11841980-11842030	AG09309	skin:	n/a
6	chr8:11839138-11839188	NH-A	brain:	n/a
7	chr8:11832261-11832311	Hela-S3	cervix:	n/a
8	chr8:11839780-11839830	H1-hESC	embryonic stem cell:	embryo
9	chr8:11853878-11853928	HCT-116	colon:	n/a
10	chr8:11832565-11832615	ECC-1	luminal epithelium:	n/a
11	chr8:11831823-11831873	MCF10A-Er-Src	breast:	n/a
12	chr8:11843807-11843857	Caco-2	colon:	n/a
13	chr8:11832039-11832089	AoSMC	blood vessel:	n/a
14	chr8:11832261-11832311	AG04450	lung:	fetal
15	chr8:11833039-11833089	NB4	blood:	n/a
16	chr8:11838532-11838582	AoSMC	blood vessel:	n/a
17	chr8:11843971-11844021	ECC-1	luminal epithelium:	n/a
18	chr8:11813211-11813261	BE2_C	brain:	n/a
19	chr8:11839780-11839830	HAEpiC	amniotic membrane:	n/a
20	chr8:11835607-11835657	HEK293	kidney:	embryo
21	chr8:11839780-11839830	NT2-D1	testis:	n/a
22	chr8:11813211-11813261	HCF	heart:	n/a
23	chr8:11831823-11831873	T-47D	breast:	n/a
24	chr8:11839764-11839814	HIPEpiC	eye:	n/a
25	chr8:11832565-11832615	NH-A	brain:	n/a
26	chr8:11839138-11839188	RPTEC	kidney:	n/a
27	chr8:11843971-11844021	HNPCEpiC	eye:	n/a
28	chr8:11838843-11838893	AoSMC	blood vessel:	n/a
29	chr8:11839844-11839894	HIPEpiC	eye:	n/a
30	chr8:11843816-11843866	AoSMC	blood vessel:	n/a
31	chr8:11813211-11813261	SK-N-MC	brain:	n/a
32	chr8:11832039-11832089	HL-60	blood:	n/a
33	chr8:11832762-11832812	AG10803	skin:	n/a
34	chr8:11853121-11853171	H1-hESC	embryonic stem cell:	embryo
35	chr8:11832039-11832089	MCF10A-Er-Src	breast:	n/a
36	chr8:11843807-11843857	SK-N-SH_RA	brain:	n/a
37	chr8:11853920-11853970	PrEC	prostate:	n/a
38	chr8:11839764-11839814	H1-hESC	embryonic stem cell:	embryo
39	chr8:11843807-11843857	HRE	kidney:	n/a
40	chr8:11841980-11842030	LNCaP	prostate:	n/a
41	chr8:11832762-11832812	Hela-S3	cervix:	n/a
42	chr8:11833039-11833089	ovcar-3	ovarian:	n/a
43	chr8:11839138-11839188	ECC-1	luminal epithelium:	n/a
44	chr8:11839844-11839894	HEK293	kidney:	embryo
45	chr8:11843807-11843857	GM06990	blood:	n/a
46	chr8:11839764-11839814	MCF10A-Er-Src	breast:	n/a
47	chr8:11853121-11853171	AG09309	skin:	n/a
48	chr8:11839138-11839188	HIPEpiC	eye:	n/a
49	chr8:11831823-11831873	GM12878	blood:	n/a
50	chr8:11843807-11843857	HL-60	blood:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:11835676..11838476-chr8:11840654..11843385,2	K562	blood:
2	chr8:11816060..11816951-chr8:11827752..11828579,2	MCF-7	breast:
3	chr8:11835676..11838476-chr8:11840654..11843385,2	K562	blood:
4	chr8:11830756..11832686-chr8:11834027..11835713,2	K562	blood:
5	chr8:11838617..11840884-chr8:11844089..11846019,2	K562	blood:
6	chr8:11424139..11425217-chr8:11815416..11817027,6	K562	blood:
7	chr8:11421778..11422656-chr8:11816114..11817045,3	MCF-7	breast:
8	chr8:11622750..11623420-chr8:11815244..11815854,2	MCF-7	breast:
9	chr8:11421707..11422824-chr8:11816126..11817083,9	K562	blood:
10	chr8:11851923..11853652-chr8:11853797..11856578,2	K562	blood:
11	chr8:11759912..11760480-chr8:11816112..11816711,2	K562	blood:
12	chr8:11833455..11835537-chr8:11843531..11845955,2	K562	blood:
13	chr8:11816131..11817071-chr8:11827985..11828641,3	K562	blood:
14	chr8:11827300..11830194-chr8:11832454..11834607,2	K562	blood:
15	chr8:11816131..11817071-chr8:11827985..11828641,3	K562	blood:
16	chr8:11820183..11822422-chr8:11827376..11829261,2	K562	blood:
17	chr8:11819737..11820672-chr8:11872272..11872975,3	MCF-7	breast:
18	chr8:11835676..11837241-chr8:11840654..11843342,2	K562	blood:
19	chr8:11658805..11661004-chr8:11802756..11805427,2	K562	blood:
20	chr8:11816060..11816951-chr8:11827752..11828579,2	MCF-7	breast:
21	chr8:11836841..11840054-chr8:11842955..11845395,3	MCF-7	breast:
22	chr8:11820183..11822422-chr8:11827376..11829261,2	K562	blood:
23	chr8:11827300..11830194-chr8:11832454..11834607,2	K562	blood:
24	chr8:11798435..11800299-chr8:11803537..11805187,2	K562	blood:
25	chr8:11835676..11837241-chr8:11840654..11843342,2	K562	blood:
26	chr8:11801089..11802817-chr8:11804319..11806900,3	K562	blood:
27	chr8:11619764..11620442-chr8:11816053..11817012,3	K562	blood:
28	chr8:11833455..11835537-chr8:11843531..11845955,2	K562	blood:
29	chr8:11801089..11802817-chr8:11804319..11806900,3	K562	blood:
30	chr8:11622903..11623629-chr8:11815893..11817036,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB135-1	chr8:11856596-11856977	NONHSAT125105

No data

Variant related genes	Relation type
DEFB134	TF binding region
DEFB136	TF binding region
DEFB135	TF binding region
ENSG00000255174	TF binding region
DEFB134	CpG island
DEFB136	CpG island
DEFB135	CpG island
ENSG00000255174	CpG island
ENSG00000079459	chromatin interactions
ENSG00000205883	chromatin interactions
ENSG00000255046	chromatin interactions
ENSG00000205882	chromatin interactions
ENSG00000205884	chromatin interactions

Extended variants
information (count: 3091 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:3091 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528063414	chr8:11802339-11802340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540175449	chr8:11802357-11802358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112815413	chr8:11802368-11802369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561950068	chr8:11802369-11802370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs4240678	chr8:11802426-11802427	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs550783092	chr8:11802453-11802454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534527322	chr8:11802457-11802458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533267625	chr8:11802489-11802490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187745484	chr8:11802518-11802519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559441548	chr8:11802567-11802568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566767433	chr8:11802572-11802573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534179667	chr8:11802574-11802575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555667807	chr8:11802589-11802590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12681142	chr8:11802601-11802602	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs146731942	chr8:11802653-11802654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs578088777	chr8:11802654-11802655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs367763763	chr8:11802659-11802660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545606175	chr8:11802682-11802683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557801165	chr8:11802699-11802700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568796102	chr8:11802703-11802704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572787794	chr8:11802704-11802705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs4841648	chr8:11802711-11802712	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs562002630	chr8:11802715-11802716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs193138152	chr8:11802738-11802739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542747758	chr8:11802752-11802753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544469023	chr8:11802778-11802779	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs562693841	chr8:11802808-11802809	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs533115842	chr8:11802811-11802812	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs551615461	chr8:11802817-11802818	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs560612337	chr8:11802833-11802834	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs527732254	chr8:11802879-11802880	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs530128117	chr8:11802883-11802884	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs111529443	chr8:11802891-11802892	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs548666845	chr8:11802897-11802898	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs538152622	chr8:11802929-11802930	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs150344294	chr8:11802935-11802936	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs571766905	chr8:11802938-11802939	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs576050844	chr8:11802939-11802940	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs188528584	chr8:11802955-11802956	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs546663552	chr8:11802964-11802965	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs34446502	chr8:11802976-11802977	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs570149477	chr8:11802979-11802980	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs572882309	chr8:11802980-11802981	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs192180678	chr8:11802984-11802985	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs7013084	chr8:11802995-11802996	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs573648207	chr8:11803030-11803031	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs138114040	chr8:11803034-11803035	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs573388829	chr8:11803040-11803041	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs78001271	chr8:11803065-11803066	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs577789030	chr8:11803071-11803072	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:140)

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
Breast cancer	22522925	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:744 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11800200-11804600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:11800400-11804200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr8:11800800-11804400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr8:11800800-11807200	Weak transcription	Right Atrium	heart
5	chr8:11801600-11806800	Weak transcription	Fetal Heart	heart
6	chr8:11804200-11804600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr8:11804400-11804600	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr8:11804600-11804800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr8:11804600-11804800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr8:11804800-11805400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr8:11804800-11805800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr8:11805400-11805800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr8:11805800-11806600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr8:11805800-11807000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr8:11806600-11809000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr8:11806800-11807000	Enhancers	Fetal Heart	heart
17	chr8:11807000-11807200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr8:11807000-11807200	Flanking Active TSS	Fetal Heart	heart
19	chr8:11807000-11807400	Bivalent Enhancer	K562	blood
20	chr8:11807200-11807600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr8:11807200-11807600	Enhancers	Fetal Heart	heart
22	chr8:11807200-11807600	Enhancers	Right Atrium	heart
23	chr8:11807200-11807800	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
24	chr8:11807200-11808800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr8:11807400-11807600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr8:11807600-11807800	Bivalent Enhancer	Placenta	Placenta
27	chr8:11807600-11808800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr8:11807600-11812200	Weak transcription	Fetal Heart	heart
29	chr8:11807600-11812600	Weak transcription	Right Atrium	heart
30	chr8:11808800-11810800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr8:11808800-11810800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr8:11809000-11810800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:11810800-11811400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:11810800-11813000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr8:11810800-11813000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr8:11811200-11811400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr8:11811200-11811400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:11811400-11812200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr8:11811400-11812800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr8:11811600-11812600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr8:11812000-11813000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr8:11812200-11812600	Enhancers	Stomach Smooth Muscle	stomach
43	chr8:11812200-11813800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr8:11812200-11814200	Enhancers	Fetal Heart	heart
45	chr8:11812400-11812600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr8:11812400-11812600	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr8:11812400-11812600	Enhancers	Colon Smooth Muscle	Colon
48	chr8:11812400-11812600	Enhancers	Rectal Smooth Muscle	rectum
49	chr8:11812400-11813000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr8:11812400-11813000	Enhancers	Right Ventricle	heart

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