Variant report

Variant	nsv891274
Chromosome Location	chr8:110224047-110308776
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1082)
CpG islands
(count:245)
Chromatin interactive
region (count:65)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1082 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:110241055-110242143	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:110289281-110289645	HepG2	liver:	n/a	n/a
3	ATF2	chr8:110274349-110274803	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr8:110241124-110242274	HCT-116	colon:	n/a	n/a
5	ATF3	chr8:110241073-110242231	HCT-116	colon:	n/a	n/a
6	BACH1	chr8:110241938-110241939	K562	blood:	n/a	n/a
7	BHLHE40	chr8:110241242-110241883	HepG2	liver:	n/a	n/a
8	BHLHE40	chr8:110307193-110307196	HepG2	liver:	n/a	n/a
9	BRCA1	chr8:110294420-110294571	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr8:110283892-110284221	K562	blood:	n/a	n/a
11	CBX3	chr8:110225784-110226023	K562	blood:	n/a	n/a
12	CBX3	chr8:110241092-110242211	HCT-116	colon:	n/a	n/a
13	CBX3	chr8:110304602-110305153	HCT-116	colon:	n/a	n/a
14	CBX3	chr8:110283791-110284340	HCT-116	colon:	n/a	n/a
15	CBX3	chr8:110241027-110242231	HCT-116	colon:	n/a	n/a
16	CBX3	chr8:110283781-110284300	HCT-116	colon:	n/a	n/a
17	CBX3	chr8:110283811-110284240	K562	blood:	n/a	n/a
18	CBX3	chr8:110295193-110295518	K562	blood:	n/a	n/a
19	CEBPB	chr8:110289326-110289508	HepG2	liver:	n/a	n/a
20	CEBPB	chr8:110265965-110266292	HepG2	liver:	n/a	chr8:110266104-110266117 chr8:110266104-110266115
21	CEBPB	chr8:110304424-110305358	HCT-116	colon:	n/a	chr8:110304939-110304952
22	CEBPB	chr8:110304600-110305096	IMR90	lung:	n/a	chr8:110304939-110304952
23	CEBPB	chr8:110240941-110242384	HCT-116	colon:	n/a	chr8:110241297-110241308
24	CEBPB	chr8:110258117-110258334	HepG2	liver:	n/a	chr8:110258218-110258229
25	CEBPB	chr8:110304827-110305100	A549	lung:	n/a	chr8:110304939-110304952
26	CEBPB	chr8:110241114-110241597	HepG2	liver:	n/a	chr8:110241297-110241308
27	CEBPB	chr8:110241215-110241469	HepG2	liver:	n/a	chr8:110241297-110241308
28	CEBPB	chr8:110258049-110258387	IMR90	lung:	n/a	chr8:110258218-110258229
29	CEBPB	chr8:110265987-110266274	H1-hESC	embryonic stem cell:	n/a	chr8:110266104-110266117 chr8:110266104-110266115
30	CEBPB	chr8:110265971-110266273	IMR90	lung:	n/a	chr8:110266104-110266117 chr8:110266104-110266115
31	CEBPB	chr8:110266003-110266249	A549	lung:	n/a	chr8:110266104-110266117 chr8:110266104-110266115
32	CEBPB	chr8:110278818-110278920	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr8:110278754-110278970	MCF-7	breast:	n/a	n/a
34	CEBPB	chr8:110289230-110289603	HepG2	liver:	n/a	n/a
35	CEBPB	chr8:110278803-110278974	K562	blood:	n/a	n/a
36	CEBPB	chr8:110241135-110241634	HepG2	liver:	n/a	chr8:110241297-110241308
37	CEBPB	chr8:110241016-110242195	HCT-116	colon:	n/a	chr8:110241297-110241308
38	CEBPB	chr8:110258108-110258384	A549	lung:	n/a	chr8:110258218-110258229
39	CEBPB	chr8:110294414-110294618	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr8:110294169-110294703	MCF-7	breast:	n/a	n/a
41	CEBPB	chr8:110265928-110266293	K562	blood:	n/a	chr8:110266104-110266117 chr8:110266104-110266115
42	CEBPB	chr8:110280529-110280673	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr8:110241186-110241421	HepG2	liver:	n/a	chr8:110241297-110241308
44	CEBPB	chr8:110304659-110305178	A549	lung:	n/a	chr8:110304939-110304952
45	CEBPB	chr8:110304601-110305135	Hela-S3	cervix:	n/a	chr8:110304939-110304952
46	CEBPB	chr8:110304560-110305134	HCT-116	colon:	n/a	chr8:110304939-110304952
47	CHD1	chr8:110274336-110274349	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr8:110294401-110294667	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr8:110274460-110274867	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr8:110241130-110241759	HepG2	liver:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:110274914-110274964	LNCaP	prostate:	n/a
2	chr8:110274914-110274964	LNCaP	prostate:	n/a
3	chr8:110272720-110272770	RPTEC	kidney:	n/a
4	chr8:110253782-110253832	SK-N-MC	brain:	n/a
5	chr8:110280928-110280978	Hela-S3	cervix:	n/a
6	chr8:110272720-110272770	K562	blood:	n/a
7	chr8:110280928-110280978	K562	blood:	n/a
8	chr8:110274914-110274964	HRPEpiC	eye:	n/a
9	chr8:110280928-110280978	GM19239	blood:	n/a
10	chr8:110253782-110253832	HCM	heart:	n/a
11	chr8:110272720-110272770	BJ	skin:	n/a
12	chr8:110274914-110274964	GM12892	blood:	n/a
13	chr8:110280928-110280978	HEEpiC	esophagus:	n/a
14	chr8:110272720-110272770	T-47D	breast:	n/a
15	chr8:110253782-110253832	CMK	blood:	n/a
16	chr8:110274914-110274964	PrEC	prostate:	n/a
17	chr8:110280928-110280978	SAEC	small airway:	n/a
18	chr8:110280928-110280978	ProgFib	skin:	n/a
19	chr8:110274914-110274964	Jurkat	blood:	n/a
20	chr8:110253782-110253832	HAEpiC	amniotic membrane:	n/a
21	chr8:110272720-110272770	SKMC	muscle:	n/a
22	chr8:110274914-110274964	NH-A	brain:	n/a
23	chr8:110274914-110274964	HCM	heart:	n/a
24	chr8:110274914-110274964	ovcar-3	ovarian:	n/a
25	chr8:110253782-110253832	H1-hESC	embryonic stem cell:	embryo
26	chr8:110274914-110274964	A549	lung:	n/a
27	chr8:110280928-110280978	GM12891	blood:	n/a
28	chr8:110253782-110253832	IMR90	lung:	fetal
29	chr8:110253782-110253832	HCT-116	colon:	n/a
30	chr8:110272720-110272770	HPAEpiC	pulmonary alveolar:	n/a
31	chr8:110274914-110274964	NB4	blood:	n/a
32	chr8:110280928-110280978	PANC-1	pancreas:	n/a
33	chr8:110253782-110253832	MCF-7	breast:	n/a
34	chr8:110280928-110280978	A549	lung:	n/a
35	chr8:110280928-110280978	HCPEpiC	choroid plexus:	n/a
36	chr8:110274914-110274964	GM19239	blood:	n/a
37	chr8:110274914-110274964	Hela-S3	cervix:	n/a
38	chr8:110272720-110272770	CMK	blood:	n/a
39	chr8:110280928-110280978	ECC-1	luminal epithelium:	n/a
40	chr8:110280928-110280978	Hepatocyte	liver:	n/a
41	chr8:110272720-110272770	GM06990	blood:	n/a
42	chr8:110272720-110272770	PrEC	prostate:	n/a
43	chr8:110272720-110272770	SK-N-SH	brain:	n/a
44	chr8:110280928-110280978	NT2-D1	testis:	n/a
45	chr8:110274914-110274964	HAEpiC	amniotic membrane:	n/a
46	chr8:110274914-110274964	HNPCEpiC	eye:	n/a
47	chr8:110272720-110272770	HCF	heart:	n/a
48	chr8:110272720-110272770	U87	brain:	n/a
49	chr8:110272720-110272770	HAEpiC	amniotic membrane:	n/a
50	chr8:110274914-110274964	CMK	blood:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:110273357..110276985-chr8:110278828..110281749,3	K562	blood:
2	chr8:110242575..110246884-chr8:110247305..110250446,3	MCF-7	breast:
3	chr8:110284939..110287374-chr8:110293583..110295372,2	MCF-7	breast:
4	chr8:110267160..110271575-chr8:110275719..110280785,4	MCF-7	breast:
5	chr8:110266910..110269823-chr8:110274098..110276440,2	MCF-7	breast:
6	chr8:110305748..110308660-chr8:110346435..110347987,2	K562	blood:
7	chr8:110236599..110237927-chr8:110328052..110329074,4	MCF-7	breast:
8	chr8:110284939..110287374-chr8:110293583..110295372,2	MCF-7	breast:
9	chr8:110284682..110286826-chr8:110289156..110291459,2	MCF-7	breast:
10	chr8:110284180..110285865-chr8:110286825..110289616,2	K562	blood:
11	chr8:110276401..110278429-chr8:110280186..110282933,2	MCF-7	breast:
12	chr8:110298680..110300639-chr8:110303623..110306620,2	K562	blood:
13	chr8:110265183..110267675-chr8:110271618..110273789,2	K562	blood:
14	chr8:110237132..110238315-chr8:110294080..110295100,5	MCF-7	breast:
15	chr8:110293214..110295684-chr8:110300331..110302859,2	MCF-7	breast:
16	chr8:110251271..110254204-chr8:110279241..110281441,2	K562	blood:
17	chr8:110237132..110238315-chr8:110294080..110295100,5	MCF-7	breast:
18	chr8:110238617..110240882-chr8:110264919..110266571,2	MCF-7	breast:
19	chr8:110051446..110054408-chr8:110240885..110242830,2	MCF-7	breast:
20	chr8:110245513..110246299-chr8:110328099..110328844,2	MCF-7	breast:
21	chr8:110302918..110306043-chr8:110308192..110310489,3	MCF-7	breast:
22	chr8:109931267..109933961-chr8:110239914..110241556,2	MCF-7	breast:
23	chr8:110293214..110295684-chr8:110300331..110302859,2	MCF-7	breast:
24	chr8:110298680..110300639-chr8:110303623..110306620,2	K562	blood:
25	chr8:110273357..110276985-chr8:110278828..110281749,3	K562	blood:
26	chr8:109930335..109931225-chr8:110235196..110236060,2	MCF-7	breast:
27	chr8:110249700..110252178-chr8:110258243..110259912,2	K562	blood:
28	chr8:110282798..110284490-chr8:110290384..110293883,3	K562	blood:
29	chr8:110265183..110267675-chr8:110271618..110273789,2	K562	blood:
30	chr8:110296774..110299286-chr8:110348162..110350315,2	K562	blood:
31	chr8:110293728..110295786-chr8:110296881..110298730,2	MCF-7	breast:
32	chr8:110276401..110278429-chr8:110280186..110282933,2	MCF-7	breast:
33	chr8:110284682..110286826-chr8:110289156..110291459,2	MCF-7	breast:
34	chr8:110238617..110240882-chr8:110264919..110266571,2	MCF-7	breast:
35	chr8:110271725..110274616-chr8:110342573..110345047,2	K562	blood:
36	chr8:110282798..110284490-chr8:110290384..110293883,3	K562	blood:
37	chr8:110267160..110271575-chr8:110275719..110280785,4	MCF-7	breast:
38	chr8:110249700..110252178-chr8:110258243..110259912,2	K562	blood:
39	chr8:110237564..110238071-chr8:110338220..110338727,2	MCF-7	breast:
40	chr8:110284180..110285865-chr8:110286825..110289616,2	K562	blood:
41	chr8:109930431..109931332-chr8:110293724..110294960,8	MCF-7	breast:
42	chr8:110251256..110254212-chr8:110254485..110256380,2	K562	blood:
43	chr8:110274391..110276446-chr8:110278687..110281148,2	MCF-7	breast:
44	chr8:110234924..110237282-chr8:110242100..110245071,2	K562	blood:
45	chr8:110300725..110303179-chr8:110304720..110306354,2	MCF-7	breast:
46	chr8:110274484..110277076-chr8:110350109..110352539,2	K562	blood:
47	chr8:110251271..110254204-chr8:110279241..110281441,2	K562	blood:
48	chr8:110252631..110254624-chr8:110265466..110267437,3	MCF-7	breast:
49	chr8:110302918..110306043-chr8:110308192..110310489,3	MCF-7	breast:
50	chr8:110242575..110246884-chr8:110247305..110250446,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDCD1-1	chr8:110243904-110244239	NONHSAT128287

No data

Variant related genes	Relation type
ENSG00000250267	TF binding region
ENSG00000250267	CpG island
ENSG00000120533	chromatin interactions
ENSG00000253796	chromatin interactions
ENSG00000147654	chromatin interactions
ENSG00000120526	chromatin interactions

Extended variants
information (count: 3162 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3162 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4735119	chr8:110224047-110224048	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538961889	chr8:110224099-110224100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189901866	chr8:110224106-110224107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs199914710	chr8:110224121-110224122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs66982660	chr8:110224122-110224123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs56395614	chr8:110224123-110224124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182526699	chr8:110224189-110224190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537856268	chr8:110224212-110224213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142296715	chr8:110224221-110224222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77031422	chr8:110224245-110224246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540416967	chr8:110224286-110224287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs56358144	chr8:110224294-110224295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573844906	chr8:110224295-110224296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201733593	chr8:110224296-110224297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs202064529	chr8:110224324-110224325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs72409696	chr8:110224325-110224326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185709407	chr8:110224328-110224329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191828040	chr8:110224329-110224330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531563430	chr8:110224361-110224362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369319356	chr8:110224365-110224366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200432230	chr8:110224384-110224385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543057821	chr8:110224393-110224394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542255497	chr8:110224402-110224403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183598074	chr8:110224405-110224406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527821196	chr8:110224448-110224449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188994134	chr8:110224477-110224478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560360043	chr8:110224485-110224486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532361264	chr8:110224491-110224492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145916001	chr8:110224527-110224528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531740171	chr8:110224542-110224543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201374519	chr8:110224556-110224557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs193128131	chr8:110224616-110224617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551836258	chr8:110224628-110224629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116163014	chr8:110224703-110224704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568046247	chr8:110224716-110224717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138863459	chr8:110224720-110224721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553468522	chr8:110224726-110224727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374809298	chr8:110224761-110224762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375535665	chr8:110224769-110224770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141207683	chr8:110224774-110224775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556576244	chr8:110224779-110224780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576713675	chr8:110224858-110224859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143523274	chr8:110224871-110224872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562141477	chr8:110224872-110224873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140324584	chr8:110224896-110224897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541502009	chr8:110224897-110224898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564580425	chr8:110224943-110224944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184148797	chr8:110224944-110224945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186546197	chr8:110224975-110224976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562627920	chr8:110224978-110224979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Multiple myeloma	16461302	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1617 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:110191400-110237400	Weak transcription	Left Ventricle	heart
2	chr8:110204800-110230600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:110211200-110311600	Weak transcription	Right Ventricle	heart
4	chr8:110225600-110231000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:110225800-110226000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr8:110225800-110241800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr8:110226000-110230600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr8:110230000-110230600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
9	chr8:110230000-110230600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr8:110230200-110231200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr8:110230400-110241000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr8:110230600-110230800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:110230600-110231800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr8:110230600-110231800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr8:110231000-110231800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:110231000-110231800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr8:110231000-110238600	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr8:110231200-110233600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
19	chr8:110231400-110232200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
20	chr8:110231400-110233200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
21	chr8:110231400-110236800	Weak transcription	Ovary	ovary
22	chr8:110231600-110235600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr8:110231800-110233000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:110231800-110234800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr8:110231800-110235400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr8:110231800-110235400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr8:110231800-110237400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr8:110231800-110242200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr8:110232200-110232800	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr8:110232800-110233200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
31	chr8:110233400-110233600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
32	chr8:110233600-110239000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr8:110233800-110235800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr8:110233800-110236200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr8:110233800-110237400	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr8:110234200-110237400	Weak transcription	Pancreas	Pancrea
37	chr8:110234200-110241200	Weak transcription	HUVEC	blood vessel
38	chr8:110234400-110235400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
39	chr8:110234400-110235800	Weak transcription	Brain Germinal Matrix	brain
40	chr8:110234400-110236000	Weak transcription	A549	lung
41	chr8:110234400-110237400	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr8:110234600-110237400	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr8:110234600-110240400	Weak transcription	HMEC	breast
44	chr8:110234800-110235000	ZNF genes & repeats	Liver	Liver
45	chr8:110234800-110238000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr8:110234800-110264200	Weak transcription	Primary B cells from peripheral blood	blood
47	chr8:110235000-110237400	Weak transcription	Fetal Muscle Trunk	muscle
48	chr8:110235000-110239000	Weak transcription	Liver	Liver
49	chr8:110235000-110239800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr8:110235000-110240600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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