Variant report

Variant	nsv891647
Chromosome Location	chr8:143920340-143984880
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:583)
CpG islands
(count:915)
Chromatin interactive
region (count:30)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:583 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:143943119-143943687	HepG2	liver:	n/a	n/a
2	ATF1	chr8:143926111-143926335	K562	blood:	n/a	n/a
3	BATF	chr8:143952169-143952426	GM12878	blood:	n/a	chr8:143952314-143952325
4	BHLHE40	chr8:143959425-143959448	K562	blood:	n/a	n/a
5	BHLHE40	chr8:143975344-143975622	K562	blood:	n/a	n/a
6	BHLHE40	chr8:143946391-143946484	K562	blood:	n/a	n/a
7	BHLHE40	chr8:143975332-143975632	HepG2	liver:	n/a	n/a
8	BHLHE40	chr8:143955812-143956123	K562	blood:	n/a	n/a
9	BHLHE40	chr8:143952207-143952419	GM12878	blood:	n/a	n/a
10	CBX3	chr8:143955785-143956085	K562	blood:	n/a	n/a
11	CEBPB	chr8:143943419-143943642	HepG2	liver:	n/a	n/a
12	CEBPB	chr8:143975315-143975613	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr8:143955958-143956450	K562	blood:	n/a	chr8:143956304-143956317
14	CHD2	chr8:143968205-143968520	K562	blood:	n/a	n/a
15	CREB1	chr8:143946856-143947217	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr8:143946702-143947270	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr8:143946780-143946930	AG04449	skin:	n/a	n/a
18	CTCF	chr8:143922228-143922359	MCF-7	breast:	n/a	n/a
19	CTCF	chr8:143946324-143946574	LNCaP	prostate:	n/a	n/a
20	CTCF	chr8:143946316-143946598	LNCaP	prostate:	n/a	n/a
21	CTCF	chr8:143922240-143922390	HCT-116	colon:	n/a	n/a
22	CTCF	chr8:143946420-143946570	HCM	heart:	n/a	n/a
23	CTCF	chr8:143922215-143922388	GM12878	blood:	n/a	n/a
24	CTCF	chr8:143922180-143922330	GM12873	blood:	n/a	n/a
25	CTCF	chr8:143922200-143922350	GM12875	blood:	n/a	n/a
26	CTCF	chr8:143946380-143946530	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr8:143946420-143946570	HFF	foreskin:	n/a	n/a
28	CTCF	chr8:143955840-143955990	MCF-7	breast:	n/a	n/a
29	CTCF	chr8:143946400-143946550	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr8:143945428-143947117	A549	lung:	n/a	n/a
31	CTCF	chr8:143946250-143946601	K562	blood:	n/a	n/a
32	CTCF	chr8:143946328-143946610	GM19239	blood:	n/a	n/a
33	CTCF	chr8:143946240-143946664	K562	blood:	n/a	n/a
34	CTCF	chr8:143922046-143922489	K562	blood:	n/a	n/a
35	CTCF	chr8:143946345-143946602	HepG2	liver:	n/a	n/a
36	CTCF	chr8:143922180-143922330	NB4	blood:	n/a	n/a
37	CTCF	chr8:143946293-143946655	A549	lung:	n/a	n/a
38	CTCF	chr8:143946400-143946550	AG04450	lung:	n/a	n/a
39	CTCF	chr8:143946380-143946530	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr8:143946420-143946570	HMEC	breast:	n/a	n/a
41	CTCF	chr8:143946286-143946544	ECC-1	luminal epithelium:	n/a	n/a
42	CTCF	chr8:143946322-143946574	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr8:143946329-143946588	GM13977	blood:	n/a	n/a
44	CTCF	chr8:143946330-143946568	GM10266	blood:	n/a	n/a
45	CTCF	chr8:143946400-143946550	GM12874	blood:	n/a	n/a
46	CTCF	chr8:143922236-143922349	HepG2	liver:	n/a	n/a
47	CTCF	chr8:143946360-143946510	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr8:143922272-143922305	MCF-7	breast:	n/a	n/a
49	CTCF	chr8:143946380-143946530	GM12872	blood:	n/a	n/a
50	CTCF	chr8:143946315-143946595	Medullo	brain:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:143946809-143946859	T-47D	breast:	n/a
2	chr8:143926325-143926375	BE2_C	brain:	n/a
3	chr8:143958385-143958435	CMK	blood:	n/a
4	chr8:143958577-143958627	HCF	heart:	n/a
5	chr8:143955181-143955231	HNPCEpiC	eye:	n/a
6	chr8:143958385-143958435	NHBE	bronchial:	n/a
7	chr8:143958385-143958435	Jurkat	blood:	n/a
8	chr8:143958385-143958435	NB4	blood:	n/a
9	chr8:143961341-143961391	NHDF-neo	bronchial:	n/a
10	chr8:143925513-143925563	NB4	blood:	n/a
11	chr8:143960794-143960844	HNPCEpiC	eye:	n/a
12	chr8:143960794-143960844	AG09319	gingival:	n/a
13	chr8:143958577-143958627	HNPCEpiC	eye:	n/a
14	chr8:143956517-143956567	GM19239	blood:	n/a
15	chr8:143961291-143961341	MCF-7	breast:	n/a
16	chr8:143958385-143958435	Hela-S3	cervix:	n/a
17	chr8:143958577-143958627	NH-A	brain:	n/a
18	chr8:143961341-143961391	A549	lung:	n/a
19	chr8:143961291-143961341	SK-N-SH_RA	brain:	n/a
20	chr8:143961145-143961195	PFSK-1	brain:	n/a
21	chr8:143957347-143957397	U87	brain:	n/a
22	chr8:143960794-143960844	K562	blood:	n/a
23	chr8:143958385-143958435	RPTEC	kidney:	n/a
24	chr8:143961341-143961391	NB4	blood:	n/a
25	chr8:143961145-143961195	HUVEC	blood vessel:	n/a
26	chr8:143946809-143946859	HCT-116	colon:	n/a
27	chr8:143926325-143926375	NH-A	brain:	n/a
28	chr8:143961141-143961191	PANC-1	pancreas:	n/a
29	chr8:143926325-143926375	ovcar-3	ovarian:	n/a
30	chr8:143958385-143958435	AG09319	gingival:	n/a
31	chr8:143961141-143961191	A549	lung:	n/a
32	chr8:143946809-143946859	HNPCEpiC	eye:	n/a
33	chr8:143961341-143961391	ovcar-3	ovarian:	n/a
34	chr8:143957347-143957397	SAEC	small airway:	n/a
35	chr8:143957809-143957859	HRPEpiC	eye:	n/a
36	chr8:143926325-143926375	HCPEpiC	choroid plexus:	n/a
37	chr8:143961291-143961341	HEK293	kidney:	embryo
38	chr8:143960794-143960844	GM06990	blood:	n/a
39	chr8:143961341-143961391	NT2-D1	testis:	n/a
40	chr8:143946809-143946859	HRCEpiC	kidney:	n/a
41	chr8:143946809-143946859	HRE	kidney:	n/a
42	chr8:143961145-143961195	H1-hESC	embryonic stem cell:	embryo
43	chr8:143925513-143925563	HNPCEpiC	eye:	n/a
44	chr8:143946809-143946859	A549	lung:	n/a
45	chr8:143960794-143960844	PANC-1	pancreas:	n/a
46	chr8:143961291-143961341	IMR90	lung:	fetal
47	chr8:143955181-143955231	BE2_C	brain:	n/a
48	chr8:143925513-143925563	U87	brain:	n/a
49	chr8:143946809-143946859	NT2-D1	testis:	n/a
50	chr8:143958385-143958435	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:143946808..143950749-chr8:143951745..143954647,3	MCF-7	breast:
2	chr8:143915524..143917551-chr8:143919721..143921570,2	K562	blood:
3	chr8:143937339..143939539-chr8:143943827..143946799,2	K562	blood:
4	chr8:143922239..143923851-chr8:143929533..143932108,2	K562	blood:
5	chr8:143946454..143948817-chr8:144107214..144108998,2	MCF-7	breast:
6	chr8:143956006..143958994-chr8:144119486..144121629,2	MCF-7	breast:
7	chr8:143945983..143946553-chr8:144110469..144111073,2	MCF-7	breast:
8	chr8:143916939..143918538-chr8:143919157..143921821,2	MCF-7	breast:
9	chr8:143945790..143948477-chr8:144097861..144100482,4	MCF-7	breast:
10	chr8:143920958..143925881-chr8:143926446..143930514,5	MCF-7	breast:
11	chr8:143946808..143950749-chr8:143951745..143954647,3	MCF-7	breast:
12	chr8:143928685..143930379-chr8:143986753..143989580,2	K562	blood:
13	chr8:143945984..143947341-chr8:144065118..144066440,13	MCF-7	breast:
14	chr8:143970505..143972946-chr8:143997611..144000246,2	MCF-7	breast:
15	chr8:143911313..143913922-chr8:143922454..143924635,2	MCF-7	breast:
16	chr8:143976851..143979156-chr8:143982564..143985353,2	MCF-7	breast:
17	chr8:143954490..143957417-chr8:144098775..144100679,3	MCF-7	breast:
18	chr8:143913018..143915383-chr8:143919740..143921369,2	MCF-7	breast:
19	chr8:143914444..143917340-chr8:143923491..143925641,2	MCF-7	breast:
20	chr8:143945972..143946899-chr8:144015017..144015972,3	MCF-7	breast:
21	chr8:143937339..143939539-chr8:143943827..143946799,2	K562	blood:
22	chr8:143947786..143949833-chr8:144110474..144112075,2	K562	blood:
23	chr8:143982631..143984699-chr8:143987404..143990195,2	K562	blood:
24	chr8:143976851..143979156-chr8:143982564..143985353,2	MCF-7	breast:
25	chr8:143945596..143947202-chr8:144065141..144066639,16	MCF-7	breast:
26	chr8:143920958..143925881-chr8:143926446..143930514,5	MCF-7	breast:
27	chr8:143945981..143946890-chr8:144129351..144130428,4	MCF-7	breast:
28	chr8:143897585..143899463-chr8:143921203..143923883,2	MCF-7	breast:
29	chr8:143922239..143923851-chr8:143929533..143932108,2	K562	blood:
30	chr8:143952603..143954565-chr8:144064385..144066432,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LY6E-4	chr8:143957598-143957980	NONHSAT129503
2	lnc-LY6E-4	chr8:143959812-143960330	NONHSAT129503
3	lnc-CYP11B1-2	chr8:143950348-143952878	NONHSAT129502

No data

Variant related genes	Relation type
CYP11B1	TF binding region
ENSG00000253728	TF binding region
ZNHIT1P1	TF binding region
CYP11B1	CpG island
ENSG00000253728	CpG island
ZNHIT1P1	CpG island
ENSG00000179142	chromatin interactions
ENSG00000160932	chromatin interactions
ENSG00000253728	chromatin interactions
ENSG00000104499	chromatin interactions
ENSG00000247317	chromatin interactions
ENSG00000177335	chromatin interactions

Extended variants
information (count: 2787 )
Associated
traits (count: 149 )

Variant overlapped rSNPs/rCNVs (count:2787 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4736338	chr8:143920340-143920341	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs4736339	chr8:143920343-143920344	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs4736340	chr8:143920373-143920374	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs118008245	chr8:143920378-143920379	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs553557432	chr8:143920446-143920447	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs535778388	chr8:143920467-143920468	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs2027890	chr8:143920538-143920539	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs4736341	chr8:143920557-143920558	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs144049001	chr8:143920558-143920559	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs539475233	chr8:143920562-143920563	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs543699908	chr8:143920565-143920566	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs114333336	chr8:143920572-143920573	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs2027891	chr8:143920574-143920575	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs572998697	chr8:143920581-143920582	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs2027892	chr8:143920583-143920584	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs11445904	chr8:143920588-143920589	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs2717568	chr8:143920625-143920626	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs75880477	chr8:143920643-143920644	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs555280515	chr8:143920666-143920667	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs74345639	chr8:143920685-143920686	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs549122373	chr8:143920687-143920688	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs75280229	chr8:143920733-143920734	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs2717569	chr8:143920762-143920763	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs76003351	chr8:143920772-143920773	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs545820186	chr8:143920776-143920777	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs77513604	chr8:143920787-143920788	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs183407481	chr8:143920828-143920829	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs573682342	chr8:143920851-143920852	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs116280313	chr8:143920860-143920861	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs529532407	chr8:143920873-143920874	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs186639772	chr8:143920897-143920898	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs375172013	chr8:143920905-143920906	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs191292195	chr8:143920906-143920907	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs369412096	chr8:143920907-143920908	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs540112170	chr8:143920908-143920909	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs115446880	chr8:143920914-143920915	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs75991734	chr8:143920924-143920925	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs533874094	chr8:143920957-143920958	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs114662302	chr8:143920958-143920959	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs573642386	chr8:143920960-143920961	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs376657299	chr8:143920975-143920976	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs377389794	chr8:143921006-143921007	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs544427385	chr8:143921036-143921037	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs556062111	chr8:143921037-143921038	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs577538229	chr8:143921064-143921065	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs544867968	chr8:143921079-143921080	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs144931590	chr8:143921080-143921081	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs1016935	chr8:143921083-143921084	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs756551	chr8:143921095-143921096	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs540256898	chr8:143921096-143921097	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:149)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	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
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	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
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	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
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Developmental delay	21147756	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	16616336	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Gastric cancer	24379144	CNVD
Sezary syndrome	18413736	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20409316	CNVD
Colorectal cancer	16272173	CNVD
Glioma	17123091	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Esophageal squamous carcinoma	17470683	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Astrocytoma	22246337	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	21806811	CNVD
Chylomicronemia	22008945	CNVD
Heart disease	21282601	CNVD
Chordoma	21602918	CNVD
Neuroblastoma	18923191	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	16397240	CNVD
Colorectal cancer	19455253	CNVD
Myxofibrosarcoma	16751306	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
Oral cancer	22144094	CNVD
XY gonadal dysgenesis	20685758	CNVD
Cancer	20581869	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Pancreatic cancer	21811587	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	16824018	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:143913200-143922000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:143916000-143922200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:143919200-143921000	Enhancers	HSMMtube	muscle
4	chr8:143919400-143924600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr8:143919600-143920600	Enhancers	NH-A	brain
6	chr8:143919800-143920400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:143919800-143920600	Bivalent Enhancer	NHEK	skin
8	chr8:143919800-143920800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr8:143920000-143920400	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr8:143920000-143920400	Enhancers	HMEC	breast
11	chr8:143920000-143920400	Enhancers	Osteobl	bone
12	chr8:143920000-143920600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr8:143920000-143920600	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr8:143920000-143920600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
15	chr8:143920000-143921000	Enhancers	HSMM	muscle
16	chr8:143920000-143921200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr8:143920000-143921800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr8:143920000-143923600	Enhancers	Primary T cells fromperipheralblood	blood
19	chr8:143920000-143927400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr8:143920400-143920600	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:143920400-143920800	Enhancers	Placenta Amnion	Placenta Amnion
22	chr8:143920600-143920800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr8:143920600-143921000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr8:143920600-143922400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr8:143920600-143926200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr8:143921200-143921400	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr8:143921600-143921800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr8:143921600-143921800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
29	chr8:143922000-143922400	Active TSS	Gastric	stomach
30	chr8:143922000-143923000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr8:143922200-143922400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr8:143922400-143924000	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr8:143922600-143922800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
34	chr8:143922600-143924200	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr8:143922600-143927400	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr8:143922600-143927600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr8:143922800-143923200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr8:143922800-143924200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr8:143922800-143924200	Enhancers	Fetal Thymus	thymus
40	chr8:143922800-143924600	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr8:143922800-143924800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr8:143922800-143926000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr8:143922800-143927200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr8:143922800-143927600	Enhancers	Primary T cells from cord blood	blood
45	chr8:143922800-143927600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr8:143922800-143927600	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr8:143923000-143924200	Enhancers	Primary hematopoietic stem cells	blood
48	chr8:143923200-143923600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr8:143923600-143923800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
50	chr8:143923600-143926200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood

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