Variant report

Variant	nsv533559
Chromosome Location	chr8:92116009-92175700
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:247)
CpG islands
(count:183)
Chromatin interactive
region (count:29)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:247 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:92121937-92122001	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:92130895-92131095	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:92119585-92120834	HepG2	liver:	n/a	n/a
4	ATF1	chr8:92126805-92126814	K562	blood:	n/a	n/a
5	ATF2	chr8:92157649-92158115	GM12878	blood:	n/a	n/a
6	BACH1	chr8:92130210-92130270	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr8:92120097-92120425	HepG2	liver:	n/a	n/a
8	BHLHE40	chr8:92119659-92120741	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:92148641-92148988	K562	blood:	n/a	chr8:92148804-92148815
10	CEBPB	chr8:92130918-92131377	IMR90	lung:	n/a	n/a
11	CEBPB	chr8:92120574-92120772	IMR90	lung:	n/a	n/a
12	CEBPB	chr8:92148557-92148979	MCF-7	breast:	n/a	chr8:92148804-92148815
13	CEBPB	chr8:92123908-92124201	HepG2	liver:	n/a	n/a
14	CEBPB	chr8:92152343-92152575	HepG2	liver:	n/a	chr8:92152445-92152458 chr8:92152447-92152456 chr8:92152447-92152456 chr8:92152445-92152458 chr8:92152447-92152456 chr8:92152447-92152456 chr8:92152447-92152458 chr8:92152445-92152456 chr8:92152447-92152458
15	CEBPB	chr8:92119569-92119750	HepG2	liver:	n/a	n/a
16	CEBPB	chr8:92152325-92152560	IMR90	lung:	n/a	chr8:92152445-92152458 chr8:92152447-92152456 chr8:92152447-92152456 chr8:92152445-92152458 chr8:92152447-92152456 chr8:92152447-92152456 chr8:92152447-92152458 chr8:92152445-92152456 chr8:92152447-92152458
17	CEBPB	chr8:92164320-92164536	A549	lung:	n/a	n/a
18	CEBPB	chr8:92148613-92148967	MCF-7	breast:	n/a	chr8:92148804-92148815
19	CEBPB	chr8:92148672-92148965	HepG2	liver:	n/a	chr8:92148804-92148815
20	CEBPB	chr8:92148653-92148976	IMR90	lung:	n/a	chr8:92148804-92148815
21	CEBPB	chr8:92120050-92120860	HepG2	liver:	n/a	chr8:92120199-92120211
22	CHD2	chr8:92124549-92124557	HepG2	liver:	n/a	n/a
23	CHD2	chr8:92120111-92120465	HepG2	liver:	n/a	n/a
24	CREB1	chr8:92157732-92158202	GM12878	blood:	n/a	n/a
25	CTCF	chr8:92129900-92130050	BJ	skin:	n/a	n/a
26	CTCF	chr8:92129980-92130130	AG04449	skin:	n/a	n/a
27	CTCF	chr8:92120500-92120650	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr8:92152201-92152298	LNCaP	prostate:	n/a	n/a
29	CTCF	chr8:92120480-92120630	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr8:92120551-92120591	GM20000	blood:	n/a	n/a
31	CTCF	chr8:92120540-92120690	RPTEC	kidney:	n/a	n/a
32	CTCF	chr8:92120480-92120630	AG04449	skin:	n/a	n/a
33	CTCF	chr8:92120440-92120590	AG09319	gingival:	n/a	n/a
34	CTCF	chr8:92129900-92130050	AG10803	skin:	n/a	n/a
35	CTCF	chr8:92129880-92130030	BJ	skin:	n/a	n/a
36	CTCF	chr8:92120480-92120630	MCF-7	breast:	n/a	n/a
37	CTCF	chr8:92120546-92120549	K562	blood:	n/a	n/a
38	CTCF	chr8:92120480-92120630	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr8:92120564-92120587	GM12878	blood:	n/a	n/a
40	CTCF	chr8:92120385-92120778	K562	blood:	n/a	n/a
41	CTCF	chr8:92120518-92120587	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr8:92120517-92120624	HepG2	liver:	n/a	n/a
43	CTCF	chr8:92120480-92120628	Medullo	brain:	n/a	n/a
44	CTCF	chr8:92120497-92120621	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr8:92175640-92175790	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr8:92120400-92120550	BE2_C	brain:	n/a	n/a
47	CTCF	chr8:92120460-92120610	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr8:92120440-92120590	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr8:92120477-92120670	MCF-7	breast:	n/a	n/a
50	CTCF	chr8:92120501-92120636	MCF-7	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:92129661-92129711	HL-60	blood:	n/a
2	chr8:92130454-92130504	CMK	blood:	n/a
3	chr8:92129661-92129711	ovcar-3	ovarian:	n/a
4	chr8:92129661-92129711	Hepatocyte	liver:	n/a
5	chr8:92130454-92130504	ProgFib	skin:	n/a
6	chr8:92130025-92130075	SK-N-SH	brain:	n/a
7	chr8:92130454-92130504	HCPEpiC	choroid plexus:	n/a
8	chr8:92129661-92129711	HCM	heart:	n/a
9	chr8:92130454-92130504	HCM	heart:	n/a
10	chr8:92130025-92130075	GM19239	blood:	n/a
11	chr8:92129661-92129711	ProgFib	skin:	n/a
12	chr8:92129661-92129711	NT2-D1	testis:	n/a
13	chr8:92130454-92130504	GM12878	blood:	n/a
14	chr8:92130025-92130075	RPTEC	kidney:	n/a
15	chr8:92130025-92130075	NHBE	bronchial:	n/a
16	chr8:92129661-92129711	SAEC	small airway:	n/a
17	chr8:92130454-92130504	HCF	heart:	n/a
18	chr8:92130025-92130075	AG09319	gingival:	n/a
19	chr8:92129661-92129711	BE2_C	brain:	n/a
20	chr8:92129661-92129711	HCT-116	colon:	n/a
21	chr8:92130025-92130075	HEEpiC	esophagus:	n/a
22	chr8:92130025-92130075	HIPEpiC	eye:	n/a
23	chr8:92130025-92130075	HNPCEpiC	eye:	n/a
24	chr8:92130025-92130075	HRCEpiC	kidney:	n/a
25	chr8:92129661-92129711	HRCEpiC	kidney:	n/a
26	chr8:92129661-92129711	GM06990	blood:	n/a
27	chr8:92130025-92130075	HCM	heart:	n/a
28	chr8:92130454-92130504	HIPEpiC	eye:	n/a
29	chr8:92129661-92129711	IMR90	lung:	fetal
30	chr8:92130025-92130075	CMK	blood:	n/a
31	chr8:92129661-92129711	NB4	blood:	n/a
32	chr8:92130454-92130504	K562	blood:	n/a
33	chr8:92130025-92130075	A549	lung:	n/a
34	chr8:92129661-92129711	Caco-2	colon:	n/a
35	chr8:92130454-92130504	GM12892	blood:	n/a
36	chr8:92129661-92129711	SK-N-SH_RA	brain:	n/a
37	chr8:92129661-92129711	K562	blood:	n/a
38	chr8:92130025-92130075	PFSK-1	brain:	n/a
39	chr8:92129661-92129711	HEK293	kidney:	embryo
40	chr8:92130454-92130504	U87	brain:	n/a
41	chr8:92130025-92130075	SK-N-SH_RA	brain:	n/a
42	chr8:92129661-92129711	SK-N-MC	brain:	n/a
43	chr8:92130454-92130504	PrEC	prostate:	n/a
44	chr8:92130454-92130504	ovcar-3	ovarian:	n/a
45	chr8:92130454-92130504	RPTEC	kidney:	n/a
46	chr8:92130025-92130075	Hepatocyte	liver:	n/a
47	chr8:92130454-92130504	HepG2	liver:	n/a
48	chr8:92130025-92130075	LNCaP	prostate:	n/a
49	chr8:92129661-92129711	CMK	blood:	n/a
50	chr8:92129661-92129711	BJ	skin:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:92119859..92121552-chr8:92126272..92127780,2	K562	blood:
2	chr8:92132436..92135251-chr8:92135477..92137033,2	K562	blood:
3	chr8:92154407..92157062-chr8:92186719..92188314,2	K562	blood:
4	chr8:92120160..92121035-chr8:92355245..92356052,2	MCF-7	breast:
5	chr8:92110951..92113555-chr8:92117926..92119500,2	MCF-7	breast:
6	chr8:92120884..92123955-chr8:92135517..92137332,3	K562	blood:
7	chr8:92134168..92136932-chr8:92139678..92141512,2	MCF-7	breast:
8	chr8:92120884..92123342-chr8:92135640..92137332,2	K562	blood:
9	chr8:92119728..92121505-chr8:92405339..92406291,6	MCF-7	breast:
10	chr8:92119859..92121552-chr8:92126272..92127780,2	K562	blood:
11	chr8:92144011..92145737-chr8:92157940..92159530,2	K562	blood:
12	chr8:92155872..92157525-chr8:92209191..92211411,2	K562	blood:
13	chr8:92120884..92123342-chr8:92135640..92137332,2	K562	blood:
14	chr8:92144011..92145737-chr8:92157940..92159530,2	K562	blood:
15	chr8:92120202..92121198-chr8:92265328..92266332,4	MCF-7	breast:
16	chr8:92110664..92112974-chr8:92115701..92118510,3	MCF-7	breast:
17	chr8:92081085..92084002-chr8:92118821..92120627,2	MCF-7	breast:
18	chr8:92134168..92136932-chr8:92139678..92141512,2	MCF-7	breast:
19	chr8:92120884..92123955-chr8:92135517..92137332,3	K562	blood:
20	chr8:92120448..92121074-chr8:92405403..92406245,2	MCF-7	breast:
21	chr8:92150726..92152514-chr8:92154521..92157433,2	MCF-7	breast:
22	chr8:92117994..92121552-chr8:92125286..92129221,4	K562	blood:
23	chr8:92052048..92053750-chr8:92131275..92133087,2	K562	blood:
24	chr8:92148959..92151184-chr8:92158932..92161122,2	K562	blood:
25	chr8:92117994..92121552-chr8:92125286..92129221,4	K562	blood:
26	chr8:92098468..92101361-chr8:92119773..92121850,2	K562	blood:
27	chr8:92132436..92135251-chr8:92135477..92137033,2	K562	blood:
28	chr8:92148959..92151184-chr8:92158932..92161122,2	K562	blood:
29	chr8:92110691..92113252-chr8:92118062..92119956,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OTUD6B-3	chr8:92136721-92137011	NONHSAT127671
2	lnc-OTUD6B-4	chr8:92142987-92143064	NONHSAT127672
3	lnc-TMEM55A-4	chr8:92151335-92151500	ucscGeneNc_uc003yet_1
4	lnc-OTUD6B-5	chr8:92147909-92147967	NONHSAT127673
5	lnc-OTUD6B-4	chr8:92145338-92145592	NONHSAT127672
6	lnc-TMEM55A-4	chr8:92149320-92151226	ucscGeneNc_uc003yet_1
7	lnc-OTUD6B-6	chr8:92151489-92151751	NONHSAT127674
8	lnc-OTUD6B-4	chr8:92142582-92142645	NONHSAT127672
9	lnc-OTUD6B-5	chr8:92150995-92151423	NONHSAT127673

No data

Variant related genes	Relation type
RN7SL777P	TF binding region
ENSG00000253525	TF binding region
LRRC69	TF binding region
RN7SL777P	CpG island
ENSG00000253525	CpG island
LRRC69	CpG island
ENSG00000155099	chromatin interactions
ENSG00000147606	chromatin interactions
ENSG00000155100	chromatin interactions
ENSG00000253738	chromatin interactions
ENSG00000263888	chromatin interactions

Extended variants
information (count: 1768 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:1768 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537527692	chr8:92116084-92116085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555764669	chr8:92116116-92116117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376092563	chr8:92116118-92116119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs57004380	chr8:92116154-92116155	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs141955814	chr8:92116159-92116160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553987628	chr8:92116166-92116167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572248302	chr8:92116173-92116174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374399862	chr8:92116181-92116182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542848757	chr8:92116198-92116199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs71528764	chr8:92116204-92116205	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs113816753	chr8:92116219-92116220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567572584	chr8:92116229-92116230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141903288	chr8:92116237-92116238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs79164164	chr8:92116243-92116244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs578040531	chr8:92116264-92116265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548701441	chr8:92116278-92116279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531878820	chr8:92116295-92116296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190364495	chr8:92116306-92116307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545715987	chr8:92116342-92116343	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs76055342	chr8:92116351-92116352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181452494	chr8:92116367-92116368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185755179	chr8:92116460-92116461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561109509	chr8:92116477-92116478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561298326	chr8:92116517-92116518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs77132893	chr8:92116518-92116519	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549428077	chr8:92116520-92116521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189382587	chr8:92116555-92116556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs116455818	chr8:92116556-92116557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139862053	chr8:92116603-92116604	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571490338	chr8:92116650-92116651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112253057	chr8:92116741-92116742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566000809	chr8:92116748-92116749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536135138	chr8:92116773-92116774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554769343	chr8:92116778-92116779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576270036	chr8:92116792-92116793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144860716	chr8:92116801-92116802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556644738	chr8:92116912-92116913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538784647	chr8:92116914-92116915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs578140083	chr8:92116932-92116933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545423584	chr8:92116943-92116944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181746192	chr8:92116976-92116977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572723067	chr8:92116979-92116980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186092175	chr8:92116985-92116986	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190750061	chr8:92117005-92117006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561543153	chr8:92117010-92117011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114349583	chr8:92117206-92117207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183408991	chr8:92117237-92117238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554210955	chr8:92117238-92117239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564680291	chr8:92117276-92117277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs147534940	chr8:92117314-92117315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	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
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:92083000-92147800	Weak transcription	Spleen	Spleen
2	chr8:92083400-92124400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:92083600-92150800	Weak transcription	Pancreas	Pancrea
4	chr8:92084000-92124600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr8:92085000-92125800	Weak transcription	Small Intestine	intestine
6	chr8:92091200-92133800	Weak transcription	NHLF	lung
7	chr8:92091800-92137800	Weak transcription	Rectal Smooth Muscle	rectum
8	chr8:92092600-92116800	Weak transcription	Brain Hippocampus Middle	brain
9	chr8:92092600-92147800	Weak transcription	Right Ventricle	heart
10	chr8:92092800-92124400	Weak transcription	Brain Cingulate Gyrus	brain
11	chr8:92094200-92125200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr8:92095200-92124400	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr8:92095200-92130800	Weak transcription	HSMMtube	muscle
14	chr8:92095800-92126600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr8:92096800-92135000	Weak transcription	Hela-S3	cervix
16	chr8:92097200-92127000	Weak transcription	Colon Smooth Muscle	Colon
17	chr8:92097400-92126400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr8:92097400-92130800	Weak transcription	Osteobl	bone
19	chr8:92097400-92146200	Weak transcription	Psoas Muscle	Psoas
20	chr8:92098200-92124600	Weak transcription	HUVEC	blood vessel
21	chr8:92098600-92122800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr8:92100800-92130800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr8:92101400-92118800	Weak transcription	Fetal Brain Female	brain
24	chr8:92104400-92117800	Weak transcription	Brain Angular Gyrus	brain
25	chr8:92104400-92124400	Weak transcription	Gastric	stomach
26	chr8:92104600-92116800	Weak transcription	Stomach Smooth Muscle	stomach
27	chr8:92104600-92117000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr8:92104600-92126000	Weak transcription	Fetal Intestine Large	intestine
29	chr8:92104600-92129600	Weak transcription	Brain Anterior Caudate	brain
30	chr8:92104800-92124400	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr8:92104800-92124400	Weak transcription	Ovary	ovary
32	chr8:92104800-92125400	Weak transcription	Fetal Muscle Trunk	muscle
33	chr8:92104800-92126200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr8:92104800-92130600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr8:92104800-92134200	Weak transcription	Thymus	Thymus
36	chr8:92104800-92148000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr8:92105000-92119800	Weak transcription	Placenta	Placenta
38	chr8:92105800-92125800	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr8:92106000-92120000	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr8:92106000-92125800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr8:92106000-92126400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr8:92106800-92127400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr8:92107000-92117200	Weak transcription	A549	lung
44	chr8:92107200-92141000	Weak transcription	HMEC	breast
45	chr8:92107400-92117200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr8:92107400-92119800	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr8:92107400-92123200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr8:92107600-92117200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr8:92108400-92124400	Weak transcription	GM12878-XiMat	blood
50	chr8:92109000-92117200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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Variant report

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