Variant report

Variant	esv2752207
Chromosome Location	chr8:122869651-122961848
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:243)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:243 , 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	BHLHE40	chr8:122875611-122875613	A549	lung:	n/a	n/a
2	CEBPB	chr8:122909299-122909528	A549	lung:	n/a	n/a
3	CEBPB	chr8:122954678-122955065	IMR90	lung:	n/a	n/a
4	CEBPB	chr8:122940279-122940567	IMR90	lung:	n/a	n/a
5	CEBPB	chr8:122905954-122906426	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr8:122931294-122931701	IMR90	lung:	n/a	chr8:122931424-122931435 chr8:122931319-122931332
7	CEBPB	chr8:122906058-122906417	A549	lung:	n/a	n/a
8	CEBPB	chr8:122931295-122931718	Hela-S3	cervix:	n/a	chr8:122931424-122931435 chr8:122931319-122931332
9	CEBPB	chr8:122909048-122909561	Hela-S3	cervix:	n/a	chr8:122909263-122909274
10	CEBPB	chr8:122905886-122906443	IMR90	lung:	n/a	n/a
11	CEBPB	chr8:122875460-122875622	IMR90	lung:	n/a	n/a
12	CEBPB	chr8:122887770-122887949	IMR90	lung:	n/a	chr8:122887898-122887907
13	CTCF	chr8:122906040-122906190	HMF	breast:	n/a	n/a
14	CTCF	chr8:122906060-122906210	HMEC	breast:	n/a	n/a
15	CTCF	chr8:122906020-122906170	HMF	breast:	n/a	n/a
16	CTCF	chr8:122906080-122906230	AoAF	blood vessel:	n/a	n/a
17	CTCF	chr8:122886220-122886370	BE2_C	brain:	n/a	n/a
18	CTCF	chr8:122907374-122907429	GM10248	blood:	n/a	n/a
19	CTCF	chr8:122906100-122906250	HVMF	connective:	n/a	n/a
20	CTCF	chr8:122906000-122906150	BJ	skin:	n/a	n/a
21	CTCF	chr8:122906080-122906230	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr8:122890460-122890610	AG04450	lung:	n/a	n/a
23	CTCF	chr8:122906060-122906210	A549	lung:	n/a	n/a
24	CTCF	chr8:122931780-122931930	Caco-2	colon:	n/a	n/a
25	CTCF	chr8:122883520-122883670	HCT-116	colon:	n/a	n/a
26	CTCF	chr8:122870774-122870859	Lung_OC	lung:	n/a	n/a
27	CTCF	chr8:122906020-122906170	BJ	skin:	n/a	n/a
28	CTCF	chr8:122871400-122871550	GM12867	blood:	n/a	n/a
29	CTCF	chr8:122954400-122954550	GM12878	blood:	n/a	n/a
30	CTCF	chr8:122906060-122906210	AG04449	skin:	n/a	n/a
31	CTCF	chr8:122900098-122900162	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr8:122901034-122901070	LNCaP	prostate:	n/a	n/a
33	CTCF	chr8:122906080-122906230	AG10803	skin:	n/a	n/a
34	E2F4	chr8:122936967-122937136	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr8:122905973-122906225	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr8:122954594-122955072	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr8:122871485-122871662	MCF10A-Er-Src	breast:	n/a	n/a
38	EP300	chr8:122954816-122955184	SK-N-SH_RA	brain:	n/a	chr8:122955121-122955131 chr8:122954886-122954895 chr8:122954887-122954896
39	EP300	chr8:122881799-122882208	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr8:122905933-122906345	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr8:122881843-122882178	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr8:122908725-122909330	Hela-S3	cervix:	n/a	chr8:122909284-122909298 chr8:122909160-122909169 chr8:122909161-122909170
43	EP300	chr8:122905896-122906351	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr8:122958517-122959147	SK-N-SH_RA	brain:	n/a	chr8:122959024-122959038 chr8:122959027-122959041
45	EP300	chr8:122931395-122931640	Hela-S3	cervix:	n/a	chr8:122931510-122931524
46	EP300	chr8:122958531-122959097	SK-N-SH_RA	brain:	n/a	chr8:122959024-122959038 chr8:122959027-122959041
47	EP300	chr8:122957776-122959803	SK-N-SH	brain:	n/a	chr8:122959024-122959038 chr8:122959027-122959041
48	EP300	chr8:122954431-122955348	SK-N-SH	brain:	n/a	chr8:122955121-122955131 chr8:122954886-122954895 chr8:122954887-122954896
49	FAM48A	chr8:122892567-122892767	GM12878	blood:	n/a	n/a
50	FOS	chr8:122937220-122937436	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:122954569-122954619	HNPCEpiC	eye:	n/a
2	chr8:122954569-122954619	LNCaP	prostate:	n/a
3	chr8:122954569-122954619	HRCEpiC	kidney:	n/a
4	chr8:122954569-122954619	U87	brain:	n/a
5	chr8:122954569-122954619	Hepatocyte	liver:	n/a
6	chr8:122954569-122954619	HCPEpiC	choroid plexus:	n/a
7	chr8:122954569-122954619	SK-N-SH_RA	brain:	n/a
8	chr8:122954569-122954619	A549	lung:	n/a
9	chr8:122954569-122954619	BE2_C	brain:	n/a
10	chr8:122954569-122954619	IMR90	lung:	fetal
11	chr8:122954569-122954619	ECC-1	luminal epithelium:	n/a
12	chr8:122954569-122954619	GM12878	blood:	n/a
13	chr8:122954569-122954619	HRPEpiC	eye:	n/a
14	chr8:122954569-122954619	AG09309	skin:	n/a
15	chr8:122954569-122954619	ovcar-3	ovarian:	n/a
16	chr8:122954569-122954619	NH-A	brain:	n/a
17	chr8:122954569-122954619	HRE	kidney:	n/a
18	chr8:122954569-122954619	SKMC	muscle:	n/a
19	chr8:122954569-122954619	Caco-2	colon:	n/a
20	chr8:122954569-122954619	GM19239	blood:	n/a
21	chr8:122954569-122954619	K562	blood:	n/a
22	chr8:122954569-122954619	GM06990	blood:	n/a
23	chr8:122954569-122954619	PANC-1	pancreas:	n/a
24	chr8:122954569-122954619	HCF	heart:	n/a
25	chr8:122954569-122954619	AG04449	skin:	fetal
26	chr8:122954569-122954619	HAEpiC	amniotic membrane:	n/a
27	chr8:122954569-122954619	RPTEC	kidney:	n/a
28	chr8:122954569-122954619	NB4	blood:	n/a
29	chr8:122954569-122954619	SAEC	small airway:	n/a
30	chr8:122954569-122954619	PFSK-1	brain:	n/a
31	chr8:122954569-122954619	HUVEC	blood vessel:	n/a
32	chr8:122954569-122954619	AoSMC	blood vessel:	n/a
33	chr8:122954569-122954619	PrEC	prostate:	n/a
34	chr8:122954569-122954619	HCT-116	colon:	n/a
35	chr8:122954569-122954619	SK-N-MC	brain:	n/a
36	chr8:122954569-122954619	HEEpiC	esophagus:	n/a
37	chr8:122954569-122954619	AG09319	gingival:	n/a
38	chr8:122954569-122954619	Hela-S3	cervix:	n/a
39	chr8:122954569-122954619	MCF10A-Er-Src	breast:	n/a
40	chr8:122954569-122954619	NT2-D1	testis:	n/a
41	chr8:122954569-122954619	SK-N-SH	brain:	n/a
42	chr8:122954569-122954619	NHBE	bronchial:	n/a
43	chr8:122954569-122954619	HepG2	liver:	n/a
44	chr8:122954569-122954619	GM12891	blood:	n/a
45	chr8:122954569-122954619	HMEC	breast:	n/a
46	chr8:122954569-122954619	NHDF-neo	bronchial:	n/a
47	chr8:122954569-122954619	AG10803	skin:	n/a
48	chr8:122954569-122954619	HCM	heart:	n/a
49	chr8:122954569-122954619	GM12892	blood:	n/a
50	chr8:122954569-122954619	H1-hESC	embryonic stem cell:	embryo

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:122881369..122883762-chr8:122885140..122886791,2	K562	blood:
2	chr8:122951001..122953487-chr8:122956796..122959609,2	MCF-7	breast:
3	chr8:122881369..122883762-chr8:122885140..122886791,2	K562	blood:
4	chr8:122926458..122928257-chr8:122928422..122931077,2	MCF-7	breast:
5	chr8:122948060..122951012-chr8:122952144..122954901,2	MCF-7	breast:
6	chr8:122948060..122951012-chr8:122952144..122954901,2	MCF-7	breast:
7	chr8:122926458..122928257-chr8:122928422..122931077,2	MCF-7	breast:
8	chr8:122951001..122953487-chr8:122956796..122959609,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-785H20.1.1-1	chr8:122915678-122915779	ENSG00000254018.1
2	lnc-RP11-785H20.1.1-1	chr8:122901064-122901216	XLOC_006911
3	lnc-RP11-785H20.1.1-1	chr8:122897017-122897123	XLOC_006911
4	lnc-RP11-785H20.1.1-1	chr8:122891869-122892004	XLOC_006911
5	lnc-RP11-785H20.1.1-1	chr8:122891869-122892004	XLOC_006911
6	lnc-RP11-785H20.1.1-1	chr8:122916318-122916512	ENSG00000254018.1
7	lnc-RP11-785H20.1.1-1	chr8:122901064-122901216	XLOC_006911
8	lnc-RP11-785H20.1.1-1	chr8:122915678-122915779	XLOC_006911
9	lnc-RP11-785H20.1.1-1	chr8:122926093-122926132	NONHSAT128482
10	lnc-RP11-785H20.1.1-1	chr8:122896963-122897123	ENSG00000254018.1
11	lnc-RP11-785H20.1.1-1	chr8:122891869-122892004	XLOC_006911
12	lnc-RP11-785H20.1.1-1	chr8:122897017-122897123	XLOC_006911
13	lnc-RP11-785H20.1.1-1	chr8:122901064-122901216	XLOC_006911
14	lnc-RP11-785H20.1.1-1	chr8:122901064-122901216	ENSG00000254018.1
15	lnc-RP11-785H20.1.1-1	chr8:122891869-122892004	XLOC_006911
16	lnc-RP11-785H20.1.1-1	chr8:122901064-122901216	XLOC_006911
17	lnc-RP11-785H20.1.1-1	chr8:122926094-122926132	XLOC_006911
18	lnc-RP11-785H20.1.1-1	chr8:122915678-122915779	XLOC_006911
19	lnc-RP11-785H20.1.1-3	chr8:122961050-122961228	l_3672_chr8:122779024-122961228_testes

No data

Variant related genes	Relation type
ENSG00000254018	TF binding region
ENSG00000254018	CpG island
FAM123B	miRNA target sites
MXD1	miRNA target sites

Extended variants
information (count: 2356 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:2356 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10101403	chr8:122869651-122869652	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147623936	chr8:122869662-122869663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs142133389	chr8:122869695-122869696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562391824	chr8:122869707-122869708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575861826	chr8:122869738-122869739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs536030627	chr8:122869745-122869746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs147068015	chr8:122869793-122869794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560010098	chr8:122869807-122869808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs9297655	chr8:122869832-122869833	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs552241507	chr8:122869845-122869846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547551518	chr8:122869898-122869899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183078911	chr8:122869922-122869923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547946725	chr8:122870009-122870010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533025946	chr8:122870032-122870033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568046953	chr8:122870047-122870048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs386729398	chr8:122870048-122870049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs4320548	chr8:122870050-122870051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs370685446	chr8:122870077-122870078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570813794	chr8:122870090-122870091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1397347	chr8:122870120-122870121	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs548976017	chr8:122870135-122870136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs76602209	chr8:122870151-122870152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs377349586	chr8:122870176-122870177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573345344	chr8:122870216-122870217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567347571	chr8:122870235-122870236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185996631	chr8:122870315-122870316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190996480	chr8:122870326-122870327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575879526	chr8:122870365-122870366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183215803	chr8:122870368-122870369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563178092	chr8:122870372-122870373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188176157	chr8:122870455-122870456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs16896256	chr8:122870511-122870512	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs559045969	chr8:122870522-122870523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs16896259	chr8:122870557-122870558	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs556250362	chr8:122870618-122870619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565572415	chr8:122870649-122870650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs16896262	chr8:122870661-122870662	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs561917002	chr8:122870696-122870697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534784230	chr8:122870752-122870753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs571114917	chr8:122870771-122870772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550858479	chr8:122870795-122870796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371918857	chr8:122870801-122870802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192582206	chr8:122870803-122870804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570606524	chr8:122870930-122870931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112757524	chr8:122870972-122870973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113346525	chr8:122871033-122871034	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567007476	chr8:122871078-122871079	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535933361	chr8:122871086-122871087	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183106780	chr8:122871147-122871148	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10108701	chr8:122871164-122871165	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:138)

Disease	PMID	Source
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
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	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
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
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
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	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
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD

Chromatin state (count:186 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:122869400-122873600	Enhancers	Fetal Lung	lung
2	chr8:122869600-122871600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr8:122870000-122870800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:122870200-122870400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:122870200-122871200	Enhancers	Fetal Stomach	stomach
6	chr8:122870400-122870600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr8:122870400-122870600	Enhancers	NHDF-Ad	bronchial
8	chr8:122870400-122871200	Enhancers	Liver	Liver
9	chr8:122870400-122871400	Enhancers	Fetal Kidney	kidney
10	chr8:122870600-122871000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:122870600-122881800	Weak transcription	NHDF-Ad	bronchial
12	chr8:122871000-122871600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:122871200-122873600	Weak transcription	Fetal Stomach	stomach
14	chr8:122872800-122874000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr8:122873000-122873200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr8:122873200-122873600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:122873600-122874400	Weak transcription	Fetal Lung	lung
18	chr8:122873600-122874600	Enhancers	Fetal Stomach	stomach
19	chr8:122873600-122876400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr8:122874400-122875200	Enhancers	Fetal Lung	lung
21	chr8:122876200-122877000	Enhancers	Fetal Brain Male	brain
22	chr8:122876400-122876800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr8:122878200-122878800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr8:122881600-122881800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr8:122881800-122882400	Enhancers	NHDF-Ad	bronchial
26	chr8:122881800-122896800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr8:122882000-122882600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr8:122892000-122892800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:122893600-122894600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr8:122893800-122895200	Enhancers	HSMM	muscle
31	chr8:122893800-122895400	Enhancers	Fetal Lung	lung
32	chr8:122894600-122895000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr8:122894600-122895600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr8:122895000-122896000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:122895600-122897000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr8:122896000-122896800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr8:122896800-122897000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr8:122896800-122897600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:122896800-122897800	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr8:122897000-122897200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr8:122897400-122898200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr8:122897600-122898800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr8:122898800-122899600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:122899200-122906000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr8:122904600-122904800	Enhancers	NHDF-Ad	bronchial
46	chr8:122904600-122906600	Enhancers	HUVEC	blood vessel
47	chr8:122904800-122905800	Weak transcription	NHDF-Ad	bronchial
48	chr8:122905400-122905800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr8:122905400-122906600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr8:122905400-122906800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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