Variant report

Variant	esv33063
Chromosome Location	chr8:8247056-8249234
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:59)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:59 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:8247278-8248517	GM12878	blood:	n/a	n/a
2	ATF2	chr8:8247266-8248601	GM12878	blood:	n/a	n/a
3	BATF	chr8:8248010-8248462	GM12878	blood:	n/a	n/a
4	BATF	chr8:8247515-8248005	GM12878	blood:	n/a	n/a
5	BATF	chr8:8248034-8248454	GM12878	blood:	n/a	n/a
6	BCL11A	chr8:8248056-8248500	GM12878	blood:	n/a	n/a
7	BCL11A	chr8:8248164-8248420	GM12878	blood:	n/a	n/a
8	BCL3	chr8:8248024-8248457	GM12878	blood:	n/a	n/a
9	CHD2	chr8:8247533-8247839	GM12878	blood:	n/a	n/a
10	CHD2	chr8:8247582-8247829	H1-hESC	embryonic stem cell:	n/a	n/a
11	CUX1	chr8:8247511-8247707	GM12878	blood:	n/a	n/a
12	EBF1	chr8:8247488-8248470	GM12878	blood:	n/a	chr8:8248230-8248241
13	EBF1	chr8:8248000-8248474	GM12878	blood:	n/a	chr8:8248230-8248241
14	EBF1	chr8:8247983-8248426	GM12878	blood:	n/a	chr8:8248230-8248241
15	EP300	chr8:8247971-8248471	GM12878	blood:	n/a	n/a
16	EP300	chr8:8247501-8247757	GM12878	blood:	n/a	n/a
17	FOXM1	chr8:8247347-8248604	GM12878	blood:	n/a	n/a
18	GATA2	chr8:8247700-8248122	SH-SY5Y	brain:	n/a	n/a
19	GATA2	chr8:8248465-8249066	SH-SY5Y	brain:	n/a	n/a
20	GATA3	chr8:8247678-8248261	SH-SY5Y	brain:	n/a	n/a
21	IKZF1	chr8:8247789-8248504	GM12878	blood:	n/a	n/a
22	IRF4	chr8:8247430-8248472	GM12878	blood:	n/a	n/a
23	JUN	chr8:8247623-8247867	H1-hESC	embryonic stem cell:	n/a	n/a
24	JUND	chr8:8247761-8247883	HepG2	liver:	n/a	n/a
25	KAP1	chr8:8246660-8247165	U2OS	brain:	n/a	n/a
26	KAP1	chr8:8247588-8248863	U2OS	brain:	n/a	n/a
27	KAP1	chr8:8246576-8248773	HEK293	kidney:	n/a	n/a
28	MAX	chr8:8247825-8248190	GM12878	blood:	n/a	n/a
29	MAZ	chr8:8247587-8247690	GM12878	blood:	n/a	n/a
30	MAZ	chr8:8247985-8248340	GM12878	blood:	n/a	n/a
31	MEF2A	chr8:8248056-8248462	GM12878	blood:	n/a	n/a
32	MTA3	chr8:8247396-8248522	GM12878	blood:	n/a	n/a
33	MTA3	chr8:8247244-8248605	GM12878	blood:	n/a	n/a
34	NFIC	chr8:8247227-8248647	GM12878	blood:	n/a	chr8:8247607-8247635
35	NFIC	chr8:8247908-8248809	GM12878	blood:	n/a	n/a
36	NFIC	chr8:8247245-8247852	GM12878	blood:	n/a	chr8:8247607-8247635
37	NRF1	chr8:8248108-8248270	GM12878	blood:	n/a	n/a
38	RAD21	chr8:8248085-8248374	GM12878	blood:	n/a	n/a
39	RCOR1	chr8:8247509-8247810	K562	blood:	n/a	n/a
40	RELA	chr8:8248079-8248455	GM12892	blood:	n/a	n/a
41	RELA	chr8:8247474-8248548	GM15510	blood:	n/a	chr8:8247612-8247621 chr8:8247612-8247621
42	RELA	chr8:8247459-8247817	GM19099	blood:	n/a	chr8:8247612-8247621 chr8:8247612-8247621
43	RELA	chr8:8247428-8248679	GM18505	blood:	n/a	chr8:8247612-8247621 chr8:8247612-8247621
44	RELA	chr8:8247443-8248510	GM18951	blood:	n/a	chr8:8247612-8247621 chr8:8247612-8247621
45	RELA	chr8:8247432-8248456	GM12878	blood:	n/a	chr8:8247612-8247621 chr8:8247612-8247621
46	RELA	chr8:8247429-8248621	GM12891	blood:	n/a	chr8:8247612-8247621 chr8:8247612-8247621
47	RELA	chr8:8247477-8247820	GM19193	blood:	n/a	chr8:8247612-8247621 chr8:8247612-8247621
48	RELA	chr8:8248030-8248443	GM19099	blood:	n/a	n/a
49	RUNX3	chr8:8247318-8248655	GM12878	blood:	n/a	n/a
50	RUNX3	chr8:8247417-8248547	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8247802-8247852	GM12892	blood:	n/a
2	chr8:8247802-8247852	HMEC	breast:	n/a
3	chr8:8247802-8247852	HEEpiC	esophagus:	n/a
4	chr8:8247802-8247852	H1-hESC	embryonic stem cell:	embryo
5	chr8:8247802-8247852	Jurkat	blood:	n/a
6	chr8:8247802-8247852	ProgFib	skin:	n/a
7	chr8:8247802-8247852	SKMC	muscle:	n/a
8	chr8:8247802-8247852	ovcar-3	ovarian:	n/a
9	chr8:8247802-8247852	GM12878	blood:	n/a
10	chr8:8247802-8247852	U87	brain:	n/a
11	chr8:8247802-8247852	AG10803	skin:	n/a
12	chr8:8247802-8247852	NHBE	bronchial:	n/a
13	chr8:8247802-8247852	HIPEpiC	eye:	n/a
14	chr8:8247802-8247852	BJ	skin:	n/a
15	chr8:8247802-8247852	MCF10A-Er-Src	breast:	n/a
16	chr8:8247802-8247852	NT2-D1	testis:	n/a
17	chr8:8247802-8247852	NHDF-neo	bronchial:	n/a
18	chr8:8247802-8247852	HPAEpiC	pulmonary alveolar:	n/a
19	chr8:8247802-8247852	PANC-1	pancreas:	n/a
20	chr8:8247802-8247852	A549	lung:	n/a
21	chr8:8247802-8247852	AG09319	gingival:	n/a
22	chr8:8247802-8247852	CMK	blood:	n/a
23	chr8:8247802-8247852	BE2_C	brain:	n/a
24	chr8:8247802-8247852	K562	blood:	n/a
25	chr8:8247802-8247852	HepG2	liver:	n/a
26	chr8:8247802-8247852	AG04450	lung:	fetal
27	chr8:8247802-8247852	NH-A	brain:	n/a
28	chr8:8247802-8247852	RPTEC	kidney:	n/a
29	chr8:8247802-8247852	HAEpiC	amniotic membrane:	n/a
30	chr8:8247802-8247852	NB4	blood:	n/a
31	chr8:8247802-8247852	AG04449	skin:	fetal
32	chr8:8247802-8247852	MCF-7	breast:	n/a
33	chr8:8247802-8247852	HCT-116	colon:	n/a
34	chr8:8247802-8247852	HRCEpiC	kidney:	n/a
35	chr8:8247802-8247852	HL-60	blood:	n/a
36	chr8:8247802-8247852	ECC-1	luminal epithelium:	n/a
37	chr8:8247802-8247852	SAEC	small airway:	n/a
38	chr8:8247802-8247852	LNCaP	prostate:	n/a
39	chr8:8247802-8247852	HCM	heart:	n/a
40	chr8:8247802-8247852	T-47D	breast:	n/a
41	chr8:8247802-8247852	SK-N-SH_RA	brain:	n/a
42	chr8:8247802-8247852	AoSMC	blood vessel:	n/a
43	chr8:8247802-8247852	HNPCEpiC	eye:	n/a
44	chr8:8247802-8247852	Hela-S3	cervix:	n/a
45	chr8:8247802-8247852	Hepatocyte	liver:	n/a
46	chr8:8247802-8247852	HCPEpiC	choroid plexus:	n/a
47	chr8:8247802-8247852	SK-N-SH	brain:	n/a
48	chr8:8247802-8247852	Caco-2	colon:	n/a
49	chr8:8247802-8247852	PrEC	prostate:	n/a
50	chr8:8247802-8247852	HUVEC	blood vessel:	n/a

No data

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC068020.1-3	chr8:8246546-8247206	NONHSAT124871
2	lnc-PRAGMIN.1-5	chr8:8247672-8248105	NONHSAT124872
3	lnc-PRAGMIN.1-5	chr8:8248563-8248678	FPKM1_group_30826_transcript_2
4	lnc-PRAGMIN.1-5	chr8:8247672-8248105	FPKM1_group_30826_transcript_2

No data

Variant related genes	Relation type
ENSG00000182319	TF binding region
ENSG00000182319	CpG island
STRADB	miRNA target sites

Extended variants
information (count: 121 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:121 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192700871	chr8:8247068-8247069	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs558009522	chr8:8247074-8247075	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs577953834	chr8:8247098-8247099	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs184145655	chr8:8247100-8247101	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs543726754	chr8:8247109-8247110	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs377023079	chr8:8247147-8247148	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs370423970	chr8:8247169-8247170	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs563492728	chr8:8247178-8247179	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs149887271	chr8:8247197-8247198	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs2920998	chr8:8247213-8247214	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs116180214	chr8:8247232-8247233	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs567233132	chr8:8247240-8247241	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs189864411	chr8:8247254-8247255	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs575535993	chr8:8247278-8247279	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs551832982	chr8:8247280-8247281	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs571684448	chr8:8247318-8247319	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs2979157	chr8:8247323-8247324	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs192614103	chr8:8247350-8247351	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs550494630	chr8:8247364-8247365	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs570260555	chr8:8247365-8247366	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs538842603	chr8:8247379-8247380	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs78165388	chr8:8247432-8247433	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs373864046	chr8:8247462-8247463	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs368609975	chr8:8247463-8247464	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs113308726	chr8:8247464-8247465	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs565823099	chr8:8247470-8247471	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs534468118	chr8:8247474-8247475	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs201004675	chr8:8247475-8247476	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs386412000	chr8:8247476-8247477	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs10665801	chr8:8247478-8247479	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs115869315	chr8:8247479-8247480	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs559073847	chr8:8247504-8247505	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs184601361	chr8:8247566-8247567	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs147556292	chr8:8247598-8247599	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs189010372	chr8:8247611-8247612	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs111754981	chr8:8247656-8247657	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs537304584	chr8:8247666-8247667	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs2920997	chr8:8247696-8247697	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs557269133	chr8:8247731-8247732	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs574148772	chr8:8247747-8247748	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs2976951	chr8:8247750-8247751	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs543233738	chr8:8247802-8247803	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs73661387	chr8:8247803-8247804	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region CpG island lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs534747398	chr8:8247814-8247815	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs573252673	chr8:8247838-8247839	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs554551868	chr8:8247857-8247858	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs147721305	chr8:8247887-8247888	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs565233426	chr8:8247890-8247891	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs530938079	chr8:8247916-8247917	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs550090171	chr8:8247946-8247947	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:139)

Disease	PMID	Source
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164919	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8244600-8248800	Weak transcription	Ovary	ovary
2	chr8:8244600-8249600	Weak transcription	Right Atrium	heart
3	chr8:8244800-8248200	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr8:8245000-8247200	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr8:8245000-8247600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr8:8245000-8248200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr8:8245000-8248200	Enhancers	Primary B cells from peripheral blood	blood
8	chr8:8245000-8249200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:8245000-8255600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr8:8245000-8256800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:8245200-8247800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr8:8245200-8248400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr8:8245400-8247400	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr8:8245400-8247400	Enhancers	GM12878-XiMat	blood
15	chr8:8245400-8247800	Weak transcription	NH-A	brain
16	chr8:8245400-8249400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr8:8245600-8247400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr8:8245600-8248200	Weak transcription	Placenta	Placenta
19	chr8:8246000-8247800	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr8:8246400-8248000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:8246600-8247200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr8:8246600-8248400	Enhancers	H1 Cell Line	embryonic stem cell
23	chr8:8246600-8248800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr8:8246600-8249000	Enhancers	Placenta Amnion	Placenta Amnion
25	chr8:8246600-8249400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr8:8246800-8247400	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:8246800-8247800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr8:8246800-8248000	Enhancers	Fetal Kidney	kidney
29	chr8:8246800-8249000	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr8:8246800-8249400	Enhancers	H9 Cell Line	embryonic stem cell
31	chr8:8247000-8247200	Flanking Active TSS	Fetal Intestine Small	intestine
32	chr8:8247000-8247200	Enhancers	HSMMtube	muscle
33	chr8:8247000-8247400	Active TSS	Duodenum Mucosa	Duodenum
34	chr8:8247000-8247400	Flanking Active TSS	Fetal Intestine Large	intestine
35	chr8:8247000-8248200	Enhancers	HepG2	liver
36	chr8:8247200-8247400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
37	chr8:8247200-8247600	Enhancers	Fetal Intestine Small	intestine
38	chr8:8247200-8247800	Weak transcription	HSMMtube	muscle
39	chr8:8247200-8249600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr8:8247400-8247600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
41	chr8:8247400-8247600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr8:8247400-8247600	Active TSS	Rectal Mucosa Donor 29	rectum
43	chr8:8247400-8248400	Flanking Active TSS	GM12878-XiMat	blood
44	chr8:8247400-8249400	Enhancers	Duodenum Mucosa	Duodenum
45	chr8:8247400-8250000	Enhancers	Fetal Intestine Large	intestine
46	chr8:8247600-8247800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr8:8247600-8247800	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr8:8247600-8247800	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr8:8247600-8248000	Flanking Active TSS	Fetal Intestine Small	intestine
50	chr8:8247800-8248000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell

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