Variant report

Variant	esv3436028
Chromosome Location	chr8:57905223-57907771
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:441)
CpG islands
(count:612)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:441 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:57906339-57906829	HepG2	liver:	n/a	n/a
2	BACH1	chr8:57905431-57905465	K562	blood:	n/a	n/a
3	BACH1	chr8:57905737-57905802	K562	blood:	n/a	n/a
4	BACH1	chr8:57905485-57907050	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr8:57905294-57905811	K562	blood:	n/a	n/a
6	BHLHE40	chr8:57906370-57906418	K562	blood:	n/a	n/a
7	BRCA1	chr8:57905816-57905887	GM12878	blood:	n/a	n/a
8	BRCA1	chr8:57905634-57905996	Hela-S3	cervix:	n/a	n/a
9	CCNT2	chr8:57905608-57906551	K562	blood:	n/a	chr8:57906265-57906274
10	CEBPB	chr8:57906275-57906900	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr8:57905417-57905720	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr8:57905589-57905789	K562	blood:	n/a	n/a
13	CEBPD	chr8:57906181-57906610	HepG2	liver:	n/a	n/a
14	CHD2	chr8:57905739-57906007	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr8:57905706-57906640	HepG2	liver:	n/a	n/a
16	CHD2	chr8:57905301-57906728	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr8:57905219-57906461	K562	blood:	n/a	n/a
18	CHD2	chr8:57905312-57905454	HepG2	liver:	n/a	n/a
19	CHD2	chr8:57905695-57906524	GM12878	blood:	n/a	n/a
20	CREB1	chr8:57906075-57906646	A549	lung:	n/a	n/a
21	CREB1	chr8:57906086-57906703	HepG2	liver:	n/a	n/a
22	CREB1	chr8:57905747-57906006	A549	lung:	n/a	n/a
23	CTBP2	chr8:57905511-57906695	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr8:57906623-57906629	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr8:57905713-57905719	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr8:57906580-57906730	SAEC	small airway:	n/a	n/a
27	CTCF	chr8:57906020-57906170	AG04449	skin:	n/a	n/a
28	CTCF	chr8:57905551-57905587	Fibrobl	skin:	n/a	n/a
29	CTCF	chr8:57906318-57906403	GM12892	blood:	n/a	n/a
30	CTCF	chr8:57906332-57906407	GM12891	blood:	n/a	n/a
31	CTCF	chr8:57906595-57906618	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr8:57905760-57905910	HEK293	kidney:	n/a	n/a
33	CTCF	chr8:57906400-57906550	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr8:57905919-57905927	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:57906019-57906104	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr8:57906500-57906650	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr8:57905789-57905822	GM19239	blood:	n/a	n/a
38	CTCF	chr8:57906336-57906480	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr8:57905980-57906130	GM12866	blood:	n/a	n/a
40	CTCF	chr8:57905751-57905916	MCF-7	breast:	n/a	n/a
41	CTCF	chr8:57906020-57906170	GM12873	blood:	n/a	n/a
42	CTCF	chr8:57905680-57905830	GM12867	blood:	n/a	n/a
43	CTCF	chr8:57905730-57905824	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:57905595-57905700	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr8:57905822-57905996	Fibrobl	skin:	n/a	n/a
46	CTCF	chr8:57905980-57906130	GM12869	blood:	n/a	n/a
47	CUX1	chr8:57905457-57905645	K562	blood:	n/a	n/a
48	E2F4	chr8:57906370-57907155	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F6	chr8:57906281-57906462	K562	blood:	n/a	n/a
50	E2F6	chr8:57906469-57906699	K562	blood:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:57907010-57907060	IMR90	lung:	fetal
2	chr8:57907010-57907060	NT2-D1	testis:	n/a
3	chr8:57907010-57907060	IMR90	lung:	fetal
4	chr8:57907010-57907060	NT2-D1	testis:	n/a
5	chr8:57906543-57906593	ovcar-3	ovarian:	n/a
6	chr8:57906166-57906216	HCPEpiC	choroid plexus:	n/a
7	chr8:57907010-57907060	H1-hESC	embryonic stem cell:	embryo
8	chr8:57906543-57906593	SK-N-MC	brain:	n/a
9	chr8:57906363-57906413	SK-N-SH	brain:	n/a
10	chr8:57905325-57905375	NT2-D1	testis:	n/a
11	chr8:57906837-57906887	HRE	kidney:	n/a
12	chr8:57906609-57906659	HRCEpiC	kidney:	n/a
13	chr8:57906609-57906659	PANC-1	pancreas:	n/a
14	chr8:57906166-57906216	GM12892	blood:	n/a
15	chr8:57905925-57905975	IMR90	lung:	fetal
16	chr8:57906166-57906216	MCF10A-Er-Src	breast:	n/a
17	chr8:57906058-57906108	IMR90	lung:	fetal
18	chr8:57906543-57906593	BJ	skin:	n/a
19	chr8:57905325-57905375	PrEC	prostate:	n/a
20	chr8:57906543-57906593	HL-60	blood:	n/a
21	chr8:57907138-57907188	HIPEpiC	eye:	n/a
22	chr8:57905325-57905375	GM19239	blood:	n/a
23	chr8:57905925-57905975	SK-N-SH_RA	brain:	n/a
24	chr8:57906363-57906413	CMK	blood:	n/a
25	chr8:57907010-57907060	AoSMC	blood vessel:	n/a
26	chr8:57905925-57905975	HNPCEpiC	eye:	n/a
27	chr8:57907138-57907188	NHBE	bronchial:	n/a
28	chr8:57906166-57906216	ovcar-3	ovarian:	n/a
29	chr8:57906609-57906659	HCF	heart:	n/a
30	chr8:57907010-57907060	HCT-116	colon:	n/a
31	chr8:57906609-57906659	HRPEpiC	eye:	n/a
32	chr8:57906363-57906413	HCT-116	colon:	n/a
33	chr8:57906363-57906413	Caco-2	colon:	n/a
34	chr8:57906058-57906108	HepG2	liver:	n/a
35	chr8:57906543-57906593	A549	lung:	n/a
36	chr8:57906166-57906216	GM12878	blood:	n/a
37	chr8:57905325-57905375	PFSK-1	brain:	n/a
38	chr8:57907138-57907188	AG09309	skin:	n/a
39	chr8:57906609-57906659	Jurkat	blood:	n/a
40	chr8:57906837-57906887	HRPEpiC	eye:	n/a
41	chr8:57905325-57905375	MCF10A-Er-Src	breast:	n/a
42	chr8:57906837-57906887	U87	brain:	n/a
43	chr8:57905925-57905975	AG09319	gingival:	n/a
44	chr8:57906058-57906108	T-47D	breast:	n/a
45	chr8:57906837-57906887	NHDF-neo	bronchial:	n/a
46	chr8:57906166-57906216	HRE	kidney:	n/a
47	chr8:57906609-57906659	HAEpiC	amniotic membrane:	n/a
48	chr8:57906837-57906887	NB4	blood:	n/a
49	chr8:57906837-57906887	NH-A	brain:	n/a
50	chr8:57906363-57906413	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:57891643..57894816-chr8:57903794..57907010,5	K562	blood:
2	chr8:57892210..57896083-chr8:57903794..57907547,6	K562	blood:
3	chr8:57891263..57893548-chr8:57905444..57907032,2	MCF-7	breast:
4	chr8:57907351..57909951-chr8:57912106..57914531,3	MCF-7	breast:

No data

Variant related genes	Relation type
IMPAD1	TF binding region
IMPAD1	CpG island
ENSG00000104331	chromatin interactions

Extended variants
information (count: 69 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:69 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566439747	chr8:57905254-57905255	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs538777815	chr8:57905258-57905259	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs10958516	chr8:57905273-57905274	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs11784432	chr8:57905297-57905298	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs552158354	chr8:57905299-57905300	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs538112627	chr8:57905325-57905326	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs554922267	chr8:57905350-57905351	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs78055210	chr8:57905372-57905373	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs540058728	chr8:57905430-57905431	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs553981574	chr8:57905488-57905489	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs75764447	chr8:57905500-57905501	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184852569	chr8:57905522-57905523	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs548900071	chr8:57905545-57905546	Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs530828633	chr8:57905601-57905602	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs13256360	chr8:57905697-57905698	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs567356359	chr8:57905712-57905713	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs372392210	chr8:57905744-57905745	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs145484021	chr8:57905798-57905799	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs148820865	chr8:57905809-57905810	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs374711732	chr8:57905817-57905818	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs559655615	chr8:57905834-57905835	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs112318196	chr8:57905840-57905841	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs367837388	chr8:57905847-57905848	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs368994525	chr8:57905864-57905865	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs371716301	chr8:57905892-57905893	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs189210871	chr8:57905903-57905904	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs530470175	chr8:57905920-57905921	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs546867419	chr8:57905925-57905926	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs377437636	chr8:57905946-57905947	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs11545960	chr8:57905962-57905963	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs147738902	chr8:57905969-57905970	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs560769519	chr8:57905973-57905974	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs532219991	chr8:57906145-57906146	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs1057409	chr8:57906269-57906270	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs568839316	chr8:57906275-57906276	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs537853348	chr8:57906290-57906291	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs548420336	chr8:57906299-57906300	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs1057407	chr8:57906313-57906314	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs534138309	chr8:57906418-57906419	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs553671090	chr8:57906420-57906421	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs28362578	chr8:57906574-57906575	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs530437689	chr8:57906575-57906576	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs538719308	chr8:57906609-57906610	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs3808630	chr8:57906730-57906731	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs575193825	chr8:57906758-57906759	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs34452109	chr8:57906792-57906793	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs192529601	chr8:57906803-57906804	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs550115163	chr8:57906818-57906819	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs184760339	chr8:57906899-57906900	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs560673393	chr8:57906999-57907000	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	22183965	CNVD
Bipolar disorder	19114987	CNVD
Recurrent pregnancy loss	19789632	CNVD

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:57896200-57905400	Weak transcription	Spleen	Spleen
2	chr8:57897200-57905400	Weak transcription	Stomach Mucosa	stomach
3	chr8:57901800-57907200	Active TSS	GM12878-XiMat	blood
4	chr8:57903200-57907000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:57903400-57907200	Active TSS	Psoas Muscle	Psoas
6	chr8:57903600-57905400	Enhancers	Fetal Heart	heart
7	chr8:57903600-57905600	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr8:57903600-57905800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr8:57903600-57906800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr8:57903600-57907200	Active TSS	HUES6 Cell Line	embryonic stem cell
11	chr8:57903600-57907200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr8:57903800-57905400	Active TSS	HUES48 Cell Line	embryonic stem cell
13	chr8:57903800-57906000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr8:57903800-57907200	Active TSS	NHDF-Ad	bronchial
15	chr8:57904000-57905400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr8:57904000-57905400	Active TSS	HepG2	liver
17	chr8:57904000-57906600	Active TSS	K562	blood
18	chr8:57904000-57907000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr8:57904000-57907000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr8:57904000-57907200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr8:57904000-57907400	Active TSS	HMEC	breast
22	chr8:57904200-57907200	Active TSS	Right Atrium	heart
23	chr8:57904200-57907400	Active TSS	Breast Myoepithelial Primary Cells	Breast
24	chr8:57904400-57905800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr8:57904400-57906800	Active TSS	Brain Angular Gyrus	brain
26	chr8:57904400-57907200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
27	chr8:57904400-57907200	Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr8:57904400-57907200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr8:57904400-57907200	Active TSS	HSMMtube	muscle
30	chr8:57904400-57907400	Active TSS	NHLF	lung
31	chr8:57904600-57905400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr8:57904600-57905800	Flanking Active TSS	Primary hematopoietic stem cells	blood
33	chr8:57904600-57906000	Flanking Active TSS	Primary B cells from cord blood	blood
34	chr8:57904600-57906800	Active TSS	Fetal Muscle Leg	muscle
35	chr8:57904600-57907000	Active TSS	Placenta	Placenta
36	chr8:57904600-57907000	Active TSS	Fetal Stomach	stomach
37	chr8:57904600-57907200	Active TSS	Ovary	ovary
38	chr8:57904600-57907200	Active TSS	Right Ventricle	heart
39	chr8:57904600-57907200	Active TSS	Thymus	Thymus
40	chr8:57904600-57907200	Active TSS	HSMM	muscle
41	chr8:57904800-57905400	Active TSS	Fetal Muscle Trunk	muscle
42	chr8:57904800-57905800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
43	chr8:57904800-57906000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
44	chr8:57904800-57906600	Active TSS	Fetal Thymus	thymus
45	chr8:57904800-57907000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr8:57904800-57907000	Active TSS	Brain Germinal Matrix	brain
47	chr8:57904800-57907000	Active TSS	A549	lung
48	chr8:57904800-57907000	Active TSS	Hela-S3	cervix
49	chr8:57904800-57907200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
50	chr8:57904800-57907200	Active TSS	Colonic Mucosa	Colon

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