Variant report

Variant	esv3375675
Chromosome Location	chr7:65669142-65671690
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:603)
CpG islands
(count:795)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:603 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:65670291-65670347	K562	blood:	n/a	n/a
2	ARID3A	chr7:65670065-65670445	HepG2	liver:	n/a	n/a
3	ATF2	chr7:65670156-65670466	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:65670068-65670544	GM12878	blood:	n/a	n/a
5	BACH1	chr7:65669695-65670290	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr7:65669926-65670427	GM12878	blood:	n/a	chr7:65670059-65670072 chr7:65670138-65670151 chr7:65670137-65670146
7	BCLAF1	chr7:65669957-65670552	GM12878	blood:	n/a	chr7:65670059-65670072 chr7:65670138-65670151 chr7:65670137-65670146
8	BCLAF1	chr7:65670100-65670520	GM12878	blood:	n/a	chr7:65670138-65670151 chr7:65670137-65670146
9	BHLHE40	chr7:65669624-65670476	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:65670143-65670384	K562	blood:	n/a	n/a
11	BHLHE40	chr7:65669947-65670428	HepG2	liver:	n/a	n/a
12	BRCA1	chr7:65670101-65670359	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr7:65670199-65670448	HepG2	liver:	n/a	n/a
14	BRCA1	chr7:65669843-65670427	GM12878	blood:	n/a	n/a
15	CBX3	chr7:65670091-65670508	K562	blood:	n/a	n/a
16	CCNT2	chr7:65669914-65670859	K562	blood:	n/a	chr7:65670138-65670147 chr7:65669970-65669979 chr7:65670636-65670645
17	CEBPB	chr7:65670167-65670429	H1-hESC	embryonic stem cell:	n/a	chr7:65670246-65670254
18	CEBPB	chr7:65670198-65670332	HepG2	liver:	n/a	chr7:65670246-65670254
19	CEBPB	chr7:65670143-65670440	Hela-S3	cervix:	n/a	chr7:65670246-65670254
20	CEBPD	chr7:65670183-65670500	HepG2	liver:	n/a	n/a
21	CHD1	chr7:65669734-65670738	GM12878	blood:	n/a	n/a
22	CHD1	chr7:65670323-65670836	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr7:65671016-65671102	GM12878	blood:	n/a	n/a
24	CHD1	chr7:65671332-65671462	GM12878	blood:	n/a	n/a
25	CHD1	chr7:65669733-65672187	IMR90	lung:	n/a	n/a
26	CHD2	chr7:65669984-65670439	K562	blood:	n/a	n/a
27	CHD2	chr7:65669862-65670845	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr7:65669718-65670476	HepG2	liver:	n/a	n/a
29	CHD2	chr7:65669612-65670934	GM12878	blood:	n/a	n/a
30	CHD2	chr7:65669966-65670528	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr7:65669618-65671079	HepG2	liver:	n/a	n/a
32	CREB1	chr7:65669873-65670586	A549	lung:	n/a	n/a
33	CREB1	chr7:65669962-65670355	A549	lung:	n/a	n/a
34	CREB1	chr7:65669823-65670597	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr7:65669861-65670655	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr7:65669734-65670635	GM12878	blood:	n/a	n/a
37	CTBP2	chr7:65669904-65671295	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr7:65670240-65670390	HVMF	connective:	n/a	n/a
39	CTCF	chr7:65670200-65670350	HPF	lung:	n/a	n/a
40	CTCF	chr7:65670240-65670390	AG10803	skin:	n/a	n/a
41	CTCF	chr7:65670260-65670410	GM12878	blood:	n/a	n/a
42	CTCF	chr7:65670040-65670527	K562	blood:	n/a	n/a
43	CTCF	chr7:65670176-65670432	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr7:65670200-65670350	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr7:65670280-65670430	GM12866	blood:	n/a	n/a
46	CTCF	chr7:65670169-65670448	Fibrobl	skin:	n/a	n/a
47	CTCF	chr7:65670220-65670370	AG04450	lung:	n/a	n/a
48	CTCF	chr7:65670170-65670429	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:65670220-65670370	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr7:65670200-65670350	GM12872	blood:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:65669728-65669778	AG04450	lung:	fetal
2	chr7:65669728-65669778	SK-N-SH	brain:	n/a
3	chr7:65669728-65669778	AG04450	lung:	fetal
4	chr7:65669728-65669778	SK-N-SH	brain:	n/a
5	chr7:65670776-65670826	AoSMC	blood vessel:	n/a
6	chr7:65669728-65669778	AG09319	gingival:	n/a
7	chr7:65670151-65670201	HRE	kidney:	n/a
8	chr7:65669728-65669778	HL-60	blood:	n/a
9	chr7:65670130-65670180	GM12878	blood:	n/a
10	chr7:65669728-65669778	HCF	heart:	n/a
11	chr7:65670776-65670826	GM12878	blood:	n/a
12	chr7:65669728-65669778	SK-N-MC	brain:	n/a
13	chr7:65669806-65669856	HCPEpiC	choroid plexus:	n/a
14	chr7:65670237-65670287	SKMC	muscle:	n/a
15	chr7:65670237-65670287	Hepatocyte	liver:	n/a
16	chr7:65669806-65669856	NHBE	bronchial:	n/a
17	chr7:65670241-65670291	Hela-S3	cervix:	n/a
18	chr7:65670841-65670891	GM06990	blood:	n/a
19	chr7:65670237-65670287	SK-N-SH_RA	brain:	n/a
20	chr7:65670130-65670180	Hepatocyte	liver:	n/a
21	chr7:65670114-65670164	HIPEpiC	eye:	n/a
22	chr7:65669806-65669856	Hela-S3	cervix:	n/a
23	chr7:65671551-65671601	NHDF-neo	bronchial:	n/a
24	chr7:65670151-65670201	NB4	blood:	n/a
25	chr7:65670237-65670287	U87	brain:	n/a
26	chr7:65669806-65669856	A549	lung:	n/a
27	chr7:65670151-65670201	LNCaP	prostate:	n/a
28	chr7:65670474-65670524	IMR90	lung:	fetal
29	chr7:65671551-65671601	GM12891	blood:	n/a
30	chr7:65669966-65670016	ovcar-3	ovarian:	n/a
31	chr7:65670151-65670201	IMR90	lung:	fetal
32	chr7:65670776-65670826	HEK293	kidney:	embryo
33	chr7:65670237-65670287	HCPEpiC	choroid plexus:	n/a
34	chr7:65670474-65670524	NB4	blood:	n/a
35	chr7:65669728-65669778	HIPEpiC	eye:	n/a
36	chr7:65670151-65670201	AG09319	gingival:	n/a
37	chr7:65670130-65670180	HEK293	kidney:	embryo
38	chr7:65669806-65669856	HIPEpiC	eye:	n/a
39	chr7:65670130-65670180	HRPEpiC	eye:	n/a
40	chr7:65670241-65670291	ECC-1	luminal epithelium:	n/a
41	chr7:65669966-65670016	HCM	heart:	n/a
42	chr7:65670151-65670201	ECC-1	luminal epithelium:	n/a
43	chr7:65669806-65669856	GM06990	blood:	n/a
44	chr7:65670130-65670180	NH-A	brain:	n/a
45	chr7:65669806-65669856	SK-N-MC	brain:	n/a
46	chr7:65670130-65670180	AG04450	lung:	fetal
47	chr7:65671551-65671601	BJ	skin:	n/a
48	chr7:65670841-65670891	Jurkat	blood:	n/a
49	chr7:65669806-65669856	HEEpiC	esophagus:	n/a
50	chr7:65669806-65669856	GM12891	blood:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CRCP-3	chr7:65670259-65670509	NONHSAT121146

No data

Variant related genes	Relation type
TPST1	TF binding region
TPST1	CpG island

Extended variants
information (count: 82 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:82 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549664856	chr7:65669179-65669180	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs566211080	chr7:65669205-65669206	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs528685335	chr7:65669230-65669231	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs62465526	chr7:65669265-65669266	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs61015518	chr7:65669296-65669297	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs537588626	chr7:65669329-65669330	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs557469028	chr7:65669351-65669352	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs567686457	chr7:65669449-65669450	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs536217536	chr7:65669467-65669468	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs555656716	chr7:65669487-65669488	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs148233294	chr7:65669488-65669489	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs145951804	chr7:65669494-65669495	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs540838284	chr7:65669528-65669529	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs187145001	chr7:65669530-65669531	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs141200204	chr7:65669536-65669537	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs532540388	chr7:65669700-65669701	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs543145773	chr7:65669728-65669729	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs190018939	chr7:65669739-65669740	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs78581407	chr7:65669763-65669764	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs542210583	chr7:65669770-65669771	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs560003428	chr7:65669814-65669815	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs556791440	chr7:65669821-65669822	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs528822961	chr7:65669866-65669867	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs568591054	chr7:65669882-65669883	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs138400229	chr7:65669906-65669907	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs571897687	chr7:65670002-65670003	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs35702556	chr7:65670043-65670044	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs531111884	chr7:65670052-65670053	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs551111249	chr7:65670093-65670094	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs567627895	chr7:65670109-65670110	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs536654219	chr7:65670114-65670115	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs546638815	chr7:65670142-65670143	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs566851125	chr7:65670148-65670149	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs370595273	chr7:65670179-65670180	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs557612160	chr7:65670199-65670200	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs577429310	chr7:65670273-65670274	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs536819640	chr7:65670284-65670285	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs557020563	chr7:65670287-65670288	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs142928539	chr7:65670371-65670372	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs542697202	chr7:65670379-65670380	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs200599650	chr7:65670430-65670431	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs182622126	chr7:65670456-65670457	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs572854397	chr7:65670495-65670496	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs545750362	chr7:65670505-65670506	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs565544203	chr7:65670522-65670523	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531152586	chr7:65670565-65670566	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187694506	chr7:65670566-65670567	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377174389	chr7:65670601-65670602	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550848923	chr7:65670617-65670618	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561445006	chr7:65670669-65670670	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Glioblastoma	21080181	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD

Chromatin state (count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65660800-65669800	Weak transcription	Spleen	Spleen
2	chr7:65661600-65669400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:65663600-65669600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:65663600-65669600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr7:65663800-65669600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr7:65664200-65669600	Weak transcription	HSMMtube	muscle
7	chr7:65665200-65669600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:65665200-65669600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:65665400-65669600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr7:65667600-65669400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr7:65667600-65669400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:65667600-65669600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr7:65667800-65669400	Weak transcription	Primary hematopoietic stem cells	blood
14	chr7:65667800-65669400	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr7:65667800-65669400	Enhancers	HepG2	liver
16	chr7:65667800-65669600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr7:65667800-65669600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr7:65668200-65669400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr7:65668400-65669400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr7:65669000-65669200	Weak transcription	Liver	Liver
21	chr7:65669200-65669400	Enhancers	Primary B cells from cord blood	blood
22	chr7:65669200-65669400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr7:65669200-65669400	Enhancers	Liver	Liver
24	chr7:65669200-65669400	Enhancers	Stomach Mucosa	stomach
25	chr7:65669200-65669400	Enhancers	GM12878-XiMat	blood
26	chr7:65669200-65669400	Enhancers	Hela-S3	cervix
27	chr7:65669200-65669600	Enhancers	Primary B cells from peripheral blood	blood
28	chr7:65669400-65669600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
29	chr7:65669400-65669600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
30	chr7:65669400-65669600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
31	chr7:65669400-65669600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr7:65669400-65669600	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr7:65669400-65669600	Flanking Active TSS	Primary T cells from cord blood	blood
34	chr7:65669400-65669600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
35	chr7:65669400-65669600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr7:65669400-65669600	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr7:65669400-65669600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
38	chr7:65669400-65669600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr7:65669400-65669600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr7:65669400-65669600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr7:65669400-65669600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr7:65669400-65669600	Enhancers	Brain Germinal Matrix	brain
43	chr7:65669400-65669600	Enhancers	Brain Hippocampus Middle	brain
44	chr7:65669400-65669600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr7:65669400-65669600	Enhancers	Brain Substantia Nigra	brain
46	chr7:65669400-65669600	Enhancers	Colon Smooth Muscle	Colon
47	chr7:65669400-65669600	Bivalent Enhancer	Duodenum Mucosa	Duodenum
48	chr7:65669400-65669600	Enhancers	Duodenum Smooth Muscle	Duodenum
49	chr7:65669400-65669600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr7:65669400-65669600	Enhancers	Fetal Brain Male	brain

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