Variant report

Variant	esv3346922
Chromosome Location	chr7:87103841-87106389
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:236)
CpG islands
(count:489)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:236 , 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	chr7:87105129-87105319	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:87103805-87104061	HepG2	liver:	n/a	n/a
3	ATF2	chr7:87103159-87104838	GM12878	blood:	n/a	chr7:87104394-87104401
4	ATF2	chr7:87103357-87104743	GM12878	blood:	n/a	chr7:87104394-87104401
5	BACH1	chr7:87104693-87104885	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr7:87103408-87104590	GM12878	blood:	n/a	chr7:87104368-87104377
7	BATF	chr7:87103714-87104408	GM12878	blood:	n/a	chr7:87104368-87104377
8	BCL11A	chr7:87103765-87104455	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:87103389-87104608	GM12878	blood:	n/a	chr7:87103426-87103435
10	BCL3	chr7:87103771-87104306	GM12878	blood:	n/a	n/a
11	BCL3	chr7:87103501-87104527	GM12878	blood:	n/a	n/a
12	BCLAF1	chr7:87103241-87104577	GM12878	blood:	n/a	chr7:87103426-87103435
13	BCLAF1	chr7:87103284-87104672	GM12878	blood:	n/a	chr7:87103426-87103435
14	BHLHE40	chr7:87103333-87105002	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:87105560-87105599	GM12878	blood:	n/a	n/a
16	BRCA1	chr7:87104037-87104253	GM12878	blood:	n/a	n/a
17	BRCA1	chr7:87105230-87105252	GM12878	blood:	n/a	n/a
18	CCNT2	chr7:87105224-87105341	K562	blood:	n/a	n/a
19	CEBPB	chr7:87104216-87104585	IMR90	lung:	n/a	n/a
20	CEBPB	chr7:87104372-87104706	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr7:87104253-87104485	K562	blood:	n/a	n/a
22	CEBPB	chr7:87104230-87104587	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:87104255-87104498	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr7:87104224-87104575	A549	lung:	n/a	n/a
25	CEBPB	chr7:87103821-87104498	GM12878	blood:	n/a	n/a
26	CEBPB	chr7:87103220-87104832	GM12878	blood:	n/a	n/a
27	CEBPD	chr7:87104723-87105270	HepG2	liver:	n/a	n/a
28	CHD1	chr7:87105625-87106080	GM12878	blood:	n/a	n/a
29	CHD1	chr7:87103651-87105326	GM12878	blood:	n/a	chr7:87104889-87104899
30	CHD1	chr7:87104723-87104848	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr7:87104791-87105412	HepG2	liver:	n/a	chr7:87104889-87104899
32	CHD2	chr7:87103416-87105339	GM12878	blood:	n/a	chr7:87104889-87104899
33	CREB1	chr7:87103692-87104672	GM12878	blood:	n/a	n/a
34	CREB1	chr7:87103262-87105411	GM12878	blood:	n/a	n/a
35	CTCF	chr7:87104680-87104830	GM12866	blood:	n/a	n/a
36	CTCF	chr7:87104560-87104710	GM12864	blood:	n/a	n/a
37	CTCF	chr7:87104020-87104170	GM12868	blood:	n/a	n/a
38	CTCF	chr7:87104699-87104753	GM12892	blood:	n/a	n/a
39	CTCF	chr7:87103764-87104264	GM12878	blood:	n/a	n/a
40	CTCF	chr7:87104690-87104698	GM12892	blood:	n/a	n/a
41	CTCF	chr7:87104638-87104938	GM12878	blood:	n/a	n/a
42	CUX1	chr7:87103336-87104667	GM12878	blood:	n/a	n/a
43	CUX1	chr7:87103902-87103919	K562	blood:	n/a	n/a
44	E2F6	chr7:87104816-87105178	K562	blood:	n/a	n/a
45	E2F6	chr7:87104617-87105204	H1-hESC	embryonic stem cell:	n/a	n/a
46	E2F6	chr7:87104631-87105103	H1-hESC	embryonic stem cell:	n/a	n/a
47	EBF1	chr7:87103689-87104361	GM12878	blood:	n/a	n/a
48	EBF1	chr7:87104512-87104905	GM12878	blood:	n/a	n/a
49	EBF1	chr7:87103433-87104837	GM12878	blood:	n/a	n/a
50	EBF1	chr7:87103678-87104343	GM12878	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:87104879-87104929	HUVEC	blood vessel:	n/a
2	chr7:87104879-87104929	HUVEC	blood vessel:	n/a
3	chr7:87105416-87105466	ECC-1	luminal epithelium:	n/a
4	chr7:87104932-87104982	Jurkat	blood:	n/a
5	chr7:87104724-87104774	SK-N-SH	brain:	n/a
6	chr7:87105293-87105343	HCM	heart:	n/a
7	chr7:87105293-87105343	RPTEC	kidney:	n/a
8	chr7:87105293-87105343	HRCEpiC	kidney:	n/a
9	chr7:87105022-87105072	HRPEpiC	eye:	n/a
10	chr7:87105022-87105072	NHBE	bronchial:	n/a
11	chr7:87104932-87104982	HCM	heart:	n/a
12	chr7:87105416-87105466	MCF-7	breast:	n/a
13	chr7:87105398-87105448	HRPEpiC	eye:	n/a
14	chr7:87105416-87105466	Caco-2	colon:	n/a
15	chr7:87105216-87105266	HEK293	kidney:	embryo
16	chr7:87105293-87105343	MCF10A-Er-Src	breast:	n/a
17	chr7:87105398-87105448	HRE	kidney:	n/a
18	chr7:87105398-87105448	AG09319	gingival:	n/a
19	chr7:87105022-87105072	HAEpiC	amniotic membrane:	n/a
20	chr7:87105293-87105343	HCT-116	colon:	n/a
21	chr7:87104724-87104774	NT2-D1	testis:	n/a
22	chr7:87105022-87105072	SK-N-SH	brain:	n/a
23	chr7:87105398-87105448	HCF	heart:	n/a
24	chr7:87105398-87105448	GM12892	blood:	n/a
25	chr7:87105398-87105448	ProgFib	skin:	n/a
26	chr7:87105293-87105343	ProgFib	skin:	n/a
27	chr7:87105293-87105343	AG09309	skin:	n/a
28	chr7:87104879-87104929	PFSK-1	brain:	n/a
29	chr7:87105293-87105343	A549	lung:	n/a
30	chr7:87104724-87104774	BE2_C	brain:	n/a
31	chr7:87105216-87105266	HRE	kidney:	n/a
32	chr7:87105398-87105448	CMK	blood:	n/a
33	chr7:87104932-87104982	MCF-7	breast:	n/a
34	chr7:87104879-87104929	AG09319	gingival:	n/a
35	chr7:87105022-87105072	RPTEC	kidney:	n/a
36	chr7:87105293-87105343	SK-N-SH_RA	brain:	n/a
37	chr7:87104932-87104982	ProgFib	skin:	n/a
38	chr7:87105293-87105343	AG04450	lung:	fetal
39	chr7:87105216-87105266	SK-N-SH	brain:	n/a
40	chr7:87105293-87105343	GM12891	blood:	n/a
41	chr7:87105022-87105072	HL-60	blood:	n/a
42	chr7:87104724-87104774	HEK293	kidney:	embryo
43	chr7:87105216-87105266	A549	lung:	n/a
44	chr7:87105022-87105072	NH-A	brain:	n/a
45	chr7:87105216-87105266	HEEpiC	esophagus:	n/a
46	chr7:87104879-87104929	PrEC	prostate:	n/a
47	chr7:87105022-87105072	H1-hESC	embryonic stem cell:	embryo
48	chr7:87105216-87105266	HepG2	liver:	n/a
49	chr7:87105398-87105448	BE2_C	brain:	n/a
50	chr7:87105022-87105072	NB4	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:87105847..87108201-chr7:87108317..87110707,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CROT-1	chr7:87105081-87107196	NONHSAT121834

No data

Variant related genes	Relation type
ABCB4	TF binding region
ABCB4	CpG island
ENSG00000005471	chromatin interactions

Extended variants
information (count: 85 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:85 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547667440	chr7:87103935-87103936	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs45529340	chr7:87104011-87104012	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs533879949	chr7:87104040-87104041	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs533477529	chr7:87104041-87104042	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185000452	chr7:87104055-87104056	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189461774	chr7:87104101-87104102	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs559103071	chr7:87104105-87104106	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551323430	chr7:87104136-87104137	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs117431116	chr7:87104142-87104143	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs537097730	chr7:87104145-87104146	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528173794	chr7:87104174-87104175	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555548975	chr7:87104201-87104202	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs567461415	chr7:87104228-87104229	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs534850016	chr7:87104229-87104230	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs367855915	chr7:87104230-87104231	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs76538400	chr7:87104238-87104239	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577129521	chr7:87104257-87104258	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs45597334	chr7:87104270-87104271	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs544981160	chr7:87104352-87104353	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558082148	chr7:87104357-87104358	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs576404670	chr7:87104433-87104434	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544454755	chr7:87104442-87104443	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs151095285	chr7:87104450-87104451	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561879383	chr7:87104460-87104461	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529804002	chr7:87104479-87104480	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs45615437	chr7:87104565-87104566	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs45619531	chr7:87104588-87104589	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs559711712	chr7:87104601-87104602	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs375156842	chr7:87104611-87104612	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs533636525	chr7:87104617-87104618	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs182365784	chr7:87104640-87104641	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs373325153	chr7:87104661-87104662	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs186976987	chr7:87104697-87104698	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs369649919	chr7:87104726-87104727	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs141141860	chr7:87104728-87104729	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs542027378	chr7:87104770-87104771	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs374204436	chr7:87104781-87104782	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs45449704	chr7:87104782-87104783	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs8187785	chr7:87104791-87104792	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs373480624	chr7:87104815-87104816	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs201514328	chr7:87104827-87104828	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs370942845	chr7:87104830-87104831	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs375260707	chr7:87104831-87104832	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs546742784	chr7:87104844-87104845	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs571354175	chr7:87104866-87104867	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs34690247	chr7:87104879-87104880	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs183287902	chr7:87104962-87104963	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs72552782	chr7:87104978-87104979	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs563192312	chr7:87105067-87105068	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs72559420	chr7:87105087-87105088	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	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
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	16616336	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:87095000-87104000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:87101600-87105200	Active TSS	Liver	Liver
3	chr7:87102400-87104000	Flanking Active TSS	HepG2	liver
4	chr7:87102600-87104000	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr7:87102600-87104000	Enhancers	Primary B cells from peripheral blood	blood
6	chr7:87102800-87104000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:87102800-87104000	Weak transcription	Psoas Muscle	Psoas
8	chr7:87103000-87104000	Active TSS	Skeletal Muscle Male	skeletal muscle
9	chr7:87103000-87104000	Active TSS	Skeletal Muscle Female	skeletal muscle
10	chr7:87103200-87104000	Enhancers	Colon Smooth Muscle	Colon
11	chr7:87103200-87104000	Enhancers	HSMMtube	muscle
12	chr7:87103400-87104000	Weak transcription	Colonic Mucosa	Colon
13	chr7:87103400-87104000	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr7:87103400-87104000	Enhancers	Osteobl	bone
15	chr7:87103400-87104200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:87103400-87104400	Bivalent Enhancer	Fetal Intestine Large	intestine
17	chr7:87103400-87104400	Active TSS	Stomach Smooth Muscle	stomach
18	chr7:87103400-87104600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr7:87103400-87104800	Flanking Active TSS	NHDF-Ad	bronchial
20	chr7:87103400-87105000	Flanking Active TSS	GM12878-XiMat	blood
21	chr7:87103600-87104000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr7:87103600-87104800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr7:87103600-87104800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:87103600-87105200	Active TSS	Right Atrium	heart
25	chr7:87103600-87105400	Active TSS	Aorta	Aorta
26	chr7:87103600-87105400	Active TSS	Fetal Heart	heart
27	chr7:87103600-87105400	Active TSS	Right Ventricle	heart
28	chr7:87103600-87105600	Active TSS	Duodenum Smooth Muscle	Duodenum
29	chr7:87103600-87105800	Active TSS	Rectal Smooth Muscle	rectum
30	chr7:87103800-87104000	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
31	chr7:87103800-87104000	Flanking Bivalent TSS/Enh	ES-WA7 Cell Line	embryonic stem cell
32	chr7:87103800-87104000	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr7:87103800-87104000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
34	chr7:87103800-87104000	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr7:87103800-87104000	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
36	chr7:87103800-87104000	Active TSS	Duodenum Mucosa	Duodenum
37	chr7:87103800-87104000	Enhancers	Fetal Brain Female	brain
38	chr7:87103800-87104000	Bivalent Enhancer	Fetal Intestine Small	intestine
39	chr7:87103800-87104000	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
40	chr7:87103800-87104000	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr7:87103800-87104200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr7:87103800-87104200	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
43	chr7:87103800-87104200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr7:87103800-87104200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr7:87103800-87104400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
46	chr7:87103800-87104400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
47	chr7:87103800-87104400	Active TSS	Primary B cells from cord blood	blood
48	chr7:87103800-87104400	Flanking Active TSS	Primary hematopoietic stem cells	blood
49	chr7:87103800-87104400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr7:87103800-87104400	Bivalent Enhancer	Fetal Lung	lung

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