Variant report

Variant	esv3406129
Chromosome Location	chr7:70595641-70598589
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:76)
CpG islands
(count:794)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:76 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:70596126-70596870	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:70597821-70597985	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr7:70597911-70597916	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chr7:70597727-70598099	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD1	chr7:70596637-70597085	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr7:70596719-70596950	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr7:70597431-70597433	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTBP2	chr7:70596159-70597435	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr7:70596374-70596725	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr7:70596533-70596602	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr7:70596501-70596530	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr7:70596475-70596611	Pancreas_OC	pancreas:	n/a	n/a
13	CTCF	chr7:70596361-70596716	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr7:70596505-70596604	Medullo	brain:	n/a	n/a
15	CTCF	chr7:70596513-70596573	Fibrobl	skin:	n/a	n/a
16	E2F6	chr7:70597674-70598316	H1-hESC	embryonic stem cell:	n/a	n/a
17	E2F6	chr7:70596160-70597030	H1-hESC	embryonic stem cell:	n/a	chr7:70596767-70596776
18	E2F6	chr7:70596113-70596585	H1-hESC	embryonic stem cell:	n/a	n/a
19	E2F6	chr7:70597518-70598565	H1-hESC	embryonic stem cell:	n/a	n/a
20	E2F6	chr7:70596606-70597220	H1-hESC	embryonic stem cell:	n/a	chr7:70597032-70597041 chr7:70597092-70597101 chr7:70596767-70596776
21	EP300	chr7:70596146-70596579	H1-hESC	embryonic stem cell:	n/a	chr7:70596414-70596423 chr7:70596479-70596495 chr7:70596483-70596499
22	GABPA	chr7:70596487-70597048	H1-hESC	embryonic stem cell:	n/a	chr7:70596767-70596776 chr7:70596493-70596507 chr7:70596490-70596504
23	GABPA	chr7:70596151-70596426	H1-hESC	embryonic stem cell:	n/a	n/a
24	GTF2F1	chr7:70597789-70597981	H1-hESC	embryonic stem cell:	n/a	n/a
25	GTF2F1	chr7:70596455-70596678	H1-hESC	embryonic stem cell:	n/a	n/a
26	GTF2F1	chr7:70596950-70597000	H1-hESC	embryonic stem cell:	n/a	n/a
27	JUND	chr7:70596155-70596372	H1-hESC	embryonic stem cell:	n/a	chr7:70596272-70596286
28	JUND	chr7:70596571-70596794	H1-hESC	embryonic stem cell:	n/a	n/a
29	JUND	chr7:70596027-70596983	H1-hESC	embryonic stem cell:	n/a	chr7:70596110-70596124 chr7:70596272-70596286
30	MAX	chr7:70597378-70598434	H1-hESC	embryonic stem cell:	n/a	n/a
31	MAX	chr7:70597622-70598363	H1-hESC	embryonic stem cell:	n/a	n/a
32	MAX	chr7:70596114-70597192	H1-hESC	embryonic stem cell:	n/a	chr7:70596476-70596486
33	MAX	chr7:70596150-70597151	H1-hESC	embryonic stem cell:	n/a	chr7:70596476-70596486
34	MXI1	chr7:70597943-70598162	H1-hESC	embryonic stem cell:	n/a	n/a
35	MXI1	chr7:70597508-70597621	H1-hESC	embryonic stem cell:	n/a	n/a
36	MXI1	chr7:70596294-70596477	H1-hESC	embryonic stem cell:	n/a	n/a
37	MYC	chr7:70596294-70596597	H1-hESC	embryonic stem cell:	n/a	chr7:70596476-70596486
38	MYC	chr7:70597973-70598173	H1-hESC	embryonic stem cell:	n/a	n/a
39	NRF1	chr7:70596402-70596574	H1-hESC	embryonic stem cell:	n/a	chr7:70596493-70596507 chr7:70596490-70596504
40	POLR2A	chr7:70597480-70597885	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr7:70596070-70598893	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr7:70597472-70598216	H1-neurons	neurons:	n/a	n/a
43	POLR2A	chr7:70596172-70597347	H1-neurons	neurons:	n/a	n/a
44	POLR2A	chr7:70596212-70597318	H1-neurons	neurons:	n/a	n/a
45	POLR2A	chr7:70596195-70596584	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr7:70596152-70596574	SK-N-MC	brain:	n/a	n/a
47	POLR2A	chr7:70597374-70598047	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr7:70596203-70596987	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr7:70596239-70596507	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr7:70596611-70597314	SK-N-MC	brain:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70598282-70598332	RPTEC	kidney:	n/a
2	chr7:70598282-70598332	RPTEC	kidney:	n/a
3	chr7:70596377-70596427	PrEC	prostate:	n/a
4	chr7:70597921-70597971	K562	blood:	n/a
5	chr7:70597774-70597824	HAEpiC	amniotic membrane:	n/a
6	chr7:70596308-70596358	HRPEpiC	eye:	n/a
7	chr7:70597058-70597108	LNCaP	prostate:	n/a
8	chr7:70596308-70596358	Jurkat	blood:	n/a
9	chr7:70597921-70597971	PFSK-1	brain:	n/a
10	chr7:70597713-70597763	MCF10A-Er-Src	breast:	n/a
11	chr7:70597774-70597824	PrEC	prostate:	n/a
12	chr7:70598282-70598332	MCF-7	breast:	n/a
13	chr7:70597687-70597737	HCF	heart:	n/a
14	chr7:70597687-70597737	Jurkat	blood:	n/a
15	chr7:70597091-70597141	AG09319	gingival:	n/a
16	chr7:70597599-70597649	BE2_C	brain:	n/a
17	chr7:70597778-70597828	HAEpiC	amniotic membrane:	n/a
18	chr7:70598282-70598332	T-47D	breast:	n/a
19	chr7:70597599-70597649	AG09309	skin:	n/a
20	chr7:70597774-70597824	NHBE	bronchial:	n/a
21	chr7:70597065-70597115	HEK293	kidney:	embryo
22	chr7:70597778-70597828	NH-A	brain:	n/a
23	chr7:70597458-70597508	GM12891	blood:	n/a
24	chr7:70596377-70596427	HRE	kidney:	n/a
25	chr7:70597921-70597971	Jurkat	blood:	n/a
26	chr7:70597599-70597649	SAEC	small airway:	n/a
27	chr7:70598282-70598332	HRCEpiC	kidney:	n/a
28	chr7:70597774-70597824	HPAEpiC	pulmonary alveolar:	n/a
29	chr7:70597458-70597508	HPAEpiC	pulmonary alveolar:	n/a
30	chr7:70596377-70596427	HEK293	kidney:	embryo
31	chr7:70597599-70597649	HCPEpiC	choroid plexus:	n/a
32	chr7:70597458-70597508	HCPEpiC	choroid plexus:	n/a
33	chr7:70597774-70597824	MCF10A-Er-Src	breast:	n/a
34	chr7:70597921-70597971	HCT-116	colon:	n/a
35	chr7:70597599-70597649	AG10803	skin:	n/a
36	chr7:70597778-70597828	HMEC	breast:	n/a
37	chr7:70597778-70597828	SAEC	small airway:	n/a
38	chr7:70597774-70597824	HRPEpiC	eye:	n/a
39	chr7:70598282-70598332	ECC-1	luminal epithelium:	n/a
40	chr7:70597774-70597824	HepG2	liver:	n/a
41	chr7:70597065-70597115	NHDF-neo	bronchial:	n/a
42	chr7:70597713-70597763	A549	lung:	n/a
43	chr7:70597091-70597141	Hepatocyte	liver:	n/a
44	chr7:70597599-70597649	HAEpiC	amniotic membrane:	n/a
45	chr7:70597713-70597763	AoSMC	blood vessel:	n/a
46	chr7:70597713-70597763	AG10803	skin:	n/a
47	chr7:70597713-70597763	SKMC	muscle:	n/a
48	chr7:70597458-70597508	LNCaP	prostate:	n/a
49	chr7:70597687-70597737	A549	lung:	n/a
50	chr7:70596308-70596358	AG09319	gingival:	n/a

No data

Variant related genes	Relation type
WBSCR17	TF binding region
WBSCR17	CpG island

Extended variants
information (count: 129 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:129 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7783769	chr7:70595648-70595649	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567347413	chr7:70595699-70595700	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs537816547	chr7:70595704-70595705	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs556823743	chr7:70595708-70595709	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs7810849	chr7:70595730-70595731	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs372720729	chr7:70595758-70595759	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs545083807	chr7:70595802-70595803	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs146896954	chr7:70595804-70595805	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs200647135	chr7:70595809-70595810	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs139251580	chr7:70595857-70595858	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs542814336	chr7:70595865-70595866	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs144868961	chr7:70595876-70595877	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs149830467	chr7:70595880-70595881	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs73706796	chr7:70595894-70595895	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs184556631	chr7:70595903-70595904	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs28485392	chr7:70595906-70595907	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs576126967	chr7:70595923-70595924	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs190142429	chr7:70595932-70595933	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs115011006	chr7:70596024-70596025	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs543816128	chr7:70596044-70596045	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs562848770	chr7:70596106-70596107	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs150441049	chr7:70596121-70596122	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs545223576	chr7:70596150-70596151	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs544592712	chr7:70596197-70596198	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs564924213	chr7:70596202-70596203	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs556783685	chr7:70596216-70596217	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs369639778	chr7:70596232-70596233	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs13230586	chr7:70596239-70596240	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs117754510	chr7:70596300-70596301	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs531733063	chr7:70596314-70596315	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs182172404	chr7:70596384-70596385	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs549903221	chr7:70596424-70596425	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs138206824	chr7:70596438-70596439	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs538945202	chr7:70596460-70596461	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs149571444	chr7:70596499-70596500	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs58589178	chr7:70596532-70596533	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs536806953	chr7:70596559-70596560	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs555510553	chr7:70596572-70596573	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs112077594	chr7:70596579-70596580	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs544237098	chr7:70596635-70596636	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs555871647	chr7:70596654-70596655	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs569012320	chr7:70596689-70596690	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs544999405	chr7:70596696-70596697	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs531418820	chr7:70596726-70596727	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs559983935	chr7:70596782-70596783	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs572371826	chr7:70596820-70596821	Bivalent/Poised TSS Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs545604714	chr7:70596821-70596822	Bivalent/Poised TSS Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs542365036	chr7:70596831-70596832	Bivalent/Poised TSS Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs561090437	chr7:70596841-70596842	Bivalent/Poised TSS Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs531699972	chr7:70596845-70596846	Bivalent/Poised TSS Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
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
Wilms tumour	21544195	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
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
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
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70594600-70596000	Bivalent Enhancer	Fetal Muscle Leg	muscle
2	chr7:70594800-70595800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr7:70594800-70596000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:70595000-70595800	Enhancers	H1 Cell Line	embryonic stem cell
5	chr7:70595000-70595800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr7:70595000-70595800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:70595000-70596000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr7:70595000-70596000	Enhancers	Fetal Lung	lung
9	chr7:70595200-70595800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr7:70595200-70595800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr7:70595200-70596000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:70595400-70595800	Flanking Active TSS	H9 Cell Line	embryonic stem cell
13	chr7:70595400-70595800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:70595400-70595800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr7:70595400-70595800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr7:70595400-70595800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr7:70595400-70595800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr7:70595400-70596000	Active TSS	Fetal Brain Male	brain
19	chr7:70595400-70596000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr7:70595600-70595800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr7:70595600-70595800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:70595600-70595800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr7:70595600-70595800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr7:70595600-70595800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
25	chr7:70595600-70596000	Enhancers	Fetal Brain Female	brain
26	chr7:70595600-70596000	Bivalent Enhancer	Fetal Stomach	stomach
27	chr7:70595600-70596000	Enhancers	Placenta Amnion	Placenta Amnion
28	chr7:70595600-70596000	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr7:70595600-70596000	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr7:70595600-70596000	Bivalent Enhancer	NH-A	brain
31	chr7:70595600-70596400	Active TSS	Colonic Mucosa	Colon
32	chr7:70595600-70596400	Enhancers	Fetal Heart	heart
33	chr7:70595800-70596000	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr7:70595800-70596000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
35	chr7:70595800-70596000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr7:70595800-70596000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr7:70595800-70596000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr7:70595800-70596000	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
39	chr7:70595800-70596200	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
40	chr7:70595800-70596200	Enhancers	Stomach Smooth Muscle	stomach
41	chr7:70595800-70596600	Active TSS	H1 Cell Line	embryonic stem cell
42	chr7:70595800-70596800	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr7:70595800-70596800	Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr7:70595800-70597400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr7:70595800-70597400	Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr7:70595800-70597800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr7:70595800-70597800	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr7:70595800-70598600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr7:70595800-70598800	Active TSS	H9 Cell Line	embryonic stem cell
50	chr7:70595800-70598800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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