Variant report

Variant	esv3375044
Chromosome Location	chr7:6387252-6389800
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6388618-6388920	K562	blood:	n/a	n/a
2	ARID3A	chr7:6388543-6388891	HepG2	liver:	n/a	n/a
3	ATF1	chr7:6388405-6388876	K562	blood:	n/a	n/a
4	ATF2	chr7:6388420-6388909	GM12878	blood:	n/a	chr7:6388596-6388607
5	ATF2	chr7:6388529-6388924	GM12878	blood:	n/a	chr7:6388596-6388607
6	ATF2	chr7:6388437-6388937	H1-hESC	embryonic stem cell:	n/a	chr7:6388596-6388607
7	ATF2	chr7:6388443-6388988	H1-hESC	embryonic stem cell:	n/a	chr7:6388596-6388607
8	ATF3	chr7:6388442-6388841	H1-hESC	embryonic stem cell:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607
9	ATF3	chr7:6388356-6388835	K562	blood:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607
10	ATF3	chr7:6388456-6389065	K562	blood:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607
11	ATF3	chr7:6388385-6388986	A549	lung:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607
12	ATF3	chr7:6388397-6388976	HepG2	liver:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607
13	ATF3	chr7:6388437-6389070	A549	lung:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607
14	ATF3	chr7:6388479-6388902	GM12878	blood:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607
15	BACH1	chr7:6388532-6388708	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr7:6388503-6388987	A549	lung:	n/a	n/a
17	BCLAF1	chr7:6388469-6388989	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:6388098-6388876	GM12878	blood:	n/a	chr7:6388115-6388131 chr7:6388446-6388462
19	BHLHE40	chr7:6388411-6388912	K562	blood:	n/a	chr7:6388446-6388462
20	BHLHE40	chr7:6387976-6388072	K562	blood:	n/a	n/a
21	BRCA1	chr7:6388417-6388923	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr7:6388496-6388723	GM12878	blood:	n/a	n/a
23	BRCA1	chr7:6388593-6388823	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr7:6388497-6388819	HepG2	liver:	n/a	n/a
25	CBX3	chr7:6388389-6389002	K562	blood:	n/a	n/a
26	CCNT2	chr7:6388438-6388902	K562	blood:	n/a	chr7:6388639-6388648
27	CEBPB	chr7:6388607-6388900	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:6388461-6388973	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr7:6388622-6388888	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPD	chr7:6388283-6388690	HepG2	liver:	n/a	n/a
31	CHD1	chr7:6388617-6388714	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr7:6388538-6388820	HepG2	liver:	n/a	n/a
33	CHD2	chr7:6388543-6388850	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr7:6388437-6388914	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr7:6388429-6388891	GM12878	blood:	n/a	n/a
36	CHD2	chr7:6388567-6388815	K562	blood:	n/a	n/a
37	CREB1	chr7:6388413-6388868	A549	lung:	n/a	chr7:6388595-6388608
38	CREB1	chr7:6388297-6388929	H1-hESC	embryonic stem cell:	n/a	chr7:6388595-6388608
39	CREB1	chr7:6387878-6388948	HepG2	liver:	n/a	chr7:6388595-6388608
40	CREB1	chr7:6388374-6388821	ECC-1	luminal epithelium:	n/a	chr7:6388595-6388608
41	CREB1	chr7:6388282-6388943	H1-hESC	embryonic stem cell:	n/a	chr7:6388595-6388608
42	CREB1	chr7:6388198-6388883	GM12878	blood:	n/a	chr7:6388595-6388608
43	CREB1	chr7:6388212-6388980	A549	lung:	n/a	chr7:6388595-6388608
44	CREB1	chr7:6388260-6388921	K562	blood:	n/a	chr7:6388595-6388608
45	CREB1	chr7:6388283-6388940	HepG2	liver:	n/a	chr7:6388595-6388608
46	CREB1	chr7:6388317-6388831	ECC-1	luminal epithelium:	n/a	chr7:6388595-6388608
47	CREB1	chr7:6388241-6388968	K562	blood:	n/a	chr7:6388595-6388608
48	CTCF	chr7:6388588-6388897	NHEK	skin:	n/a	chr7:6388739-6388757 chr7:6388741-6388754 chr7:6388734-6388755 chr7:6388740-6388756
49	CTCF	chr7:6388680-6388830	GM12871	blood:	n/a	chr7:6388739-6388757 chr7:6388741-6388754 chr7:6388734-6388755 chr7:6388740-6388756
50	CTCF	chr7:6388700-6388850	K562	blood:	n/a	chr7:6388739-6388757 chr7:6388741-6388754 chr7:6388734-6388755 chr7:6388740-6388756

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6388620-6388670	HMEC	breast:	n/a
2	chr7:6388620-6388670	SKMC	muscle:	n/a
3	chr7:6388334-6388384	NB4	blood:	n/a
4	chr7:6388620-6388670	HMEC	breast:	n/a
5	chr7:6388620-6388670	SKMC	muscle:	n/a
6	chr7:6388334-6388384	NB4	blood:	n/a
7	chr7:6388827-6388877	AG04450	lung:	fetal
8	chr7:6388334-6388384	A549	lung:	n/a
9	chr7:6388130-6388180	PANC-1	pancreas:	n/a
10	chr7:6388601-6388651	SK-N-MC	brain:	n/a
11	chr7:6388620-6388670	AG04450	lung:	fetal
12	chr7:6388872-6388922	HNPCEpiC	eye:	n/a
13	chr7:6388872-6388922	PrEC	prostate:	n/a
14	chr7:6388872-6388922	ECC-1	luminal epithelium:	n/a
15	chr7:6388601-6388651	AG10803	skin:	n/a
16	chr7:6388620-6388670	MCF-7	breast:	n/a
17	chr7:6388618-6388668	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:6388695-6388745	SK-N-MC	brain:	n/a
19	chr7:6388601-6388651	GM12878	blood:	n/a
20	chr7:6388334-6388384	PANC-1	pancreas:	n/a
21	chr7:6388618-6388668	GM12878	blood:	n/a
22	chr7:6388872-6388922	HRPEpiC	eye:	n/a
23	chr7:6388601-6388651	IMR90	lung:	fetal
24	chr7:6388738-6388788	Jurkat	blood:	n/a
25	chr7:6388563-6388613	PrEC	prostate:	n/a
26	chr7:6388618-6388668	CMK	blood:	n/a
27	chr7:6388601-6388651	HEK293	kidney:	embryo
28	chr7:6388695-6388745	HL-60	blood:	n/a
29	chr7:6388620-6388670	HCPEpiC	choroid plexus:	n/a
30	chr7:6388591-6388641	HMEC	breast:	n/a
31	chr7:6388695-6388745	NHBE	bronchial:	n/a
32	chr7:6388620-6388670	NT2-D1	testis:	n/a
33	chr7:6388563-6388613	SK-N-MC	brain:	n/a
34	chr7:6388827-6388877	HCF	heart:	n/a
35	chr7:6388130-6388180	HRE	kidney:	n/a
36	chr7:6388620-6388670	HAEpiC	amniotic membrane:	n/a
37	chr7:6388827-6388877	HMEC	breast:	n/a
38	chr7:6388591-6388641	HCM	heart:	n/a
39	chr7:6388334-6388384	PrEC	prostate:	n/a
40	chr7:6388618-6388668	HCF	heart:	n/a
41	chr7:6388130-6388180	PFSK-1	brain:	n/a
42	chr7:6388738-6388788	Caco-2	colon:	n/a
43	chr7:6388563-6388613	SKMC	muscle:	n/a
44	chr7:6388872-6388922	HL-60	blood:	n/a
45	chr7:6388334-6388384	HEK293	kidney:	embryo
46	chr7:6388695-6388745	SK-N-SH_RA	brain:	n/a
47	chr7:6388563-6388613	IMR90	lung:	fetal
48	chr7:6388872-6388922	AoSMC	blood vessel:	n/a
49	chr7:6388601-6388651	HCF	heart:	n/a
50	chr7:6388618-6388668	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:6377795..6380161-chr7:6386976..6388780,2	MCF-7	breast:
2	chr7:6097568..6100190-chr7:6387069..6389785,3	MCF-7	breast:
3	chr7:6047922..6050389-chr7:6388573..6391369,3	K562	blood:
4	chr7:6388682..6389270-chr7:6443357..6444249,2	MCF-7	breast:
5	chr7:6386514..6388780-chr7:6439968..6442713,2	MCF-7	breast:
6	chr7:6120676..6122302-chr7:6388312..6390000,2	MCF-7	breast:
7	chr7:6046534..6048837-chr7:6387102..6390061,2	MCF-7	breast:
8	chr7:6049082..6051960-chr7:6388689..6390680,2	MCF-7	breast:
9	chr10:93169367..93170145-chr7:6388240..6389220,2	Hela-S3	cervix:
10	chr7:6387247..6388755-chr7:6413232..6415374,2	MCF-7	breast:

Variant related genes	Relation type
FAM220A	TF binding region
FAM220A	CpG island
ENSG00000136238	chromatin interactions
ENSG00000122512	chromatin interactions
ENSG00000165338	chromatin interactions
ENSG00000178397	chromatin interactions
ENSG00000231704	chromatin interactions
ENSG00000106305	chromatin interactions
ENSG00000086232	chromatin interactions

Extended variants
information (count: 130 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:130 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35458416	chr7:6387253-6387254	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs557698662	chr7:6387299-6387300	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs533947422	chr7:6387333-6387334	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs576185988	chr7:6387366-6387367	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs558999022	chr7:6387367-6387368	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs576968245	chr7:6387385-6387386	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs13242515	chr7:6387447-6387448	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs576950516	chr7:6387458-6387459	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs147113348	chr7:6387473-6387474	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs182132421	chr7:6387494-6387495	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs376869408	chr7:6387514-6387515	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs143253434	chr7:6387515-6387516	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs374442934	chr7:6387517-6387518	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs577346421	chr7:6387523-6387524	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs574307591	chr7:6387524-6387525	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs545084042	chr7:6387614-6387615	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs563769886	chr7:6387615-6387616	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs531093091	chr7:6387653-6387654	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs549415077	chr7:6387671-6387672	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs11983343	chr7:6387673-6387674	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs138512145	chr7:6387733-6387734	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs528516845	chr7:6387766-6387767	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs547042940	chr7:6387827-6387828	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs551988767	chr7:6387844-6387845	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs201696948	chr7:6387861-6387862	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs11408091	chr7:6387863-6387864	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs541675785	chr7:6387864-6387865	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs73060727	chr7:6387865-6387866	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs551048366	chr7:6387869-6387870	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs71008376	chr7:6387872-6387873	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs569762651	chr7:6387880-6387881	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs190041956	chr7:6387949-6387950	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs368544095	chr7:6387953-6387954	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs555398671	chr7:6387998-6387999	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs573628128	chr7:6388010-6388011	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs73060728	chr7:6388024-6388025	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs551933987	chr7:6388030-6388031	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs552591353	chr7:6388064-6388065	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs139709331	chr7:6388073-6388074	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs564188848	chr7:6388082-6388083	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs567200409	chr7:6388127-6388128	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs544780271	chr7:6388140-6388141	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs144113889	chr7:6388144-6388145	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs575764120	chr7:6388177-6388178	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs376026599	chr7:6388237-6388238	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs115596447	chr7:6388256-6388257	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs543176762	chr7:6388336-6388337	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs11550274	chr7:6388338-6388339	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs561443454	chr7:6388357-6388358	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs111834382	chr7:6388392-6388393	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6358200-6387600	Weak transcription	Rectal Smooth Muscle	rectum
2	chr7:6358200-6387600	Weak transcription	HSMM	muscle
3	chr7:6358200-6387600	Weak transcription	NH-A	brain
4	chr7:6362800-6387800	Weak transcription	Fetal Lung	lung
5	chr7:6363000-6387600	Weak transcription	NHEK	skin
6	chr7:6368400-6387800	Weak transcription	Colonic Mucosa	Colon
7	chr7:6368800-6387800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:6370000-6387800	Weak transcription	Brain Substantia Nigra	brain
9	chr7:6370200-6387600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr7:6370200-6387600	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr7:6370200-6387800	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr7:6370400-6387600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr7:6370400-6387600	Weak transcription	Osteobl	bone
14	chr7:6370600-6387600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr7:6370600-6387600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr7:6370600-6387600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr7:6370600-6387600	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr7:6370600-6387800	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr7:6370800-6387400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr7:6370800-6387600	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr7:6370800-6387600	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr7:6370800-6387800	Weak transcription	Liver	Liver
23	chr7:6370800-6387800	Weak transcription	HSMMtube	muscle
24	chr7:6370800-6387800	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr7:6371000-6387800	Weak transcription	Adipose Nuclei	Adipose
26	chr7:6372000-6387600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr7:6372000-6387600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr7:6373200-6387800	Weak transcription	NHDF-Ad	bronchial
29	chr7:6378800-6387600	Weak transcription	A549	lung
30	chr7:6378800-6387800	Weak transcription	Ovary	ovary
31	chr7:6378800-6387800	Weak transcription	GM12878-XiMat	blood
32	chr7:6379000-6387600	Weak transcription	Placenta	Placenta
33	chr7:6379000-6387800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr7:6379000-6387800	Weak transcription	Psoas Muscle	Psoas
35	chr7:6379600-6387600	Weak transcription	Right Atrium	heart
36	chr7:6380200-6387400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr7:6381200-6387600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr7:6382200-6387600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr7:6382800-6387800	Weak transcription	NHLF	lung
40	chr7:6383800-6387800	Weak transcription	Fetal Kidney	kidney
41	chr7:6384000-6387600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr7:6384000-6387800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr7:6384200-6387400	Weak transcription	Primary T cells from cord blood	blood
44	chr7:6384200-6387400	Strong transcription	Fetal Stomach	stomach
45	chr7:6384200-6387600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr7:6384200-6387800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr7:6385200-6387600	Weak transcription	Primary B cells from cord blood	blood
48	chr7:6385400-6387800	Weak transcription	K562	blood
49	chr7:6385600-6387800	Weak transcription	Brain Anterior Caudate	brain
50	chr7:6385800-6387600	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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