Variant report

Variant	esv3324748
Chromosome Location	chr7:70158266-70160839
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:308)
CpG islands
(count:427)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:70159737-70160179	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr7:70158188-70158571	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr7:70160128-70160685	GM12878	blood:	n/a	chr7:70160375-70160391
4	BHLHE40	chr7:70158734-70159179	GM12878	blood:	n/a	chr7:70159147-70159163
5	BRCA1	chr7:70160153-70160203	GM12878	blood:	n/a	n/a
6	CEBPB	chr7:70158609-70158963	MCF-7	breast:	n/a	chr7:70158756-70158767
7	CEBPB	chr7:70158624-70158869	HepG2	liver:	n/a	chr7:70158756-70158767
8	CEBPB	chr7:70158582-70158901	A549	lung:	n/a	chr7:70158756-70158767
9	CEBPB	chr7:70158563-70158948	H1-hESC	embryonic stem cell:	n/a	chr7:70158756-70158767
10	CEBPB	chr7:70158581-70158954	MCF-7	breast:	n/a	chr7:70158756-70158767
11	CEBPB	chr7:70158655-70158909	A549	lung:	n/a	chr7:70158756-70158767
12	CEBPB	chr7:70158492-70159079	A549	lung:	n/a	chr7:70158756-70158767
13	CEBPB	chr7:70158570-70158936	HepG2	liver:	n/a	chr7:70158756-70158767
14	CEBPB	chr7:70158502-70158961	IMR90	lung:	n/a	chr7:70158756-70158767
15	CEBPB	chr7:70158634-70158846	HepG2	liver:	n/a	chr7:70158756-70158767
16	CHD1	chr7:70159054-70159379	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr7:70159050-70161957	GM12878	blood:	n/a	n/a
18	CHD1	chr7:70159739-70162428	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr7:70158661-70159209	H1-hESC	embryonic stem cell:	n/a	chr7:70158841-70158851
20	CHD2	chr7:70159329-70159497	GM12878	blood:	n/a	n/a
21	CHD2	chr7:70158714-70158805	GM12878	blood:	n/a	n/a
22	CHD2	chr7:70159846-70160301	GM12878	blood:	n/a	n/a
23	CHD2	chr7:70159087-70159092	GM12878	blood:	n/a	n/a
24	CREB1	chr7:70159373-70159620	A549	lung:	n/a	n/a
25	CTCF	chr7:70158300-70158450	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr7:70158620-70158770	HEK293	kidney:	n/a	n/a
27	CTCF	chr7:70158680-70158830	GM12865	blood:	n/a	n/a
28	CTCF	chr7:70158600-70158750	AG09319	gingival:	n/a	n/a
29	CTCF	chr7:70158660-70158810	GM12875	blood:	n/a	n/a
30	CTCF	chr7:70159260-70159410	SAEC	small airway:	n/a	n/a
31	CTCF	chr7:70159320-70159470	AG04449	skin:	n/a	n/a
32	CTCF	chr7:70158720-70158870	GM12871	blood:	n/a	chr7:70158836-70158849
33	CTCF	chr7:70158660-70158810	HCFaa	heart:	n/a	n/a
34	CTCF	chr7:70158620-70158770	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr7:70158640-70158790	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr7:70158620-70158770	GM12864	blood:	n/a	n/a
37	CTCF	chr7:70158620-70158770	GM12873	blood:	n/a	n/a
38	CTCF	chr7:70158640-70158790	GM12873	blood:	n/a	n/a
39	CTCF	chr7:70158620-70158770	AG10803	skin:	n/a	n/a
40	CTCF	chr7:70158720-70158870	GM12872	blood:	n/a	chr7:70158836-70158849
41	CTCF	chr7:70158640-70158790	GM12866	blood:	n/a	n/a
42	CTCF	chr7:70158660-70158810	HCM	heart:	n/a	n/a
43	CTCF	chr7:70158620-70158770	HMF	breast:	n/a	n/a
44	CTCF	chr7:70159000-70159150	GM12875	blood:	n/a	chr7:70159116-70159129
45	CTCF	chr7:70158640-70158790	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr7:70158640-70158790	BE2_C	brain:	n/a	n/a
47	CTCF	chr7:70158660-70158810	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr7:70158660-70158810	GM12869	blood:	n/a	n/a
49	CTCF	chr7:70158340-70158490	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr7:70158620-70158770	SAEC	small airway:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70159215-70159265	HPAEpiC	pulmonary alveolar:	n/a
2	chr7:70160734-70160784	AG04449	skin:	fetal
3	chr7:70160498-70160548	HRCEpiC	kidney:	n/a
4	chr7:70160734-70160784	AG09309	skin:	n/a
5	chr7:70158761-70158811	LNCaP	prostate:	n/a
6	chr7:70159330-70159380	SAEC	small airway:	n/a
7	chr7:70160734-70160784	GM19239	blood:	n/a
8	chr7:70159340-70159390	NB4	blood:	n/a
9	chr7:70160006-70160056	Caco-2	colon:	n/a
10	chr7:70160734-70160784	AoSMC	blood vessel:	n/a
11	chr7:70159340-70159390	HAEpiC	amniotic membrane:	n/a
12	chr7:70160006-70160056	AG10803	skin:	n/a
13	chr7:70160006-70160056	A549	lung:	n/a
14	chr7:70159340-70159390	HRCEpiC	kidney:	n/a
15	chr7:70159215-70159265	MCF-7	breast:	n/a
16	chr7:70159215-70159265	PFSK-1	brain:	n/a
17	chr7:70158761-70158811	MCF-7	breast:	n/a
18	chr7:70160498-70160548	ECC-1	luminal epithelium:	n/a
19	chr7:70159215-70159265	HCT-116	colon:	n/a
20	chr7:70160006-70160056	HCPEpiC	choroid plexus:	n/a
21	chr7:70159340-70159390	GM12892	blood:	n/a
22	chr7:70160734-70160784	HepG2	liver:	n/a
23	chr7:70160498-70160548	Hepatocyte	liver:	n/a
24	chr7:70160734-70160784	HAEpiC	amniotic membrane:	n/a
25	chr7:70159340-70159390	Hela-S3	cervix:	n/a
26	chr7:70159340-70159390	AG10803	skin:	n/a
27	chr7:70160006-70160056	SAEC	small airway:	n/a
28	chr7:70159330-70159380	AG09319	gingival:	n/a
29	chr7:70159340-70159390	PANC-1	pancreas:	n/a
30	chr7:70159215-70159265	AG04450	lung:	fetal
31	chr7:70158761-70158811	ECC-1	luminal epithelium:	n/a
32	chr7:70158761-70158811	SK-N-SH	brain:	n/a
33	chr7:70159340-70159390	AG04449	skin:	fetal
34	chr7:70159215-70159265	HRCEpiC	kidney:	n/a
35	chr7:70159340-70159390	H1-hESC	embryonic stem cell:	embryo
36	chr7:70160734-70160784	SAEC	small airway:	n/a
37	chr7:70160498-70160548	HRE	kidney:	n/a
38	chr7:70160734-70160784	HRCEpiC	kidney:	n/a
39	chr7:70158761-70158811	NH-A	brain:	n/a
40	chr7:70158761-70158811	Caco-2	colon:	n/a
41	chr7:70160006-70160056	LNCaP	prostate:	n/a
42	chr7:70159215-70159265	ECC-1	luminal epithelium:	n/a
43	chr7:70160498-70160548	GM12892	blood:	n/a
44	chr7:70159330-70159380	LNCaP	prostate:	n/a
45	chr7:70160734-70160784	Hela-S3	cervix:	n/a
46	chr7:70159340-70159390	SK-N-MC	brain:	n/a
47	chr7:70159215-70159265	MCF10A-Er-Src	breast:	n/a
48	chr7:70158761-70158811	IMR90	lung:	fetal
49	chr7:70160006-70160056	HEEpiC	esophagus:	n/a
50	chr7:70159330-70159380	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:70157686..70159380-chr7:70159994..70162274,2	MCF-7	breast:
2	chr7:70157686..70159380-chr7:70159994..70162274,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WBSCR17-3	chr7:70159859-70160031	NONHSAT121336

No data

Variant related genes	Relation type
AUTS2	TF binding region
AUTS2	CpG island

Extended variants
information (count: 58 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:58 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113378109	chr7:70158277-70158278	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs187994398	chr7:70158283-70158284	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs147271934	chr7:70158293-70158294	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs12698914	chr7:70158370-70158371	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs60408354	chr7:70158495-70158496	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs368345929	chr7:70158513-70158514	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs547598063	chr7:70158536-70158537	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs566413285	chr7:70158627-70158628	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs372000023	chr7:70158643-70158644	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs555198960	chr7:70158670-70158671	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs567239525	chr7:70158685-70158686	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs537882123	chr7:70158712-70158713	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs556493655	chr7:70158726-70158727	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs577999886	chr7:70158757-70158758	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs545183680	chr7:70158801-70158802	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs553947152	chr7:70158819-70158820	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs572419352	chr7:70158842-70158843	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs543083500	chr7:70158846-70158847	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs12536766	chr7:70158864-70158865	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs113957304	chr7:70158865-70158866	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs531586113	chr7:70158921-70158922	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs543417654	chr7:70159012-70159013	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs368989042	chr7:70159253-70159254	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs13227734	chr7:70159290-70159291	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs13227742	chr7:70159311-70159312	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs13227743	chr7:70159316-70159317	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs532683920	chr7:70159424-70159425	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs547648725	chr7:70159480-70159481	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs566241786	chr7:70159481-70159482	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs530266703	chr7:70159492-70159493	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs181435451	chr7:70159602-70159603	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs567295279	chr7:70159619-70159620	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs545151742	chr7:70159760-70159761	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs375423788	chr7:70159822-70159823	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs530675419	chr7:70159827-70159828	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs565330064	chr7:70159854-70159855	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs556204472	chr7:70159913-70159914	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs571531192	chr7:70160003-70160004	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
39	rs538953732	chr7:70160035-70160036	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs118049787	chr7:70160045-70160046	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs186538247	chr7:70160096-70160097	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs374991416	chr7:70160213-70160214	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
43	rs555003170	chr7:70160261-70160262	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
44	rs552506486	chr7:70160292-70160293	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
45	rs113951103	chr7:70160299-70160300	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
46	rs576139237	chr7:70160378-70160379	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
47	rs543380969	chr7:70160407-70160408	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs191702244	chr7:70160460-70160461	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs181772820	chr7:70160471-70160472	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs112844975	chr7:70160499-70160500	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:363 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70155200-70158400	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr7:70156600-70158600	Enhancers	Liver	Liver
3	chr7:70157200-70158600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:70157800-70158400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
5	chr7:70157800-70158400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
6	chr7:70157800-70158400	Enhancers	Fetal Thymus	thymus
7	chr7:70157800-70158400	Bivalent Enhancer	Thymus	Thymus
8	chr7:70157800-70158400	Enhancers	HSMMtube	muscle
9	chr7:70157800-70158600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr7:70157800-70158600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:70157800-70158600	Enhancers	Right Atrium	heart
12	chr7:70157800-70158800	Enhancers	Fetal Brain Male	brain
13	chr7:70158000-70158400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
14	chr7:70158000-70158400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr7:70158000-70158400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr7:70158000-70158400	Enhancers	Fetal Brain Female	brain
17	chr7:70158000-70158400	Enhancers	Fetal Intestine Small	intestine
18	chr7:70158000-70158400	Enhancers	Fetal Muscle Trunk	muscle
19	chr7:70158000-70158400	Enhancers	Fetal Stomach	stomach
20	chr7:70158000-70158400	Enhancers	Psoas Muscle	Psoas
21	chr7:70158000-70158600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr7:70158000-70158600	Enhancers	Fetal Intestine Large	intestine
23	chr7:70158000-70158600	Enhancers	Fetal Muscle Leg	muscle
24	chr7:70158000-70158600	Enhancers	Spleen	Spleen
25	chr7:70158000-70160400	Active TSS	Duodenum Smooth Muscle	Duodenum
26	chr7:70158200-70158400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr7:70158200-70158400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr7:70158200-70158400	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr7:70158200-70158400	Enhancers	Muscle Satellite Cultured Cells	--
30	chr7:70158200-70158400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr7:70158200-70158400	Enhancers	Brain Cingulate Gyrus	brain
32	chr7:70158200-70158400	Bivalent Enhancer	Brain Germinal Matrix	brain
33	chr7:70158200-70158400	Enhancers	Duodenum Mucosa	Duodenum
34	chr7:70158200-70158400	Enhancers	Fetal Kidney	kidney
35	chr7:70158200-70158400	Enhancers	Gastric	stomach
36	chr7:70158200-70158400	Enhancers	Ovary	ovary
37	chr7:70158200-70158400	Enhancers	Dnd41	blood
38	chr7:70158200-70158400	Enhancers	HSMM	muscle
39	chr7:70158200-70158400	Enhancers	NH-A	brain
40	chr7:70158200-70158600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
41	chr7:70158200-70158600	Flanking Bivalent TSS/Enh	H9 Cell Line	embryonic stem cell
42	chr7:70158200-70158600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
43	chr7:70158200-70158600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
44	chr7:70158200-70158600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
45	chr7:70158200-70158600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
46	chr7:70158200-70158600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr7:70158200-70158600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:70158200-70158600	Enhancers	Primary T cells from cord blood	blood
49	chr7:70158200-70158600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr7:70158200-70158600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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