Variant report

Variant	esv2758141
Chromosome Location	chr7:153001173-153298779
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1480)
CpG islands
(count:793)
Chromatin interactive
region (count:240)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1480 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:153109096-153109296	K562	blood:	n/a	n/a
2	ARID3A	chr7:153078807-153079063	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:153108540-153108589	K562	blood:	n/a	n/a
4	ARID3A	chr7:153103307-153103458	K562	blood:	n/a	n/a
5	ARID3A	chr7:153103753-153104234	K562	blood:	n/a	n/a
6	ARID3A	chr7:153109739-153110062	K562	blood:	n/a	n/a
7	ARID3A	chr7:153082623-153082873	K562	blood:	n/a	n/a
8	ARID3A	chr7:153043449-153043453	K562	blood:	n/a	n/a
9	ARID3A	chr7:153110322-153112174	K562	blood:	n/a	n/a
10	ARID3A	chr7:153143735-153143934	K562	blood:	n/a	n/a
11	ARID3A	chr7:153130385-153130583	K562	blood:	n/a	n/a
12	ARID3A	chr7:153104655-153106258	K562	blood:	n/a	n/a
13	ATF1	chr7:153130251-153130554	K562	blood:	n/a	n/a
14	ATF1	chr7:153154941-153155221	K562	blood:	n/a	n/a
15	ATF1	chr7:153112718-153113068	K562	blood:	n/a	n/a
16	ATF1	chr7:153074161-153074244	K562	blood:	n/a	n/a
17	ATF1	chr7:153119688-153120319	K562	blood:	n/a	n/a
18	ATF1	chr7:153034781-153034828	K562	blood:	n/a	n/a
19	ATF1	chr7:153104526-153104952	K562	blood:	n/a	n/a
20	ATF1	chr7:153110923-153111307	K562	blood:	n/a	n/a
21	ATF3	chr7:153119989-153120275	K562	blood:	n/a	n/a
22	BACH1	chr7:153031945-153032120	K562	blood:	n/a	n/a
23	BACH1	chr7:153100843-153101026	K562	blood:	n/a	n/a
24	BACH1	chr7:153109751-153110110	K562	blood:	n/a	n/a
25	BACH1	chr7:153108498-153108636	K562	blood:	n/a	n/a
26	BACH1	chr7:153111122-153111267	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr7:153110739-153112141	K562	blood:	n/a	n/a
28	BACH1	chr7:153099558-153099965	K562	blood:	n/a	n/a
29	BACH1	chr7:153055076-153055079	K562	blood:	n/a	n/a
30	BACH1	chr7:153203925-153204059	K562	blood:	n/a	n/a
31	BACH1	chr7:153113244-153113564	K562	blood:	n/a	n/a
32	BACH1	chr7:153244736-153244872	K562	blood:	n/a	n/a
33	BACH1	chr7:153133123-153133319	K562	blood:	n/a	n/a
34	BACH1	chr7:153097892-153097911	K562	blood:	n/a	n/a
35	BACH1	chr7:153200611-153200865	H1-hESC	embryonic stem cell:	n/a	n/a
36	BCL3	chr7:153103242-153103537	K562	blood:	n/a	n/a
37	BCL3	chr7:153101811-153102227	K562	blood:	n/a	n/a
38	BCL3	chr7:153109499-153110250	K562	blood:	n/a	n/a
39	BCL3	chr7:153105524-153106503	K562	blood:	n/a	n/a
40	BCL3	chr7:153104489-153105071	K562	blood:	n/a	n/a
41	BCLAF1	chr7:153104261-153105189	K562	blood:	n/a	n/a
42	BCLAF1	chr7:153110402-153111174	K562	blood:	n/a	n/a
43	BCLAF1	chr7:153107687-153111130	K562	blood:	n/a	n/a
44	BCLAF1	chr7:153105443-153107677	K562	blood:	n/a	n/a
45	BHLHE40	chr7:153150901-153150904	K562	blood:	n/a	n/a
46	BHLHE40	chr7:153167374-153167638	K562	blood:	n/a	n/a
47	BHLHE40	chr7:153099774-153100192	K562	blood:	n/a	n/a
48	BHLHE40	chr7:153055739-153055799	K562	blood:	n/a	n/a
49	BHLHE40	chr7:153108552-153108560	K562	blood:	n/a	n/a
50	BHLHE40	chr7:153121524-153121702	K562	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:153110492-153110542	AG04450	lung:	fetal
2	chr7:153110762-153110812	SAEC	small airway:	n/a
3	chr7:153078797-153078847	HCM	heart:	n/a
4	chr7:153109538-153109588	HAEpiC	amniotic membrane:	n/a
5	chr7:153110492-153110542	GM06990	blood:	n/a
6	chr7:153108684-153108734	AG10803	skin:	n/a
7	chr7:153108684-153108734	AoSMC	blood vessel:	n/a
8	chr7:153109375-153109425	AG04449	skin:	fetal
9	chr7:153109538-153109588	HMEC	breast:	n/a
10	chr7:153110492-153110542	NHDF-neo	bronchial:	n/a
11	chr7:153108684-153108734	K562	blood:	n/a
12	chr7:153110762-153110812	HMEC	breast:	n/a
13	chr7:153287752-153287802	NHBE	bronchial:	n/a
14	chr7:153287529-153287579	NH-A	brain:	n/a
15	chr7:153287591-153287641	ovcar-3	ovarian:	n/a
16	chr7:153108642-153108692	SK-N-SH_RA	brain:	n/a
17	chr7:153012895-153012945	HCF	heart:	n/a
18	chr7:153108726-153108776	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:153110994-153111044	AG10803	skin:	n/a
20	chr7:153110994-153111044	HRCEpiC	kidney:	n/a
21	chr7:153108642-153108692	K562	blood:	n/a
22	chr7:153078797-153078847	GM12878	blood:	n/a
23	chr7:153287591-153287641	GM12891	blood:	n/a
24	chr7:153287591-153287641	RPTEC	kidney:	n/a
25	chr7:153287529-153287579	RPTEC	kidney:	n/a
26	chr7:153110994-153111044	HepG2	liver:	n/a
27	chr7:153108642-153108692	PFSK-1	brain:	n/a
28	chr7:153110492-153110542	GM19239	blood:	n/a
29	chr7:153110492-153110542	ovcar-3	ovarian:	n/a
30	chr7:153108642-153108692	AG04449	skin:	fetal
31	chr7:153287752-153287802	GM12878	blood:	n/a
32	chr7:153108684-153108734	GM12878	blood:	n/a
33	chr7:153109538-153109588	AG10803	skin:	n/a
34	chr7:153012895-153012945	HRCEpiC	kidney:	n/a
35	chr7:153108726-153108776	PANC-1	pancreas:	n/a
36	chr7:153109538-153109588	U87	brain:	n/a
37	chr7:153078797-153078847	T-47D	breast:	n/a
38	chr7:153078797-153078847	IMR90	lung:	fetal
39	chr7:153078797-153078847	HRCEpiC	kidney:	n/a
40	chr7:153012895-153012945	H1-hESC	embryonic stem cell:	embryo
41	chr7:153108726-153108776	HRPEpiC	eye:	n/a
42	chr7:153287591-153287641	ECC-1	luminal epithelium:	n/a
43	chr7:153108726-153108776	Hepatocyte	liver:	n/a
44	chr7:153287591-153287641	MCF-7	breast:	n/a
45	chr7:153110994-153111044	U87	brain:	n/a
46	chr7:153078797-153078847	AoSMC	blood vessel:	n/a
47	chr7:153287752-153287802	NT2-D1	testis:	n/a
48	chr7:153012895-153012945	T-47D	breast:	n/a
49	chr7:153287591-153287641	NT2-D1	testis:	n/a
50	chr7:153110492-153110542	HL-60	blood:	n/a

(count:240 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr7:153104012..153105714-chr7:153166504..153168791,2	K562	blood:
2	chr7:153103866..153106849-chr7:153334968..153337420,2	K562	blood:
3	chr7:153298050..153299925-chr7:153304254..153305961,2	K562	blood:
4	chr7:153065822..153067507-chr7:153075563..153078240,2	K562	blood:
5	chr7:153054753..153057546-chr7:153057782..153059510,2	K562	blood:
6	chr7:153103427..153106418-chr7:153612695..153615251,3	K562	blood:
7	chr7:153105650..153108822-chr7:153162776..153165855,3	K562	blood:
8	chr7:153109482..153112162-chr7:153199634..153202345,2	K562	blood:
9	chr7:153105266..153107285-chr7:153207203..153209217,2	K562	blood:
10	chr7:153098213..153100977-chr7:153153610..153156518,2	K562	blood:
11	chr7:152724247..152725784-chr7:153100492..153103483,2	K562	blood:
12	chr7:153133971..153136584-chr7:153144727..153146368,2	K562	blood:
13	chr7:153094292..153096861-chr7:153257977..153260330,2	K562	blood:
14	chr7:152592588..152594175-chr7:153102302..153103832,2	K562	blood:
15	chr7:153080633..153085077-chr7:153085115..153088222,5	K562	blood:
16	chr16:1825198..1826827-chr7:153150973..153152473,2	K562	blood:
17	chr7:152890009..152890763-chr7:153066469..153067438,2	MCF-7	breast:
18	chr7:153205000..153206676-chr7:153209443..153211203,2	K562	blood:
19	chr7:152788621..152790562-chr7:153104603..153106199,2	K562	blood:
20	chr7:153102748..153104810-chr7:153194160..153196266,2	K562	blood:
21	chr7:153018926..153020911-chr7:153105135..153106975,2	K562	blood:
22	chr2:84104828..84106331-chr7:153109556..153111137,2	K562	blood:
23	chr7:153098583..153101313-chr7:153228583..153231539,3	K562	blood:
24	chr7:153110155..153112303-chr7:153247620..153250543,3	K562	blood:
25	chr7:153094372..153097321-chr7:153253930..153256627,2	K562	blood:
26	chr7:153137391..153139228-chr7:153141759..153143841,2	K562	blood:
27	chr7:153100820..153103410-chr7:153246584..153249087,2	K562	blood:
28	chr7:153033175..153035096-chr7:153059959..153061462,2	K562	blood:
29	chr7:152600593..152604431-chr7:153104940..153107829,3	K562	blood:
30	chr7:152947748..152949504-chr7:153104988..153107669,2	K562	blood:
31	chr7:153145961..153147522-chr7:153147556..153149926,2	K562	blood:
32	chr7:153106993..153109091-chr7:153192344..153194750,2	K562	blood:
33	chr7:153130431..153132961-chr7:153133375..153135450,3	K562	blood:
34	chr7:152981185..152983494-chr7:153101027..153103155,2	K562	blood:
35	chr7:153104450..153106704-chr7:153631945..153634979,3	K562	blood:
36	chr7:153104483..153106622-chr7:154809652..154811276,2	K562	blood:
37	chr7:153207860..153209582-chr7:153211240..153212900,2	K562	blood:
38	chr7:153291103..153293422-chr7:153317816..153319821,2	K562	blood:
39	chr7:153150343..153152572-chr7:153153820..153155844,2	K562	blood:
40	chr7:153179767..153181427-chr7:153183794..153186407,2	K562	blood:
41	chr7:153103154..153105187-chr7:153228223..153229957,2	K562	blood:
42	chr7:153100549..153102656-chr7:153210062..153212505,2	K562	blood:
43	chr7:153094563..153096914-chr7:153326913..153328518,2	K562	blood:
44	chr7:153103693..153106480-chr7:153169343..153171365,2	K562	blood:
45	chr7:153107803..153110775-chr7:153221727..153224014,2	K562	blood:
46	chr7:153168165..153169692-chr7:153180801..153182343,2	K562	blood:
47	chr7:153137391..153141168-chr7:153141506..153146066,7	K562	blood:
48	chr7:153065822..153067507-chr7:153075563..153078240,2	K562	blood:
49	chr7:153104012..153105714-chr7:153166504..153168791,2	K562	blood:
50	chr7:153078275..153079219-chr7:153531525..153532699,6	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DPP6-3	chr7:153092527-153092639	XLOC_006297
2	lnc-XRCC2-3	chr7:153220300-153220910	XLOC_006658
3	lnc-XRCC2-2	chr7:153120803-153121101	XLOC_006657
4	lnc-XRCC2-1	chr7:153102577-153102683	ENSG00000234722.3
5	lnc-XRCC2-1	chr7:153109176-153109319	ENSG00000234722.3
6	lnc-DPP6-3	chr7:153092498-153092703	XLOC_006297
7	lnc-DPP6-2	chr7:153119376-153119626	XLOC_006298
8	lnc-XRCC2-1	chr7:153109178-153109319	ENSG00000234722
9	lnc-XRCC2-1	chr7:153102578-153102683	ENSG00000234722
10	lnc-XRCC2-3	chr7:153221094-153221300	XLOC_006658
11	lnc-XRCC2-1	chr7:153097005-153097631	ENSG00000234722.3
12	lnc-XRCC2-1	chr7:153104041-153104169	ENSG00000234722.3
13	lnc-XRCC2-1	chr7:153097005-153097631	ENSG00000234722
14	lnc-DPP6-3	chr7:153093149-153093207	XLOC_006297
15	lnc-XRCC2-1	chr7:153104041-153104171	ENSG00000234722
16	lnc-XRCC2-2	chr7:153125396-153125424	XLOC_006657
17	lnc-DPP6-7	chr7:153146514-153146960	NONHSAT124301
18	lnc-XRCC2-1	chr7:153110698-153111021	ENSG00000234722
19	lnc-XRCC2-1	chr7:153102577-153102683	ENSG00000234722
20	lnc-DPP6-3	chr7:153086676-153086815	XLOC_006297
21	lnc-DPP6-2	chr7:153120526-153120601	XLOC_006298

No data

Variant related genes	Relation type
ENSG00000234722	TF binding region
ENSG00000233489	TF binding region
ENSG00000234722	CpG island
ENSG00000233489	CpG island
ENSG00000222281	chromatin interactions
ENSG00000234722	chromatin interactions
ENSG00000155380	chromatin interactions
ENSG00000236198	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000141371	chromatin interactions
ENSG00000170832	chromatin interactions
ENSG00000223700	chromatin interactions
ENSG00000197774	chromatin interactions
ENSG00000171222	chromatin interactions
ENSG00000234338	chromatin interactions
ENSG00000233489	chromatin interactions
ENSG00000261455	chromatin interactions
CCT2	miRNA target sites
APAF1	miRNA target sites
DHX57	miRNA target sites
LRRC1	miRNA target sites

Extended variants
information (count: 6173 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:6173 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189281664	chr7:153016454-153016455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs2166121	chr7:153016471-153016472	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs537358047	chr7:153016478-153016479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570232803	chr7:153016480-153016481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs566927304	chr7:153016496-153016497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534274931	chr7:153016546-153016547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs55948708	chr7:153016550-153016551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577446870	chr7:153016551-153016552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535737053	chr7:153016569-153016570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557320628	chr7:153016574-153016575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs151111320	chr7:153016597-153016598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546042177	chr7:153016626-153016627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs75132916	chr7:153016689-153016690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558235721	chr7:153016717-153016718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575023783	chr7:153016732-153016733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200394372	chr7:153016738-153016739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573382814	chr7:153016744-153016745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs367771752	chr7:153016755-153016756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs443734	chr7:153016774-153016775	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs199520862	chr7:153016815-153016816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200537641	chr7:153016843-153016844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562108955	chr7:153016892-153016893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149816825	chr7:153016893-153016894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145813827	chr7:153016940-153016941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541480124	chr7:153016971-153016972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562860491	chr7:153016979-153016980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181320249	chr7:153017004-153017005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs396672	chr7:153017006-153017007	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs570173711	chr7:153017022-153017023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528181203	chr7:153017039-153017040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs565615171	chr7:153017103-153017104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs141604863	chr7:153017153-153017154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs397065	chr7:153017182-153017183	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs35033170	chr7:153017225-153017226	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs147059442	chr7:153017228-153017229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569174937	chr7:153017263-153017264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539602094	chr7:153017268-153017269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537125146	chr7:153017317-153017318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs74674148	chr7:153017350-153017351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572998150	chr7:153017360-153017361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs435736	chr7:153017392-153017393	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs372000059	chr7:153017403-153017404	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs389153	chr7:153017421-153017422	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs185441096	chr7:153017439-153017440	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs562798246	chr7:153017463-153017464	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs73154476	chr7:153017479-153017480	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs190678169	chr7:153017509-153017510	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs641865	chr7:153017565-153017566	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs28595404	chr7:153017585-153017586	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs546659617	chr7:153017594-153017595	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	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
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Ovarian cancer	21720365	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Nasopharyngeal cancer	20548289	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21509527	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:153016400-153017400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr7:153017000-153017800	Enhancers	Colon Smooth Muscle	Colon
3	chr7:153017000-153018400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr7:153017400-153017800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr7:153017800-153018600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:153018000-153018200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:153018200-153019000	Enhancers	Spleen	Spleen
8	chr7:153018400-153020400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr7:153018600-153020200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr7:153019800-153020400	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr7:153020200-153020400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr7:153020400-153020600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr7:153020400-153020600	Enhancers	Brain Hippocampus Middle	brain
14	chr7:153020400-153021000	Enhancers	Fetal Brain Female	brain
15	chr7:153023600-153024200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:153026200-153026400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:153034800-153035200	Active TSS	Fetal Heart	heart
18	chr7:153046000-153046400	Active TSS	Fetal Heart	heart
19	chr7:153047400-153047600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:153067200-153067600	Enhancers	K562	blood
21	chr7:153067600-153082400	Weak transcription	K562	blood
22	chr7:153071000-153071200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr7:153071800-153072000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr7:153078000-153078800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr7:153078200-153078800	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr7:153078400-153078600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr7:153078400-153078600	Enhancers	Brain Anterior Caudate	brain
28	chr7:153078400-153078600	Active TSS	Duodenum Smooth Muscle	Duodenum
29	chr7:153078400-153078600	Enhancers	Fetal Kidney	kidney
30	chr7:153078400-153078600	Enhancers	Fetal Stomach	stomach
31	chr7:153078400-153078800	Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr7:153078400-153078800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr7:153078400-153078800	Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr7:153078400-153078800	Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr7:153078400-153078800	Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr7:153078400-153078800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
37	chr7:153078400-153078800	Enhancers	Brain Hippocampus Middle	brain
38	chr7:153078400-153079000	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr7:153078400-153079000	Enhancers	Rectal Smooth Muscle	rectum
40	chr7:153078400-153079000	Active TSS	Stomach Smooth Muscle	stomach
41	chr7:153078400-153082000	Enhancers	Colon Smooth Muscle	Colon
42	chr7:153078600-153078800	Enhancers	H1 Cell Line	embryonic stem cell
43	chr7:153078600-153078800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr7:153078600-153078800	Flanking Active TSS	Brain Anterior Caudate	brain
45	chr7:153078600-153078800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
46	chr7:153078600-153079000	Flanking Active TSS	Fetal Kidney	kidney
47	chr7:153078600-153079000	Enhancers	Fetal Muscle Trunk	muscle
48	chr7:153078600-153079800	Enhancers	Fetal Muscle Leg	muscle
49	chr7:153078600-153082000	Enhancers	Adipose Nuclei	Adipose
50	chr7:153078800-153079000	Active TSS	Brain Anterior Caudate	brain

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