Variant report

Variant	nsv547854
Chromosome Location	chr1:152145661-152165878
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	BHLHE40	chr1:152161151-152161308	K562	blood:	n/a	n/a
2	BHLHE40	chr1:152158100-152158292	K562	blood:	n/a	n/a
3	BRCA1	chr1:152163059-152163431	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr1:152159405-152159950	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr1:152163061-152163590	MCF-7	breast:	n/a	n/a
6	CEBPB	chr1:152159205-152159696	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:152162334-152163555	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr1:152158157-152158357	K562	blood:	n/a	n/a
9	CEBPB	chr1:152155579-152155919	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:152153939-152154005	A549	lung:	n/a	n/a
11	CEBPB	chr1:152153872-152154057	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr1:152161204-152161213	K562	blood:	n/a	n/a
13	CHD2	chr1:152159398-152159656	Hela-S3	cervix:	n/a	chr1:152159419-152159426
14	CREB1	chr1:152161498-152161928	A549	lung:	n/a	n/a
15	CTCF	chr1:152162297-152162657	A549	lung:	n/a	chr1:152162484-152162497 chr1:152162481-152162499 chr1:152162483-152162504 chr1:152162321-152162329 chr1:152162484-152162492
16	CTCF	chr1:152162332-152162628	K562	blood:	n/a	chr1:152162484-152162497 chr1:152162481-152162499 chr1:152162483-152162504 chr1:152162484-152162492
17	CTCF	chr1:152155000-152155150	HEEpiC	esophagus:	n/a	chr1:152155090-152155111 chr1:152155095-152155113
18	CTCF	chr1:152162360-152162510	GM12865	blood:	n/a	chr1:152162484-152162497 chr1:152162481-152162499 chr1:152162483-152162504 chr1:152162484-152162492
19	CTCF	chr1:152159560-152159710	GM12872	blood:	n/a	n/a
20	CTCF	chr1:152162360-152162593	GM10248	blood:	n/a	chr1:152162484-152162497 chr1:152162481-152162499 chr1:152162483-152162504 chr1:152162484-152162492
21	CTCF	chr1:152162420-152162570	K562	blood:	n/a	chr1:152162484-152162497 chr1:152162481-152162499 chr1:152162483-152162504 chr1:152162484-152162492
22	CTCF	chr1:152161116-152161308	SK-N-SH_RA	brain:	n/a	chr1:152161238-152161256 chr1:152161241-152161254 chr1:152161243-152161253 chr1:152161239-152161255 chr1:152161240-152161261 chr1:152161241-152161254 chr1:152161241-152161250
23	CTCF	chr1:152161540-152161690	HMEC	breast:	n/a	n/a
24	CTCF	chr1:152155020-152155170	GM12868	blood:	n/a	chr1:152155090-152155111 chr1:152155095-152155113
25	CTCF	chr1:152162340-152162602	Lung_OC	lung:	n/a	chr1:152162484-152162497 chr1:152162481-152162499 chr1:152162483-152162504 chr1:152162484-152162492
26	CTCF	chr1:152158140-152158290	AG10803	skin:	n/a	chr1:152158233-152158242 chr1:152158227-152158245
27	CTCF	chr1:152162440-152162590	AG09309	skin:	n/a	chr1:152162484-152162497 chr1:152162481-152162499 chr1:152162483-152162504 chr1:152162484-152162492
28	CTCF	chr1:152155060-152155210	AG09319	gingival:	n/a	chr1:152155090-152155111 chr1:152155095-152155113
29	CTCF	chr1:152161160-152161310	HPAF	blood vessel:	n/a	chr1:152161238-152161256 chr1:152161241-152161254 chr1:152161243-152161253 chr1:152161239-152161255 chr1:152161240-152161261 chr1:152161241-152161254 chr1:152161241-152161250
30	CTCF	chr1:152161140-152161290	GM12864	blood:	n/a	chr1:152161238-152161256 chr1:152161241-152161254 chr1:152161243-152161253 chr1:152161239-152161255 chr1:152161240-152161261 chr1:152161241-152161254 chr1:152161241-152161250
31	CTCF	chr1:152155040-152155190	GM12867	blood:	n/a	chr1:152155090-152155111 chr1:152155095-152155113
32	CTCF	chr1:152155021-152155179	Fibrobl	skin:	n/a	chr1:152155090-152155111 chr1:152155095-152155113
33	CTCF	chr1:152162400-152162550	HPF	lung:	n/a	chr1:152162484-152162497 chr1:152162481-152162499 chr1:152162483-152162504 chr1:152162484-152162492
34	CTCF	chr1:152158140-152158290	GM12865	blood:	n/a	chr1:152158233-152158242 chr1:152158227-152158245
35	CTCF	chr1:152158143-152158345	GM12891	blood:	n/a	chr1:152158233-152158242 chr1:152158227-152158245
36	CTCF	chr1:152158172-152158319	H1-hESC	embryonic stem cell:	n/a	chr1:152158233-152158242 chr1:152158227-152158245
37	CTCF	chr1:152155000-152155150	GM12873	blood:	n/a	chr1:152155090-152155111 chr1:152155095-152155113
38	CTCF	chr1:152161160-152161310	GM12868	blood:	n/a	chr1:152161238-152161256 chr1:152161241-152161254 chr1:152161243-152161253 chr1:152161239-152161255 chr1:152161240-152161261 chr1:152161241-152161254 chr1:152161241-152161250
39	CTCF	chr1:152158160-152158310	GM12873	blood:	n/a	chr1:152158233-152158242 chr1:152158227-152158245
40	CTCF	chr1:152161160-152161310	HEK293	kidney:	n/a	chr1:152161238-152161256 chr1:152161241-152161254 chr1:152161243-152161253 chr1:152161239-152161255 chr1:152161240-152161261 chr1:152161241-152161254 chr1:152161241-152161250
41	CTCF	chr1:152154900-152155050	GM12874	blood:	n/a	n/a
42	CTCF	chr1:152161840-152161990	HPF	lung:	n/a	n/a
43	CTCF	chr1:152155000-152155150	GM12864	blood:	n/a	chr1:152155090-152155111 chr1:152155095-152155113
44	CTCF	chr1:152161180-152161330	GM12868	blood:	n/a	chr1:152161238-152161256 chr1:152161241-152161254 chr1:152161243-152161253 chr1:152161239-152161255 chr1:152161240-152161261 chr1:152161241-152161254 chr1:152161241-152161250
45	CTCF	chr1:152155020-152155170	GM12864	blood:	n/a	chr1:152155090-152155111 chr1:152155095-152155113
46	CTCF	chr1:152155040-152155190	HMF	breast:	n/a	chr1:152155090-152155111 chr1:152155095-152155113
47	CTCF	chr1:152162420-152162570	Hela-S3	cervix:	n/a	chr1:152162484-152162497 chr1:152162481-152162499 chr1:152162483-152162504 chr1:152162484-152162492
48	CTCF	chr1:152158099-152158332	A549	lung:	n/a	chr1:152158233-152158242 chr1:152158227-152158245
49	CTCF	chr1:152155416-152155464	GM19240	blood:	n/a	n/a
50	CTCF	chr1:152162266-152162659	T-47D	breast:	n/a	chr1:152162484-152162497 chr1:152162481-152162499 chr1:152162483-152162504 chr1:152162321-152162329 chr1:152162484-152162492

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:152162025-152162075	Hepatocyte	liver:	n/a
2	chr1:152161885-152161935	ECC-1	luminal epithelium:	n/a
3	chr1:152158135-152158185	MCF-7	breast:	n/a
4	chr1:152161683-152161733	ProgFib	skin:	n/a
5	chr1:152161885-152161935	K562	blood:	n/a
6	chr1:152161927-152161977	BJ	skin:	n/a
7	chr1:152161927-152161977	PrEC	prostate:	n/a
8	chr1:152161885-152161935	PFSK-1	brain:	n/a
9	chr1:152161237-152161287	AG04450	lung:	fetal
10	chr1:152161885-152161935	GM12878	blood:	n/a
11	chr1:152158135-152158185	HUVEC	blood vessel:	n/a
12	chr1:152158135-152158185	HepG2	liver:	n/a
13	chr1:152161885-152161935	HCF	heart:	n/a
14	chr1:152164017-152164067	HCT-116	colon:	n/a
15	chr1:152161237-152161287	PrEC	prostate:	n/a
16	chr1:152161683-152161733	HUVEC	blood vessel:	n/a
17	chr1:152161927-152161977	A549	lung:	n/a
18	chr1:152161237-152161287	SAEC	small airway:	n/a
19	chr1:152161397-152161447	GM12892	blood:	n/a
20	chr1:152161521-152161571	BE2_C	brain:	n/a
21	chr1:152164017-152164067	ECC-1	luminal epithelium:	n/a
22	chr1:152161237-152161287	SK-N-SH_RA	brain:	n/a
23	chr1:152161397-152161447	HMEC	breast:	n/a
24	chr1:152161521-152161571	AG10803	skin:	n/a
25	chr1:152158135-152158185	AG09309	skin:	n/a
26	chr1:152161397-152161447	GM19239	blood:	n/a
27	chr1:152162025-152162075	HCM	heart:	n/a
28	chr1:152161521-152161571	HMEC	breast:	n/a
29	chr1:152161237-152161287	HCPEpiC	choroid plexus:	n/a
30	chr1:152161927-152161977	LNCaP	prostate:	n/a
31	chr1:152162507-152162557	AG09309	skin:	n/a
32	chr1:152161885-152161935	HIPEpiC	eye:	n/a
33	chr1:152161927-152161977	ProgFib	skin:	n/a
34	chr1:152164017-152164067	HepG2	liver:	n/a
35	chr1:152158135-152158185	PFSK-1	brain:	n/a
36	chr1:152161885-152161935	U87	brain:	n/a
37	chr1:152161885-152161935	HRCEpiC	kidney:	n/a
38	chr1:152161237-152161287	AG04449	skin:	fetal
39	chr1:152161683-152161733	SK-N-SH	brain:	n/a
40	chr1:152161521-152161571	LNCaP	prostate:	n/a
41	chr1:152161397-152161447	T-47D	breast:	n/a
42	chr1:152161397-152161447	BJ	skin:	n/a
43	chr1:152162025-152162075	AG04450	lung:	fetal
44	chr1:152162025-152162075	HRPEpiC	eye:	n/a
45	chr1:152161927-152161977	HAEpiC	amniotic membrane:	n/a
46	chr1:152161927-152161977	AoSMC	blood vessel:	n/a
47	chr1:152161237-152161287	HIPEpiC	eye:	n/a
48	chr1:152161237-152161287	GM12878	blood:	n/a
49	chr1:152161237-152161287	LNCaP	prostate:	n/a
50	chr1:152162507-152162557	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:152034141..152035088-chr1:152154621..152155465,4	MCF-7	breast:
2	chr1:152160624..152161417-chr1:152199475..152200038,4	MCF-7	breast:
3	chr1:152146040..152146767-chr1:152158008..152158869,2	MCF-7	breast:
4	chr1:152025124..152025656-chr1:152161097..152161675,2	MCF-7	breast:
5	chr1:152006732..152007276-chr1:152157793..152158293,2	MCF-7	breast:
6	chr1:152024872..152025692-chr1:152156993..152157536,2	K562	blood:
7	chr1:152160815..152161721-chr1:152320660..152321540,3	MCF-7	breast:
8	chr1:152026285..152026873-chr1:152154304..152154844,2	MCF-7	breast:
9	chr1:152162374..152163052-chr1:152320634..152321136,2	MCF-7	breast:
10	chr1:152034269..152035066-chr1:152153200..152153993,2	MCF-7	breast:
11	chr1:152162116..152162772-chr1:152319294..152319814,2	MCF-7	breast:
12	chr1:152162395..152164443-chr1:152410728..152413718,2	MCF-7	breast:
13	chr1:152015810..152018390-chr1:152153370..152155715,2	K562	blood:
14	chr1:152160785..152161519-chr1:152413069..152413968,2	K562	blood:
15	chr1:152114275..152115072-chr1:152153697..152154247,2	MCF-7	breast:
16	chr1:152024794..152025624-chr1:152157743..152158320,3	K562	blood:
17	chr1:152024529..152025807-chr1:152157754..152158654,6	MCF-7	breast:
18	chr1:152023865..152025668-chr1:152157560..152159687,2	MCF-7	breast:
19	chr1:152033820..152035009-chr1:152157797..152158750,5	MCF-7	breast:
20	chr1:152111927..152114607-chr1:152153105..152155250,3	MCF-7	breast:
21	chr1:152024776..152025649-chr1:152154319..152155043,2	K562	blood:
22	chr1:152145123..152147434-chr1:152151128..152152716,2	MCF-7	breast:
23	chr1:152161041..152161774-chr1:152423855..152424586,2	MCF-7	breast:
24	chr1:152161168..152161696-chr3:64015970..64016664,2	MCF-7	breast:
25	chr1:152113593..152115138-chr1:152157487..152158735,36	MCF-7	breast:
26	chr1:152140940..152143889-chr1:152152084..152153950,2	MCF-7	breast:
27	chr1:152163573..152164481-chr1:152430706..152431340,2	MCF-7	breast:
28	chr1:152160950..152161743-chr1:152199424..152200319,5	MCF-7	breast:
29	chr1:152024690..152025712-chr1:152154629..152155833,16	MCF-7	breast:
30	chr1:152160802..152161752-chr1:152430569..152431282,4	MCF-7	breast:
31	chr1:152007310..152009058-chr1:152155234..152157493,3	MCF-7	breast:
32	chr1:152025717..152026500-chr1:152154875..152155620,2	MCF-7	breast:
33	chr1:151985750..151986659-chr1:152155001..152155545,2	MCF-7	breast:
34	chr1:152160487..152160988-chr1:152413455..152414286,2	MCF-7	breast:
35	chr1:152163614..152164697-chr1:152319285..152320275,3	MCF-7	breast:
36	chr1:152023780..152024525-chr1:152154631..152155596,5	MCF-7	breast:
37	chr1:152021638..152025256-chr1:152144689..152147457,3	MCF-7	breast:
38	chr1:152004874..152008437-chr1:152153479..152155850,3	MCF-7	breast:
39	chr1:152005022..152006958-chr1:152156350..152158073,2	MCF-7	breast:
40	chr1:152019877..152021951-chr1:152154042..152156834,2	MCF-7	breast:
41	chr1:152162013..152163026-chr1:152320678..152321307,3	MCF-7	breast:
42	chr1:152114175..152115930-chr1:152155659..152158204,3	MCF-7	breast:
43	chr1:152162203..152163021-chr1:152413054..152413609,4	K562	blood:
44	chr1:152162006..152163447-chr1:152318869..152320295,9	MCF-7	breast:
45	chr1:152024690..152025212-chr1:152160729..152161691,2	MCF-7	breast:
46	chr1:152019081..152021323-chr1:152144362..152146461,2	MCF-7	breast:
47	chr1:152024797..152025791-chr1:152154887..152155573,4	MCF-7	breast:
48	chr1:152160966..152161616-chr1:152433035..152433995,2	MCF-7	breast:
49	chr1:152162008..152163068-chr1:152430225..152431533,6	K562	blood:
50	chr1:152126007..152128051-chr1:152155968..152157757,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LCE5A-2	chr1:152161827-152161984	ENSG00000237975

Variant related genes	Relation type
FLG-AS1	TF binding region
FLG-AS1	CpG island
ENSG00000163191	chromatin interactions
ENSG00000237975	chromatin interactions
PLSCR4	miRNA target sites

Extended variants
information (count: 695 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:695 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16833867	chr1:152145661-152145662	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186567956	chr1:152145677-152145678	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs367837174	chr1:152145688-152145689	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs143021391	chr1:152145706-152145707	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs375098210	chr1:152145708-152145709	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs188911777	chr1:152145710-152145711	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs563755653	chr1:152145712-152145713	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs532824830	chr1:152145714-152145715	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs552560161	chr1:152145725-152145726	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs566053414	chr1:152145734-152145735	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs146747881	chr1:152145871-152145872	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs10494273	chr1:152145872-152145873	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs533661917	chr1:152145908-152145909	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs568213155	chr1:152145990-152145991	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs201293369	chr1:152146009-152146010	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs200459153	chr1:152146011-152146012	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs397713593	chr1:152146012-152146013	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs181610590	chr1:152146059-152146060	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs10494272	chr1:152146060-152146061	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs557104731	chr1:152146109-152146110	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs570521975	chr1:152146125-152146126	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs539644574	chr1:152146152-152146153	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs553259085	chr1:152146166-152146167	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs563906419	chr1:152146187-152146188	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs573185772	chr1:152146198-152146199	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs145411481	chr1:152146202-152146203	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs547287316	chr1:152146228-152146229	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs555447220	chr1:152146248-152146249	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs368252992	chr1:152146264-152146265	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs530950754	chr1:152146277-152146278	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs565878041	chr1:152146290-152146291	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs11204928	chr1:152146298-152146299	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs137985514	chr1:152146304-152146305	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs543442511	chr1:152146325-152146326	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs555482614	chr1:152146331-152146332	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs532568851	chr1:152146352-152146353	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs71582215	chr1:152146394-152146395	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs60630123	chr1:152146467-152146468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149058533	chr1:152146496-152146497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116364006	chr1:152146497-152146498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143049297	chr1:152146592-152146593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568150677	chr1:152146608-152146609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148189786	chr1:152146612-152146613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76905795	chr1:152146621-152146622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12033248	chr1:152146648-152146649	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs539220383	chr1:152146653-152146654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143345698	chr1:152146654-152146655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35301955	chr1:152146661-152146662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566767166	chr1:152146770-152146771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11204929	chr1:152146789-152146790	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:122)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152131400-152145800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr1:152142200-152151800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:152151600-152152800	Enhancers	NHEK	skin
4	chr1:152151800-152152200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr1:152151800-152152200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:152151800-152152800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:152151800-152152800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr1:152151800-152153400	Enhancers	HMEC	breast
9	chr1:152151800-152158600	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr1:152152000-152152200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr1:152152000-152152200	Enhancers	Right Atrium	heart
12	chr1:152152000-152152400	Enhancers	Esophagus	oesophagus
13	chr1:152152000-152152400	Enhancers	Osteobl	bone
14	chr1:152152000-152152600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:152152000-152152600	Enhancers	Muscle Satellite Cultured Cells	--
16	chr1:152152000-152152600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr1:152152000-152152800	Enhancers	Spleen	Spleen
18	chr1:152152000-152152800	Enhancers	NHDF-Ad	bronchial
19	chr1:152152200-152153600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr1:152152200-152154800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:152152200-152161200	Weak transcription	Right Atrium	heart
22	chr1:152152400-152154000	Weak transcription	Esophagus	oesophagus
23	chr1:152152400-152154600	Weak transcription	Osteobl	bone
24	chr1:152152400-152155000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr1:152152600-152154000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr1:152152600-152154200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr1:152152600-152154200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
28	chr1:152152600-152154600	Enhancers	Brain Substantia Nigra	brain
29	chr1:152152600-152154800	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr1:152152600-152154800	Enhancers	Brain Hippocampus Middle	brain
31	chr1:152152800-152153800	Weak transcription	NHEK	skin
32	chr1:152152800-152154000	Weak transcription	Spleen	Spleen
33	chr1:152152800-152154200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:152152800-152154200	Weak transcription	NHDF-Ad	bronchial
35	chr1:152152800-152154600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr1:152153400-152153800	Weak transcription	HMEC	breast
37	chr1:152153400-152154400	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr1:152153600-152155400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr1:152153800-152154400	Enhancers	Brain Cingulate Gyrus	brain
40	chr1:152153800-152155200	Enhancers	NHEK	skin
41	chr1:152153800-152159800	Enhancers	HMEC	breast
42	chr1:152154000-152154400	Enhancers	Esophagus	oesophagus
43	chr1:152154000-152154400	Enhancers	Spleen	Spleen
44	chr1:152154000-152160200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr1:152154200-152158000	Enhancers	NHDF-Ad	bronchial
46	chr1:152154200-152158200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:152154200-152158200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:152154400-152155400	Weak transcription	Esophagus	oesophagus
49	chr1:152154400-152161400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr1:152154600-152157000	Enhancers	Osteobl	bone

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