Variant report

Variant	nsv834636
Chromosome Location	chr3:23138653-23301443
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1261)
CpG islands
(count:1099)
Chromatin interactive
region (count:72)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1261 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:23270274-23270325	K562	blood:	n/a	n/a
2	ATF2	chr3:23203161-23204167	GM12878	blood:	n/a	n/a
3	ATF2	chr3:23202917-23204305	GM12878	blood:	n/a	n/a
4	ATF2	chr3:23201328-23201845	GM12878	blood:	n/a	n/a
5	ATF2	chr3:23259335-23259791	GM12878	blood:	n/a	n/a
6	ATF2	chr3:23244667-23245186	GM12878	blood:	n/a	n/a
7	ATF2	chr3:23204372-23204880	GM12878	blood:	n/a	n/a
8	ATF2	chr3:23259313-23259723	GM12878	blood:	n/a	n/a
9	ATF2	chr3:23201404-23201826	GM12878	blood:	n/a	n/a
10	BACH1	chr3:23231692-23231730	K562	blood:	n/a	n/a
11	BACH1	chr3:23244708-23244923	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:23203781-23203899	K562	blood:	n/a	n/a
13	BACH1	chr3:23203524-23204001	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr3:23243944-23244445	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:23299743-23299785	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr3:23201382-23201672	GM12878	blood:	n/a	chr3:23201617-23201627
17	BATF	chr3:23203116-23204063	GM12878	blood:	n/a	n/a
18	BATF	chr3:23203671-23204037	GM12878	blood:	n/a	n/a
19	BATF	chr3:23298327-23298695	GM12878	blood:	n/a	n/a
20	BCL11A	chr3:23201395-23201734	GM12878	blood:	n/a	chr3:23201619-23201628
21	BCL11A	chr3:23203639-23204096	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:23260741-23261087	GM12878	blood:	n/a	chr3:23260800-23260807
23	BCL3	chr3:23243926-23244417	A549	lung:	n/a	n/a
24	BCL3	chr3:23202791-23203090	GM12878	blood:	n/a	n/a
25	BCL3	chr3:23244392-23244991	GM12878	blood:	n/a	chr3:23244501-23244510 chr3:23244503-23244516 chr3:23244526-23244539
26	BCLAF1	chr3:23203360-23204046	GM12878	blood:	n/a	n/a
27	BCLAF1	chr3:23244399-23245493	GM12878	blood:	n/a	chr3:23245422-23245435 chr3:23244501-23244510 chr3:23244503-23244516 chr3:23244526-23244539
28	BCLAF1	chr3:23203309-23204121	GM12878	blood:	n/a	n/a
29	BHLHE40	chr3:23270311-23270369	A549	lung:	n/a	n/a
30	BHLHE40	chr3:23204323-23204737	GM12878	blood:	n/a	n/a
31	BHLHE40	chr3:23244447-23245260	GM12878	blood:	n/a	n/a
32	BRCA1	chr3:23244081-23244202	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr3:23225286-23225628	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr3:23244476-23244666	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr3:23261437-23261514	GM12878	blood:	n/a	n/a
36	CCNT2	chr3:23244428-23245044	K562	blood:	n/a	chr3:23244500-23244509
37	CEBPB	chr3:23245231-23245522	H1-hESC	embryonic stem cell:	n/a	chr3:23245364-23245375 chr3:23245364-23245377 chr3:23245364-23245377
38	CEBPB	chr3:23214263-23214279	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr3:23154022-23154269	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr3:23237845-23238123	HepG2	liver:	n/a	chr3:23237970-23237981
41	CEBPB	chr3:23156581-23157101	MCF-7	breast:	n/a	n/a
42	CEBPB	chr3:23245158-23245462	ECC-1	luminal epithelium:	n/a	chr3:23245364-23245375 chr3:23245364-23245377 chr3:23245364-23245377
43	CEBPB	chr3:23181550-23181751	HepG2	liver:	n/a	chr3:23181655-23181668 chr3:23181656-23181667
44	CEBPB	chr3:23280694-23280996	Hela-S3	cervix:	n/a	chr3:23280843-23280854 chr3:23280807-23280818
45	CEBPB	chr3:23150179-23150492	HepG2	liver:	n/a	n/a
46	CEBPB	chr3:23237848-23238092	Hela-S3	cervix:	n/a	chr3:23237970-23237981
47	CEBPB	chr3:23245047-23245520	A549	lung:	n/a	chr3:23245364-23245375 chr3:23245364-23245377 chr3:23245364-23245377
48	CEBPB	chr3:23245239-23245532	K562	blood:	n/a	chr3:23245364-23245375 chr3:23245364-23245377 chr3:23245364-23245377
49	CEBPB	chr3:23201604-23201618	A549	lung:	n/a	n/a
50	CEBPB	chr3:23237834-23238143	A549	lung:	n/a	chr3:23237970-23237981

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:23243300-23243350	NHDF-neo	bronchial:	n/a
2	chr3:23243300-23243350	NHDF-neo	bronchial:	n/a
3	chr3:23245747-23245797	RPTEC	kidney:	n/a
4	chr3:23241154-23241204	SAEC	small airway:	n/a
5	chr3:23225524-23225574	AG09319	gingival:	n/a
6	chr3:23244068-23244118	NHDF-neo	bronchial:	n/a
7	chr3:23244051-23244101	BE2_C	brain:	n/a
8	chr3:23244681-23244731	NHBE	bronchial:	n/a
9	chr3:23244690-23244740	IMR90	lung:	fetal
10	chr3:23244068-23244118	GM12878	blood:	n/a
11	chr3:23245916-23245966	SK-N-SH_RA	brain:	n/a
12	chr3:23170838-23170888	PANC-1	pancreas:	n/a
13	chr3:23243300-23243350	T-47D	breast:	n/a
14	chr3:23244637-23244687	T-47D	breast:	n/a
15	chr3:23245916-23245966	PrEC	prostate:	n/a
16	chr3:23243300-23243350	AG04450	lung:	fetal
17	chr3:23225524-23225574	HAEpiC	amniotic membrane:	n/a
18	chr3:23241154-23241204	GM06990	blood:	n/a
19	chr3:23244637-23244687	SAEC	small airway:	n/a
20	chr3:23244068-23244118	HCF	heart:	n/a
21	chr3:23245747-23245797	U87	brain:	n/a
22	chr3:23247317-23247367	PANC-1	pancreas:	n/a
23	chr3:23245747-23245797	HUVEC	blood vessel:	n/a
24	chr3:23245400-23245450	NHBE	bronchial:	n/a
25	chr3:23241154-23241204	GM12878	blood:	n/a
26	chr3:23245747-23245797	HPAEpiC	pulmonary alveolar:	n/a
27	chr3:23170838-23170888	SK-N-SH_RA	brain:	n/a
28	chr3:23244062-23244112	HCM	heart:	n/a
29	chr3:23244125-23244175	Jurkat	blood:	n/a
30	chr3:23243625-23243675	Caco-2	colon:	n/a
31	chr3:23244681-23244731	CMK	blood:	n/a
32	chr3:23245422-23245472	GM06990	blood:	n/a
33	chr3:23244688-23244738	Hela-S3	cervix:	n/a
34	chr3:23245916-23245966	CMK	blood:	n/a
35	chr3:23244688-23244738	NB4	blood:	n/a
36	chr3:23243300-23243350	GM19239	blood:	n/a
37	chr3:23245916-23245966	GM19239	blood:	n/a
38	chr3:23244690-23244740	AG09309	skin:	n/a
39	chr3:23225524-23225574	HepG2	liver:	n/a
40	chr3:23244637-23244687	PrEC	prostate:	n/a
41	chr3:23244637-23244687	PANC-1	pancreas:	n/a
42	chr3:23244125-23244175	HCPEpiC	choroid plexus:	n/a
43	chr3:23244068-23244118	GM06990	blood:	n/a
44	chr3:23247317-23247367	SK-N-SH	brain:	n/a
45	chr3:23244637-23244687	HCPEpiC	choroid plexus:	n/a
46	chr3:23245747-23245797	HIPEpiC	eye:	n/a
47	chr3:23245916-23245966	H1-hESC	embryonic stem cell:	embryo
48	chr3:23170838-23170888	AG04450	lung:	fetal
49	chr3:23170838-23170888	Jurkat	blood:	n/a
50	chr3:23241154-23241204	T-47D	breast:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:23247004..23248744-chr3:23272999..23274643,2	K562	blood:
2	chr3:23245352..23245950-chr3:23374735..23375546,2	MCF-7	breast:
3	chr3:23266677..23268446-chr3:23270132..23272875,2	K562	blood:
4	chr3:23243585..23246598-chr3:23255369..23258477,4	MCF-7	breast:
5	chr3:23255785..23258216-chr3:23259980..23262399,2	MCF-7	breast:
6	chr3:23224961..23225741-chr3:23841911..23842898,2	MCF-7	breast:
7	chr3:23137402..23139607-chr3:23140156..23142703,3	MCF-7	breast:
8	chr3:23245657..23247808-chr3:23255813..23257344,2	K562	blood:
9	chr3:23155801..23158791-chr3:23160046..23163016,3	MCF-7	breast:
10	chr3:23266677..23268446-chr3:23270132..23272875,2	K562	blood:
11	chr3:23208542..23210812-chr3:23212932..23215034,2	MCF-7	breast:
12	chr3:23220511..23222117-chr3:23223792..23225535,2	MCF-7	breast:
13	chr3:23245270..23247157-chr3:23255844..23257640,2	K562	blood:
14	chr3:23138261..23141338-chr3:23143225..23146692,3	MCF-7	breast:
15	chr3:23247857..23249626-chr3:23258764..23261200,2	MCF-7	breast:
16	chr3:23245657..23247808-chr3:23255813..23257344,2	K562	blood:
17	chr3:23154251..23156736-chr3:23157951..23160343,2	K562	blood:
18	chr3:23245705..23247404-chr3:23258369..23260756,2	K562	blood:
19	chr3:23159093..23161060-chr3:23170078..23172221,2	MCF-7	breast:
20	chr3:23245201..23247930-chr3:23252122..23255042,2	K562	blood:
21	chr3:23245201..23247930-chr3:23252122..23255042,2	K562	blood:
22	chr3:23155580..23157104-chr3:23162253..23163789,2	K562	blood:
23	chr3:23247004..23248744-chr3:23272999..23274643,2	K562	blood:
24	chr3:23240263..23242304-chr3:23245058..23246936,2	K562	blood:
25	chr3:23243052..23244840-chr3:23256645..23259135,2	K562	blood:
26	chr3:23237186..23240059-chr3:23244524..23247449,2	K562	blood:
27	chr3:23155801..23158791-chr3:23160046..23163016,3	MCF-7	breast:
28	chr3:23208542..23210812-chr3:23212932..23215034,2	MCF-7	breast:
29	chr3:23159093..23161060-chr3:23170078..23172221,2	MCF-7	breast:
30	chr3:23224924..23225833-chr3:73897073..73898303,5	MCF-7	breast:
31	chr3:23284952..23287695-chr3:23289326..23291059,2	K562	blood:
32	chr3:23267196..23270682-chr3:23275861..23279079,3	MCF-7	breast:
33	chr3:23238476..23240188-chr3:23244080..23245921,2	MCF-7	breast:
34	chr3:23229817..23231730-chr3:23239013..23241977,2	MCF-7	breast:
35	chr3:23229817..23231730-chr3:23239013..23241977,2	MCF-7	breast:
36	chr3:23245705..23247404-chr3:23258369..23260756,2	K562	blood:
37	chr3:23166144..23168159-chr3:23169321..23171985,3	K562	blood:
38	chr3:23146246..23149153-chr3:23154916..23156444,2	MCF-7	breast:
39	chr3:23151746..23153503-chr3:23153998..23156456,2	MCF-7	breast:
40	chr3:23240535..23243490-chr3:23256250..23257758,2	MCF-7	breast:
41	chr3:23137402..23139607-chr3:23140156..23142703,3	MCF-7	breast:
42	chr3:23160635..23162852-chr3:23171582..23173150,2	MCF-7	breast:
43	chr3:23247857..23249626-chr3:23258764..23261200,2	MCF-7	breast:
44	chr3:23154251..23156736-chr3:23157951..23160343,2	K562	blood:
45	chr3:23240535..23243490-chr3:23256250..23257758,2	MCF-7	breast:
46	chr3:23284952..23287695-chr3:23289326..23291059,2	K562	blood:
47	chr3:23220511..23222117-chr3:23223792..23225535,2	MCF-7	breast:
48	chr3:23119484..23121007-chr3:23156209..23158438,2	MCF-7	breast:
49	chr3:23158636..23161578-chr3:23165993..23167885,2	MCF-7	breast:
50	chr3:23243031..23244851-chr3:23845499..23848237,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NKIRAS1-6	chr3:23211305-23211380	l_2332_chr3:23211304-23219228_testes
2	lnc-NKIRAS1-3	chr3:23244112-23244249	XLOC_003065
3	lnc-NKIRAS1-3	chr3:23243883-23244034	XLOC_003065
4	lnc-NKIRAS1-3	chr3:23236301-23236905	XLOC_003065
5	lnc-NKIRAS1-3	chr3:23236561-23236905	XLOC_003065
6	lnc-NKIRAS1-3	chr3:23236463-23236905	XLOC_003065
7	lnc-NKIRAS1-6	chr3:23219359-23219452	l_2332_chr3:23211304-23219228_testes
8	lnc-NKIRAS1-6	chr3:23218887-23219280	l_2332_chr3:23211304-23219228_testes
9	lnc-NKIRAS1-3	chr3:23236561-23236905	XLOC_003065
10	lnc-NKIRAS1-3	chr3:23236561-23236905	ENSG00000233153.1
11	lnc-NKIRAS1-3	chr3:23243883-23244024	ENSG00000233153.1
12	lnc-NKIRAS1-3	chr3:23244355-23244446	XLOC_003065
13	lnc-NKIRAS1-6	chr3:23214595-23214712	l_2332_chr3:23211304-23219228_testes
14	lnc-NKIRAS1-3	chr3:23243916-23244069	XLOC_003065
15	lnc-NKIRAS1-6	chr3:23211427-23211909	l_2332_chr3:23211304-23219228_testes

No data

Variant related genes	Relation type
RPL24P7	TF binding region
UBE2E2	TF binding region
UBE2E2-AS1	TF binding region
RPL24P7	CpG island
UBE2E2	CpG island
UBE2E2-AS1	CpG island
ENSG00000214021	chromatin interactions
ENSG00000170142	chromatin interactions
ENSG00000182247	chromatin interactions
ENSG00000233153	chromatin interactions
C1orf77	miRNA target sites
SDCBP	miRNA target sites
GOLT1B	miRNA target sites
C6orf134	miRNA target sites

Extended variants
information (count: 5131 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:5131 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115769254	chr3:23138654-23138655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs116751305	chr3:23138697-23138698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368976439	chr3:23138701-23138702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553514859	chr3:23138729-23138730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372650851	chr3:23138739-23138740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190277291	chr3:23138748-23138749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79680636	chr3:23138754-23138755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369139189	chr3:23138755-23138756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138414992	chr3:23138767-23138768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112704018	chr3:23138805-23138806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs76055997	chr3:23138806-23138807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533295963	chr3:23138822-23138823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538248381	chr3:23138847-23138848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551237812	chr3:23138857-23138858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372217410	chr3:23138883-23138884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183277103	chr3:23138885-23138886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141027914	chr3:23138903-23138904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576633111	chr3:23138978-23138979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs77733509	chr3:23139018-23139019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113539275	chr3:23139020-23139021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187860263	chr3:23139029-23139030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs578156860	chr3:23139079-23139080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73037593	chr3:23139102-23139103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6789879	chr3:23139118-23139119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6792470	chr3:23139119-23139120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567588855	chr3:23139141-23139142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538062185	chr3:23139168-23139169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6800955	chr3:23139179-23139180	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs572946673	chr3:23139223-23139224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150274562	chr3:23139225-23139226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78305426	chr3:23139250-23139251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553821214	chr3:23139281-23139282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570782464	chr3:23139284-23139285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs193168138	chr3:23139290-23139291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138964029	chr3:23139297-23139298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149430908	chr3:23139315-23139316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564780645	chr3:23139466-23139467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34625919	chr3:23139488-23139489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377362994	chr3:23139498-23139499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73037594	chr3:23139502-23139503	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs543718498	chr3:23139503-23139504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs6801272	chr3:23139511-23139512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576961411	chr3:23139514-23139515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183356791	chr3:23139791-23139792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114997230	chr3:23139799-23139800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555682908	chr3:23139815-23139816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370260714	chr3:23139827-23139828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542575811	chr3:23139879-23139880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76318071	chr3:23139884-23139885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9681439	chr3:23139892-23139893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1776 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23137600-23140200	Weak transcription	HUVEC	blood vessel
2	chr3:23140200-23140800	Enhancers	HUVEC	blood vessel
3	chr3:23140200-23141800	Enhancers	Primary B cells from cord blood	blood
4	chr3:23140600-23141800	Enhancers	Primary B cells from peripheral blood	blood
5	chr3:23140800-23141800	Flanking Active TSS	HUVEC	blood vessel
6	chr3:23141000-23141400	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr3:23141000-23141400	Enhancers	Placenta Amnion	Placenta Amnion
8	chr3:23141800-23142600	Enhancers	HUVEC	blood vessel
9	chr3:23142600-23146200	Weak transcription	HUVEC	blood vessel
10	chr3:23145000-23145600	Enhancers	Gastric	stomach
11	chr3:23145400-23145600	Enhancers	Esophagus	oesophagus
12	chr3:23146200-23147200	Enhancers	HUVEC	blood vessel
13	chr3:23148400-23148800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:23148800-23150000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:23150000-23150200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:23150400-23150600	Enhancers	Fetal Lung	lung
17	chr3:23150600-23154400	Weak transcription	Fetal Lung	lung
18	chr3:23152800-23153200	Enhancers	HSMMtube	muscle
19	chr3:23153000-23153200	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr3:23153200-23153600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr3:23153200-23155400	Weak transcription	HSMMtube	muscle
22	chr3:23153400-23154200	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr3:23153800-23156400	Enhancers	NHEK	skin
24	chr3:23153800-23157400	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr3:23154000-23154200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr3:23154000-23154200	Enhancers	Hela-S3	cervix
27	chr3:23154000-23154400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr3:23154000-23154400	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr3:23154000-23154400	Enhancers	Colon Smooth Muscle	Colon
30	chr3:23154000-23155200	Enhancers	Fetal Muscle Trunk	muscle
31	chr3:23154000-23155200	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
32	chr3:23154000-23156200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr3:23154000-23156200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr3:23154000-23156400	Enhancers	HMEC	breast
35	chr3:23154000-23157200	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr3:23154000-23157600	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr3:23154200-23154400	Enhancers	Esophagus	oesophagus
38	chr3:23154200-23154600	Enhancers	Fetal Thymus	thymus
39	chr3:23154200-23154800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr3:23154200-23154800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr3:23154200-23156400	Enhancers	Rectal Smooth Muscle	rectum
42	chr3:23154400-23154600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr3:23154400-23154800	Weak transcription	Colon Smooth Muscle	Colon
44	chr3:23154400-23155000	Weak transcription	Esophagus	oesophagus
45	chr3:23154400-23155200	Weak transcription	Hela-S3	cervix
46	chr3:23154400-23156000	Enhancers	Fetal Lung	lung
47	chr3:23154400-23158600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr3:23154400-23159400	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr3:23154600-23154800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr3:23154600-23154800	Weak transcription	Fetal Thymus	thymus

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