Variant report

Variant	nsv1003113
Chromosome Location	chr1:174367687-174499155
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:498)
CpG islands
(count:183)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:174396120-174396181	K562	blood:	n/a	n/a
2	ARID3A	chr1:174382888-174383024	K562	blood:	n/a	n/a
3	ATF1	chr1:174397299-174397520	K562	blood:	n/a	n/a
4	ATF1	chr1:174484804-174484808	K562	blood:	n/a	n/a
5	ATF1	chr1:174493199-174493227	K562	blood:	n/a	n/a
6	ATF1	chr1:174448222-174448255	K562	blood:	n/a	n/a
7	ATF1	chr1:174428850-174428929	K562	blood:	n/a	n/a
8	ATF2	chr1:174367318-174367778	GM12878	blood:	n/a	n/a
9	ATF2	chr1:174367341-174367790	GM12878	blood:	n/a	n/a
10	BACH1	chr1:174397283-174397435	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:174414983-174415353	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr1:174497028-174497201	GM12878	blood:	n/a	n/a
13	BATF	chr1:174367368-174367758	GM12878	blood:	n/a	n/a
14	BATF	chr1:174367311-174367749	GM12878	blood:	n/a	n/a
15	BCL11A	chr1:174367324-174367782	GM12878	blood:	n/a	n/a
16	BCL11A	chr1:174367394-174367688	GM12878	blood:	n/a	n/a
17	BHLHE40	chr1:174394495-174394498	K562	blood:	n/a	n/a
18	BHLHE40	chr1:174367450-174367753	GM12878	blood:	n/a	n/a
19	CCNT2	chr1:174397284-174397510	K562	blood:	n/a	n/a
20	CEBPB	chr1:174470613-174470878	MCF-7	breast:	n/a	chr1:174470809-174470826 chr1:174470812-174470825
21	CEBPB	chr1:174375551-174375830	MCF-7	breast:	n/a	chr1:174375708-174375719 chr1:174375706-174375719
22	CEBPB	chr1:174470644-174470934	IMR90	lung:	n/a	chr1:174470809-174470826 chr1:174470812-174470825
23	CEBPB	chr1:174449527-174449790	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:174470588-174471008	MCF-7	breast:	n/a	chr1:174470809-174470826 chr1:174470812-174470825
25	CEBPB	chr1:174470574-174470858	A549	lung:	n/a	chr1:174470809-174470826 chr1:174470812-174470825
26	CEBPB	chr1:174436046-174436066	HepG2	liver:	n/a	n/a
27	CEBPB	chr1:174470560-174470966	Hela-S3	cervix:	n/a	chr1:174470809-174470826 chr1:174470812-174470825
28	CEBPB	chr1:174449511-174449685	K562	blood:	n/a	n/a
29	CEBPB	chr1:174445784-174445786	K562	blood:	n/a	n/a
30	CEBPB	chr1:174397131-174397381	A549	lung:	n/a	chr1:174397283-174397300
31	CEBPB	chr1:174470646-174470939	K562	blood:	n/a	chr1:174470809-174470826 chr1:174470812-174470825
32	CEBPB	chr1:174470537-174471042	A549	lung:	n/a	chr1:174470809-174470826 chr1:174470812-174470825
33	CEBPB	chr1:174445621-174445931	HepG2	liver:	n/a	n/a
34	CREB1	chr1:174367293-174367864	GM12878	blood:	n/a	n/a
35	CREB1	chr1:174367310-174367735	GM12878	blood:	n/a	n/a
36	CTCF	chr1:174382820-174382970	GM12866	blood:	n/a	n/a
37	CTCF	chr1:174382861-174383008	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr1:174382820-174382970	GM12872	blood:	n/a	n/a
39	CTCF	chr1:174382940-174383090	AG09319	gingival:	n/a	n/a
40	CTCF	chr1:174382760-174382910	HRE	kidney:	n/a	n/a
41	CTCF	chr1:174472201-174472208	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:174435915-174435977	Gliobla	brain:	n/a	n/a
43	CTCF	chr1:174382920-174383070	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr1:174383000-174383150	GM12870	blood:	n/a	n/a
45	CTCF	chr1:174435956-174435965	GM13977	blood:	n/a	n/a
46	CTCF	chr1:174382960-174383110	SAEC	small airway:	n/a	n/a
47	CTCF	chr1:174382840-174382990	A549	lung:	n/a	n/a
48	CTCF	chr1:174382825-174383047	Medullo	brain:	n/a	n/a
49	CTCF	chr1:174435830-174435990	MCF-7	breast:	n/a	n/a
50	CTCF	chr1:174435887-174435952	GM12891	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:174417967-174418017	HCM	heart:	n/a
2	chr1:174417967-174418017	Hela-S3	cervix:	n/a
3	chr1:174417375-174417425	AG10803	skin:	n/a
4	chr1:174417967-174418017	IMR90	lung:	fetal
5	chr1:174417967-174418017	BE2_C	brain:	n/a
6	chr1:174417967-174418017	AG09309	skin:	n/a
7	chr1:174417967-174418017	HMEC	breast:	n/a
8	chr1:174417375-174417425	BE2_C	brain:	n/a
9	chr1:174417175-174417225	HCF	heart:	n/a
10	chr1:174417175-174417225	GM12878	blood:	n/a
11	chr1:174417375-174417425	HNPCEpiC	eye:	n/a
12	chr1:174417175-174417225	NHBE	bronchial:	n/a
13	chr1:174417175-174417225	T-47D	breast:	n/a
14	chr1:174417175-174417225	NT2-D1	testis:	n/a
15	chr1:174417375-174417425	HepG2	liver:	n/a
16	chr1:174417375-174417425	Hepatocyte	liver:	n/a
17	chr1:174417375-174417425	AoSMC	blood vessel:	n/a
18	chr1:174417375-174417425	NH-A	brain:	n/a
19	chr1:174417375-174417425	K562	blood:	n/a
20	chr1:174417375-174417425	NT2-D1	testis:	n/a
21	chr1:174417375-174417425	AG04449	skin:	fetal
22	chr1:174417967-174418017	GM12878	blood:	n/a
23	chr1:174417175-174417225	GM12892	blood:	n/a
24	chr1:174417967-174418017	GM12891	blood:	n/a
25	chr1:174417967-174418017	HUVEC	blood vessel:	n/a
26	chr1:174417375-174417425	RPTEC	kidney:	n/a
27	chr1:174417375-174417425	ECC-1	luminal epithelium:	n/a
28	chr1:174417967-174418017	HRCEpiC	kidney:	n/a
29	chr1:174417175-174417225	MCF-7	breast:	n/a
30	chr1:174417967-174418017	ovcar-3	ovarian:	n/a
31	chr1:174417375-174417425	HPAEpiC	pulmonary alveolar:	n/a
32	chr1:174417175-174417225	AG04449	skin:	fetal
33	chr1:174417375-174417425	HL-60	blood:	n/a
34	chr1:174417967-174418017	ECC-1	luminal epithelium:	n/a
35	chr1:174417375-174417425	SAEC	small airway:	n/a
36	chr1:174417375-174417425	H1-hESC	embryonic stem cell:	embryo
37	chr1:174417967-174418017	T-47D	breast:	n/a
38	chr1:174417375-174417425	GM12891	blood:	n/a
39	chr1:174417375-174417425	ProgFib	skin:	n/a
40	chr1:174417175-174417225	Hela-S3	cervix:	n/a
41	chr1:174417967-174418017	SKMC	muscle:	n/a
42	chr1:174417375-174417425	A549	lung:	n/a
43	chr1:174417967-174418017	LNCaP	prostate:	n/a
44	chr1:174417967-174418017	AG10803	skin:	n/a
45	chr1:174417175-174417225	SK-N-SH	brain:	n/a
46	chr1:174417175-174417225	AG09309	skin:	n/a
47	chr1:174417967-174418017	CMK	blood:	n/a
48	chr1:174417175-174417225	NH-A	brain:	n/a
49	chr1:174417175-174417225	MCF10A-Er-Src	breast:	n/a
50	chr1:174417375-174417425	GM12892	blood:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:174478227..174480621-chr1:174484949..174486891,2	MCF-7	breast:
2	chr1:174418631..174420346-chr1:174546629..174548508,2	K562	blood:
3	chr1:174411537..174416184-chr1:174417800..174420410,5	K562	blood:
4	chr1:174420323..174421165-chr1:174695373..174696419,3	MCF-7	breast:
5	chr1:174365587..174367907-chr1:174369349..174371264,2	K562	blood:
6	chr1:174485495..174487649-chr1:174503565..174506456,2	K562	blood:
7	chr1:174392997..174395880-chr1:174397869..174401974,3	K562	blood:
8	chr1:174419001..174421193-chr1:174434649..174437565,2	K562	blood:
9	chr1:174427874..174429422-chr1:174431934..174434699,2	MCF-7	breast:
10	chr1:174447279..174449920-chr1:174453391..174456617,3	K562	blood:
11	chr1:174420516..174421195-chr1:174712811..174713329,2	MCF-7	breast:
12	chr1:174468172..174471596-chr1:174473522..174476530,3	K562	blood:
13	chr1:174458959..174461243-chr1:174465302..174467364,3	MCF-7	breast:
14	chr1:174478227..174480621-chr1:174484949..174486891,2	MCF-7	breast:
15	chr1:174411537..174416184-chr1:174417800..174420410,5	K562	blood:
16	chr1:174409687..174411251-chr1:174412999..174415751,2	K562	blood:
17	chr1:174392997..174395880-chr1:174397869..174401974,3	K562	blood:
18	chr1:174445047..174445587-chr2:186343137..186343750,2	MCF-7	breast:
19	chr1:174427874..174429422-chr1:174431934..174434699,2	MCF-7	breast:
20	chr1:174382438..174383401-chr1:174695381..174696315,3	MCF-7	breast:
21	chr1:174409528..174411154-chr1:174416998..174418836,2	MCF-7	breast:
22	chr1:174367483..174370019-chr1:174372739..174376540,3	K562	blood:
23	chr1:174420628..174423006-chr1:174424339..174426436,2	K562	blood:
24	chr1:174420628..174423006-chr1:174424339..174426436,2	K562	blood:
25	chr1:174423427..174424948-chr1:174426717..174429435,2	K562	blood:
26	chr1:174460451..174463330-chr1:174468900..174471148,2	K562	blood:
27	chr1:174361556..174363386-chr1:174366777..174369174,2	K562	blood:
28	chr1:174367483..174370019-chr1:174372739..174376540,3	K562	blood:
29	chr1:174382494..174383374-chr1:174713222..174713791,2	MCF-7	breast:
30	chr1:174419001..174421193-chr1:174434649..174437565,2	K562	blood:
31	chr1:174468172..174471596-chr1:174473522..174476530,3	K562	blood:
32	chr1:174365587..174367907-chr1:174369349..174371264,2	K562	blood:
33	chr1:174403554..174404054-chr10:47655569..47656367,2	NB4	blood:
34	chr1:174447279..174449920-chr1:174453391..174456617,3	K562	blood:
35	chr1:174409687..174411251-chr1:174412999..174415751,2	K562	blood:
36	chr1:174412862..174415441-chr1:174418910..174422017,3	K562	blood:
37	chr1:174367483..174370019-chr1:174373894..174376540,2	K562	blood:
38	chr1:174423427..174424948-chr1:174426717..174429435,2	K562	blood:
39	chr1:174460451..174463330-chr1:174468900..174471148,2	K562	blood:
40	chr1:174412862..174415441-chr1:174418910..174422017,3	K562	blood:
41	chr1:174367483..174370019-chr1:174373894..174376540,2	K562	blood:
42	chr1:174420322..174421208-chr1:174695285..174696163,4	MCF-7	breast:
43	chr1:174458959..174461243-chr1:174465302..174467364,3	MCF-7	breast:

No data

Variant related genes	Relation type
GPR52	TF binding region
GPR52	CpG island
ENSG00000259942	chromatin interactions
ENSG00000203737	chromatin interactions

Extended variants
information (count: 4543 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:4543 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538573714	chr1:174367714-174367715	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs572223175	chr1:174367720-174367721	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs376838608	chr1:174367756-174367757	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs578242672	chr1:174367837-174367838	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs560438840	chr1:174367843-174367844	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs539077691	chr1:174367849-174367850	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs368742910	chr1:174367884-174367885	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs547390993	chr1:174367891-174367892	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs185384083	chr1:174367923-174367924	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs541902819	chr1:174367927-174367928	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs561585028	chr1:174367959-174367960	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs575079142	chr1:174367989-174367990	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs543976844	chr1:174367991-174367992	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs564057577	chr1:174368073-174368074	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534301259	chr1:174368136-174368137	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533216182	chr1:174368185-174368186	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188377236	chr1:174368190-174368191	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs191839029	chr1:174368196-174368197	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557908474	chr1:174368214-174368215	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577779964	chr1:174368227-174368228	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs79257738	chr1:174368234-174368235	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372171704	chr1:174368322-174368323	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556746627	chr1:174368397-174368398	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149415875	chr1:174368446-174368447	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569501900	chr1:174368460-174368461	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144787385	chr1:174368505-174368506	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs551970162	chr1:174368522-174368523	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs140040964	chr1:174368532-174368533	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183606562	chr1:174368599-174368600	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552737445	chr1:174368643-174368644	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs145462939	chr1:174368663-174368664	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs562228770	chr1:174368672-174368673	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs555067343	chr1:174368684-174368685	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs11388080	chr1:174368741-174368742	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs398089672	chr1:174368742-174368743	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs147267033	chr1:174368747-174368748	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs140749728	chr1:174368780-174368781	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs375314085	chr1:174368840-174368841	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs564254387	chr1:174368842-174368843	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs188255008	chr1:174368843-174368844	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs144609587	chr1:174368848-174368849	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs533209425	chr1:174368931-174368932	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs375308365	chr1:174368942-174368943	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs151234419	chr1:174368960-174368961	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs529268098	chr1:174368961-174368962	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs549862043	chr1:174368981-174368982	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs376328673	chr1:174368999-174369000	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs182319177	chr1:174369006-174369007	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs140396429	chr1:174369020-174369021	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs531795317	chr1:174369055-174369056	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	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
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD

Chromatin state (count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:174318800-174369800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr1:174325800-174382800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr1:174341800-174372200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr1:174351000-174369000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr1:174353000-174382600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr1:174353600-174372000	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr1:174357800-174375000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr1:174358600-174368400	Weak transcription	Thymus	Thymus
9	chr1:174359400-174369200	Weak transcription	Fetal Muscle Trunk	muscle
10	chr1:174360000-174370800	Weak transcription	Pancreas	Pancrea
11	chr1:174360000-174383000	Weak transcription	Right Atrium	heart
12	chr1:174360200-174370200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:174361200-174369000	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr1:174361400-174375600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr1:174361600-174382800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr1:174361800-174370000	Weak transcription	K562	blood
17	chr1:174363000-174375800	Weak transcription	NHDF-Ad	bronchial
18	chr1:174363200-174374000	Weak transcription	Esophagus	oesophagus
19	chr1:174363200-174382800	Weak transcription	Left Ventricle	heart
20	chr1:174363400-174368600	Weak transcription	Ovary	ovary
21	chr1:174363400-174372800	Weak transcription	Lung	lung
22	chr1:174363400-174375800	Weak transcription	Gastric	stomach
23	chr1:174363600-174369400	Weak transcription	Dnd41	blood
24	chr1:174363800-174368200	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr1:174364000-174368200	Weak transcription	Fetal Muscle Leg	muscle
26	chr1:174364400-174374000	Weak transcription	Fetal Intestine Large	intestine
27	chr1:174365200-174371000	Weak transcription	Right Ventricle	heart
28	chr1:174365600-174368000	Weak transcription	Colon Smooth Muscle	Colon
29	chr1:174365600-174374600	Weak transcription	Liver	Liver
30	chr1:174366000-174368000	Strong transcription	Primary B cells from cord blood	blood
31	chr1:174366000-174368600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:174366200-174368000	Strong transcription	Duodenum Mucosa	Duodenum
33	chr1:174366200-174368000	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr1:174366200-174369600	Strong transcription	Primary B cells from peripheral blood	blood
35	chr1:174366400-174367800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr1:174366400-174368000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr1:174366400-174368400	ZNF genes & repeats	GM12878-XiMat	blood
38	chr1:174366400-174368600	Enhancers	NH-A	brain
39	chr1:174366400-174368800	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr1:174366600-174368000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:174366600-174371200	Strong transcription	Primary T cells fromperipheralblood	blood
42	chr1:174366800-174369600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr1:174366800-174369600	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr1:174367000-174367800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr1:174367000-174368600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr1:174367000-174382800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr1:174367200-174367800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:174367400-174368600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr1:174367400-174371000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr1:174367400-174371000	Weak transcription	Duodenum Smooth Muscle	Duodenum

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