Variant report

Variant	nsv1014753
Chromosome Location	chr1:174271770-174694838
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1403)
CpG islands
(count:611)
Chromatin interactive
region (count:100)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:174658514-174659032	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:174688382-174688690	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:174661452-174661781	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:174651647-174652006	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:174617608-174617676	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:174396120-174396181	K562	blood:	n/a	n/a
7	ARID3A	chr1:174635164-174635969	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:174683012-174683217	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:174382888-174383024	K562	blood:	n/a	n/a
10	ATF1	chr1:174577440-174577441	K562	blood:	n/a	n/a
11	ATF1	chr1:174618881-174619077	K562	blood:	n/a	n/a
12	ATF1	chr1:174428850-174428929	K562	blood:	n/a	n/a
13	ATF1	chr1:174277912-174277913	K562	blood:	n/a	n/a
14	ATF1	chr1:174493199-174493227	K562	blood:	n/a	n/a
15	ATF1	chr1:174484804-174484808	K562	blood:	n/a	n/a
16	ATF1	chr1:174448222-174448255	K562	blood:	n/a	n/a
17	ATF1	chr1:174397299-174397520	K562	blood:	n/a	n/a
18	ATF2	chr1:174367318-174367778	GM12878	blood:	n/a	n/a
19	ATF2	chr1:174367341-174367790	GM12878	blood:	n/a	n/a
20	ATF3	chr1:174661436-174661792	K562	blood:	n/a	n/a
21	ATF3	chr1:174649329-174649527	K562	blood:	n/a	n/a
22	BACH1	chr1:174397283-174397435	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr1:174661487-174661770	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr1:174414983-174415353	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr1:174367311-174367749	GM12878	blood:	n/a	n/a
26	BATF	chr1:174366370-174366656	GM12878	blood:	n/a	n/a
27	BATF	chr1:174574466-174574676	GM12878	blood:	n/a	n/a
28	BATF	chr1:174497028-174497201	GM12878	blood:	n/a	n/a
29	BATF	chr1:174367368-174367758	GM12878	blood:	n/a	n/a
30	BCL11A	chr1:174367324-174367782	GM12878	blood:	n/a	n/a
31	BCL11A	chr1:174367394-174367688	GM12878	blood:	n/a	n/a
32	BHLHE40	chr1:174635385-174635877	HepG2	liver:	n/a	n/a
33	BHLHE40	chr1:174367450-174367753	GM12878	blood:	n/a	n/a
34	BHLHE40	chr1:174394495-174394498	K562	blood:	n/a	n/a
35	BRCA1	chr1:174526022-174526025	H1-hESC	embryonic stem cell:	n/a	n/a
36	CBX3	chr1:174284403-174284874	K562	blood:	n/a	n/a
37	CBX3	chr1:174545240-174545642	K562	blood:	n/a	n/a
38	CBX3	chr1:174284427-174284759	K562	blood:	n/a	n/a
39	CBX3	chr1:174545300-174545553	K562	blood:	n/a	n/a
40	CBX3	chr1:174290094-174290435	K562	blood:	n/a	n/a
41	CBX3	chr1:174295373-174295772	K562	blood:	n/a	n/a
42	CBX3	chr1:174289992-174290425	K562	blood:	n/a	n/a
43	CCNT2	chr1:174397284-174397510	K562	blood:	n/a	n/a
44	CEBPB	chr1:174277885-174278089	K562	blood:	n/a	n/a
45	CEBPB	chr1:174539639-174539846	K562	blood:	n/a	chr1:174539752-174539763
46	CEBPB	chr1:174445621-174445931	HepG2	liver:	n/a	n/a
47	CEBPB	chr1:174617501-174617721	HepG2	liver:	n/a	chr1:174617640-174617651
48	CEBPB	chr1:174499539-174499642	K562	blood:	n/a	chr1:174499584-174499595
49	CEBPB	chr1:174436046-174436066	HepG2	liver:	n/a	n/a
50	CEBPB	chr1:174553077-174553540	MCF-7	breast:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:174352684-174352734	SKMC	muscle:	n/a
2	chr1:174352684-174352734	SKMC	muscle:	n/a
3	chr1:174417967-174418017	HEK293	kidney:	embryo
4	chr1:174417967-174418017	HMEC	breast:	n/a
5	chr1:174662459-174662509	AG09319	gingival:	n/a
6	chr1:174319673-174319723	HL-60	blood:	n/a
7	chr1:174417375-174417425	T-47D	breast:	n/a
8	chr1:174565337-174565387	HNPCEpiC	eye:	n/a
9	chr1:174680847-174680897	HCT-116	colon:	n/a
10	chr1:174680847-174680897	HCPEpiC	choroid plexus:	n/a
11	chr1:174417175-174417225	GM19239	blood:	n/a
12	chr1:174565337-174565387	SK-N-MC	brain:	n/a
13	chr1:174680847-174680897	ovcar-3	ovarian:	n/a
14	chr1:174565337-174565387	HEEpiC	esophagus:	n/a
15	chr1:174680847-174680897	ProgFib	skin:	n/a
16	chr1:174319673-174319723	H1-hESC	embryonic stem cell:	embryo
17	chr1:174319673-174319723	HNPCEpiC	eye:	n/a
18	chr1:174319673-174319723	AG10803	skin:	n/a
19	chr1:174417967-174418017	Jurkat	blood:	n/a
20	chr1:174680847-174680897	HMEC	breast:	n/a
21	chr1:174417375-174417425	AG09309	skin:	n/a
22	chr1:174565337-174565387	Jurkat	blood:	n/a
23	chr1:174680586-174680636	HL-60	blood:	n/a
24	chr1:174680586-174680636	K562	blood:	n/a
25	chr1:174417375-174417425	HCPEpiC	choroid plexus:	n/a
26	chr1:174526483-174526533	H1-hESC	embryonic stem cell:	embryo
27	chr1:174565337-174565387	PFSK-1	brain:	n/a
28	chr1:174565337-174565387	GM12878	blood:	n/a
29	chr1:174526483-174526533	SKMC	muscle:	n/a
30	chr1:174417967-174418017	MCF10A-Er-Src	breast:	n/a
31	chr1:174680847-174680897	U87	brain:	n/a
32	chr1:174417175-174417225	HUVEC	blood vessel:	n/a
33	chr1:174662459-174662509	AG04450	lung:	fetal
34	chr1:174417175-174417225	Caco-2	colon:	n/a
35	chr1:174319673-174319723	AG04450	lung:	fetal
36	chr1:174662459-174662509	NB4	blood:	n/a
37	chr1:174662459-174662509	GM12878	blood:	n/a
38	chr1:174680586-174680636	AG04450	lung:	fetal
39	chr1:174417375-174417425	NT2-D1	testis:	n/a
40	chr1:174417375-174417425	BE2_C	brain:	n/a
41	chr1:174352684-174352734	LNCaP	prostate:	n/a
42	chr1:174352684-174352734	HIPEpiC	eye:	n/a
43	chr1:174565337-174565387	HRE	kidney:	n/a
44	chr1:174662459-174662509	LNCaP	prostate:	n/a
45	chr1:174319673-174319723	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:174417375-174417425	K562	blood:	n/a
47	chr1:174680586-174680636	PFSK-1	brain:	n/a
48	chr1:174417375-174417425	U87	brain:	n/a
49	chr1:174680586-174680636	Jurkat	blood:	n/a
50	chr1:174526483-174526533	NT2-D1	testis:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:174427874..174429422-chr1:174431934..174434699,2	MCF-7	breast:
2	chr1:174365587..174367907-chr1:174369349..174371264,2	K562	blood:
3	chr1:174650389..174652208-chr1:174655181..174656888,2	K562	blood:
4	chr1:174485495..174487649-chr1:174503565..174506456,2	K562	blood:
5	chr1:174460451..174463330-chr1:174468900..174471148,2	K562	blood:
6	chr1:174536183..174536703-chr12:77045544..77046044,2	MCF-7	breast:
7	chr1:174420628..174423006-chr1:174424339..174426436,2	K562	blood:
8	chr1:174688388..174690592-chr1:174693450..174696212,2	MCF-7	breast:
9	chr1:174418631..174420346-chr1:174546629..174548508,2	K562	blood:
10	chr1:174478227..174480621-chr1:174484949..174486891,2	MCF-7	breast:
11	chr1:174423427..174424948-chr1:174426717..174429435,2	K562	blood:
12	chr1:174411537..174416184-chr1:174417800..174420410,5	K562	blood:
13	chr1:174302180..174304421-chr1:174305573..174307627,2	K562	blood:
14	chr1:174357412..174359554-chr1:174362221..174364096,2	K562	blood:
15	chr1:174420323..174421165-chr1:174695373..174696419,3	MCF-7	breast:
16	chr1:174382438..174383401-chr1:174695381..174696315,3	MCF-7	breast:
17	chr1:174537054..174539369-chr1:174541231..174544062,3	K562	blood:
18	chr1:174367483..174370019-chr1:174373894..174376540,2	K562	blood:
19	chr1:174445047..174445587-chr2:186343137..186343750,2	MCF-7	breast:
20	chr1:174458959..174461243-chr1:174465302..174467364,3	MCF-7	breast:
21	chr1:174688388..174690592-chr1:174693450..174696212,2	MCF-7	breast:
22	chr1:174357412..174359554-chr1:174362221..174364096,2	K562	blood:
23	chr1:174522506..174524469-chr1:174526591..174528326,2	K562	blood:
24	chr1:174423427..174424948-chr1:174426717..174429435,2	K562	blood:
25	chr1:174521191..174523406-chr1:174525648..174527204,2	MCF-7	breast:
26	chr1:174478227..174480621-chr1:174484949..174486891,2	MCF-7	breast:
27	chr1:174361556..174363386-chr1:174366777..174369174,2	K562	blood:
28	chr1:174392997..174395880-chr1:174397869..174401974,3	K562	blood:
29	chr1:174657293..174659127-chr1:174660705..174662538,2	K562	blood:
30	chr1:174527785..174529980-chr1:174530540..174532967,2	MCF-7	breast:
31	chr1:174409687..174411251-chr1:174412999..174415751,2	K562	blood:
32	chr1:174650389..174652208-chr1:174655181..174656888,2	K562	blood:
33	chr1:174320271..174322217-chr1:174328823..174331200,2	MCF-7	breast:
34	chr1:174411537..174416184-chr1:174417800..174420410,5	K562	blood:
35	chr1:174328732..174330689-chr1:174332303..174334086,2	K562	blood:
36	chr1:174294663..174296200-chr1:174300746..174303006,2	MCF-7	breast:
37	chr1:174292133..174293963-chr1:174301470..174303626,2	MCF-7	breast:
38	chr1:174367483..174370019-chr1:174373894..174376540,2	K562	blood:
39	chr1:173991563..173993480-chr1:174352055..174354802,2	K562	blood:
40	chr1:174669078..174670967-chr1:174674536..174677161,2	MCF-7	breast:
41	chr1:174358031..174358668-chr4:151874262..151874762,2	MCF-7	breast:
42	chr1:174521191..174523406-chr1:174525648..174527204,2	MCF-7	breast:
43	chr1:174633951..174635550-chr1:174711716..174714165,2	K562	blood:
44	chr1:174367483..174370019-chr1:174372739..174376540,3	K562	blood:
45	chr1:174537431..174539369-chr1:174541884..174544062,2	K562	blood:
46	chr1:174522506..174524469-chr1:174526591..174528326,2	K562	blood:
47	chr1:174409687..174411251-chr1:174412999..174415751,2	K562	blood:
48	chr1:174447279..174449920-chr1:174453391..174456617,3	K562	blood:
49	chr1:174544631..174547612-chr1:174552869..174554719,2	MCF-7	breast:
50	chr1:174420516..174421195-chr1:174712811..174713329,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RC3H1-4	chr1:174336243-174337177	NONHSAT007733

No data

Variant related genes	Relation type
ENSG00000237317	TF binding region
GPR52	TF binding region
RABGAP1L	TF binding region
ENSG00000266125	TF binding region
ENSG00000237317	CpG island
GPR52	CpG island
RABGAP1L	CpG island
ENSG00000266125	CpG island
ENSG00000152061	chromatin interactions
ENSG00000203737	chromatin interactions
ENSG00000224977	chromatin interactions
ENSG00000259942	chromatin interactions

Extended variants
information (count: 15304 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:15304 , 50 per page) page: 1 2 3 4 5 6 7 ... 307

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74958686	chr1:174271790-174271791	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs571500129	chr1:174271904-174271905	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs527988391	chr1:174271920-174271921	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs547637360	chr1:174272032-174272033	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566153190	chr1:174272088-174272089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188426444	chr1:174272099-174272100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555320150	chr1:174272138-174272139	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181201245	chr1:174272145-174272146	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537935835	chr1:174272159-174272160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544151060	chr1:174272178-174272179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201856820	chr1:174272179-174272180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184136300	chr1:174272221-174272222	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs6695636	chr1:174272225-174272226	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs114843376	chr1:174272232-174272233	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs554072466	chr1:174272235-174272236	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs189611094	chr1:174272239-174272240	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs542687460	chr1:174272262-174272263	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs575045284	chr1:174272281-174272282	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs539548694	chr1:174272334-174272335	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs35838570	chr1:174272351-174272352	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs182103794	chr1:174272359-174272360	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs16846840	chr1:174272379-174272380	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs545444849	chr1:174272484-174272485	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs187593576	chr1:174272496-174272497	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs565142322	chr1:174272594-174272595	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs190585493	chr1:174272643-174272644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554237971	chr1:174272731-174272732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561274561	chr1:174272793-174272794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373011133	chr1:174272795-174272796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530417586	chr1:174272822-174272823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548742914	chr1:174272843-174272844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568793665	chr1:174272898-174272899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537545073	chr1:174272914-174272915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557621136	chr1:174272932-174272933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116418461	chr1:174272939-174272940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12069450	chr1:174273004-174273005	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs77053067	chr1:174273043-174273044	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs74128340	chr1:174273057-174273058	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs546362415	chr1:174273058-174273059	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76912418	chr1:174273097-174273098	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556293091	chr1:174273124-174273125	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531489936	chr1:174273200-174273201	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576340857	chr1:174273204-174273205	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545194298	chr1:174273221-174273222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565004224	chr1:174273341-174273342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145457884	chr1:174273342-174273343	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145229324	chr1:174273344-174273345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561135237	chr1:174273348-174273349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181501295	chr1:174273400-174273401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550400640	chr1:174273434-174273435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Invasive pancreatic ductal carcinoma	16982739	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
Myelofibrosis	22110671	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
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	19404257	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1992 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:174242800-174277200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr1:174243800-174275800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr1:174244400-174274000	Weak transcription	Fetal Heart	heart
4	chr1:174246200-174284200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr1:174251200-174275800	Weak transcription	Stomach Smooth Muscle	stomach
6	chr1:174251400-174276000	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr1:174259600-174272200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr1:174259600-174276200	Weak transcription	Brain Anterior Caudate	brain
9	chr1:174259600-174277800	Weak transcription	K562	blood
10	chr1:174259800-174273800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr1:174259800-174274000	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr1:174260200-174274000	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr1:174260200-174275800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr1:174260400-174276200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr1:174260400-174277200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr1:174260600-174275600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr1:174262000-174274000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr1:174264800-174275400	Weak transcription	Fetal Muscle Trunk	muscle
19	chr1:174268400-174272000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr1:174270000-174271800	ZNF genes & repeats	GM12878-XiMat	blood
21	chr1:174270600-174274000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr1:174270600-174275400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr1:174270600-174279200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr1:174270800-174272200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr1:174270800-174274000	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr1:174270800-174274000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr1:174270800-174274000	Weak transcription	Duodenum Mucosa	Duodenum
28	chr1:174270800-174274000	Weak transcription	Fetal Intestine Large	intestine
29	chr1:174270800-174274200	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr1:174270800-174274200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr1:174270800-174274200	Weak transcription	Left Ventricle	heart
32	chr1:174270800-174274200	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr1:174270800-174275600	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr1:174270800-174275800	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr1:174270800-174276600	Weak transcription	Esophagus	oesophagus
36	chr1:174270800-174276800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr1:174270800-174281400	Weak transcription	Right Ventricle	heart
38	chr1:174270800-174284200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr1:174270800-174285800	Weak transcription	Aorta	Aorta
40	chr1:174270800-174289800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr1:174271000-174274000	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr1:174271000-174274000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr1:174271000-174274600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr1:174271000-174275800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr1:174271000-174276200	Weak transcription	Adipose Nuclei	Adipose
46	chr1:174271000-174276800	Weak transcription	Thymus	Thymus
47	chr1:174271000-174279400	Weak transcription	Fetal Stomach	stomach
48	chr1:174271000-174286400	Weak transcription	Spleen	Spleen
49	chr1:174271200-174272600	Strong transcription	Primary B cells from cord blood	blood
50	chr1:174271200-174273000	Weak transcription	Primary B cells from peripheral blood	blood

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