Variant report

Variant	nsv468227
Chromosome Location	chr1:227223736-227340790
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:601)
CpG islands
(count:122)
Chromatin interactive
region (count:78)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:601 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:227258535-227258732	K562	blood:	n/a	n/a
2	ARID3A	chr1:227282075-227282676	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:227232193-227232430	K562	blood:	n/a	n/a
4	ARID3A	chr1:227231537-227231737	K562	blood:	n/a	n/a
5	ARID3A	chr1:227319080-227319280	K562	blood:	n/a	n/a
6	ATF1	chr1:227258521-227258708	K562	blood:	n/a	n/a
7	ATF3	chr1:227258443-227258716	K562	blood:	n/a	n/a
8	ATF3	chr1:227258350-227258816	HCT-116	colon:	n/a	n/a
9	BACH1	chr1:227231445-227231759	K562	blood:	n/a	n/a
10	BACH1	chr1:227231455-227231670	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr1:227260814-227261065	GM12878	blood:	n/a	n/a
12	BATF	chr1:227260782-227261061	GM12878	blood:	n/a	n/a
13	BATF	chr1:227315567-227315918	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:227260773-227261059	GM12878	blood:	n/a	n/a
15	BRCA1	chr1:227319002-227319254	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr1:227281849-227282721	HCT-116	colon:	n/a	n/a
17	CCNT2	chr1:227334421-227334611	K562	blood:	n/a	n/a
18	CEBPB	chr1:227318964-227319214	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:227270310-227270472	K562	blood:	n/a	n/a
20	CEBPB	chr1:227338614-227338940	K562	blood:	n/a	chr1:227338774-227338785
21	CEBPB	chr1:227231468-227231709	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr1:227275650-227275866	A549	lung:	n/a	chr1:227275741-227275754 chr1:227275741-227275754
23	CEBPB	chr1:227258338-227258863	HCT-116	colon:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
24	CEBPB	chr1:227258420-227258694	K562	blood:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
25	CEBPB	chr1:227336332-227336521	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr1:227231508-227231769	K562	blood:	n/a	n/a
27	CEBPB	chr1:227319032-227319072	K562	blood:	n/a	n/a
28	CEBPB	chr1:227258288-227258871	HCT-116	colon:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
29	CEBPB	chr1:227258415-227258755	IMR90	lung:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
30	CEBPB	chr1:227246204-227246547	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:227258445-227258752	A549	lung:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
32	CEBPB	chr1:227318933-227319197	IMR90	lung:	n/a	n/a
33	CEBPB	chr1:227258330-227258746	K562	blood:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
34	CEBPB	chr1:227322718-227323063	K562	blood:	n/a	n/a
35	CEBPB	chr1:227338717-227338920	HepG2	liver:	n/a	chr1:227338774-227338785
36	CEBPB	chr1:227258415-227258759	HepG2	liver:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
37	CEBPB	chr1:227336277-227336518	K562	blood:	n/a	n/a
38	CEBPB	chr1:227231385-227231813	IMR90	lung:	n/a	n/a
39	CEBPB	chr1:227230023-227230323	K562	blood:	n/a	n/a
40	CEBPB	chr1:227231524-227231767	A549	lung:	n/a	n/a
41	CEBPB	chr1:227230055-227230283	A549	lung:	n/a	n/a
42	CEBPB	chr1:227260879-227261153	IMR90	lung:	n/a	n/a
43	CEBPB	chr1:227256353-227256415	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr1:227258453-227258691	H1-hESC	embryonic stem cell:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
45	CEBPB	chr1:227275642-227275884	K562	blood:	n/a	chr1:227275741-227275754 chr1:227275741-227275754
46	CEBPB	chr1:227258422-227258767	Hela-S3	cervix:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
47	CEBPB	chr1:227270333-227270533	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr1:227258398-227258770	K562	blood:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
49	CTCF	chr1:227319040-227319190	HVMF	connective:	n/a	n/a
50	CTCF	chr1:227319020-227319170	HCPEpiC	choroid plexus:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:227260129-227260179	BJ	skin:	n/a
2	chr1:227260129-227260179	AG09319	gingival:	n/a
3	chr1:227327429-227327479	HCF	heart:	n/a
4	chr1:227260129-227260179	HCT-116	colon:	n/a
5	chr1:227327429-227327479	MCF-7	breast:	n/a
6	chr1:227260129-227260179	NHBE	bronchial:	n/a
7	chr1:227327429-227327479	HRE	kidney:	n/a
8	chr1:227260129-227260179	NB4	blood:	n/a
9	chr1:227327429-227327479	AG09319	gingival:	n/a
10	chr1:227327429-227327479	GM06990	blood:	n/a
11	chr1:227260129-227260179	HNPCEpiC	eye:	n/a
12	chr1:227327429-227327479	Hela-S3	cervix:	n/a
13	chr1:227327429-227327479	HIPEpiC	eye:	n/a
14	chr1:227260129-227260179	K562	blood:	n/a
15	chr1:227260129-227260179	Hela-S3	cervix:	n/a
16	chr1:227327429-227327479	NT2-D1	testis:	n/a
17	chr1:227260129-227260179	GM06990	blood:	n/a
18	chr1:227327429-227327479	AoSMC	blood vessel:	n/a
19	chr1:227327429-227327479	SK-N-SH_RA	brain:	n/a
20	chr1:227260129-227260179	HIPEpiC	eye:	n/a
21	chr1:227327429-227327479	HRCEpiC	kidney:	n/a
22	chr1:227260129-227260179	HEEpiC	esophagus:	n/a
23	chr1:227327429-227327479	HMEC	breast:	n/a
24	chr1:227260129-227260179	AG04449	skin:	fetal
25	chr1:227327429-227327479	HCPEpiC	choroid plexus:	n/a
26	chr1:227260129-227260179	AoSMC	blood vessel:	n/a
27	chr1:227327429-227327479	MCF10A-Er-Src	breast:	n/a
28	chr1:227260129-227260179	BE2_C	brain:	n/a
29	chr1:227260129-227260179	A549	lung:	n/a
30	chr1:227327429-227327479	BE2_C	brain:	n/a
31	chr1:227260129-227260179	AG09309	skin:	n/a
32	chr1:227327429-227327479	AG04450	lung:	fetal
33	chr1:227260129-227260179	Jurkat	blood:	n/a
34	chr1:227327429-227327479	AG04449	skin:	fetal
35	chr1:227327429-227327479	HL-60	blood:	n/a
36	chr1:227327429-227327479	Jurkat	blood:	n/a
37	chr1:227260129-227260179	CMK	blood:	n/a
38	chr1:227260129-227260179	MCF10A-Er-Src	breast:	n/a
39	chr1:227327429-227327479	CMK	blood:	n/a
40	chr1:227260129-227260179	ovcar-3	ovarian:	n/a
41	chr1:227260129-227260179	NT2-D1	testis:	n/a
42	chr1:227327429-227327479	HCT-116	colon:	n/a
43	chr1:227327429-227327479	HEK293	kidney:	embryo
44	chr1:227260129-227260179	AG04450	lung:	fetal
45	chr1:227327429-227327479	PrEC	prostate:	n/a
46	chr1:227260129-227260179	SK-N-SH_RA	brain:	n/a
47	chr1:227260129-227260179	ProgFib	skin:	n/a
48	chr1:227260129-227260179	PFSK-1	brain:	n/a
49	chr1:227260129-227260179	HAEpiC	amniotic membrane:	n/a
50	chr1:227260129-227260179	SK-N-MC	brain:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:227236590..227238961-chr1:227241573..227243242,3	K562	blood:
2	chr1:227322546..227324104-chr1:227325475..227327194,2	K562	blood:
3	chr1:227319076..227321131-chr1:227322486..227324185,2	K562	blood:
4	chr1:227242900..227245161-chr1:227250146..227252441,3	K562	blood:
5	chr1:227312511..227315121-chr1:227315946..227317817,2	K562	blood:
6	chr1:227318905..227319442-chr1:227625175..227625871,2	MCF-7	breast:
7	chr1:227285309..227287428-chr1:227288705..227291944,3	K562	blood:
8	chr1:227256237..227258373-chr1:227281662..227284397,2	K562	blood:
9	chr1:227125600..227128392-chr1:227333735..227336576,2	MCF-7	breast:
10	chr1:227270688..227272597-chr1:227288564..227290914,2	MCF-7	breast:
11	chr1:227243831..227246541-chr1:227247776..227250757,2	K562	blood:
12	chr1:227242900..227245161-chr1:227250146..227252441,3	K562	blood:
13	chr1:227316215..227319084-chr1:227324943..227327660,2	K562	blood:
14	chr1:227314492..227316043-chr1:227318628..227320566,2	K562	blood:
15	chr1:227219115..227221995-chr1:227227439..227229511,2	K562	blood:
16	chr1:227322546..227324104-chr1:227325475..227327194,2	K562	blood:
17	chr1:227246764..227248668-chr1:227249328..227251525,2	MCF-7	breast:
18	chr1:227224836..227227359-chr1:227231406..227233044,2	K562	blood:
19	chr1:227288769..227292259-chr1:227294331..227298471,4	K562	blood:
20	chr1:227250275..227252416-chr1:227256127..227259076,3	K562	blood:
21	chr1:227247700..227249846-chr1:227255373..227257295,2	K562	blood:
22	chr1:227263840..227266585-chr1:227275633..227278048,3	K562	blood:
23	chr1:227258899..227260884-chr1:227261569..227263920,2	K562	blood:
24	chr1:227314587..227318154-chr1:227324311..227326852,3	MCF-7	breast:
25	chr1:227100489..227101122-chr1:227314586..227315189,2	MCF-7	breast:
26	chr1:227231949..227233855-chr1:227255369..227258277,2	K562	blood:
27	chr1:227339177..227341705-chr1:227470311..227471926,2	K562	blood:
28	chr1:227319022..227319798-chr1:227635073..227635816,2	MCF-7	breast:
29	chr1:227243831..227246541-chr1:227247776..227250757,2	K562	blood:
30	chr1:227319066..227320904-chr1:227331310..227334061,2	K562	blood:
31	chr1:227323669..227325656-chr1:227329676..227331291,2	K562	blood:
32	chr1:227225377..227226974-chr1:227228914..227231037,2	K562	blood:
33	chr1:227248469..227250587-chr1:227251655..227253321,2	K562	blood:
34	chr1:227319066..227320904-chr1:227331310..227334061,2	K562	blood:
35	chr1:227259676..227262107-chr1:227264453..227267335,2	K562	blood:
36	chr1:227259571..227263475-chr1:227264453..227268699,4	K562	blood:
37	chr1:227267691..227268598-chr5:174748538..174749384,2	MCF-7	breast:
38	chr1:227127149..227129305-chr1:227309091..227310783,2	MCF-7	breast:
39	chr1:227323669..227325656-chr1:227329676..227331291,2	K562	blood:
40	chr1:227127569..227129155-chr1:227257063..227258978,2	MCF-7	breast:
41	chr1:227100305..227100846-chr1:227318760..227319399,2	MCF-7	breast:
42	chr1:227236590..227238961-chr1:227241573..227243242,3	K562	blood:
43	chr1:227321877..227323599-chr1:227327325..227328877,2	K562	blood:
44	chr1:227314492..227316043-chr1:227318628..227320566,2	K562	blood:
45	chr1:227250275..227252416-chr1:227256127..227259076,3	K562	blood:
46	chr1:227316215..227319084-chr1:227324943..227327660,2	K562	blood:
47	chr1:227247700..227249846-chr1:227255373..227257295,2	K562	blood:
48	chr1:227231345..227233578-chr1:227235477..227237603,2	MCF-7	breast:
49	chr1:227315023..227317648-chr1:227321044..227323168,2	K562	blood:
50	chr1:227100437..227100984-chr1:227264267..227265039,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ITPKB-3	chr1:227297151-227297275	NONHSAT009914
2	lnc-ADCK3-5	chr1:227237319-227238751	NONHSAT009913
3	lnc-ITPKB-3	chr1:227295185-227295658	NONHSAT009914

No data

Variant related genes	Relation type
CDC42BPA	TF binding region
CDC42BPA	CpG island
ENSG00000163050	chromatin interactions
ENSG00000143776	chromatin interactions

Extended variants
information (count: 4314 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:4314 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7521639	chr1:227223736-227223737	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs36120940	chr1:227223756-227223757	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537777161	chr1:227223827-227223828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374048833	chr1:227223909-227223910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs79442428	chr1:227223957-227223958	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs12401963	chr1:227223973-227223974	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs539538189	chr1:227223980-227223981	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs12405686	chr1:227224059-227224060	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs559892784	chr1:227224120-227224121	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs536521390	chr1:227224146-227224147	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs56254464	chr1:227224147-227224148	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs189582309	chr1:227224153-227224154	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs542731260	chr1:227224169-227224170	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs12403161	chr1:227224185-227224186	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs12405707	chr1:227224219-227224220	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs550861015	chr1:227224226-227224227	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs12401993	chr1:227224256-227224257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145765197	chr1:227224259-227224260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551799030	chr1:227224275-227224276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113088438	chr1:227224291-227224292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12405723	chr1:227224365-227224366	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs182273242	chr1:227224377-227224378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567392214	chr1:227224380-227224381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538057068	chr1:227224403-227224404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556043395	chr1:227224410-227224411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34150971	chr1:227224411-227224412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs397860641	chr1:227224412-227224413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186169334	chr1:227224414-227224415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12403195	chr1:227224423-227224424	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs553839987	chr1:227224426-227224427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548270543	chr1:227224427-227224428	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143553415	chr1:227224452-227224453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568479358	chr1:227224483-227224484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs17529652	chr1:227224499-227224500	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs550901247	chr1:227224519-227224520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560981390	chr1:227224634-227224635	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs142542314	chr1:227224660-227224661	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs145069169	chr1:227224661-227224662	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs191022049	chr1:227224680-227224681	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs570615610	chr1:227224685-227224686	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs16846860	chr1:227224755-227224756	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs553070919	chr1:227224763-227224764	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs545164854	chr1:227224776-227224777	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs545360779	chr1:227224825-227224826	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs370202707	chr1:227224828-227224829	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs369799030	chr1:227224918-227224919	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs114565442	chr1:227224956-227224957	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs182853440	chr1:227225007-227225008	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs530581535	chr1:227225023-227225024	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs1929857	chr1:227225112-227225113	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Liposarcoma	21253554	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
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	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
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1816 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227154400-227294200	Weak transcription	Hela-S3	cervix
2	chr1:227177400-227255200	Weak transcription	Small Intestine	intestine
3	chr1:227178400-227271200	Weak transcription	Psoas Muscle	Psoas
4	chr1:227178600-227226200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr1:227182800-227224200	Weak transcription	Spleen	Spleen
6	chr1:227183200-227228200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:227183200-227240400	Weak transcription	Colonic Mucosa	Colon
8	chr1:227184000-227234000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:227190600-227272600	Weak transcription	Lung	lung
10	chr1:227203000-227278800	Weak transcription	Pancreas	Pancrea
11	chr1:227207600-227242000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr1:227209000-227231000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr1:227209000-227234600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr1:227209000-227272400	Weak transcription	Fetal Intestine Small	intestine
15	chr1:227209200-227301600	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr1:227210200-227226400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr1:227210600-227245800	Weak transcription	NHEK	skin
18	chr1:227212800-227226400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr1:227213600-227228000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:227214600-227226200	Weak transcription	Brain Germinal Matrix	brain
21	chr1:227214800-227329200	Weak transcription	Right Ventricle	heart
22	chr1:227215600-227230400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr1:227216600-227226400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:227216800-227226200	Weak transcription	Brain Hippocampus Middle	brain
25	chr1:227216800-227226200	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr1:227216800-227231400	Weak transcription	A549	lung
27	chr1:227216800-227235000	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr1:227216800-227239400	Weak transcription	Brain Cingulate Gyrus	brain
29	chr1:227216800-227287600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr1:227217000-227226000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:227217000-227226200	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr1:227217000-227226200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr1:227217000-227234000	Weak transcription	Fetal Brain Male	brain
34	chr1:227217000-227264400	Weak transcription	NHLF	lung
35	chr1:227217000-227271400	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr1:227217000-227278800	Weak transcription	Placenta	Placenta
37	chr1:227217200-227241800	Weak transcription	HepG2	liver
38	chr1:227217400-227226400	Weak transcription	HSMMtube	muscle
39	chr1:227219000-227224000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr1:227219000-227226400	Weak transcription	HMEC	breast
41	chr1:227219400-227228400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr1:227219600-227226200	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr1:227219600-227234800	Weak transcription	NH-A	brain
44	chr1:227220400-227224800	Weak transcription	NHDF-Ad	bronchial
45	chr1:227220600-227225800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr1:227220600-227226600	Weak transcription	Fetal Stomach	stomach
47	chr1:227220600-227231000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr1:227220600-227236800	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr1:227220600-227255800	Weak transcription	Gastric	stomach
50	chr1:227220600-227272600	Weak transcription	Aorta	Aorta

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