Variant report

Variant	nsv873239
Chromosome Location	chr1:227222125-227361072
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:705)
CpG islands
(count:122)
Chromatin interactive
region (count:86)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:705 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:227282075-227282676	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:227319080-227319280	K562	blood:	n/a	n/a
3	ARID3A	chr1:227232193-227232430	K562	blood:	n/a	n/a
4	ARID3A	chr1:227358074-227358482	K562	blood:	n/a	n/a
5	ARID3A	chr1:227258535-227258732	K562	blood:	n/a	n/a
6	ARID3A	chr1:227231537-227231737	K562	blood:	n/a	n/a
7	ATF1	chr1:227357826-227358453	K562	blood:	n/a	n/a
8	ATF1	chr1:227258521-227258708	K562	blood:	n/a	n/a
9	ATF3	chr1:227258350-227258816	HCT-116	colon:	n/a	n/a
10	ATF3	chr1:227258443-227258716	K562	blood:	n/a	n/a
11	BACH1	chr1:227231445-227231759	K562	blood:	n/a	n/a
12	BACH1	chr1:227231455-227231670	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr1:227260782-227261061	GM12878	blood:	n/a	n/a
14	BATF	chr1:227315567-227315918	GM12878	blood:	n/a	n/a
15	BATF	chr1:227260814-227261065	GM12878	blood:	n/a	n/a
16	BCL11A	chr1:227260773-227261059	GM12878	blood:	n/a	n/a
17	BHLHE40	chr1:227357092-227357408	K562	blood:	n/a	n/a
18	BRCA1	chr1:227319002-227319254	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr1:227281849-227282721	HCT-116	colon:	n/a	n/a
20	CCNT2	chr1:227358183-227358571	K562	blood:	n/a	n/a
21	CCNT2	chr1:227334421-227334611	K562	blood:	n/a	n/a
22	CEBPB	chr1:227231468-227231709	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:227336277-227336518	K562	blood:	n/a	n/a
24	CEBPB	chr1:227318964-227319214	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr1:227336332-227336521	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr1:227256353-227256415	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr1:227319032-227319072	K562	blood:	n/a	n/a
28	CEBPB	chr1:227322718-227323063	K562	blood:	n/a	n/a
29	CEBPB	chr1:227258453-227258691	H1-hESC	embryonic stem cell:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
30	CEBPB	chr1:227270310-227270472	K562	blood:	n/a	n/a
31	CEBPB	chr1:227222245-227222399	A549	lung:	n/a	n/a
32	CEBPB	chr1:227275650-227275866	A549	lung:	n/a	chr1:227275741-227275754 chr1:227275741-227275754
33	CEBPB	chr1:227258422-227258767	Hela-S3	cervix:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
34	CEBPB	chr1:227230055-227230283	A549	lung:	n/a	n/a
35	CEBPB	chr1:227258415-227258755	IMR90	lung:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
36	CEBPB	chr1:227270333-227270533	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr1:227338717-227338920	HepG2	liver:	n/a	chr1:227338774-227338785
38	CEBPB	chr1:227346535-227346798	HepG2	liver:	n/a	n/a
39	CEBPB	chr1:227260879-227261153	IMR90	lung:	n/a	n/a
40	CEBPB	chr1:227346500-227346801	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr1:227258338-227258863	HCT-116	colon:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
42	CEBPB	chr1:227258445-227258752	A549	lung:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
43	CEBPB	chr1:227231524-227231767	A549	lung:	n/a	n/a
44	CEBPB	chr1:227258415-227258759	HepG2	liver:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
45	CEBPB	chr1:227258398-227258770	K562	blood:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
46	CEBPB	chr1:227231385-227231813	IMR90	lung:	n/a	n/a
47	CEBPB	chr1:227258288-227258871	HCT-116	colon:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
48	CEBPB	chr1:227230023-227230323	K562	blood:	n/a	n/a
49	CEBPB	chr1:227258420-227258694	K562	blood:	n/a	chr1:227258577-227258588 chr1:227258576-227258587
50	CEBPB	chr1:227231508-227231769	K562	blood:	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	HRCEpiC	kidney:	n/a
2	chr1:227260129-227260179	HCF	heart:	n/a
3	chr1:227327429-227327479	T-47D	breast:	n/a
4	chr1:227260129-227260179	NH-A	brain:	n/a
5	chr1:227260129-227260179	GM19239	blood:	n/a
6	chr1:227260129-227260179	SK-N-SH	brain:	n/a
7	chr1:227327429-227327479	NB4	blood:	n/a
8	chr1:227260129-227260179	SK-N-SH_RA	brain:	n/a
9	chr1:227327429-227327479	GM12892	blood:	n/a
10	chr1:227260129-227260179	Hepatocyte	liver:	n/a
11	chr1:227327429-227327479	GM06990	blood:	n/a
12	chr1:227327429-227327479	H1-hESC	embryonic stem cell:	embryo
13	chr1:227260129-227260179	K562	blood:	n/a
14	chr1:227260129-227260179	NB4	blood:	n/a
15	chr1:227327429-227327479	LNCaP	prostate:	n/a
16	chr1:227327429-227327479	IMR90	lung:	fetal
17	chr1:227327429-227327479	MCF-7	breast:	n/a
18	chr1:227260129-227260179	GM06990	blood:	n/a
19	chr1:227260129-227260179	ProgFib	skin:	n/a
20	chr1:227260129-227260179	NHDF-neo	bronchial:	n/a
21	chr1:227327429-227327479	Hela-S3	cervix:	n/a
22	chr1:227260129-227260179	NT2-D1	testis:	n/a
23	chr1:227327429-227327479	NHDF-neo	bronchial:	n/a
24	chr1:227260129-227260179	AG10803	skin:	n/a
25	chr1:227327429-227327479	ProgFib	skin:	n/a
26	chr1:227260129-227260179	HCPEpiC	choroid plexus:	n/a
27	chr1:227327429-227327479	SK-N-SH_RA	brain:	n/a
28	chr1:227327429-227327479	HCM	heart:	n/a
29	chr1:227327429-227327479	GM19239	blood:	n/a
30	chr1:227260129-227260179	MCF10A-Er-Src	breast:	n/a
31	chr1:227260129-227260179	Caco-2	colon:	n/a
32	chr1:227260129-227260179	ECC-1	luminal epithelium:	n/a
33	chr1:227260129-227260179	SKMC	muscle:	n/a
34	chr1:227327429-227327479	SKMC	muscle:	n/a
35	chr1:227260129-227260179	A549	lung:	n/a
36	chr1:227327429-227327479	SK-N-SH	brain:	n/a
37	chr1:227327429-227327479	NH-A	brain:	n/a
38	chr1:227260129-227260179	LNCaP	prostate:	n/a
39	chr1:227327429-227327479	A549	lung:	n/a
40	chr1:227260129-227260179	BE2_C	brain:	n/a
41	chr1:227327429-227327479	HRPEpiC	eye:	n/a
42	chr1:227327429-227327479	AoSMC	blood vessel:	n/a
43	chr1:227260129-227260179	HepG2	liver:	n/a
44	chr1:227327429-227327479	K562	blood:	n/a
45	chr1:227260129-227260179	AG09309	skin:	n/a
46	chr1:227260129-227260179	AG09319	gingival:	n/a
47	chr1:227327429-227327479	NHBE	bronchial:	n/a
48	chr1:227260129-227260179	GM12891	blood:	n/a
49	chr1:227327429-227327479	HCPEpiC	choroid plexus:	n/a
50	chr1:227260129-227260179	ovcar-3	ovarian:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:227230140..227234774-chr1:227236431..227241922,5	K562	blood:
2	chr1:227274632..227277428-chr1:227279390..227281436,2	K562	blood:
3	chr1:227236590..227238961-chr1:227241573..227243242,3	K562	blood:
4	chr1:227231949..227233855-chr1:227255369..227258277,2	K562	blood:
5	chr1:227323669..227325656-chr1:227329676..227331291,2	K562	blood:
6	chr1:227231345..227233578-chr1:227235477..227237603,2	MCF-7	breast:
7	chr1:227344361..227346262-chr1:227357856..227360838,2	K562	blood:
8	chr1:227319076..227321131-chr1:227322486..227324185,2	K562	blood:
9	chr1:227321877..227323599-chr1:227327325..227328877,2	K562	blood:
10	chr1:227322546..227324104-chr1:227325475..227327194,2	K562	blood:
11	chr1:227270688..227272597-chr1:227288564..227290914,2	MCF-7	breast:
12	chr1:227247700..227249846-chr1:227255373..227257295,2	K562	blood:
13	chr1:227236504..227239220-chr1:227240349..227243242,4	K562	blood:
14	chr1:227236590..227238961-chr1:227241573..227243242,3	K562	blood:
15	chr1:227274632..227277428-chr1:227279390..227281436,2	K562	blood:
16	chr1:227319086..227319624-chr1:227625143..227626016,2	K562	blood:
17	chr1:227259571..227263475-chr1:227264453..227268699,4	K562	blood:
18	chr1:227323669..227325656-chr1:227329676..227331291,2	K562	blood:
19	chr1:227327635..227329514-chr1:227357311..227359633,2	K562	blood:
20	chr1:227230140..227234774-chr1:227236431..227241922,5	K562	blood:
21	chr1:227327253..227330264-chr1:227332146..227336856,4	K562	blood:
22	chr1:227339177..227341705-chr1:227470311..227471926,2	K562	blood:
23	chr1:227327635..227329514-chr1:227357311..227359633,2	K562	blood:
24	chr1:227246764..227248668-chr1:227249328..227251525,2	MCF-7	breast:
25	chr1:227126988..227128747-chr1:227341911..227344210,2	MCF-7	breast:
26	chr1:227249781..227252416-chr1:227257576..227259161,2	K562	blood:
27	chr1:227317866..227320576-chr1:227321211..227323986,2	K562	blood:
28	chr1:227248469..227250587-chr1:227251655..227253321,2	K562	blood:
29	chr1:227259571..227263475-chr1:227264453..227268699,4	K562	blood:
30	chr1:227250275..227252416-chr1:227256127..227259076,3	K562	blood:
31	chr1:227100489..227101122-chr1:227314586..227315189,2	MCF-7	breast:
32	chr1:227319066..227320904-chr1:227331310..227334061,2	K562	blood:
33	chr1:227356009..227359900-chr1:227368469..227370220,4	K562	blood:
34	chr1:227250275..227252416-chr1:227256127..227259076,3	K562	blood:
35	chr1:227312511..227315121-chr1:227315946..227317817,2	K562	blood:
36	chr1:227243831..227246541-chr1:227247776..227250757,2	K562	blood:
37	chr1:227231345..227233578-chr1:227235477..227237603,2	MCF-7	breast:
38	chr1:227312511..227315121-chr1:227315946..227317817,2	K562	blood:
39	chr1:227318905..227319442-chr1:227625175..227625871,2	MCF-7	breast:
40	chr1:227225377..227226974-chr1:227228914..227231037,2	K562	blood:
41	chr1:227259676..227262107-chr1:227264453..227267335,2	K562	blood:
42	chr1:227317866..227320576-chr1:227321211..227323986,2	K562	blood:
43	chr1:227314587..227318154-chr1:227324311..227326852,3	MCF-7	breast:
44	chr1:227243831..227246541-chr1:227247776..227250757,2	K562	blood:
45	chr1:227360407..227362745-chr1:227368024..227370354,2	K562	blood:
46	chr1:227258899..227260884-chr1:227261569..227263920,2	K562	blood:
47	chr1:227357663..227359363-chr1:227504376..227506174,2	K562	blood:
48	chr1:227267691..227268598-chr5:174748538..174749384,2	MCF-7	breast:
49	chr1:227322546..227324104-chr1:227325475..227327194,2	K562	blood:
50	chr1:227256237..227258373-chr1:227281662..227284397,2	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
ENSG00000228625	TF binding region
CDC42BPA	CpG island
ENSG00000228625	CpG island
ENSG00000228625	chromatin interactions
ENSG00000163050	chromatin interactions
ENSG00000143776	chromatin interactions

Extended variants
information (count: 5181 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:5181 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11803959	chr1:227222125-227222126	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146406590	chr1:227222149-227222150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs41303115	chr1:227222194-227222195	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs369929514	chr1:227222212-227222213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs148582723	chr1:227222227-227222228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561664089	chr1:227222249-227222250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184764106	chr1:227222261-227222262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11804315	chr1:227222263-227222264	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs548922274	chr1:227222299-227222300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78115667	chr1:227222330-227222331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371086659	chr1:227222336-227222337	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375636003	chr1:227222424-227222425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs367599369	chr1:227222503-227222504	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113874316	chr1:227222515-227222516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs66835709	chr1:227222516-227222517	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147238516	chr1:227222519-227222520	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs112562427	chr1:227222520-227222521	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs61703280	chr1:227222522-227222523	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs201089998	chr1:227222540-227222541	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs181551865	chr1:227222553-227222554	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs187146366	chr1:227222563-227222564	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs74997735	chr1:227222594-227222595	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs16846854	chr1:227222617-227222618	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs528716357	chr1:227222647-227222648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142926967	chr1:227222771-227222772	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568774865	chr1:227222857-227222858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555807734	chr1:227222889-227222890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536154109	chr1:227222947-227222948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs151076820	chr1:227222953-227222954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189567191	chr1:227222955-227222956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs16846855	chr1:227222963-227222964	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs558253710	chr1:227222977-227222978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573223496	chr1:227223010-227223011	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs79485308	chr1:227223041-227223042	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374800621	chr1:227223044-227223045	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555095939	chr1:227223061-227223062	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs181107561	chr1:227223108-227223109	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs200344808	chr1:227223200-227223201	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs35369012	chr1:227223208-227223209	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs532917605	chr1:227223235-227223236	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs35357574	chr1:227223242-227223243	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs544647737	chr1:227223262-227223263	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs142183701	chr1:227223273-227223274	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs371390192	chr1:227223280-227223281	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs527338654	chr1:227223307-227223308	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs186384835	chr1:227223317-227223318	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs373886037	chr1:227223330-227223331	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs10495272	chr1:227223367-227223368	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs529651821	chr1:227223397-227223398	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs12565685	chr1:227223399-227223400	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:93)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2073 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

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	chr1:227190600-227223200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:227190600-227272600	Weak transcription	Lung	lung
11	chr1:227202600-227222600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr1:227203000-227278800	Weak transcription	Pancreas	Pancrea
13	chr1:227207600-227242000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:227208800-227222600	Strong transcription	Cortex derived primary cultured neurospheres	brain
15	chr1:227209000-227231000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr1:227209000-227234600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr1:227209000-227272400	Weak transcription	Fetal Intestine Small	intestine
18	chr1:227209200-227301600	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr1:227209800-227222800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr1:227210200-227226400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr1:227210600-227245800	Weak transcription	NHEK	skin
22	chr1:227212200-227223000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:227212800-227226400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:227213200-227222400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr1:227213600-227228000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr1:227214000-227222600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:227214600-227226200	Weak transcription	Brain Germinal Matrix	brain
28	chr1:227214800-227329200	Weak transcription	Right Ventricle	heart
29	chr1:227215000-227222400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr1:227215600-227230400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr1:227216600-227226400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr1:227216800-227222400	Weak transcription	Brain Angular Gyrus	brain
33	chr1:227216800-227223000	Strong transcription	HUVEC	blood vessel
34	chr1:227216800-227223200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr1:227216800-227226200	Weak transcription	Brain Hippocampus Middle	brain
36	chr1:227216800-227226200	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr1:227216800-227231400	Weak transcription	A549	lung
38	chr1:227216800-227235000	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr1:227216800-227239400	Weak transcription	Brain Cingulate Gyrus	brain
40	chr1:227216800-227287600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr1:227217000-227226000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr1:227217000-227226200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr1:227217000-227226200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr1:227217000-227234000	Weak transcription	Fetal Brain Male	brain
45	chr1:227217000-227264400	Weak transcription	NHLF	lung
46	chr1:227217000-227271400	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr1:227217000-227278800	Weak transcription	Placenta	Placenta
48	chr1:227217200-227241800	Weak transcription	HepG2	liver
49	chr1:227217400-227226400	Weak transcription	HSMMtube	muscle
50	chr1:227218200-227222600	Strong transcription	Adipose Nuclei	Adipose

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