Variant report

Variant	nsv871100
Chromosome Location	chr1:70859397-70928786
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:957)
CpG islands
(count:855)
Chromatin interactive
region (count:75)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:957 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:70876387-70877951	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:70876483-70878063	K562	blood:	n/a	n/a
3	ARID3A	chr1:70925521-70925801	K562	blood:	n/a	n/a
4	ATF1	chr1:70877804-70878137	K562	blood:	n/a	n/a
5	ATF1	chr1:70876211-70877154	K562	blood:	n/a	n/a
6	ATF2	chr1:70876275-70877277	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:70876343-70877186	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:70876164-70877171	GM12878	blood:	n/a	n/a
9	ATF2	chr1:70876279-70876691	GM12878	blood:	n/a	n/a
10	ATF2	chr1:70877669-70878244	GM12878	blood:	n/a	n/a
11	ATF2	chr1:70877713-70878134	GM12878	blood:	n/a	n/a
12	ATF3	chr1:70877705-70878136	K562	blood:	n/a	n/a
13	ATF3	chr1:70925548-70925779	K562	blood:	n/a	n/a
14	ATF3	chr1:70925444-70925865	K562	blood:	n/a	n/a
15	BACH1	chr1:70876190-70877200	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr1:70874854-70875195	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr1:70925503-70925703	K562	blood:	n/a	n/a
18	BACH1	chr1:70874834-70875200	K562	blood:	n/a	n/a
19	BATF	chr1:70877797-70878186	GM12878	blood:	n/a	n/a
20	BATF	chr1:70918172-70918437	GM12878	blood:	n/a	n/a
21	BATF	chr1:70877808-70878134	GM12878	blood:	n/a	n/a
22	BCLAF1	chr1:70876260-70877169	GM12878	blood:	n/a	n/a
23	BDP1	chr1:70877798-70878147	Hela-S3	cervix:	n/a	n/a
24	BHLHE40	chr1:70877691-70878144	K562	blood:	n/a	n/a
25	BHLHE40	chr1:70923815-70923991	K562	blood:	n/a	n/a
26	BHLHE40	chr1:70876093-70877175	GM12878	blood:	n/a	n/a
27	BHLHE40	chr1:70877736-70878153	GM12878	blood:	n/a	n/a
28	BHLHE40	chr1:70925626-70925833	K562	blood:	n/a	n/a
29	BHLHE40	chr1:70891974-70891992	GM12878	blood:	n/a	n/a
30	BHLHE40	chr1:70876226-70877300	HepG2	liver:	n/a	n/a
31	BHLHE40	chr1:70876322-70877320	K562	blood:	n/a	n/a
32	BRCA1	chr1:70876776-70877186	HepG2	liver:	n/a	n/a
33	BRCA1	chr1:70876020-70878123	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr1:70876289-70877098	GM12878	blood:	n/a	n/a
35	BRCA1	chr1:70876175-70877301	H1-hESC	embryonic stem cell:	n/a	n/a
36	CBX3	chr1:70876184-70877323	K562	blood:	n/a	n/a
37	CBX3	chr1:70925255-70925898	K562	blood:	n/a	n/a
38	CCNT2	chr1:70875995-70877441	K562	blood:	n/a	n/a
39	CCNT2	chr1:70897738-70897933	K562	blood:	n/a	n/a
40	CCNT2	chr1:70878303-70878668	K562	blood:	n/a	n/a
41	CCNT2	chr1:70877744-70878032	K562	blood:	n/a	n/a
42	CEBPB	chr1:70877863-70878044	MCF-7	breast:	n/a	chr1:70877957-70877968
43	CEBPB	chr1:70909083-70909145	K562	blood:	n/a	chr1:70909130-70909143 chr1:70909130-70909141
44	CEBPB	chr1:70877778-70878144	H1-hESC	embryonic stem cell:	n/a	chr1:70877957-70877968
45	CEBPB	chr1:70875970-70877522	IMR90	lung:	n/a	n/a
46	CEBPB	chr1:70875817-70878169	Hela-S3	cervix:	n/a	chr1:70877957-70877968
47	CEBPB	chr1:70909012-70909201	HepG2	liver:	n/a	chr1:70909130-70909143 chr1:70909057-70909069 chr1:70909130-70909141
48	CEBPB	chr1:70877830-70878114	K562	blood:	n/a	chr1:70877957-70877968
49	CEBPB	chr1:70880050-70880156	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr1:70871818-70872445	K562	blood:	n/a	chr1:70872278-70872289 chr1:70871828-70871837 chr1:70871828-70871839 chr1:70872279-70872288 chr1:70871826-70871839

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:70876879-70876929	IMR90	lung:	fetal
2	chr1:70876879-70876929	IMR90	lung:	fetal
3	chr1:70876492-70876542	AoSMC	blood vessel:	n/a
4	chr1:70876492-70876542	NH-A	brain:	n/a
5	chr1:70876865-70876915	MCF-7	breast:	n/a
6	chr1:70876953-70877003	HL-60	blood:	n/a
7	chr1:70877381-70877431	HCF	heart:	n/a
8	chr1:70879924-70879974	LNCaP	prostate:	n/a
9	chr1:70876492-70876542	HNPCEpiC	eye:	n/a
10	chr1:70876623-70876673	SK-N-MC	brain:	n/a
11	chr1:70879924-70879974	HAEpiC	amniotic membrane:	n/a
12	chr1:70876865-70876915	HRE	kidney:	n/a
13	chr1:70876879-70876929	GM06990	blood:	n/a
14	chr1:70876729-70876779	NB4	blood:	n/a
15	chr1:70876888-70876938	CMK	blood:	n/a
16	chr1:70876492-70876542	HRE	kidney:	n/a
17	chr1:70873816-70873866	Caco-2	colon:	n/a
18	chr1:70877088-70877138	PFSK-1	brain:	n/a
19	chr1:70876598-70876648	HIPEpiC	eye:	n/a
20	chr1:70876801-70876851	U87	brain:	n/a
21	chr1:70873816-70873866	HCT-116	colon:	n/a
22	chr1:70876918-70876968	NT2-D1	testis:	n/a
23	chr1:70876801-70876851	PANC-1	pancreas:	n/a
24	chr1:70876598-70876648	NT2-D1	testis:	n/a
25	chr1:70877381-70877431	ECC-1	luminal epithelium:	n/a
26	chr1:70876888-70876938	IMR90	lung:	fetal
27	chr1:70876865-70876915	ovcar-3	ovarian:	n/a
28	chr1:70873816-70873866	HRPEpiC	eye:	n/a
29	chr1:70876879-70876929	GM12878	blood:	n/a
30	chr1:70879924-70879974	AG10803	skin:	n/a
31	chr1:70876888-70876938	GM06990	blood:	n/a
32	chr1:70876801-70876851	GM06990	blood:	n/a
33	chr1:70876598-70876648	HCF	heart:	n/a
34	chr1:70876598-70876648	CMK	blood:	n/a
35	chr1:70876729-70876779	HepG2	liver:	n/a
36	chr1:70876598-70876648	SAEC	small airway:	n/a
37	chr1:70876953-70877003	IMR90	lung:	fetal
38	chr1:70876865-70876915	HUVEC	blood vessel:	n/a
39	chr1:70876729-70876779	Jurkat	blood:	n/a
40	chr1:70876953-70877003	HEEpiC	esophagus:	n/a
41	chr1:70879924-70879974	ProgFib	skin:	n/a
42	chr1:70876888-70876938	HCM	heart:	n/a
43	chr1:70876879-70876929	HIPEpiC	eye:	n/a
44	chr1:70876888-70876938	PANC-1	pancreas:	n/a
45	chr1:70877381-70877431	IMR90	lung:	fetal
46	chr1:70876729-70876779	HL-60	blood:	n/a
47	chr1:70876623-70876673	ECC-1	luminal epithelium:	n/a
48	chr1:70876879-70876929	ECC-1	luminal epithelium:	n/a
49	chr1:70876729-70876779	GM19239	blood:	n/a
50	chr1:70876729-70876779	CMK	blood:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:70894381..70896682-chr1:70899372..70901619,2	K562	blood:
2	chr1:70876680..70877237-chrX:47076703..47077310,2	Hela-S3	cervix:
3	chr1:70886970..70888577-chr1:70891879..70893523,2	K562	blood:
4	chr1:70876550..70877428-chr9:127420306..127420837,2	NB4	blood:
5	chr1:70876951..70877911-chr1:155196685..155197597,2	Hela-S3	cervix:
6	chr1:70876737..70877459-chr17:39844968..39845649,2	Hela-S3	cervix:
7	chr1:70902079..70902916-chr1:70952867..70953793,2	MCF-7	breast:
8	chr1:70898237..70900336-chr1:70907691..70909600,2	K562	blood:
9	chr1:70883854..70886042-chr1:70886893..70888962,2	K562	blood:
10	chr1:70900549..70904581-chr1:70906967..70911006,5	K562	blood:
11	chr1:70898237..70900336-chr1:70907691..70909600,2	K562	blood:
12	chr1:70820167..70822627-chr1:70859878..70861873,2	MCF-7	breast:
13	chr1:70819219..70821978-chr1:70864563..70866134,2	K562	blood:
14	chr1:70925833..70928012-chr1:70929131..70931181,2	K562	blood:
15	chr1:70881141..70883419-chr1:70894353..70896787,2	K562	blood:
16	chr1:70819218..70821908-chr1:70867099..70869465,2	K562	blood:
17	chr1:70920653..70923423-chr1:70924273..70927501,3	K562	blood:
18	chr1:70883854..70885367-chr1:70886893..70889267,2	K562	blood:
19	chr1:70818087..70822177-chr1:70874224..70879265,8	K562	blood:
20	chr1:70876314..70877183-chr7:30065902..30066426,2	Hela-S3	cervix:
21	chr1:70880695..70883325-chr1:70886922..70888578,2	K562	blood:
22	chr1:70871257..70873394-chr1:70875235..70877484,2	MCF-7	breast:
23	chr1:70876810..70879492-chr1:70904587..70906471,2	K562	blood:
24	chr1:70875690..70877876-chr1:70887625..70890211,3	MCF-7	breast:
25	chr1:70876465..70877378-chr22:43010860..43011843,2	Hela-S3	cervix:
26	chr1:70881885..70883677-chr1:70886826..70889376,3	K562	blood:
27	chr1:70819400..70822032-chr1:70880139..70881848,2	K562	blood:
28	chr1:70902352..70904589-chr1:70911480..70913047,2	K562	blood:
29	chr1:70876562..70877348-chr2:44223071..44223588,2	Hela-S3	cervix:
30	chr1:70891788..70893936-chr1:70895573..70898086,2	K562	blood:
31	chr1:70876855..70877420-chr11:65728563..65729238,2	Hela-S3	cervix:
32	chr1:70876400..70877374-chr15:85259317..85260196,2	Hela-S3	cervix:
33	chr1:70876042..70876746-chr4:89444423..89445254,2	NB4	blood:
34	chr1:70881141..70883419-chr1:70894353..70896787,2	K562	blood:
35	chr1:70856727..70858585-chr1:70873316..70875351,2	K562	blood:
36	chr1:70902352..70904589-chr1:70911480..70913047,2	K562	blood:
37	chr1:70883854..70886042-chr1:70886893..70888962,2	K562	blood:
38	chr1:70878824..70881393-chr1:70902317..70904279,2	MCF-7	breast:
39	chr1:70803471..70806193-chr1:70890743..70892737,2	K562	blood:
40	chr1:70886970..70888577-chr1:70891879..70893523,2	K562	blood:
41	chr1:70812176..70814908-chr1:70864607..70866509,2	K562	blood:
42	chr1:70819028..70821982-chr1:70865141..70867182,2	MCF-7	breast:
43	chr1:70876526..70879847-chr1:71510519..71513789,3	K562	blood:
44	chr1:70876707..70877432-chr16:20817683..20818263,2	Hela-S3	cervix:
45	chr1:70876874..70877654-chr11:62608483..62609471,3	Hela-S3	cervix:
46	chr1:70897918..70900216-chr1:70902173..70904051,2	K562	blood:
47	chr1:70889416..70891152-chr1:70898818..70901184,2	K562	blood:
48	chr1:70902037..70902591-chr1:70953270..70954260,2	K562	blood:
49	chr1:70881885..70883677-chr1:70886826..70889376,3	K562	blood:
50	chr1:70877825..70880614-chr1:70884736..70887414,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTH-8	chr1:70910754-70911219	ENSG00000271992.1

No data

Variant related genes	Relation type
CTH	TF binding region
ENSG00000271992	TF binding region
CTH	CpG island
ENSG00000271992	CpG island
ENSG00000138641	chromatin interactions
ENSG00000005189	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000100227	chromatin interactions
ENSG00000224020	chromatin interactions
ENSG00000050628	chromatin interactions
ENSG00000197568	chromatin interactions
ENSG00000175467	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000271992	chromatin interactions
ENSG00000140612	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000102225	chromatin interactions
ENSG00000196678	chromatin interactions
ENSG00000198964	chromatin interactions
ENSG00000270022	chromatin interactions
ENSG00000118454	chromatin interactions
ENSG00000106080	chromatin interactions
ENSG00000116761	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000138095	chromatin interactions
ENSG00000145337	chromatin interactions

Extended variants
information (count: 2313 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2313 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143099603	chr1:70859933-70859934	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs527541353	chr1:70859969-70859970	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs540644906	chr1:70860029-70860030	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs560482720	chr1:70860078-70860079	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs529292178	chr1:70860128-70860129	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs192137374	chr1:70860129-70860130	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs528540386	chr1:70860139-70860140	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs12065320	chr1:70860168-70860169	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs546406668	chr1:70860199-70860200	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs551912042	chr1:70860222-70860223	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs12034101	chr1:70860232-70860233	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs150354861	chr1:70860269-70860270	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs828350	chr1:70860297-70860298	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs550590123	chr1:70860306-70860307	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs828351	chr1:70860321-70860322	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs528448201	chr1:70860322-70860323	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs536234462	chr1:70860327-70860328	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs556031331	chr1:70860382-70860383	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs185066881	chr1:70860407-70860408	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs137981734	chr1:70860436-70860437	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs828352	chr1:70860458-70860459	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs572389580	chr1:70860467-70860468	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs551367429	chr1:70860489-70860490	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs142667922	chr1:70860502-70860503	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs561160618	chr1:70860558-70860559	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs369996687	chr1:70860583-70860584	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs542963131	chr1:70860608-70860609	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs562852934	chr1:70860610-70860611	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs189301710	chr1:70860616-70860617	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs112267487	chr1:70860689-70860690	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs139539702	chr1:70860703-70860704	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs551705154	chr1:70860739-70860740	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs192719038	chr1:70860782-70860783	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs533829634	chr1:70860785-70860786	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs527863755	chr1:70860788-70860789	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs531880	chr1:70860819-70860820	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs545470145	chr1:70860832-70860833	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs542842	chr1:70860841-70860842	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs535872430	chr1:70860882-70860883	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs549707621	chr1:70860999-70861000	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs184195560	chr1:70861012-70861013	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs538696109	chr1:70861021-70861022	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs189910043	chr1:70861031-70861032	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs59856193	chr1:70861039-70861040	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs111742308	chr1:70861044-70861045	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs370367657	chr1:70861064-70861065	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs554908210	chr1:70861100-70861101	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs536186319	chr1:70861104-70861105	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs181415939	chr1:70861120-70861121	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs542673210	chr1:70861127-70861128	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	22522925	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1210 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70862400-70862800	Enhancers	GM12878-XiMat	blood
2	chr1:70865200-70866600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr1:70865600-70866600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:70865800-70866800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:70866000-70866600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr1:70866200-70866600	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr1:70869200-70869800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr1:70869400-70869800	Enhancers	H1 Cell Line	embryonic stem cell
9	chr1:70870600-70871600	Enhancers	HUVEC	blood vessel
10	chr1:70871400-70871800	Enhancers	Fetal Lung	lung
11	chr1:70871400-70872800	Enhancers	Liver	Liver
12	chr1:70871600-70872800	Enhancers	Adipose Nuclei	Adipose
13	chr1:70871600-70875800	Weak transcription	HUVEC	blood vessel
14	chr1:70871800-70872800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr1:70871800-70875800	Weak transcription	Fetal Lung	lung
16	chr1:70872800-70875200	Weak transcription	Liver	Liver
17	chr1:70872800-70875800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr1:70872800-70876000	Weak transcription	Adipose Nuclei	Adipose
19	chr1:70873200-70874800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr1:70874400-70874800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr1:70874800-70875800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:70874800-70876200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr1:70875200-70875800	Enhancers	Liver	Liver
24	chr1:70875400-70875600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr1:70875400-70875800	Enhancers	Hela-S3	cervix
26	chr1:70875400-70876000	Active TSS	HepG2	liver
27	chr1:70875600-70875800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr1:70875600-70875800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr1:70875600-70875800	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr1:70875600-70875800	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr1:70875600-70875800	Enhancers	Primary B cells from cord blood	blood
32	chr1:70875600-70875800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr1:70875600-70875800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr1:70875600-70875800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:70875600-70875800	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr1:70875600-70875800	Enhancers	Brain Angular Gyrus	brain
37	chr1:70875600-70875800	Enhancers	Brain Anterior Caudate	brain
38	chr1:70875600-70875800	Enhancers	Brain Hippocampus Middle	brain
39	chr1:70875600-70875800	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr1:70875600-70875800	Enhancers	Fetal Brain Female	brain
41	chr1:70875600-70875800	Enhancers	Rectal Smooth Muscle	rectum
42	chr1:70875600-70875800	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr1:70875600-70875800	Enhancers	Stomach Smooth Muscle	stomach
44	chr1:70875600-70875800	Enhancers	A549	lung
45	chr1:70875600-70875800	Enhancers	Dnd41	blood
46	chr1:70875600-70875800	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr1:70875600-70876000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr1:70875600-70876000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr1:70875600-70876400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr1:70875600-70878000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived

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