Variant report

Variant	nsv1033935
Chromosome Location	chr8:6262180-6275753
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:799)
CpG islands
(count:550)
Chromatin interactive
region (count:18)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:799 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:6270786-6270943	K562	blood:	n/a	n/a
2	ARID3A	chr8:6263882-6264269	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:6263893-6264043	K562	blood:	n/a	n/a
4	ATF2	chr8:6273689-6274273	GM12878	blood:	n/a	n/a
5	ATF2	chr8:6274572-6275754	GM12878	blood:	n/a	n/a
6	ATF2	chr8:6263711-6264270	GM12878	blood:	n/a	n/a
7	ATF2	chr8:6274564-6275935	GM12878	blood:	n/a	n/a
8	BACH1	chr8:6263916-6264157	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr8:6274761-6275058	GM12878	blood:	n/a	n/a
10	BATF	chr8:6275084-6275784	GM12878	blood:	n/a	n/a
11	BATF	chr8:6274819-6275423	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:6275121-6275398	GM12878	blood:	n/a	n/a
13	BCL11A	chr8:6274723-6275701	GM12878	blood:	n/a	n/a
14	BCLAF1	chr8:6274613-6275965	GM12878	blood:	n/a	n/a
15	BCLAF1	chr8:6263829-6264318	GM12878	blood:	n/a	chr8:6264126-6264139
16	BCLAF1	chr8:6275116-6275837	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:6263973-6264241	HepG2	liver:	n/a	n/a
18	BHLHE40	chr8:6264014-6264335	K562	blood:	n/a	n/a
19	BHLHE40	chr8:6273910-6274154	GM12878	blood:	n/a	n/a
20	BHLHE40	chr8:6274528-6275764	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:6263950-6264244	GM12878	blood:	n/a	n/a
22	BRCA1	chr8:6264893-6265173	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr8:6264076-6264244	HepG2	liver:	n/a	n/a
24	BRCA1	chr8:6263831-6264259	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr8:6274702-6274765	GM12878	blood:	n/a	n/a
26	BRCA1	chr8:6263394-6263395	HepG2	liver:	n/a	n/a
27	CBX3	chr8:6263841-6264326	K562	blood:	n/a	n/a
28	CCNT2	chr8:6263266-6264300	K562	blood:	n/a	n/a
29	CEBPB	chr8:6274761-6275124	A549	lung:	n/a	n/a
30	CEBPB	chr8:6266446-6266581	K562	blood:	n/a	n/a
31	CEBPB	chr8:6274796-6275153	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr8:6274778-6275140	HepG2	liver:	n/a	n/a
33	CEBPB	chr8:6274756-6275110	K562	blood:	n/a	n/a
34	CEBPB	chr8:6274739-6275622	GM12878	blood:	n/a	n/a
35	CEBPB	chr8:6274791-6275145	K562	blood:	n/a	n/a
36	CEBPB	chr8:6274802-6275022	HepG2	liver:	n/a	n/a
37	CEBPB	chr8:6274826-6275059	A549	lung:	n/a	n/a
38	CEBPB	chr8:6263329-6263440	Hela-S3	cervix:	n/a	n/a
39	CEBPD	chr8:6263754-6264176	HepG2	liver:	n/a	n/a
40	CHD1	chr8:6263588-6264217	GM12878	blood:	n/a	n/a
41	CHD1	chr8:6274611-6275958	GM12878	blood:	n/a	n/a
42	CHD1	chr8:6263250-6263306	GM12878	blood:	n/a	n/a
43	CHD1	chr8:6264568-6264722	GM12878	blood:	n/a	n/a
44	CHD2	chr8:6263959-6264320	K562	blood:	n/a	n/a
45	CHD2	chr8:6263887-6264324	GM12878	blood:	n/a	n/a
46	CHD2	chr8:6264774-6265023	HepG2	liver:	n/a	n/a
47	CHD2	chr8:6263891-6264254	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr8:6263579-6263691	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr8:6274656-6275905	GM12878	blood:	n/a	n/a
50	CHD2	chr8:6264640-6264823	H1-hESC	embryonic stem cell:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6264171-6264221	HUVEC	blood vessel:	n/a
2	chr8:6264171-6264221	HUVEC	blood vessel:	n/a
3	chr8:6263875-6263925	BJ	skin:	n/a
4	chr8:6263875-6263925	A549	lung:	n/a
5	chr8:6263875-6263925	PANC-1	pancreas:	n/a
6	chr8:6263789-6263839	AG10803	skin:	n/a
7	chr8:6264959-6265009	LNCaP	prostate:	n/a
8	chr8:6264181-6264231	K562	blood:	n/a
9	chr8:6264193-6264243	AG04449	skin:	fetal
10	chr8:6264959-6265009	PFSK-1	brain:	n/a
11	chr8:6263268-6263318	SKMC	muscle:	n/a
12	chr8:6263363-6263413	NHBE	bronchial:	n/a
13	chr8:6264181-6264231	T-47D	breast:	n/a
14	chr8:6264171-6264221	ovcar-3	ovarian:	n/a
15	chr8:6264181-6264231	HUVEC	blood vessel:	n/a
16	chr8:6263789-6263839	IMR90	lung:	fetal
17	chr8:6263363-6263413	AG04449	skin:	fetal
18	chr8:6264171-6264221	U87	brain:	n/a
19	chr8:6263623-6263673	MCF-7	breast:	n/a
20	chr8:6264171-6264221	HepG2	liver:	n/a
21	chr8:6264193-6264243	T-47D	breast:	n/a
22	chr8:6263623-6263673	LNCaP	prostate:	n/a
23	chr8:6263623-6263673	AoSMC	blood vessel:	n/a
24	chr8:6263623-6263673	NH-A	brain:	n/a
25	chr8:6263363-6263413	RPTEC	kidney:	n/a
26	chr8:6264193-6264243	Hela-S3	cervix:	n/a
27	chr8:6264193-6264243	ProgFib	skin:	n/a
28	chr8:6264959-6265009	RPTEC	kidney:	n/a
29	chr8:6263363-6263413	K562	blood:	n/a
30	chr8:6264171-6264221	GM12892	blood:	n/a
31	chr8:6263623-6263673	K562	blood:	n/a
32	chr8:6263268-6263318	HEEpiC	esophagus:	n/a
33	chr8:6263789-6263839	NHDF-neo	bronchial:	n/a
34	chr8:6264171-6264221	GM06990	blood:	n/a
35	chr8:6264181-6264231	HCM	heart:	n/a
36	chr8:6264181-6264231	U87	brain:	n/a
37	chr8:6263268-6263318	RPTEC	kidney:	n/a
38	chr8:6264193-6264243	HEK293	kidney:	embryo
39	chr8:6263875-6263925	Hepatocyte	liver:	n/a
40	chr8:6264959-6265009	AG10803	skin:	n/a
41	chr8:6263875-6263925	AoSMC	blood vessel:	n/a
42	chr8:6264171-6264221	IMR90	lung:	fetal
43	chr8:6263363-6263413	NB4	blood:	n/a
44	chr8:6264171-6264221	RPTEC	kidney:	n/a
45	chr8:6263268-6263318	K562	blood:	n/a
46	chr8:6264181-6264231	GM06990	blood:	n/a
47	chr8:6264959-6265009	T-47D	breast:	n/a
48	chr8:6264959-6265009	SK-N-MC	brain:	n/a
49	chr8:6264959-6265009	HAEpiC	amniotic membrane:	n/a
50	chr8:6264181-6264231	NH-A	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:6261231..6262782-chr8:6268049..6270486,2	K562	blood:
2	chr8:6274685..6276639-chr8:6565162..6567770,2	MCF-7	breast:
3	chr8:6263912..6265972-chr8:6565205..6568456,4	K562	blood:
4	chr8:6260743..6265726-chr8:6271007..6273930,5	K562	blood:
5	chr8:6267107..6268741-chr8:6565301..6567337,2	K562	blood:
6	chr8:6269409..6272361-chr8:6283113..6285800,2	K562	blood:
7	chr8:6266687..6268429-chr8:6271780..6273371,2	K562	blood:
8	chr8:6262086..6265734-chr8:6266423..6270611,6	MCF-7	breast:
9	chr8:6245309..6247015-chr8:6262084..6263587,2	MCF-7	breast:
10	chr8:6266687..6268429-chr8:6271780..6273371,2	K562	blood:
11	chr8:6262444..6265412-chr8:6565205..6567179,2	K562	blood:
12	chr8:6263561..6264353-chrX:135962392..135963076,2	NB4	blood:
13	chr8:6262974..6265715-chr8:6564962..6567789,4	MCF-7	breast:
14	chr8:6260700..6262859-chr8:6263480..6266725,3	K562	blood:
15	chr8:6261231..6262782-chr8:6268049..6270486,2	K562	blood:
16	chr17:49196178..49198302-chr8:6264048..6265705,2	K562	blood:
17	chr8:6257664..6260408-chr8:6262144..6263812,2	MCF-7	breast:
18	chr8:6263426..6264997-chr8:6273721..6275248,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-2	chr8:6264603-6264663	ENSG00000246089
2	lnc-ANGPT2-2	chr8:6264049-6264229	ENSG00000246089
3	lnc-ANGPT2-2	chr8:6263118-6263892	ENSG00000246089
4	lnc-ANGPT2-2	chr8:6262438-6264096	NONHSAT124771
5	lnc-ANGPT2-2	chr8:6263227-6264069	XLOC_006985
6	lnc-ANGPT2-2	chr8:6261079-6262641	XLOC_006985
7	lnc-ANGPT2-2	chr8:6264049-6264055	XLOC_006985
8	lnc-ANGPT2-2	chr8:6261077-6262641	NR_040040
9	lnc-ANGPT2-2	chr8:6262927-6264063	ENSG00000246089.3
10	lnc-ANGPT2-2	chr8:6263227-6264069	NR_040040
11	lnc-ANGPT2-2	chr8:6262449-6263892	XLOC_006985

No data

Variant related genes	Relation type
MCPH1	TF binding region
ENSG00000246089	TF binding region
MCPH1	CpG island
ENSG00000246089	CpG island
ENSG00000147316	chromatin interactions
ENSG00000008294	chromatin interactions
ENSG00000155189	chromatin interactions
ENSG00000249898	chromatin interactions
ENSG00000246089	chromatin interactions
ENSG00000147274	chromatin interactions

Extended variants
information (count: 987 )
Associated
traits (count: 136 )

Variant overlapped rSNPs/rCNVs (count:987 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572923838	chr8:6262197-6262198	Weak transcription Enhancers Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs545012962	chr8:6262202-6262203	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs2440453	chr8:6262215-6262216	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs575318800	chr8:6262236-6262237	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs13279928	chr8:6262247-6262248	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs191211145	chr8:6262262-6262263	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs147565464	chr8:6262271-6262272	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs529828222	chr8:6262302-6262303	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs200196057	chr8:6262303-6262304	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs540180187	chr8:6262306-6262307	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs560004149	chr8:6262335-6262336	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs73196742	chr8:6262389-6262390	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs552159221	chr8:6262395-6262396	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs569132132	chr8:6262414-6262415	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs531850423	chr8:6262421-6262422	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs548380268	chr8:6262425-6262426	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs568666022	chr8:6262438-6262439	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs188400540	chr8:6262441-6262442	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs554546936	chr8:6262467-6262468	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
20	rs540291908	chr8:6262468-6262469	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
21	rs374244749	chr8:6262476-6262477	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
22	rs560233666	chr8:6262480-6262481	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
23	rs76426324	chr8:6262501-6262502	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
24	rs571172267	chr8:6262508-6262509	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
25	rs529415831	chr8:6262510-6262511	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
26	rs1550688	chr8:6262572-6262573	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs575115556	chr8:6262580-6262581	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
28	rs544322253	chr8:6262581-6262582	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
29	rs140142779	chr8:6262607-6262608	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
30	rs574330228	chr8:6262632-6262633	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
31	rs1073908	chr8:6262637-6262638	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs559866115	chr8:6262638-6262639	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
33	rs112265102	chr8:6262644-6262645	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
34	rs545660286	chr8:6262645-6262646	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
35	rs376767235	chr8:6262648-6262649	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
36	rs78958516	chr8:6262661-6262662	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
37	rs372470440	chr8:6262662-6262663	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
38	rs377252070	chr8:6262663-6262664	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
39	rs191081359	chr8:6262696-6262697	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
40	rs182951314	chr8:6262718-6262719	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
41	rs548710716	chr8:6262743-6262744	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
42	rs562032686	chr8:6262759-6262760	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
43	rs202118477	chr8:6262770-6262771	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
44	rs725437	chr8:6262771-6262772	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs548014425	chr8:6262811-6262812	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
46	rs725438	chr8:6262831-6262832	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs148799823	chr8:6262838-6262839	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
48	rs540170209	chr8:6262852-6262853	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
49	rs145424979	chr8:6262854-6262855	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
50	rs192528055	chr8:6262876-6262877	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:136)

Disease	PMID	Source
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	21364760	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Autism	20685689	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1114 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6255600-6262400	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr8:6256400-6263200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:6256600-6263000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr8:6256800-6263000	Weak transcription	HSMM	muscle
5	chr8:6257200-6262800	Weak transcription	K562	blood
6	chr8:6258600-6263200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:6260400-6263200	Weak transcription	Pancreas	Pancrea
8	chr8:6260600-6262600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:6260600-6263000	Weak transcription	Thymus	Thymus
10	chr8:6261000-6262600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr8:6261400-6263000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr8:6261600-6262600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr8:6261600-6262800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr8:6261800-6262800	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr8:6262000-6262200	Enhancers	NHDF-Ad	bronchial
16	chr8:6262000-6265200	Active TSS	GM12878-XiMat	blood
17	chr8:6262200-6262400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr8:6262200-6262400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr8:6262200-6262400	Enhancers	Dnd41	blood
20	chr8:6262200-6262400	Enhancers	HMEC	breast
21	chr8:6262200-6262800	Enhancers	Fetal Kidney	kidney
22	chr8:6262200-6262800	Active TSS	NHDF-Ad	bronchial
23	chr8:6262200-6263000	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr8:6262200-6263000	Enhancers	Fetal Lung	lung
25	chr8:6262200-6265400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr8:6262400-6262600	Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr8:6262400-6262600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
28	chr8:6262400-6262600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr8:6262400-6262600	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr8:6262400-6262600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr8:6262400-6262800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr8:6262400-6262800	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr8:6262400-6262800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr8:6262400-6262800	Enhancers	HepG2	liver
35	chr8:6262400-6262800	Enhancers	NHEK	skin
36	chr8:6262400-6262800	Enhancers	NHLF	lung
37	chr8:6262400-6263000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr8:6262400-6263000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr8:6262400-6263000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr8:6262400-6263000	Enhancers	Adipose Nuclei	Adipose
41	chr8:6262400-6263000	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr8:6262400-6263200	Flanking Active TSS	HMEC	breast
43	chr8:6262400-6263600	Flanking Active TSS	Dnd41	blood
44	chr8:6262600-6262800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr8:6262600-6262800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr8:6262600-6262800	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr8:6262600-6262800	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr8:6262600-6262800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
49	chr8:6262600-6262800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr8:6262600-6262800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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