Variant report

Variant	esv3435412
Chromosome Location	chr9:96924949-96935312
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:96927870-96929609	HepG2	liver:	n/a	chr9:96928579-96928591
2	ARID3A	chr9:96928894-96929348	K562	blood:	n/a	n/a
3	ARID3A	chr9:96928165-96928645	K562	blood:	n/a	chr9:96928579-96928591
4	ARID3A	chr9:96930892-96931092	HepG2	liver:	n/a	n/a
5	ATF1	chr9:96928024-96928609	K562	blood:	n/a	n/a
6	ATF1	chr9:96928847-96929611	K562	blood:	n/a	n/a
7	ATF2	chr9:96927739-96928431	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr9:96928861-96929320	GM12878	blood:	n/a	chr9:96929117-96929128
9	ATF2	chr9:96928732-96929443	GM12878	blood:	n/a	chr9:96929117-96929128
10	ATF2	chr9:96928855-96929549	H1-hESC	embryonic stem cell:	n/a	chr9:96929117-96929128
11	ATF2	chr9:96928818-96929687	H1-hESC	embryonic stem cell:	n/a	chr9:96929117-96929128
12	ATF3	chr9:96928088-96928273	GM12878	blood:	n/a	chr9:96928197-96928206
13	ATF3	chr9:96928007-96928366	H1-hESC	embryonic stem cell:	n/a	chr9:96928197-96928206
14	ATF3	chr9:96928015-96928323	HepG2	liver:	n/a	chr9:96928197-96928206
15	ATF3	chr9:96928394-96929393	A549	lung:	n/a	chr9:96929116-96929126 chr9:96928893-96928913 chr9:96929115-96929130 chr9:96929116-96929126 chr9:96929119-96929126 chr9:96929115-96929128 chr9:96929116-96929127 chr9:96929119-96929127 chr9:96929116-96929129
16	ATF3	chr9:96928912-96929310	K562	blood:	n/a	chr9:96929116-96929126 chr9:96929115-96929130 chr9:96929116-96929126 chr9:96929119-96929126 chr9:96929115-96929128 chr9:96929116-96929127 chr9:96929119-96929127 chr9:96929116-96929129
17	ATF3	chr9:96927949-96928329	H1-hESC	embryonic stem cell:	n/a	chr9:96928197-96928206
18	ATF3	chr9:96928929-96929203	K562	blood:	n/a	chr9:96929116-96929126 chr9:96929115-96929130 chr9:96929116-96929126 chr9:96929119-96929126 chr9:96929115-96929128 chr9:96929116-96929127 chr9:96929119-96929127 chr9:96929116-96929129
19	ATF3	chr9:96928041-96928383	K562	blood:	n/a	chr9:96928197-96928206
20	ATF3	chr9:96927985-96928366	GM12878	blood:	n/a	chr9:96928197-96928206
21	BACH1	chr9:96927881-96929597	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr9:96928179-96928374	K562	blood:	n/a	n/a
23	BCL3	chr9:96927754-96928567	A549	lung:	n/a	chr9:96928209-96928222
24	BCL3	chr9:96928836-96929584	A549	lung:	n/a	chr9:96929331-96929344 chr9:96929125-96929134 chr9:96928900-96928913 chr9:96929332-96929345
25	BCL3	chr9:96928805-96929498	A549	lung:	n/a	chr9:96929331-96929344 chr9:96929125-96929134 chr9:96928900-96928913 chr9:96929332-96929345
26	BCLAF1	chr9:96928334-96929093	GM12878	blood:	n/a	chr9:96928900-96928913
27	BHLHE40	chr9:96927883-96929485	HepG2	liver:	n/a	chr9:96928375-96928391
28	BHLHE40	chr9:96927145-96927295	K562	blood:	n/a	n/a
29	BHLHE40	chr9:96927543-96929793	GM12878	blood:	n/a	chr9:96928375-96928391
30	BHLHE40	chr9:96932011-96932057	GM12878	blood:	n/a	n/a
31	BHLHE40	chr9:96927561-96929947	K562	blood:	n/a	chr9:96928375-96928391
32	BHLHE40	chr9:96927838-96928353	A549	lung:	n/a	n/a
33	BRCA1	chr9:96928340-96928573	GM12878	blood:	n/a	n/a
34	BRCA1	chr9:96927920-96928676	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr9:96928942-96929302	GM12878	blood:	n/a	n/a
36	BRCA1	chr9:96928900-96929877	Hela-S3	cervix:	n/a	chr9:96929828-96929835
37	BRCA1	chr9:96928546-96929196	HepG2	liver:	n/a	n/a
38	BRCA1	chr9:96928980-96929886	H1-hESC	embryonic stem cell:	n/a	chr9:96929828-96929835
39	CBX3	chr9:96927594-96928476	K562	blood:	n/a	n/a
40	CBX3	chr9:96927804-96928288	K562	blood:	n/a	n/a
41	CBX3	chr9:96928558-96929598	K562	blood:	n/a	n/a
42	CCNT2	chr9:96928025-96929759	K562	blood:	n/a	chr9:96929356-96929365 chr9:96928882-96928891 chr9:96928961-96928970
43	CEBPB	chr9:96930959-96931224	HepG2	liver:	n/a	chr9:96931039-96931052 chr9:96931039-96931050
44	CEBPB	chr9:96929362-96929690	HepG2	liver:	n/a	n/a
45	CEBPB	chr9:96928939-96929617	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr9:96928997-96929183	HepG2	liver:	n/a	n/a
47	CEBPB	chr9:96929382-96929675	A549	lung:	n/a	n/a
48	CEBPB	chr9:96930832-96931310	IMR90	lung:	n/a	chr9:96931039-96931052 chr9:96931039-96931050
49	CEBPB	chr9:96928022-96929691	Hela-S3	cervix:	n/a	chr9:96928241-96928249
50	CEBPB	chr9:96930860-96931307	K562	blood:	n/a	chr9:96931039-96931052 chr9:96931039-96931050

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:96925970-96926020	HepG2	liver:	n/a
2	chr9:96928252-96928302	SK-N-SH	brain:	n/a
3	chr9:96928252-96928302	HRCEpiC	kidney:	n/a
4	chr9:96925970-96926020	Hepatocyte	liver:	n/a
5	chr9:96929332-96929382	AG10803	skin:	n/a
6	chr9:96925970-96926020	NHDF-neo	bronchial:	n/a
7	chr9:96928252-96928302	ECC-1	luminal epithelium:	n/a
8	chr9:96929106-96929156	HMEC	breast:	n/a
9	chr9:96929332-96929382	HRE	kidney:	n/a
10	chr9:96929332-96929382	SKMC	muscle:	n/a
11	chr9:96925970-96926020	NHBE	bronchial:	n/a
12	chr9:96929106-96929156	HRE	kidney:	n/a
13	chr9:96928252-96928302	MCF-7	breast:	n/a
14	chr9:96929106-96929156	A549	lung:	n/a
15	chr9:96925970-96926020	HL-60	blood:	n/a
16	chr9:96929332-96929382	HUVEC	blood vessel:	n/a
17	chr9:96929332-96929382	HCT-116	colon:	n/a
18	chr9:96929106-96929156	AG09319	gingival:	n/a
19	chr9:96925970-96926020	GM06990	blood:	n/a
20	chr9:96928252-96928302	BJ	skin:	n/a
21	chr9:96929332-96929382	HEEpiC	esophagus:	n/a
22	chr9:96925970-96926020	H1-hESC	embryonic stem cell:	embryo
23	chr9:96925970-96926020	ProgFib	skin:	n/a
24	chr9:96925970-96926020	SAEC	small airway:	n/a
25	chr9:96929106-96929156	BE2_C	brain:	n/a
26	chr9:96928252-96928302	Hela-S3	cervix:	n/a
27	chr9:96925970-96926020	GM19239	blood:	n/a
28	chr9:96929332-96929382	HIPEpiC	eye:	n/a
29	chr9:96925970-96926020	Hela-S3	cervix:	n/a
30	chr9:96929106-96929156	Caco-2	colon:	n/a
31	chr9:96928252-96928302	HUVEC	blood vessel:	n/a
32	chr9:96929106-96929156	H1-hESC	embryonic stem cell:	embryo
33	chr9:96929106-96929156	MCF-7	breast:	n/a
34	chr9:96928252-96928302	PANC-1	pancreas:	n/a
35	chr9:96925970-96926020	HIPEpiC	eye:	n/a
36	chr9:96929106-96929156	AG10803	skin:	n/a
37	chr9:96925970-96926020	AG09309	skin:	n/a
38	chr9:96928252-96928302	SK-N-MC	brain:	n/a
39	chr9:96929106-96929156	LNCaP	prostate:	n/a
40	chr9:96929106-96929156	SK-N-SH	brain:	n/a
41	chr9:96928252-96928302	AG04449	skin:	fetal
42	chr9:96929106-96929156	Jurkat	blood:	n/a
43	chr9:96925970-96926020	CMK	blood:	n/a
44	chr9:96925970-96926020	GM12891	blood:	n/a
45	chr9:96928252-96928302	SKMC	muscle:	n/a
46	chr9:96925970-96926020	BE2_C	brain:	n/a
47	chr9:96925970-96926020	NT2-D1	testis:	n/a
48	chr9:96928252-96928302	GM12878	blood:	n/a
49	chr9:96925970-96926020	GM12878	blood:	n/a
50	chr9:96929332-96929382	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:96924444..96926701-chr9:99178289..99180741,2	MCF-7	breast:
2	chr9:96573741..96576396-chr9:96929581..96932062,2	K562	blood:
3	chr9:96834076..96836577-chr9:96929876..96932048,2	K562	blood:
4	chr9:96827846..96829961-chr9:96932041..96934679,2	MCF-7	breast:
5	chr9:96337657..96339290-chr9:96927321..96930180,2	K562	blood:
6	chr9:96934105..96937234-chr9:96943114..96945589,3	MCF-7	breast:
7	chr9:96902444..96903976-chr9:96934492..96936431,2	K562	blood:
8	chr9:96873193..96875324-chr9:96934781..96937611,2	K562	blood:
9	chr10:75757238..75757954-chr9:96929118..96929804,2	Hela-S3	cervix:
10	chr9:34328775..34329333-chr9:96928109..96928991,2	Hela-S3	cervix:
11	chr9:96911236..96913938-chr9:96926952..96928493,2	MCF-7	breast:
12	chr17:62207103..62207853-chr9:96928435..96929056,2	Hela-S3	cervix:
13	chr1:201979347..201980302-chr9:96928844..96929674,2	Hela-S3	cervix:
14	chr9:96931258..96933517-chr9:97020161..97023083,3	K562	blood:
15	chr9:96913449..96915470-chr9:96932041..96933932,2	MCF-7	breast:
16	chr11:35159898..35160664-chr9:96928460..96928999,2	Hela-S3	cervix:
17	chr9:96905663..96907940-chr9:96926715..96928230,2	K562	blood:
18	chr9:96773280..96775592-chr9:96928831..96930974,2	K562	blood:
19	chr19:12901906..12902802-chr9:96928364..96929361,2	Hela-S3	cervix:
20	chr9:96885338..96887288-chr9:96929216..96930886,2	MCF-7	breast:
21	chr1:113247853..113250339-chr9:96928983..96930846,2	K562	blood:
22	chr6:27860274..27861052-chr9:96928480..96929585,3	Hela-S3	cervix:
23	chr9:96845151..96850974-chr9:96927067..96931575,8	K562	blood:
24	chr12:53296484..53299330-chr9:96928573..96930295,2	MCF-7	breast:
25	chr9:96840095..96841913-chr9:96929412..96931188,2	K562	blood:
26	chr6:136610448..136611121-chr9:96929034..96929855,2	Hela-S3	cervix:
27	chr9:96861428..96863422-chr9:96927160..96928732,2	MCF-7	breast:
28	chr1:152008579..152009679-chr9:96928359..96929023,3	Hela-S3	cervix:
29	chr9:96829354..96831525-chr9:96932462..96934545,2	K562	blood:
30	chr9:96791956..96794354-chr9:96926207..96931491,6	MCF-7	breast:
31	chr9:96790823..96795467-chr9:96925835..96932235,7	K562	blood:
32	chr15:91497959..91498724-chr9:96927748..96928648,2	Hela-S3	cervix:
33	chr9:96212877..96215443-chr9:96928941..96930763,2	K562	blood:
34	chr9:96845151..96851769-chr9:96927067..96931565,10	K562	blood:
35	chr9:96791533..96793413-chr9:96923327..96926026,2	MCF-7	breast:
36	chr9:96933308..96934893-chr9:96957370..96959656,2	MCF-7	breast:
37	chr9:96790341..96794271-chr9:96926817..96931236,5	K562	blood:
38	chr9:96792323..96794528-chr9:96927672..96930924,4	MCF-7	breast:
39	chr14:20937169..20937695-chr9:96928145..96928840,2	Hela-S3	cervix:
40	chr9:96927010..96929542-chr9:97400485..97402088,2	MCF-7	breast:
41	chr3:184529756..184530532-chr9:96928301..96928834,2	Hela-S3	cervix:
42	chr9:96927406..96930148-chr9:97007636..97010398,2	MCF-7	breast:
43	chr9:96771017..96773474-chr9:96932074..96933586,2	MCF-7	breast:
44	chr14:90862960..90863497-chr9:96928700..96929562,2	Hela-S3	cervix:
45	chr9:96901268..96903625-chr9:96924526..96926573,2	MCF-7	breast:
46	chr9:96845064..96846581-chr9:96932043..96934956,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPDC1-7	chr9:96928535-96928663	NONHSAT133286
2	lnc-PTPDC1-7	chr9:96928571-96928663	ENSG00000269946.1
3	lnc-PTPDC1-7	chr9:96931457-96932304	NONHSAT133286

Variant related genes	Relation type
MIRLET7F1	TF binding region
MIRLET7A1	TF binding region
ENSG00000269929	TF binding region
ENSG00000269946	TF binding region
MIRLET7F1	CpG island
MIRLET7A1	CpG island
ENSG00000269929	CpG island
ENSG00000269946	CpG island
ENSG00000178607	chromatin interactions
ENSG00000175787	chromatin interactions
ENSG00000258384	chromatin interactions
ENSG00000158079	chromatin interactions
ENSG00000170421	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000252723	chromatin interactions
ENSG00000163191	chromatin interactions
ENSG00000155366	chromatin interactions
ENSG00000197724	chromatin interactions
ENSG00000029363	chromatin interactions
ENSG00000165244	chromatin interactions
ENSG00000198668	chromatin interactions
ENSG00000163435	chromatin interactions
ENSG00000026508	chromatin interactions
ENSG00000048828	chromatin interactions
ENSG00000035403	chromatin interactions
ENSG00000156931	chromatin interactions
ENSG00000198805	chromatin interactions
ENSG00000233224	chromatin interactions
ENSG00000234678	chromatin interactions
ENSG00000166965	chromatin interactions
ENSG00000165140	chromatin interactions
ENSG00000171223	chromatin interactions
ENSG00000188938	chromatin interactions
ENSG00000186638	chromatin interactions

Extended variants
information (count: 411 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:411 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12337981	chr9:96924963-96924964	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554400681	chr9:96924964-96924965	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs374337785	chr9:96925010-96925011	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs377121089	chr9:96925032-96925033	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs182981040	chr9:96925042-96925043	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs59862147	chr9:96925153-96925154	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs56121723	chr9:96925172-96925173	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs558635270	chr9:96925206-96925207	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs10993075	chr9:96925233-96925234	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs113820627	chr9:96925236-96925237	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs531872834	chr9:96925239-96925240	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs201752811	chr9:96925256-96925257	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs201400228	chr9:96925257-96925258	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs200028896	chr9:96925258-96925259	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs541104609	chr9:96925269-96925270	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs531707017	chr9:96925281-96925282	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs553048826	chr9:96925369-96925370	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs544312608	chr9:96925406-96925407	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs370512593	chr9:96925409-96925410	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs199869608	chr9:96925434-96925435	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs140323698	chr9:96925442-96925443	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs374148084	chr9:96925472-96925473	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs542544022	chr9:96925504-96925505	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs563800803	chr9:96925568-96925569	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs145585251	chr9:96925594-96925595	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs9792534	chr9:96925661-96925662	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs564683920	chr9:96925683-96925684	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs528611956	chr9:96925689-96925690	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs148067843	chr9:96925690-96925691	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs11788788	chr9:96925737-96925738	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs141779148	chr9:96925758-96925759	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs112896373	chr9:96925764-96925765	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs534510021	chr9:96925783-96925784	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs187558443	chr9:96925784-96925785	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs537336750	chr9:96925795-96925796	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs138381880	chr9:96925885-96925886	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs376022625	chr9:96925891-96925892	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs553179899	chr9:96925916-96925917	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs534718942	chr9:96925941-96925942	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs533449219	chr9:96925951-96925952	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs564062581	chr9:96925961-96925962	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs192676455	chr9:96925970-96925971	Weak transcription Enhancers ZNF genes & repeats	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs551623151	chr9:96925995-96925996	Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs570134107	chr9:96926048-96926049	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs556903695	chr9:96926054-96926055	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs575879469	chr9:96926096-96926097	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs184740420	chr9:96926204-96926205	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs78071555	chr9:96926280-96926281	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs536604069	chr9:96926304-96926305	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs75508358	chr9:96926382-96926383	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD
Effusion lymphoma	18079361	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:880 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96904000-96927200	Weak transcription	Thymus	Thymus
2	chr9:96919400-96925800	Weak transcription	Spleen	Spleen
3	chr9:96919400-96927600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr9:96919400-96927800	Weak transcription	Psoas Muscle	Psoas
5	chr9:96919600-96926000	Weak transcription	Primary T cells from cord blood	blood
6	chr9:96919600-96927800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr9:96919600-96927800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr9:96919800-96927200	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr9:96920000-96927400	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr9:96920000-96927800	Weak transcription	Fetal Muscle Trunk	muscle
11	chr9:96920000-96927800	Weak transcription	Left Ventricle	heart
12	chr9:96920000-96927800	Weak transcription	Pancreas	Pancrea
13	chr9:96920000-96927800	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr9:96920200-96927600	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr9:96921600-96926000	Weak transcription	Primary hematopoietic stem cells	blood
16	chr9:96921600-96927600	Weak transcription	Brain Substantia Nigra	brain
17	chr9:96921800-96927800	Weak transcription	HSMM	muscle
18	chr9:96922000-96926000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr9:96922200-96927400	Weak transcription	Brain Angular Gyrus	brain
20	chr9:96922200-96927600	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr9:96922200-96927800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr9:96922200-96927800	Weak transcription	Brain Hippocampus Middle	brain
23	chr9:96922200-96927800	Weak transcription	Fetal Lung	lung
24	chr9:96922400-96926000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr9:96922400-96927400	Weak transcription	Fetal Heart	heart
26	chr9:96922400-96927400	Weak transcription	Rectal Smooth Muscle	rectum
27	chr9:96922400-96927600	Weak transcription	Brain Anterior Caudate	brain
28	chr9:96922400-96927600	Weak transcription	Fetal Kidney	kidney
29	chr9:96922400-96927800	Weak transcription	Brain Cingulate Gyrus	brain
30	chr9:96922400-96927800	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr9:96922400-96927800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr9:96922400-96927800	Weak transcription	Placenta	Placenta
33	chr9:96922400-96927800	Weak transcription	NH-A	brain
34	chr9:96922600-96927800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr9:96922600-96927800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr9:96922800-96927800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr9:96923000-96926000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr9:96923000-96927600	Weak transcription	Fetal Intestine Large	intestine
39	chr9:96923200-96926000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr9:96923200-96927000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr9:96923200-96927200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr9:96923200-96927600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr9:96923200-96927600	Weak transcription	A549	lung
44	chr9:96923200-96927800	Weak transcription	Stomach Smooth Muscle	stomach
45	chr9:96923200-96928000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr9:96923400-96927600	Weak transcription	Fetal Intestine Small	intestine
47	chr9:96923400-96927800	Weak transcription	Fetal Muscle Leg	muscle
48	chr9:96923800-96927400	Weak transcription	Colon Smooth Muscle	Colon
49	chr9:96924000-96926800	Weak transcription	K562	blood
50	chr9:96924000-96927800	Weak transcription	Placenta Amnion	Placenta Amnion

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