Variant report

Variant	nsv540201
Chromosome Location	chr9:115883978-116003980
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	chr9:115983506-115983747	K562	blood:	n/a	n/a
2	ARID3A	chr9:115905739-115905943	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:115983338-115984123	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:115901124-115902211	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:115913003-115913279	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:115990291-115990958	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:115984342-115985124	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:115993968-115994315	K562	blood:	n/a	n/a
9	ATF1	chr9:115990413-115990708	K562	blood:	n/a	n/a
10	ATF1	chr9:115983423-115983901	K562	blood:	n/a	n/a
11	ATF2	chr9:115983337-115983806	H1-hESC	embryonic stem cell:	n/a	chr9:115983730-115983741
12	ATF2	chr9:115983017-115983980	H1-hESC	embryonic stem cell:	n/a	chr9:115983730-115983741
13	ATF2	chr9:115983357-115983928	GM12878	blood:	n/a	chr9:115983730-115983741
14	ATF2	chr9:115981259-115982696	GM12878	blood:	n/a	n/a
15	ATF2	chr9:115983304-115984037	GM12878	blood:	n/a	chr9:115983730-115983741
16	ATF2	chr9:115981374-115982764	GM12878	blood:	n/a	n/a
17	ATF3	chr9:115983220-115983829	HepG2	liver:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
18	ATF3	chr9:115983440-115983907	K562	blood:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
19	ATF3	chr9:115983419-115983792	H1-hESC	embryonic stem cell:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
20	ATF3	chr9:115983170-115983797	K562	blood:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
21	ATF3	chr9:115983233-115983781	HepG2	liver:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
22	ATF3	chr9:115913051-115913311	GM12878	blood:	n/a	chr9:115913211-115913220 chr9:115913220-115913240
23	ATF3	chr9:115912920-115913440	H1-hESC	embryonic stem cell:	n/a	chr9:115913211-115913220 chr9:115913220-115913240
24	ATF3	chr9:115983440-115983712	GM12878	blood:	n/a	n/a
25	ATF3	chr9:115983213-115983792	GM12878	blood:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
26	ATF3	chr9:115912959-115913376	K562	blood:	n/a	chr9:115913211-115913220 chr9:115913220-115913240
27	ATF3	chr9:115913083-115913325	H1-hESC	embryonic stem cell:	n/a	chr9:115913211-115913220 chr9:115913220-115913240
28	ATF3	chr9:115912933-115913396	GM12878	blood:	n/a	chr9:115913211-115913220 chr9:115913220-115913240
29	ATF3	chr9:115984765-115985094	K562	blood:	n/a	n/a
30	ATF3	chr9:115983301-115983851	H1-hESC	embryonic stem cell:	n/a	chr9:115983729-115983740 chr9:115983731-115983739 chr9:115983729-115983742 chr9:115983730-115983741 chr9:115983731-115983742 chr9:115983729-115983742 chr9:115983732-115983739
31	ATF3	chr9:115913054-115913384	HepG2	liver:	n/a	chr9:115913211-115913220 chr9:115913220-115913240
32	BACH1	chr9:115977514-115977791	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr9:115984091-115984099	K562	blood:	n/a	n/a
34	BACH1	chr9:115982879-115982887	K562	blood:	n/a	n/a
35	BACH1	chr9:115977469-115977786	K562	blood:	n/a	n/a
36	BATF	chr9:115982119-115982632	GM12878	blood:	n/a	n/a
37	BATF	chr9:115982206-115982623	GM12878	blood:	n/a	n/a
38	BATF	chr9:115981447-115981779	GM12878	blood:	n/a	chr9:115981724-115981732
39	BATF	chr9:115981439-115981805	GM12878	blood:	n/a	chr9:115981724-115981732
40	BCL11A	chr9:115981417-115981873	GM12878	blood:	n/a	chr9:115981634-115981643
41	BCL11A	chr9:115982153-115982635	GM12878	blood:	n/a	n/a
42	BCLAF1	chr9:115981212-115982657	GM12878	blood:	n/a	chr9:115981634-115981643
43	BCLAF1	chr9:115981455-115982653	GM12878	blood:	n/a	chr9:115981634-115981643
44	BCLAF1	chr9:115983290-115983801	GM12878	blood:	n/a	chr9:115983759-115983768 chr9:115983750-115983763 chr9:115983606-115983615
45	BHLHE40	chr9:115983468-115983999	HepG2	liver:	n/a	n/a
46	BHLHE40	chr9:115990316-115990750	HepG2	liver:	n/a	n/a
47	BHLHE40	chr9:115995278-115995394	GM12878	blood:	n/a	n/a
48	BHLHE40	chr9:115901592-115902043	HepG2	liver:	n/a	n/a
49	BHLHE40	chr9:115913008-115913338	HepG2	liver:	n/a	n/a
50	BHLHE40	chr9:115982127-115984239	GM12878	blood:	n/a	chr9:115984103-115984119

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115913052-115913102	HEEpiC	esophagus:	n/a
2	chr9:115987035-115987085	HNPCEpiC	eye:	n/a
3	chr9:115949783-115949833	T-47D	breast:	n/a
4	chr9:115987035-115987085	NB4	blood:	n/a
5	chr9:115913052-115913102	HEEpiC	esophagus:	n/a
6	chr9:115987035-115987085	HNPCEpiC	eye:	n/a
7	chr9:115949783-115949833	T-47D	breast:	n/a
8	chr9:115987035-115987085	NB4	blood:	n/a
9	chr9:115910751-115910801	HCPEpiC	choroid plexus:	n/a
10	chr9:115915001-115915051	BJ	skin:	n/a
11	chr9:115915892-115915942	RPTEC	kidney:	n/a
12	chr9:115926922-115926972	A549	lung:	n/a
13	chr9:115913052-115913102	HPAEpiC	pulmonary alveolar:	n/a
14	chr9:115987035-115987085	PFSK-1	brain:	n/a
15	chr9:115915892-115915942	BJ	skin:	n/a
16	chr9:115912047-115912097	HL-60	blood:	n/a
17	chr9:115926922-115926972	PANC-1	pancreas:	n/a
18	chr9:115910751-115910801	GM12878	blood:	n/a
19	chr9:115949783-115949833	GM19239	blood:	n/a
20	chr9:115912047-115912097	H1-hESC	embryonic stem cell:	embryo
21	chr9:115913515-115913565	GM12891	blood:	n/a
22	chr9:115926922-115926972	MCF10A-Er-Src	breast:	n/a
23	chr9:115949783-115949833	HRCEpiC	kidney:	n/a
24	chr9:115913783-115913833	AG04449	skin:	fetal
25	chr9:115926922-115926972	HRPEpiC	eye:	n/a
26	chr9:115913783-115913833	GM06990	blood:	n/a
27	chr9:115912047-115912097	AG09309	skin:	n/a
28	chr9:115983636-115983686	NHDF-neo	bronchial:	n/a
29	chr9:115912974-115913024	SAEC	small airway:	n/a
30	chr9:115949783-115949833	HIPEpiC	eye:	n/a
31	chr9:115987035-115987085	HEEpiC	esophagus:	n/a
32	chr9:115915892-115915942	K562	blood:	n/a
33	chr9:115983636-115983686	SAEC	small airway:	n/a
34	chr9:115913781-115913831	ovcar-3	ovarian:	n/a
35	chr9:115913052-115913102	CMK	blood:	n/a
36	chr9:115912974-115913024	SK-N-SH_RA	brain:	n/a
37	chr9:115913515-115913565	H1-hESC	embryonic stem cell:	embryo
38	chr9:115984268-115984318	Hepatocyte	liver:	n/a
39	chr9:115912974-115913024	GM12878	blood:	n/a
40	chr9:115913515-115913565	HPAEpiC	pulmonary alveolar:	n/a
41	chr9:115987035-115987085	GM12878	blood:	n/a
42	chr9:115915001-115915051	NH-A	brain:	n/a
43	chr9:115912974-115913024	NT2-D1	testis:	n/a
44	chr9:115910751-115910801	AG09309	skin:	n/a
45	chr9:115983049-115983099	U87	brain:	n/a
46	chr9:115984268-115984318	IMR90	lung:	fetal
47	chr9:115915892-115915942	A549	lung:	n/a
48	chr9:115983984-115984034	ovcar-3	ovarian:	n/a
49	chr9:115910751-115910801	Jurkat	blood:	n/a
50	chr9:115912047-115912097	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:115946798..115949789-chr9:116049459..116051897,2	K562	blood:
2	chr9:115968725..115971196-chr9:115981878..115984279,2	MCF-7	breast:
3	chr9:115872624..115875532-chr9:115912017..115913734,2	MCF-7	breast:
4	chr9:115983573..115985886-chr9:115986006..115988568,3	MCF-7	breast:
5	chr9:115932248..115934923-chr9:115939803..115942130,2	MCF-7	breast:
6	chr9:115904438..115911145-chr9:115911174..115916685,7	K562	blood:
7	chr9:115912871..115915332-chr9:115935674..115937488,2	K562	blood:
8	chr9:115961079..115963509-chr9:115965175..115968224,3	MCF-7	breast:
9	chr9:115932248..115934923-chr9:115939803..115942130,2	MCF-7	breast:
10	chr9:115882399..115884999-chr9:115891613..115894561,3	MCF-7	breast:
11	chr9:115952878..115954594-chr9:115956098..115958292,2	K562	blood:
12	chr9:115963672..115965977-chr9:115972388..115974143,2	MCF-7	breast:
13	chr9:115887611..115890231-chr9:115913519..115916345,2	MCF-7	breast:
14	chr9:115882894..115884462-chr9:115915677..115917990,2	MCF-7	breast:
15	chr9:115887611..115890231-chr9:115913519..115916345,2	MCF-7	breast:
16	chr9:115887976..115889749-chr9:115910119..115911972,2	MCF-7	breast:
17	chr9:115910740..115913540-chr9:115929210..115931968,2	K562	blood:
18	chr9:115929480..115931440-chr9:115950780..115952442,2	MCF-7	breast:
19	chr9:115975066..115976588-chr9:115978815..115981431,2	MCF-7	breast:
20	chr9:115912109..115914573-chr9:115927637..115929668,2	MCF-7	breast:
21	chr9:115893647..115895768-chr9:115898797..115900868,2	K562	blood:
22	chr9:115938252..115939800-chr9:115981732..115984062,2	K562	blood:
23	chr9:115904166..115905985-chr9:115907508..115909495,2	K562	blood:
24	chr11:67275557..67276131-chr9:115984372..115984872,2	Hela-S3	cervix:
25	chr9:115990891..115993253-chr9:115993931..115999009,4	K562	blood:
26	chr9:115961079..115963509-chr9:115965175..115968224,3	MCF-7	breast:
27	chr9:115881515..115883241-chr9:115913395..115914943,2	MCF-7	breast:
28	chr9:115975066..115976588-chr9:115978815..115981431,2	MCF-7	breast:
29	chr9:115886679..115889181-chr9:115895702..115897217,2	MCF-7	breast:
30	chr9:115916182..115918262-chr9:115925062..115927268,3	MCF-7	breast:
31	chr9:115959480..115961457-chr9:115966488..115968182,2	K562	blood:
32	chr9:115982005..115986983-chr9:116035777..116039702,5	K562	blood:
33	chr9:115913631..115915237-chr9:115923889..115925758,2	K562	blood:
34	chr9:115990891..115993253-chr9:115993931..115999009,4	K562	blood:
35	chr9:115991545..115993932-chr9:115995693..115997298,2	K562	blood:
36	chr9:115887976..115889749-chr9:115910119..115911972,2	MCF-7	breast:
37	chr9:115884874..115886487-chr9:115927190..115929312,2	K562	blood:
38	chr9:115952251..115954367-chr9:115960312..115963132,2	K562	blood:
39	chr9:115916182..115918262-chr9:115925062..115927268,3	MCF-7	breast:
40	chr9:115959480..115961457-chr9:115966488..115968182,2	K562	blood:
41	chr9:115996965..115999527-chr9:116002148..116004164,2	K562	blood:
42	chr9:115988089..115990143-chr9:115997118..115999123,2	MCF-7	breast:
43	chr9:115910740..115914842-chr9:115929210..115933817,4	K562	blood:
44	chr9:115942350..115944024-chr9:115948967..115951918,2	K562	blood:
45	chr9:115995531..115997450-chr9:115998162..116001080,2	MCF-7	breast:
46	chr9:115979271..115982033-chr9:115982056..115983606,2	MCF-7	breast:
47	chr9:115888226..115890685-chr9:115891498..115893833,2	MCF-7	breast:
48	chr9:115952251..115954367-chr9:115960312..115963132,2	K562	blood:
49	chr12:53894115..53894858-chr9:115983781..115984688,2	Hela-S3	cervix:
50	chr9:115913232..115915242-chr9:115917477..115919096,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC31A1-4	chr9:115913931-115914596	NONHSAT134319
2	lnc-SLC31A1-1	chr9:115983867-115983958	NONHSAT134329
3	lnc-SLC31A1-1	chr9:115989558-115989940	NONHSAT134329
4	lnc-CDC26-2	chr9:115968291-115968858	NONHSAT134327
5	lnc-SLC31A1-3	chr9:115920002-115920073	NONHSAT134321
6	lnc-SLC31A1-1	chr9:115983808-115983958	NONHSAT134328
7	lnc-CDC26-2	chr9:115969492-115969576	NONHSAT134327
8	lnc-SLC31A1-3	chr9:115925030-115925194	NONHSAT134321
9	lnc-SLC31A1-4	chr9:115913256-115913360	NONHSAT134319
10	lnc-FKBP15-1	chr9:115923286-115924232	NONHSAT134322
11	lnc-SLC31A1-3	chr9:115923790-115923978	NONHSAT134321

No.	miRNA target gene	miRNA name	Chromosome Location
1	SLC31A2	hsa-miR-124-3p	chr9:115925588-115925607
2	SLC31A2	hsa-miR-124-3p	chr9:115925600-115925607
3	FKBP15	hsa-miR-192-5p	chr9:115927845-115927865

Variant related genes	Relation type
FKBP15	TF binding region
SLC31A1	TF binding region
SLC31A2	TF binding region
FKBP15	CpG island
SLC31A1	CpG island
SLC31A2	CpG island
ENSG00000148229	chromatin interactions
ENSG00000119321	chromatin interactions
ENSG00000267598	chromatin interactions
ENSG00000160888	chromatin interactions
ENSG00000167797	chromatin interactions
ENSG00000136867	chromatin interactions
ENSG00000136875	chromatin interactions
ENSG00000231528	chromatin interactions
ENSG00000139546	chromatin interactions
ENSG00000270175	chromatin interactions
ENSG00000157653	chromatin interactions
ENSG00000225684	chromatin interactions
ENSG00000077454	chromatin interactions
ENSG00000176386	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000136868	chromatin interactions
ENSG00000106336	chromatin interactions

Extended variants
information (count: 4520 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:4520 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375879054	chr9:115883980-115883981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs561745645	chr9:115883999-115884000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553963146	chr9:115884012-115884013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149012770	chr9:115884024-115884025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs112267611	chr9:115884031-115884032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs117906238	chr9:115884049-115884050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564635751	chr9:115884096-115884097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533630159	chr9:115884098-115884099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545920359	chr9:115884156-115884157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs113096070	chr9:115884157-115884158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572146230	chr9:115884197-115884198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550049672	chr9:115884205-115884206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192986351	chr9:115884208-115884209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529225657	chr9:115884242-115884243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs151039256	chr9:115884251-115884252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112788288	chr9:115884260-115884261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184312921	chr9:115884272-115884273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141266464	chr9:115884327-115884328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs71384296	chr9:115884328-115884329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs398011921	chr9:115884349-115884350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs60562897	chr9:115884354-115884355	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs138892679	chr9:115884375-115884376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557778722	chr9:115884377-115884378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570550331	chr9:115884450-115884451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539784815	chr9:115884470-115884471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556483441	chr9:115884473-115884474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs56026613	chr9:115884522-115884523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576134275	chr9:115884532-115884533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535413593	chr9:115884534-115884535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140601395	chr9:115884546-115884547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576358693	chr9:115884574-115884575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572068681	chr9:115884611-115884612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145473945	chr9:115884612-115884613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562160823	chr9:115884678-115884679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs568962392	chr9:115884740-115884741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs537569108	chr9:115884765-115884766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561651022	chr9:115884769-115884770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543733041	chr9:115884772-115884773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs138008411	chr9:115884852-115884853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79889534	chr9:115884866-115884867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573808475	chr9:115884943-115884944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188340309	chr9:115885010-115885011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74545203	chr9:115885045-115885046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10817441	chr9:115885060-115885061	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs560777503	chr9:115885109-115885110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs80075890	chr9:115885116-115885117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs58210619	chr9:115885122-115885123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570661366	chr9:115885148-115885149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149538439	chr9:115885156-115885157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73655803	chr9:115885160-115885161	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:58)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	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
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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3645 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115875200-115884400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr9:115882000-115884800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:115883600-115884200	Enhancers	Brain Inferior Temporal Lobe	brain
4	chr9:115883800-115884000	Enhancers	Brain Cingulate Gyrus	brain
5	chr9:115884200-115892200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr9:115884600-115884800	Enhancers	Brain Cingulate Gyrus	brain
7	chr9:115886600-115886800	Enhancers	Left Ventricle	heart
8	chr9:115887200-115888000	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr9:115887200-115888400	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr9:115887600-115888000	Enhancers	Primary B cells from peripheral blood	blood
11	chr9:115887600-115888000	Enhancers	GM12878-XiMat	blood
12	chr9:115892000-115892600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr9:115892000-115893200	Enhancers	Placenta	Placenta
14	chr9:115892000-115894800	Enhancers	Brain Hippocampus Middle	brain
15	chr9:115892200-115894800	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr9:115892800-115893000	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr9:115892800-115893200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
18	chr9:115892800-115894800	Enhancers	Brain Substantia Nigra	brain
19	chr9:115893000-115894800	Enhancers	Brain Angular Gyrus	brain
20	chr9:115893000-115894800	Enhancers	Brain Cingulate Gyrus	brain
21	chr9:115893000-115895000	Enhancers	Brain Anterior Caudate	brain
22	chr9:115893200-115893600	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr9:115893200-115893600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr9:115893200-115897400	Weak transcription	Placenta	Placenta
25	chr9:115893600-115894400	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr9:115893600-115894800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr9:115893800-115894000	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
28	chr9:115893800-115894600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr9:115893800-115894800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr9:115894000-115894200	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr9:115894000-115894600	Enhancers	Right Ventricle	heart
32	chr9:115894000-115894800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr9:115894000-115894800	Enhancers	Fetal Heart	heart
34	chr9:115894400-115894600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr9:115894800-115896000	Weak transcription	Brain Hippocampus Middle	brain
36	chr9:115894800-115896200	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr9:115894800-115896400	Weak transcription	Brain Cingulate Gyrus	brain
38	chr9:115894800-115896400	Weak transcription	Brain Substantia Nigra	brain
39	chr9:115894800-115899800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr9:115894800-115900000	Weak transcription	Brain Angular Gyrus	brain
41	chr9:115895000-115896000	Weak transcription	Brain Anterior Caudate	brain
42	chr9:115896000-115896600	Enhancers	Brain Hippocampus Middle	brain
43	chr9:115896000-115897000	Enhancers	Brain Anterior Caudate	brain
44	chr9:115896200-115896800	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr9:115896400-115897400	Enhancers	Brain Substantia Nigra	brain
46	chr9:115896400-115897600	Enhancers	Brain Cingulate Gyrus	brain
47	chr9:115896600-115897400	Weak transcription	Brain Hippocampus Middle	brain
48	chr9:115896800-115897200	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr9:115897000-115899000	Weak transcription	Brain Anterior Caudate	brain
50	chr9:115897200-115897400	Enhancers	Brain Inferior Temporal Lobe	brain

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